We acknowledge the Laboratory Animal Center staff at National Cheng Kung University (NCKU) for caring for the animals. This work was supported by the scholarship from Prof. Kun-Yen Huang Education Fund of CHENG-HSING Medical Foundation to C.-W.L.; the funds from the Ministry of Science and Technology (MOST) in Taiwan: (Undergraduate Research MOST 109-2813-C-006-095-B) to T.-H.Y.; (MOST 107-2320-B-006-072-MY3; 109-2314-B-006-046; 110-2314-B-006-114; 110-2320-B-006-018-MY3) to W.-L.W.; and the Higher Education Sprout Project, Ministry of Education to the Headquarters of University Advancement at NCKU to W.-L.W.

All the experimental protocols and the animals&#39; care were approved by the National Cheng Kung University (NCKU) Institutional Animal Care and Use Committee (IACUC).
1. Preparation for the experimental animal
<ol>
	<li>Obtain 6-8-week-old wild-type C57BL/6JNarl male mice from a vendor.</li>
	<li>House the mice in a standard mouse cage with standard mouse chow and sterilized water ad libitum. 
	&#8203;NOTE: The housing conditions for the Laboratory Animal Cen...

The authors have no conflicts of interest related to this work.

Gut-derived metabolites have been associated with brain-mediated diseases without much precise mechanism, partially due to their multiple binding sites in the body6,12,24. Previous reports indicated that SCFAs could serve as ligands for G protein-coupled receptors, epigenetic regulators, and sources for energy production at multiple sites in the body6,12. To bypass the c...

The human gastrointestinal tract harbors diverse microorganisms impacting the host1,2,3. These gut bacteria can secrete gut-derived metabolites during their utilization of dietary components consumed by the host4,5. Interestingly, the gut metabolites not metabolized in the periphery can be transported to other organs via circulation6. Of note, these secreted metabolites can serve as mediators for the gut-brain axis, defined as the bidirectional communication between the central nervous system and the gut7. Previous studies have shown that gut-derived metabolites can modulate complex behavior and emotion in animals8,9,10,11.
Short-chain fatty acids (SCFAs) are the main metabolites produced by gut microbiota during the fermentation of dietary fiber and indigestible carbohydrates6. Acetate, propionate, and butyrate are the most abundant SCFAs in the gut12. SCFAs serve as the energy source for cells in the gastrointestinal tract. Unmetabolized SCFAs in the gut can be transported to the brain through the portal vein, thus modulating brain and behavior6,12. Previous studies have suggested that SCFAs might play a critical role in neuropsychiatric disorders6,12. For example, intraperitoneal injection of butyrate in BTBR T+ Itpr3tf/J (BTBR) mice, an animal model of autism spectrum disorder (ASD), rescued their social deficits13. Antibiotic-treated rats receiving microbiota from depressive subjects showed an increase in anxiety-like behaviors and fecal SCFAs14. Clinically, alterations in fecal SCFAs levels were observed in people with ASD compared to typically developing controls15,16. People with depression have lower fecal SCFAs levels than healthy subjects17,18. These studies suggested that SCFAs can alter behavior in animals and humans through various routes.
Microbial metabolites exert diverse effects on multiple sites in the body, impacting host physiology and behaviors4,19, including the gastrointestinal tract, vagus nerve, and sympathetic nerve. It is difficult to pinpoint the precise role of gut-derived metabolites in the brain when administering the metabolites via peripheral routes. This paper presents a video-based protocol to investigate the effects of gut-derived metabolites in the brain of a freely moving mouse (Figure 1). We showed that SCFAs could be acutely given through the guide cannula during behavioral tests. The type, volume, and infusion rate of metabolites can be modified depending on the purpose. The site of cannulization can be adjusted to explore the impact of gut metabolites in a specific brain region. We aim to provide scientists with a method to explore the potential impact of gut-derived microbial metabolites on the brain and behavior.

<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>Material</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Advil Liqui-Gels Solubilized Ibuprofen A2:D41</td>
			<td>Pfizer</td>
			<td>n/a</td>
			<td></td>
		</tr>
		<tr>
			<td>Alexa Fