We are grateful the supported from the Ministry of Science and Technology, Taiwan &#8211; MOST105-2628-B-038-005-MY3(1-3) and Health and welfare surcharge of tobacco products - MOHW106-TDU-B-212-144001 to S-Y C.

NOTE: All the protocols and methods used in animal subjects have been approved by Institutional Animal Care and Use Committees (IACUC) of the Taipei Medical University (Protocol numbers: LAC-2014-0387)
1. Preparation of Micro-Osmotic Pump Infusion Systems
NOTE: Prepare the pump, artificial cerebrospinal fluid (aCSF) buffer, and drug (Met-CCL5/RANTES protein solution (10 ng/mL in aCSF)) under sterile conditions using buffers filtered with 0.2 &#181;m filters and conduct all the procedures under the culture hood with gloves. The surgery procedures are conducted as follows:
<ol>
	<li>Prepare the micro-osmotic pumps one day before surgery: Fill the brain micro-osmotic pump with artificial cerebrospinal fluid (aCSF) with a 1 mL syringe and blunt-head needle provided along with the kit. Immerse the micro-osmotic pump in aCSF and place it on a shaker and gently shake overnight. 
	CAUTION: The pump should be filled with aCSF, and air bubbles should be avoided inside the pump (Figure 1A).</li>
	<li>Before starting surgery, prepare the recombinant Met-CCL5/RANTES protein solution (10 ng/mL, diluted in aCSF) to be used in the experiment. Remove aCSF from the pump and fill the pump with the drug solution slowly until excess leaks out. 
	NOTE: 15 mL aCSF or Met-CCL5/RANTES solution is sufficient for 5-8 pumps. 
	CAUTION: Repeat the procedure to ensure that the pump is completely filled with the drug without bubbles inside.</li>
	<li>Cut the catheter tubes into the desired length and attach them with the blunt-end brain infusion needle in the brain infusion kit. Fill the infusion kit and tubes with the drug.</li>
	<li>Finally, assemble and attach the brain infusion kit to the micro-osmotic pump. 
	CAUTION: No bubbles should be formed in the tube or the pump (Figure 1A).</li>
	<li>Immerse the entire osmotic pump-brain fusion set in aCSF in a sterilized 50 mL tube to prevent the pump from drying out. The osmotic pump-brain fusion set is now ready to be used for surgery. 
	NOTE: The micro-osmotic pump systems can be used for long-term drug infusion. This ensures a safe and convenient mode of drug delivery into the mouse brain.</li>
</ol>
2. Intracerebral Ventricular Surgery &#8211; implantation of the micro osmotic pump
CAUTION: Sterilize the surgical environment with 75% ethanol and ensure that the people involved in the study are wearing sterile gloves and a clean lab coat. Surgical tools/ instruments must be autoclaved and dried before use, and subsequently sterilized with 75% ethanol in-between mice surgeries.
<ol>
	<li>Weigh the mouse and anesthetize it using intra-peritoneal injection (IP) with Ketamine/Xylazine (Ketamine 50 mg/kg, Xylazine 10 mg/kg). 
	CAUTION: Mice body weights lower than 24 g are not recommended for osmotic pump implantation surgery.</li>
	<li>Mount and fix the mouse head onto the stereotactic apparatus (Figure 1B).</li>
	<li>Use a pair of surgical scissors and pincers to cut open the outer skin covering the skull. Use iodine to clean the peripheral skull.</li>
	<li>Separate the outermost layer of skin from the subcutaneous skin with the help of a pair of blunt-head pincers near the neck region for the osmotic pump-brain fusion set implantation (Figure 1C).</li>
	<li>Mark the infusion point with reference to the brain map (Figure 1D) using the stereotactic apparatus. In this experiment, the needle needs to be implanted in the 3rd ventricle region (Bregma: 0.0 mm lateral, 1.3 mm posterior, 5.7 mm ventral).</li>
	<li>Drill a hole using a nail drill around the area marked on the skull (Figure 1E). 
	CAUTION: Be careful not to break the mouse meninges and blood vessels, thus avoiding the disruption of micro-blood vessels in the brain.</li>
	<li>Place the micro-osmotic pump-brain fusion set containing aCSF (as control) or drug (Met-CCL5/RANTES protein solution) under the skin behind the neck region and insert the brain infusion needle into the drilled hole to infuse the drug into the mouse brain (Figure 1E). The needle will penetrate the meninges and get into the ventricle. Fix the needle in place on the skull using surface desensitizing gel (Figure 1F) and wait 1-2 min until the glue dries. Next, cut off the projecting part on top of the needle (Figure 1G-H).</li>
	<li>Use a tissue adhesive glue to heal the operation wound on the head. Apply 50 &#181;L of the glue on top of the wound, pull both sides of the skin together, and hold on for 30 s to allow the skin to seal (Figure 1I). 
	&#160;CAUTION: Use 100% alcohol pad to clean the wound after surgery and 100 ul penicillin with streptomycin to prevent infection.&#160;NOTE: Mouse skin will form scar tissue and heal in a few days following the administration of the surgical glue. The main advantage of the glue is the avoidance of surgical stitches which may cause skin irritation or inflammation.</li>
	<li>Place the mouse in a clean cage kept on a warm plate (heated up to 37 &#176;C) and wait until the mouse recovers from the anesthetic effect.&#160; 
	CAUTION: It is critical to maintain the mouse&#39;s body temperature to enhance the chance of survival after surgery.</li>
	<li>After a one-week recovery period, the mice will be ready for further experiments, such as the Oral Glucose Tolerance Test (OGTT) and Insulin Tolerance Test (ITT).</li>
</ol>
3. Oral Glucose Tolerance Test (OGTT)
NOTE: Perform the oral glucose tolerance test 7 days after the infusion of aCSF and MetCCL5/RANTES (10 ng/mL, 100 &#181;L). Maintain a 6 h fast for the mice before OGTT with sufficient water supply. Keep the animals on the same work bench where the experiments will be performed so that they can acclimatize to the environment to reduce stress during the procedure.
<ol>
	<li>Glucose solution preparation: Before conducting the experiment, prepare the glucose solution by dissolving 3.75 g glucose in 15 mL distilled H2O.</li>
	<li>Set up a timetable to record the readings during the experimental procedure (Table 1). 
	NOTE: It is important to set up a time-table with proper intervals between each blood examination to allow accurate recording during the experiment.</li>
	<li>Weigh each mouse after fasting and calculate the appropriate amount of glucose to be injected. For example, if the mouse weighs 30 g, the amount of glucose solution to be administered should be 300 &#181;L.</li>
	<li>Prepare the following instruments at the work bench:
	<ol>
		<li>Glucometer (Press the start button to check the battery status, make sure it is functioning before the test.)</li>
		<li>Glucose chip</li>
		<li>Insulin syringe (0.3 mL Insulin syringe)</li>
		<li>Razor blades</li>
		<li>Timer</li>
	</ol>
	</li>
	<li>Once the bench is set up, measure and record the blood glucose level as follows: Put a clean and new glucose chip into the glucometer and press the start button to zero it.</li>
	<li>Pick up the mouse by the back of the neck and stroke the tail a few times to ensure sufficient blood flow to the tail region.</li>
	<li>Using a new razor blade to cut off a small piece of the tail and squeeze out one small drop of blood (about 10-20 &#181;L) into the glucose chip. The blood should fill the chip to allow accurate measurement. The glucometer will display the glucose level immediately. If the machine shows &#34;error&#34;, repeat the procedure with a new glucose chip. 
	NOTE: The glucose chip requires only one drop of blood. When the blood sample needs to be collected more than once, simply apply pressure by running your fingers along the mouse&#39;s tail several times while holding the end of the tail directly on top of the chip to collect blood. It is not necessary to cut the tail end each time while collecting blood samples.</li>
	<li>Next, feed the mice glucose (0.25 g/mL) orally by using the intragastric gavage technique. The amount of glucose to be administered should be calculated by using the formula: 10X body weight (BW) &#181;L glucose solution (for example, if the mouse weighs 30 g, the amount of glucose solution to be administered will be 300 &#181;L). Start the timer immediately after administering oral glucose.</li>
	<li>Repeat the glucose measurement procedure at 15, 30, 60, 90, and 120 min.</li>
	<li>After all the glucose level readings have been recorded, discard the razor blades and glucose chips in a biohazard container. Put the food back into the mice cages and return them to the animal room.</li>
</ol>
4. Insulin Tolerance Test (ITT)
NOTE: The insulin tolerance test and oral glucose tolerance test should be scheduled at least 7 days apart to reduce the fasting effect on animals. For the insulin tolerance test (ITT), human insulin (0.75 U/Kg) will be administered through IP injection.
<ol>
	<li>Preparation of 0.25 U insulin solution: Dilute 100U human insulin to the ratio of 1:400 in saline solution.</li>
	<li>Weigh each mouse after fasting, and calculate the injected amount of insulin accordingly: the volume (&#181;L) of 0.25 U insulin to be injected IP = 3 X BW (0.75 U insulin/Kg body weight). For example: for a mouse weighing 28.8 g, inject: 28.8 X 3 = 86.4 &#181;L (0.25 U diluted insulin) (Table 2). 
	CAUTION: The same animals might have different body weights after 6 h fasting on different days. Thus, it is necessary to measure the body weight right before and after fasting and conduct the OGTT and ITT test. Mouse body weight could drop depending on the species, gender, and fasting duration. Higher dosages of insulin could cause insulin shock and would lead to the death of the animal.</li>
	<li>Set up a table (Table 2) to record the readings during the experimental procedure. Repeat the steps 3.4. to 3.8. for the measurement blood glucose levels.</li>
</ol>

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	<li>Plata-Salaman, C. R., Borkoski, J. P. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Chemokines/intercrines+and+central+regulation+of+feeding.">Chemokines/intercrines and central regulation of feeding.</a> Am J Physiol. 266, R1711-R1715 (1994).</li><li>Milanski, M., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Inhibition+of+hypothalamic+inflammation+reverses+diet-induced+insulin+resistance+in+the+liver.">Inhibition of hypothalamic inflammation reverses diet-induced insulin resistance in the liver.</a> Diabetes. 61, 1455-1462 (2012).</li><li>Wang, X., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Increased+hypothalamic+inflammation+associated+with+the+susceptibility+to+obesity+in+rats+exposed+to+high-fat+diet.">Increased hypothalamic inflammation associated with the susceptibility to obesity in rats exposed to high-fat diet.</a> Experimental diabetes research. 2012, 847246 (2012).</li><li>Benomar, Y., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Insulin+and+leptin+induce+Glut4+plasma+membrane+translocation+and+glucose+uptake+in+a+human+neuronal+cell+line+by+a+phosphatidylinositol+3-kinase-+dependent+mechanism.">Insulin and leptin induce Glut4 plasma membrane translocation and glucose uptake in a human neuronal cell line by a phosphatidylinositol 3-kinase- dependent mechanism.</a> Endocrinology. 147, 2550-2556 (2006).</li><li>Gual, P., Le Marchand-Brustel, Y., Tanti, J. 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E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Insulin+resistance+due+to+phosphorylation+of+insulin+receptor+substrate-1+at+serine+302.">Insulin resistance due to phosphorylation of insulin receptor substrate-1 at serine 302.</a> The Journal of biological chemistry. 279, 35298-35305 (2004).</li><li>Boura-Halfon, S., Zick, Y. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Phosphorylation+of+IRS+proteins,+insulin+action,+and+insulin+resistance.">Phosphorylation of IRS proteins, insulin action, and insulin resistance.</a> American journal of physiology. Endocrinology and metabolism. 296, E581-E591 (2009).</li><li>Chou, S. Y., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=CCL5/RANTES+contributes+to+hypothalamic+insulin+signaling+for+systemic+insulin+responsiveness+through+CCR5.">CCL5/RANTES contributes to hypothalamic insulin signaling for systemic insulin responsiveness through CCR5.</a> Sci Rep. 6, 37659 (2016).</li><li>Calegari, V. C., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Inflammation+of+the+hypothalamus+leads+to+defective+pancreatic+islet+function.">Inflammation of the hypothalamus leads to defective pancreatic islet function.</a> J Biol Chem. 286, 12870-12880 (2011).</li><li>Mighiu, P. I., Filippi, B. M., Lam, T. K. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Linking+inflammation+to+the+brain-liver+axis.">Linking inflammation to the brain-liver axis.</a> Diabetes. 61, 1350-1352 (2012).</li><li>Tavares, E., Minano, F. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=RANTES:+a+new+prostaglandin+dependent+endogenous+pyrogen+in+the+rat.">RANTES: a new prostaglandin dependent endogenous pyrogen in the rat.</a> Neuropharmacology. 39, 2505-2513 (2000).</li><li>Appay, V., Rowland-Jones, S. L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=RANTES:+a+versatile+and+controversial+chemokine.">RANTES: a versatile and controversial chemokine.</a> Trends in immunology. 22, 83-87 (2001).</li><li>DeVos, S. L., Miller, T. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Direct+intraventricular+delivery+of+drugs+to+the+rodent+central+nervous+system.">Direct intraventricular delivery of drugs to the rodent central nervous system.</a> J Vis Exp. , e50326 (2013).</li><li>Wang, N., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Admission+blood+glucose+and+in-hospital+clinical+outcome+among+patients+with+acute+stroke+in+Inner+Mongolia,+China.">Admission blood glucose and in-hospital clinical outcome among patients with acute stroke in Inner Mongolia, China.</a> Clin Invest Med. 32, E151-E157 (2009).</li><li>Olsen, T. S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Blood+glucose+in+acute+stroke.">Blood glucose in acute stroke.</a> Expert Rev Neurother. 9, 409-419 (2009).</li><li>De Jong, W. H., Borm, P. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Drug+delivery+and+nanoparticles:applications+and+hazards.">Drug delivery and nanoparticles:applications and hazards.</a> Int J Nanomedicine. 3, 133-149 (2008).</li><li>Kitade, H., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=CCR5+plays+a+critical+role+in+obesity-induced+adipose+tissue+inflammation+and+insulin+resistance+by+regulating+both+macrophage+recruitment+and+M1/M2+status.">CCR5 plays a critical role in obesity-induced adipose tissue inflammation and insulin resistance by regulating both macrophage recruitment and M1/M2 status.</a> Diabetes. 61, 1680-1690 (2012).</li><li>Kennedy, A., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Loss+of+CCR5+results+in+glucose+intolerance+in+diet-induced+obese+mice.">Loss of CCR5 results in glucose intolerance in diet-induced obese mice.</a> Am J Physiol Endocrinol Metab. 305, E897-E906 (2013).</li></ol>

The authors have nothing to disclose.

The mechanism of chronic inflammation and related chemokines such as CCL5 and its receptor &#8211; CCR5 in the development of type-2 diabetes remains unclear. Chronic inflammation causes macrophage infiltration into adipose tissues and affects the regulation of adipokines; in the meantime, it also attracts &#946;-cells and impairs insulin secretion from the islets of Langerhans in response to blood glucose. Hypothalamus in the brain plays an important role as a control center in coordinating insulin and adipokine signals from the systemic peripheral tissues in regulating appetite, peripheral blood glucose metabolism, and insulin response. Many studies also indicate that hypothalamic inflammation leads to defective regulation of energy homeostasis as well as defective pancreatic islet and liver function2,3,9,10. CCL5 in the brain contributes to food intake and body temperature regulation in the hypothalamus11,12; however, the correlation of CCL5 to hypothalamic and systemic insulin signaling is unclear. A CCL5 whole body knockout mouse (CCL5-/-) has been generated to address this question, which shows an insulin resistance phenotype with higher insulin levels and high blood glucose levels in blood8. However, it requires a long time to develop the T2DM phenotype and it is difficult to investigate the role and mechanism of CCL5 in hypothalamic insulin signal due to possible long-term compensatory effects. Therefore, a direct manipulation of CCL5 signaling in hypothalamic neurons is the best approach. There are, however, multiple types of neurons in the hypothalamic region and it is quite expensive and time-consuming to generate cell specific knockout mice. Utilizing an ICV infusion system can thus save time and provide a more specific approach to manipulate CCL5 function directly in the brain, bypassing possible peripheral inflammatory reactions.
Studies utilizing osmotic pumps have already been published previously, providing great examples and demonstrations of techniques involved in the implantation of osmotic pumps in rodents13. However, we faced a few challenges while following these protocols in our study. First, some of the equipment used in the protocol is quite expensive, including 1) the electric system to reach the location, drawing and inserting the needle into mouse brain, 2) the thermo system for maintaining mouse body temperature and 3) the oxygen-isoflurane supply system for administering anesthesia to mice. Second, the techniques described in other articles were difficult to replicate because we were only able to use animals within a small range of body weights and at certain ages for our study. We are aware that larger mice are more suitable for surgery and implantation. However, in our study, we had to use smaller and younger mice to avoid the overweight and aging effects on insulin and blood glucose regulation: only male mice with body weight 25 &#177; 2 g and age around 2 months old were chosen in the study. Thus, it is difficult to perform surgery and suture the wound on the mouse head. Third, the inflammatory response has to be minimized after surgery since an inflammatory cytokine is the target in this study. Mice and rats can remove suture and open wounds easily after surgery, which will result in inflammation and increase chemokine reactions. Therefore, a strategy to reach the location and draw and insert the needle into mouse brain that avoids secondary infection is necessary. Therefore, we modified the previously described protocols to make this technique cost effective, easier, and less harmful to the animals, as described in the following paragraph.
Firstly, we used a nail drill to manually drill a hole around the target area marked on the skull, as described in step 2.6. This method is cost effective and allows us to monitor the entire procedure so as to avoid damaging the mouse meninges and blood vessels. Blood glucose regulation is impaired after acute stroke, such as a hemorrhage in the brain. Acute hyperglycemia and diabetes-like syndromes were also observed after stroke in clinical settings14,15. Similarly, we also found impaired glucose level and insulin response in mice with hemorrhage and pus in the brain. We are aware that better control of manual-based surgery is necessary to ensure consistency of the results. Secondly, we took advantage of a newly developed medical biomaterial commonly used in clinics, tissue adhesive glue (Step 2.8), to seal the skin on the mouse head following surgery, hence, avoiding stitches and accelerating the rate of healing. This makes surgical procedures easier to perform and reduces the chance of secondary inflammation. Thirdly, the time required to perform the entire surgical procedure is comparatively shorter, which increases the chance of survival for the mice and lowers the dosage of anesthetic drug being injected intraperitoneally. We observed a high survival rate (95%) and obtained relatively accurate results by following this modified protocol.
The limitation of this technique is the relatively short time frame of drug delivery. Although an osmotic pump can be placed into the mouse body alternatively without re-opening the brain, our study only focuses on the inflammatory chemokine effect on the brain to regulate the peripheral systemic insulin signaling. Additional surgery in peripheral tissues could possibly induce an inflammatory reaction in peripheral tissues, which would then increase inflammatory chemokine expression and affect the results. Secondly, the half-life of the drug also limits the duration of the study. Recombinant proteins such as chemokine usually have a shorter half-life, which loses its activity over time, though it also allows us to study the effect of blocking CCL5 signaling in the brain over the short term. Our previous studies have also described a genetic modification approach for generating a CCL5 knockout mouse, which provides a model with long-term effects8.
There are some new techniques and alternative methods to deliver drugs into the brain. Nanotechnology is a powerful technique, which can be used to deliver drugs into the central nervous system. However, many drugs are thermosensitive and can be destroyed when trying to package them into nanoparticles16. In addition, nanoparticles can pass through BBB and be uptaken by cells that are suitable for siRNA or most common drugs, but it is not an ideal method for ligand-receptor binding. CCL5 requires binding to its receptor, CCR5, in the hypothalamus ARC neurons to take effect8, and the delivery of CCL5 antagonist MetCCL5 into neurons through nanoparticles might cause a loss of the ability to bind and block CCR5 on the cell surface.
The blood glucose level was significantly higher in mice administered with the CCL5-antagonist MetCCL5 as compared to the controls (mice administered with aCSF) in the oral glucose tolerance test. Additional insulin administration (insulin tolerance test) was also unable to lower the blood glucose level in MetCCL5 receiving mice (Figure 4B), which suggests that both endogenous and external insulin cannot reduce blood glucose levels when blocking hypothalamic CCL5 signaling. Mice became insulin resistant without CCL5 activity in the hypothalamus. Increased serine302 phosphorylation of IRS-1 was found in the mice receiving Met-CCL5 compared to control mice receiving aCSF (Figure 5A-B). Serine 302 phosphorylation of IRS-1 has been shown to induce a physical dissociation of IRS-1 from the insulin receptor, which is a major cause of insulin resistance6; insulin is unable to activate downstream signals such as the PI3K-Akt pathway. An ex vivo insulin stimulation study confirmed the insulin downstream signaling molecule Akt (p-AktS473) was not activated by insulin in mouse hypothalamic tissue infused with Met-CCL5 and, instead, the serine 302 phosphorylation increased. Altogether, both physiological data (OGTT and ITT) and molecular study demonstrate that hypothalamic CCL5 signaling mediates the hypothalamic insulin signal regulation, which contributes to systematic insulin resistance and glucose metabolism.
The role and mechanism of CCL5 and CCR5 in obesity-associated diabetes remains unclear. Kitade et al. reported that CCR5 deficiency protected mice from obesity-induced inflammation, macrophage recruitment, and insulin resistance17. However, other studies by Kennedy et al. found opposite results indicating that CCR5 deficiency impairs systemic glucose tolerance as well as adipocyte and muscle insulin signaling18. Both studies applied a high-fat diet to induce obesity, which leads to whole body chronic inflammation and compensatory response. These studies did not provide clean and clear mechanisms of CCL5 and CCR5 in insulin signaling regulation. On the other hand, the osmotic pump technique allows a brain specific infusion and avoids compensatory response with its time-limited delivery.
In conclusion, although the osmotic pump with the brain infusion system seems to be an &#34;old-fashioned&#34; technique, it does provide a cheaper, easier, and less harmful method of drug delivery and helps investigate the function of ligand-receptor signaling in the brain.

Insulin affects a wide variety of tissues including the brain. Insulin passes through blood-brain barrier, enters the central nervous system (CNS), and binds with insulin receptor (IR) in the hypothalamus to regulate food intake, sympathetic activity, and peripheral insulin response. Chronic inflammation in peripheral adipose tissues has been proposed to contribute to type 2 diabetes mellitus (T2DM), but how these inflammatory reactions affect insulin signals in the hypothalamus to mediate systemic insulin response and glucose intolerance remains unclear. Some chemokines participate in appetite regulation and body temperature regulation in the hypothalamus1 such as tumor necrosis factor-alpha (TNF&#945;), interleukin (IL)-6, IL-1&#946;, monocyte chemoattractant protein-1 (MCP-1), and CCL5 (C-C motif ligand 5). In addition, inflammation in the hypothalamus leads to insulin resistance in T2DM2,3.
Among these chemokines, the alteration of expression levels of chemokine CCL5 and its receptor, CCR5, in adipose tissues has been associated with arteriosclerosis and glucose intolerance in T2DM in humans as well as animals. CCL5 also has neuroendocrine functions, including the regulation of food intake and body temperature, in the hypothalamus. It is thus important to investigate whether CCL5 participates in insulin signal activation within the hypothalamus or the peripheral tissues.
Insulin signaling is tightly regulated within cells. The binding of insulin to insulin receptors (IR) activates insulin receptor substrate (IRS) proteins, followed by phosphatidylinositol 3-kinase (PI3K) and protein kinase B (PKB/AKT) activation and glucose transporter-4 (GLUT4) membrane translocation4. IRS proteins are the key regulators in this signaling pathway: they have multiple tyrosine and serine residues, which can be phosphorylated in response to positive or negative insulin signals5. For example, serine 302 phosphorylation on IRS-1 can lead to the physical dissociation of IRS-1 from IR and block insulin signal transduction, leading to insulin resistance6. The activity impairment of IRS proteins in the hypothalamus has been shown to induce insulin resistance and glucose intolerance in mice7.
One common way to study the function of a specific gene is the manipulation of the expression of target genes distributed throughout the entire body of the organism. However, this may have several drawbacks: 1) it could generate different feedback regulatory or compensatory effects over time and 2) this method does not help us illustrate the role of the target protein in the specific brain regions. Also, tissue- and cell-specific gene knockout animals take a long time to breed and are costly. Thus, we use a short-term brain infusion osmotic pump system - a relatively quick and convenient way to interfere with the signaling of the target protein in the brain using the antagonist drug to overcome the aforementioned issues. Stereotactic injections used to require intricate surgical skill and extensive investment in instrumentation and time. In this protocol, we provide a simple and safe way to perform stereotactic injection and a quick, less harmful, and instantaneous method to detect the concentration of blood glucose and investigate the role of CCL5 in hypothalamic insulin signaling regulation.

<table><tbody><tr><td>Vetbond Tissue Adhesive</td><td>3M</td><td>#1049SB</td><td>The glue used to seal the lesion site on the mouse head</td></tr><tr><td>LOCTITE 454 instant adhesive</td><td>Durect Corporation</td><td>#8670</td><td>The glue used to fix the needle on the mouse skull</td></tr><tr><td>Alzet Micro- Osmotic Pump</td><td>Durect Corporation</td><td>#9922</td><td>0.11 &amp;mu;l per hour, 28 days</td></tr><tr><td>Brain infusion system</td><td>Durect Corporation</td><td>#8851</td><td>1-3 mm, used to perfuse the drug in to the mice brain</td></tr><tr><td>Glucometer</td><td>Roche</td><td>#06870244001</td><td>Used to measure the blood glucose level</td></tr><tr><td>Glucose chip</td><td>Roche</td><td>#06454011020</td><td>Used to load the blood sample</td></tr><tr><td>Evan&#039;s blue</td><td>Sigma</td><td>#MKBK0523V</td><td>To demonstrate the drug infusion area</td></tr><tr><td>Insulin syringe</td><td>Becton, Dickinson and Company</td><td>#3232145 C</td><td>Used to administer insulin intraperitoneally</td></tr><tr><td>MIO NE116 CONTROL UNIT&lt;br/&gt; (nail drill)</td><td>Mio System</td><td>#E235-015</td><td>To drill a hole in the skull of the mouse</td></tr><tr><td>CCL5/Met-RANTES Protein</td><td>R&amp;amp;D</td><td>#ADB0111081</td><td>Recombinant Human CCL5, E-coli derived</td></tr><tr><td>aCSF formula</td><td>119 mM NaCl&lt;br/&gt; 26.2 mM NaHCO&lt;sub&gt;3&lt;/sub&gt;&lt;br/&gt; 2.5 mM KCl&lt;br/&gt; 1 mM NaH&lt;sub&gt;2&lt;/sub&gt;PO&lt;sub&gt;4&lt;/sub&gt;&lt;br/&gt; 1.3 mM MgCl&lt;sub&gt;2&lt;/sub&gt;&lt;br/&gt; 10 mM glucose</td><td></td><td>Filter sterilize with a 0.22 &amp;mu;m filter apparatus, and store at 4&amp;deg;C.&lt;br/&gt; aCSF is stable for 3-4 weeks</td></tr><tr><td>Phospho-IRS-1 Serine302 antibody</td><td>Cell Signaling</td><td>#12879</td><td>1:1000 dilution</td></tr><tr><td>IRS-1 (D23G12) antibody</td><td>Cell Signaling</td><td>#12879</td><td>1:1000 dilution</td></tr><tr><td>Phospho-Akt Serine 473 antibody</td><td>Cell Signaling</td><td>#9916</td><td>1:2000 dilution</td></tr><tr><td>Akt (pan) (C67E7) antibody</td><td>Cell Signaling</td><td>#9916</td><td>1:1000 dilution</td></tr><tr><td>Animals: C57BL/6</td><td>NAR Labs</td><td></td><td>Wild type mice strain used in the study</td></tr></tbody></table>

studying the hypothalamic insulin signal to peripheral glucose intolerance with a continuous drug infusion system into the mouse brain

Insulin regulates systematic metabolism in the hypothalamus and the peripheral insulin response. An inflammatory reaction in peripheral adipose tissues contributes to type 2 diabetes mellitus (T2DM) development and appetite regulation in the hypothalamus. Chemokine CCL5 and C-C chemokine receptor type 5 (CCR5) levels have been suggested to mediate arteriosclerosis and glucose intolerance in type 2 diabetes mellitus (T2DM). In addition, CCL5 plays a neuroendocrine role in the hypothalamus by regulating food intake and body temperature, thus, prompting us to investigate its function in hypothalamic insulin signaling and the regulation of peripheral glucose metabolism.
The micro-osmotic pump brain infusion system is a quick and precise way to manipulate CCL5 function and study its effect in the brain. It also provides a convenient alternative approach to generating a transgenic knockout animal. In this system, CCL5 signaling was blocked by intracerebroventricular (ICV) infusion of its antagonist, MetCCL5, using a micro-osmotic pump. The peripheral glucose metabolism and insulin responsiveness was detected by the Oral Glucose Tolerance Test (OGTT) and Insulin Tolerance Test (ITT). Insulin signaling activity was then analyzed by protein blot from tissue samples derived from the animals.
After 7-14 days of MetCCL5 infusion, the glucose metabolism and insulin responsiveness was impaired in mice, as seen in the results of the OGTT and ITT. The IRS-1 serine302 phosphorylation was increased and the Akt activity was reduced in mice hypothalamic neurons following CCL5 inhibition. Altogether, our data suggest that blocking CCL5 in the mouse brain increases the phosphorylation of IRS-1 S302 and interrupts hypothalamic insulin signaling, leading to a decrease in insulin function in peripheral tissues as well as the impairment of glucose metabolism.

Surgical implantations of osmotic infusion pumps containing either aCSF as control or CCL5 antagonist MetCCL5 (to block CCL5 effects in the brain) were conducted on the mice. At 7 and 14 days after surgery, the peripheral glucose tolerance and insulin responsiveness of mice were analyzed using OGTT (after 7 days) and ITT (after 14 days) as mentioned in the protocol. The oral glucose tolerance test (OGTT) and insulin tolerance test (ITT) of mice were performed after 6 hours fasting. Mice were administered with glucose orally, with the amount based on their respective body weights. The changes in blood glucose levels were recorded, as shown in Figure 3. The insulin sensitivity test was performed by intraperitoneal (IP) insulin injection into mice and the change of blood glucose level was measured immediately. The changes of blood glucose levels upon insulin stimulation in mice with different infusion drugs were recorded, as shown in Figure 4. The blood glucose level was only slightly reduced after glucose administration (Figure 3B) and insulin injection (Figure 4B) in mice with CCL5 antagonist (MetCCL5) infusion as compared to mice with aCSF infusion. These results suggest impairments in insulin function on peripheral glucose metabolism in mice with MetCCL5 administered in the brain.
Next, we analyzed the activation of insulin signal by evaluating the IRS-1 phosphorylation and Akt activation levels in hypothalamic tissues. The serine phosphorylation on 302 of IRS-1 was upregulated in mice treated with antagonist (MetCCL5) (Figure 5B-C) when mice were fed normally. In the control group, aCSF was administrated to the mice hypothalamus and the insulin challenge activated the downstream signal molecule Akt (phosphorylated Akt Serine 473) (Figure 5D, F) without increasing IRS-1 serine302 activation (Figure 5D-E) and Akt serine473 phosphorylation. In contrast, the Akt signal was not increased in mice infused with MetCCL5, but there was an increase in phosphorylation of IRS-1 serine 302 instead. Meanwhile, blocking the CCL5 signal in the mouse brain interrupted insulin activity in the hypothalamus and impaired peripheral insulin function. From our overall findings, such as the results from the ITT, OGTT, and ex vivo insulin challenge, we concluded that CCL5 in the hypothalamus contributes to insulin signal activation and peripheral glucose metabolism upon insulin stimulation.
<img alt="Figure 1" class="xfigimg" src="/files/ftp_upload/56410/56410fig1.jpg" /> 
Figure 1. Osmotic pump preparation and implantation surgical procedure in mouse. (A) The brain infusion kit and pump preparation perfused with drug solution. Red arrows indicate the catheter tubes filled with liquid. (B) Fix and mount the mouse head onto the stereotactic apparatus. (C) Separate the outermost layer of the skin from the subcutaneous skin for the implantation of micro-osmotic pump-brain infusion set; dash lines indicate the location of osmotic pump implants. (D) The arrow indicates the infusion side. (E) Drill a hole around the marked area on the skull. (F) Place the osmotic pump-brain infusion set into the back of the mouse and insert the brain infusion needle into the drilled hole (dash circled). (G) Fix the needle onto the skull using tissue-adhesive glue and detach the top of the needle (Scissor pointed in G) as shown in (H). (I) Seal the wound using tissue adhesive glue. <a href="https://cloudflare.jove.com/files/ftp_upload/56410/56410fig1large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 2" class="xfigimg" src="/files/ftp_upload/56410/56410fig2.jpg" /> 
Figure 2. Representative images of the drug diffusion area when the drug is administered in the ventricular region using the osmotic pump. Evan&#39;s blue is the representative drug used in the osmotic pump drug infusion illustration into the ventricular region (A) and diffusion into lateral and third ventricles (B). Scale bar = 0.5 cm. <a href="https://cloudflare.jove.com/files/ftp_upload/56410/56410fig2large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 3" class="xfigimg" src="/files/ftp_upload/56410/56410fig3.jpg" /> 
Figure 3. Glucose metabolism of the mice after surgery measured by the oral glucose tolerance test (OGTT). The distribution of blood glucose levels changed following the oral administration of glucose in WT mice infused with aCSF (A) and antagonist, MCCL5 (B). Data shown as mean &#177; SE. (Figure modified from8). *p&#60;0.05, by two-way ANOVA. <a href="https://cloudflare.jove.com/files/ftp_upload/56410/56410fig3large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 4" class="xfigimg" src="/files/ftp_upload/56410/56410fig4.jpg" /> 
Figure 4. Insulin function in mice blood glucose - the insulin tolerance test (ITT). The distribution of blood glucose levels changed following insulin injection in WT mice infused with aCSF (A), and infused with antagonist, MCCL5 (B). Data presented as mean &#177; SE (Figure modified from8). ***p&#60;0.001, by two-way ANOVA. <a href="https://cloudflare.jove.com/files/ftp_upload/56410/56410fig4large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 5" class="xfigimg" src="/files/ftp_upload/56410/56410fig5.jpg" /> 
Figure 5. Insulin signal activity in mice after surgery. (A) Western blotting of the inhibitory Serine 302 phosphorylation form of IRS-1 (insulin response substrate-1, pIRS1S302) in mice hypothalamus tissues treated with aCSF or CCL5 antagonist, MetCCL5 (MCCL5) infusion pump. (B) Related levels of phosphor-IRS-1S302 after infusion in mice hypothalamus with normal feeding. (C) Western blotting of the S302 phosphorylation of IRS-1 and Akt activation (phosphor-Akt S473, pAktS473) with or without insulin stimulation in hypothalamic tissue after aCSF or METCCL5 infusion. (D-E) Relative levels of pIRS-1S302, pS6KT421, and pAktS473. (&#34;2&#34; in each bar graph stands for: n=2 for all quantifications). (The blank bars in 5D-E, left: without insulin; the strips bars in 5D-E, right: with insulin). <a href="https://cloudflare.jove.com/files/ftp_upload/56410/56410fig5large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>#</td>
			<td>Mouse ID</td>
			<td>Body</td>
			<td>Glucose</td>
			<td>Start</td>
			<td>0</td>
			<td>15</td>
			<td>30</td>
			<td>60</td>
			<td>90</td>
		</tr>
		<tr>
			<td></td>
			<td></td>
			<td>weight</td>
			<td>&#956;L =10xBW</td>
			<td>time</td>
			<td>mins</td>
			<td>mins</td>
			<td>mins</td>
			<td>mins</td>
			<td>mins</td>
		</tr>
		<tr>
			<td>1</td>
			<td>501</td>
			<td>25.8g</td>
			<td>258</td>
			<td>9:00</td>
			<td>9:00</td>
			<td>9:00</td>
			<td>9:15</td>
			<td>9:30</td>
			<td>10:00</td>
		</tr>
		<tr>
			<td>2</td>
			<td>502</td>
			<td>25.3g</td>
			<td>253</td>
			<td>9:07</td>
			<td>9:07</td>
			<td>9:07</td>
			<td>9:22</td>
			<td>9:37</td>
			<td>10:07</td>
		</tr>
	</tbody>
</table>
Table 1. Timetable for Oral Glucose Tolerance Test (OGTT) recording
<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>#</td>
			<td>Mouse ID</td>
			<td>Body</td>
			<td>Insulin 0.25IU</td>
			<td>Start</td>
			<td>0</td>
			<td>15</td>
			<td>30</td>
			<td>60</td>
			<td>90</td>
		</tr>
		<tr>
			<td></td>
			<td></td>
			<td>weight</td>
			<td>&#956;L =3xBW</td>
			<td>time</td>
			<td>mins</td>
			<td>mins</td>
			<td>mins</td>
			<td>mins</td>
			<td>mins</td>
		</tr>
		<tr>
			<td>1</td>
			<td>501</td>
			<td>28.8g</td>
			<td>86.4</td>
			<td>9:00</td>
			<td>9:00</td>
			<td>9:15</td>
			<td>9:30</td>
			<td>10:00</td>
			<td>10:30</td>
		</tr>
		<tr>
			<td>2</td>
			<td>502</td>
			<td>25.3g</td>
			<td>75.9</td>
			<td>9:07</td>
			<td>9:07</td>
			<td>9:22</td>
			<td>9:37</td>
			<td>10:07</td>
			<td>10:37</td>
		</tr>
	</tbody>
</table>
Table 2. Timetable for Insulin Tolerance Test (ITT) recording

Watch this Scientific Journal Video about Studying the Hypothalamic Insulin Signal to Peripheral Glucose Intolerance with a Continuous Drug Infusion System into the Mouse Brain at JoVE.com

Studying the Hypothalamic Insulin Signal to Peripheral Glucose Intolerance with a Continuous Drug Infusion System into the Mouse Brain

This protocol studies the role of chemokine (C-C motif) ligand 5 (CCL5) in the hypothalamus by delivering an antagonist, MetCCL5, into the mouse brain using a micro-osmotic pump brain infusion system. This transient inhibition of CCL5 activity interrupted hypothalamic insulin signaling, leading to glucose intolerance and peripheral systemic insulin sensitivity.

Insulin regulates systematic metabolism in the hypothalamus and the peripheral insulin response. An inflammatory reaction in peripheral adipose tissues ...

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10.2K Views.  Taipei Medical University and National Health Research. Dit protocol bestudeert de rol van chemokine (C-C motief) ligand 5 (CCL5) in de hypothalamus door het leveren van een antagonist, MetCCL5, in de hersenen van de muis met behulp van een micro-osmotische hersenen infusie pompsysteem. Deze tijdelijke remming van CCL5 activiteit onderbroken hypothalame insuline signalering, wat leidt tot glucose-intolerantie en perifere systemische insulinegevoeligheid.

Video: Studying the Hypothalamic Insulin Signal to Peripheral Glucose Intolerance with a Continuous Drug Infusion System into the Mouse Brain

Hyperinsulinemic-Euglycemic Clamp in the Conscious Rat

Type 2 diabetes (T2D) is rapidly rising in prevalence. Characterized by either inadequate insulin production or the inability to utilize insulin produced, T2D results in elevated blood glucose levels. The "gold-standard" in assessing insulin sensitivity is a hyperinsulinemic-euglycemic clamp or insulin clamp. In this procedure, insulin is infused at a constant rate resulting in a drop in blood glucose. To maintain blood glucose at a constant level, exogenous glucose (D50) is infused into the venous circulation. The amount of glucose infused to maintain homeostasis is indicative of insulin sensitivity. Here, we show the basic clamp procedure in the chronically catheterized, unrestrained, conscious rat. This model allows blood to be collected with minimal stress to the animal. Following the induction of anesthesia, a midline incision is made and the left common carotid artery and right jugular vein are catheterized. Inserted catheters are flushed with heparinized saline, then exteriorized and secured. Animals are allowed to recover for 4-5 days prior to experiments, with weight gain monitored daily. Only those animals who regain weight to pre-surgery levels are used for experiments. On the day of the experiment, rats are fasted and connected to pumps containing insulin and D50. Baseline glucose is assessed from the arterial line and used a benchmark throughout the experiment (euglycemia). Following this, insulin is infused at a constant rate into the venous circulation. To match the drop in blood glucose, D50 is infused. If the rate of D50 infusion is greater than the rate of uptake, a rise in glucose will occur. Similarly, if the rate is insufficient to match whole body glucose uptake, a drop will occur. Titration of glucose continues until stable glucose readings are achieved. Glucose levels and glucose infusion rates during this stable period are recorded and reported. Results provide an index of whole body insulin sensitivity. The technique can be refined to meet specific experimental requirements. It is further enhanced by the use of radioactive tracers that can determine tissue specific insulin-stimulated glucose uptake as well as whole body glucose turnover.

The hyperinsulinemic-euglycemic clamp is the "gold standard" for the assessment of insulin action. Insulin is infused at a constant rate stimulating glucose uptake. The amount of exogenous glucose infused to counter this drop is indicative of insulin sensitivity. Here the procedure is performed on a conscious, unrestrained rat.

Type 2 diabetes (T2D) is rapidly rising in prevalence. Characterized by either inadequate insulin production or the inability to utilize insulin produced, ...

Hyperinsulinemic-euglycemic Clamps in Conscious, Unrestrained Mice

Type 2 diabetes is characterized by a defect in insulin action. The hyperinsulinemic-euglycemic clamp, or insulin clamp, is widely considered the "gold standard" method for assessing insulin action in vivo. During an insulin clamp, hyperinsulinemia is achieved by a constant insulin infusion. Euglycemia is maintained via a concomitant glucose infusion at a variable rate. This variable glucose infusion rate (GIR) is determined by measuring blood glucose at brief intervals throughout the experiment and adjusting the GIR accordingly. The GIR is indicative of whole-body insulin action, as mice with enhanced insulin action require a greater GIR. The insulin clamp can incorporate administration of isotopic 2[14C]deoxyglucose to assess tissue-specific glucose uptake and [3-3H]glucose to assess the ability of insulin to suppress the rate of endogenous glucose appearance (endoRa), a marker of hepatic glucose production, and to stimulate the rate of whole-body glucose disappearance (Rd).
The miniaturization of the insulin clamp for use in genetic mouse models of metabolic disease has led to significant advances in diabetes research. Methods for performing insulin clamps vary between laboratories. It is important to note that the manner in which an insulin clamp is performed can significantly affect the results obtained. We have published a comprehensive assessment of different approaches to performing insulin clamps in conscious mice1 as well as an evaluation of the metabolic response of four commonly used inbred mouse strains using various clamp techniques2. Here we present a protocol for performing insulin clamps on conscious, unrestrained mice developed by the Vanderbilt Mouse Metabolic Phenotyping Center (MMPC; URL: www.mc.vanderbilt.edu/mmpc). This includes a description of the method for implanting catheters used during the insulin clamp. The protocol employed by the Vanderbilt MMPC utilizes a unique two-catheter system3. One catheter is inserted into the jugular vein for infusions. A second catheter is inserted into the carotid artery, which allows for blood sampling without the need to restrain or handle the mouse. This technique provides a significant advantage to the most common method for obtaining blood samples during insulin clamps which is to sample from the severed tip of the tail. Unlike this latter method, sampling from an arterial catheter is not stressful to the mouse1. We also describe methods for using isotopic tracer infusions to assess tissue-specific insulin action. We also provide guidelines for the appropriate presentation of results obtained from insulin clamps.

The hyperinsulinemic-euglycemic clamp, or insulin clamp, is the gold standard for assessing insulin action in vivo. A method for performing insulin clamps in mice is described. This includes a method for arterial catheterization that permits experiments to be performed in conscious, unrestrained mice with minimal stress.

Type 2 diabetes is characterized by a defect in insulin action. The hyperinsulinemic-euglycemic clamp, or insulin clamp, is widely considered the "gold ...

Hippocampal Insulin Microinjection and In vivo Microdialysis During Spatial Memory Testing

Glucose metabolism is a useful marker for local neural activity, forming the basis of methods such as 2-deoxyglucose and functional magnetic resonance imaging. However, use of such methods in animal models requires anesthesia and hence both alters the brain state and prevents behavioral measures. An alternative method is the use of in vivo microdialysis to take continuous measurement of brain extracellular fluid concentrations of glucose, lactate, and related metabolites in awake, unrestrained animals. This technique is especially useful when combined with tasks designed to rely on specific brain regions and/or acute pharmacological manipulation; for example, hippocampal measurements during a spatial working memory task (spontaneous alternation) show a dip in extracellular glucose and rise in lactate that are suggestive of enhanced glycolysis1-3,4-5, and intrahippocampal insulin administration both improves memory and increases hippocampal glycolysis6. Substances such as insulin can be delivered to the hippocampus via the same microdialysis probe used to measure metabolites. The use of spontaneous alternation as a measure of hippocampal function is designed to avoid any confound from stressful motivators (e.g. footshock), restraint, or rewards (e.g. food), all of which can alter both task performance and metabolism; this task also provides a measure of motor activity that permits control for nonspecific effects of treatment. Combined, these methods permit direct measurement of the neurochemical and metabolic variables regulating behavior.

Hippocampal Insulin Microinjection and In vivo Microdialysis During Spatial Memory Testing

Modulation of hippocampally-dependent spatial working memory by direct intrahippocampal microinjection, accompanied and followed by in vivo microdialysis for metabolites in conscious, behaving animals.

Glucose metabolism is a useful marker for local neural activity, forming the basis of methods such as 2-deoxyglucose and functional magnetic resonance ...

Neuroscience

Study of In Vivo Glucose Metabolism in High-fat Diet-fed Mice Using Oral Glucose Tolerance Test (OGTT) and Insulin Tolerance Test (ITT)

Obesity represents the most important single risk factor in the pathogenesis of type 2 diabetes, a disease which is characterized by a resistance to insulin-stimulated glucose uptake and a gross decompensation of systemic glucose metabolism. Despite considerable progress in the understanding of glucose metabolism, the molecular mechanisms of its regulation in health and disease remain under-investigated, while novel approaches to prevent and treat diabetes are urgently needed. Diet derived glucose stimulates the pancreatic secretion of insulin, which serves as the principal regulator of cellular anabolic processes during the fed-state and thus balances blood glucose levels to maintain systemic energy status. Chronic overfeeding triggers meta-inflammation, which leads to alterations in peripheral insulin receptor-associated signaling and thus reduces the sensitivity to insulin-mediated glucose disposal. These events ultimately result in elevated fasting glucose and insulin levels as well as a reduction in glucose tolerance, which in turn serve as important indicators of insulin resistance. Here, we present a protocol for the generation and metabolic characterization of high-fat diet (HFD)-fed mice as a frequently used model of diet-induced insulin resistance. We illustrate in detail the oral glucose tolerance test (OGTT), which monitors the peripheral disposal of an orally administered glucose load and insulin secretion over time. Additionally, we present a protocol for the insulin tolerance test (ITT) to monitor whole-body insulin action. Together, these methods and their downstream applications represent powerful tools to characterize the general metabolic phenotype of mice as well as to specifically assess alterations in glucose metabolism. They may be especially useful in the broad research field of insulin resistance, diabetes and obesity to provide a better understanding of pathogenesis as well as to test the effects of therapeutic interventions.

Study of In Vivo Glucose Metabolism in High-fat Diet-fed Mice Using Oral Glucose Tolerance Test OGTT and Insulin Tolerance Test ITT

The current article describes the generation and metabolic characterization of high-fat diet-fed mice as a model of diet-induced insulin resistance and obesity. It further features detailed protocols to perform the oral glucose tolerance test and the insulin tolerance test, monitoring whole-body alterations of glucose metabolism in vivo.

Obesity represents the most important single risk factor in the pathogenesis of type 2 diabetes, a disease which is characterized by a resistance to ...

Acclimation Prior to an Intraperitoneal Insulin Tolerance Test to Mitigate Stress-Induced Hyperglycemia in Conscious Mice

The insulin tolerance test is commonly used in metabolic studies to assess whole body insulin sensitivity in rodents. It is a relatively simple test that involves measurement of blood glucose levels over time following a single intraperitoneal injection of insulin. Given that it is performed in the conscious state and blood is often collected via a tail snip, it has the potential to elicit a stress response from animals due to anxiety associated with handling and blood collection. As such, a stress-induced rise in blood glucose can occur, making it difficult to detect and interpret the primary endpoint measure, namely an insulin-mediated reduction in blood glucose. This has been seen in many mouse strains, and is quite common in diabetic db/db mice, where glucose levels can increase, rather than decrease, after insulin administration. Here, we describe a method of acclimating mice to handling, injections and blood sampling prior to performing the insulin tolerance test. We find that this lowers stress-induced hyperglycemia and results in data that more accurately reflects whole body insulin sensitivity.

Stress-induced elevations in glucose levels can confound interpretation of data derived from a conscious intraperitoneal insulin tolerance test in mice. In this article, we describe a method to acclimate the mice to handling, injections and blood sampling prior to performing the insulin tolerance test in order to limit stress-induced hyperglycemia.

The insulin tolerance test is commonly used in metabolic studies to assess whole body insulin sensitivity in rodents. It is a relatively simple test that ...

Surgical Installation of Hyperglycemic and Hypoglycemic Clamps in Mice

Hyperglycemic Clamp and Hypoglycemic Clamp in Conscious Mice

Diabetes mellitus (DM) is caused by insufficient insulin release from the pancreatic &#946;-cells (Type1 DM) and insulin sensitivity in muscles, liver, and adipose tissues (Type2 DM). Insulin injection treats DM patients but leads to hypoglycemia as a side effect. Cortisol and catecholamines are released to activate glucose production from the liver to recover hypoglycemia, called counter-regulatory responses (CRR). In DM research using rodent models, glucose tolerance tests and 2-deoxy-glucose injection are used to measure insulin release and CRR, respectively. However, blood glucose concentrations change persistently during experiments, causing difficulties in assessing net insulin release and CRR. This article describes a method in which blood glucose is kept at 250 mg/dL or 50 mg/dL in conscious mice to compare the release of insulin and CRR hormones, respectively.
Polyethylene tubing is implanted in the mice's carotid artery and jugular vein, and the mice are allowed to recover from the surgery. The jugular vein tubing is connected to a Hamilton syringe with a syringe pump to enable insulin or glucose infusion at a constant and variable rate. The carotid artery tubing is for blood collection. For the hyperglycemic clamp, 30% glucose is infused into the vein, and blood glucose levels are measured from the arterial blood every 5 min or 10 min. The infusion rate of 30% glucose is increased until the blood glucose level becomes 250 mg/dL. Blood is collected to measure insulin concentrations. For hypoglycemic clamp, 10 mU/kg/min insulin is infused together with 30% glucose, whose infusion rate is variable to maintain 50 mg/dL of blood glucose level. Blood is collected to measure counter-regulatory hormones when both glucose infusion and blood glucose reach a steady state. Both hyperglycemic and hypoglycemic clamps have the same surgical procedure and experimental setups. Thus, this method is useful for researchers of systemic glucose metabolism.

Author Spotlight: Investigating the Blood Glucose Homeostasis in Murine Brain Using a Cost-Effective Hyperglycemic And Hypoglycemic Clamp Technique

A hyperglycemic clamp is used for measuring insulin release with a maintained higher blood glucose concentration. A hypoglycemic clamp is for measuring glucose production induced by counter-regulatory responses. Both methods use the same surgical procedure. Here, we present a clamp technique to assess systemic glucose metabolism.

Diabetes mellitus (DM) is caused by insufficient insulin release from the pancreatic &#946;-cells (Type1 DM) and insulin sensitivity in muscles, liver, ...

Simple Continuous Glucose Monitoring in Freely Moving Mice

Mice are a common model organism used to study metabolic diseases such as diabetes mellitus. Glucose levels are typically measured by tail-bleeding, which requires handling the mice, causes stress, and does not provide data on freely behaving mice during the dark cycle. State-of-the-art continuous glucose measurement in mice requires inserting a probe into the aortic arch of the mouse, as well as a specialized telemetry system. This challenging and expensive method has not been adopted by most labs. Here, we present a simple protocol involving the utilization of commercially available continuous glucose monitors used by millions of patients to measure glucose continuously in mice as a part of basic research. The glucose-sensing probe is inserted into the subcutaneous space in the back of the mouse through a small incision to the skin and is held in place tightly using a couple of sutures. The device is sutured to the mouse skin to ensure it remains in place. The device can measure glucose levels for up to 2 weeks and sends the data to a nearby receiver without any need to handle the mice. Scripts for the basic data analysis of glucose levels recorded are provided. This method, from surgery to computational analysis, is cost-effective and potentially very useful in metabolic research.

Here, we describe a simple method to implant a commercial continuous glucose monitor designed for patients onto mice and provide the scripts to analyze the results.

Mice are a common model organism used to study metabolic diseases such as diabetes mellitus. Glucose levels are typically measured by tail-bleeding, which ...

Biology

Osmotic Minipump Implantation for Increasing Glucose Concentration in Mouse Cerebrospinal Fluid

Diabetes increases the risk of cognitive decline and impairs brain function. Whether or not this relationship between high glucose and cognitive deficits is causal remains elusive. Moreover, whether these deficits are mediated by an increase in glucose levels in cerebrospinal fluid (CSF) and/or blood is also unclear. There are very few studies investigating the direct effects of high CSF glucose levels on central nervous system (CNS) function, especially on learning and memory, since current diabetes models are not sufficiently developed to address such research questions. This article describes a method to chronically increase CSF glucose levels for 4 weeks by continuously infusing glucose into the lateral ventricle using osmotic minipumps in mice. The protocol was validated by measuring glucose levels in CSF. This protocol increased CSF glucose levels to ~328 mg/dL after infusion of a 50% glucose solution at a 0.25 &#181;L/h flow rate, compared to a CSF glucose concentration of ~56 mg/dL in mice that received artificial cerebrospinal fluid (aCSF). Furthermore, this protocol did not affect blood glucose levels. Therefore, this method can be used to determine the direct effects of high CSF glucose on brain function or a specific neural pathway independently of changes in blood glucose levels. Overall, the approach described here will facilitate the development of animal models for testing the role of high CSF glucose in mediating features of Alzheimer&#39;s disease and/or other neurodegenerative disorders associated with diabetes.

This article describes a detailed protocol to increase glucose concentration in the cerebrospinal fluid (CSF) of mice. This approach can be useful for studying the effects of high CSF glucose on neurodegeneration, cognition, and peripheral glucose metabolism in mice.

Diabetes increases the risk of cognitive decline and impairs brain function. Whether or not this relationship between high glucose and cognitive deficits ...

Oral Glucose Tolerance Test (OGTT): Measuring Glucose Metabolism in Mice

Source: Ajoy, R. and Chou, S. Y. <a href="https://www.jove.com/video/56410/studying-hypothalamic-insulin-signal-to-peripheral-glucose">Studying the Hypothalamic Insulin Signal to Peripheral Glucose Intolerance with a Continuous Drug Infusion System into the Mouse Brain</a>.&#160;J. Vis. Exp. (2018).
This video introduces how to perform an oral glucose tolerance test on a laboratory mouse.

Source: Ajoy, R. and Chou, S. Y. Studying the Hypothalamic Insulin Signal to Peripheral Glucose Intolerance with a Continuous Drug Infusion System into ...

JoVE Encyclopedia of Experiments

Rodent Models

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Continuous Drug Infusion System in Mouse Model: A Surgical Procedure to Implant Micro-osmotic Pump Infusion System in the Mouse Brain for Continuous Drug Delivery

Source: Ajoy, R., Chou, S. Y. <a href="https://www.jove.com/v/56410">Studying the Hypothalamic Insulin Signal to Peripheral Glucose Intolerance with a Continuous Drug Infusion System into the Mouse Brain.</a> J. Vis. Exp. (2018)
In this video, we demonstrate the assembly of a micro-osmotic pump brain infusion system followed by its surgical implantation in the mouse skull. This system enables continuous delivery of potential drugs and facilitates the study of their effects on the brain and brain tissue.

Source: Ajoy, R., Chou, S. Y. Studying the Hypothalamic Insulin Signal to Peripheral Glucose Intolerance with a Continuous Drug Infusion System into the ...

Studying the Hypothalamic Insulin Signal to Peripheral Glucose Intolerance with a Continuous Drug Infusion System into the Mouse Brain

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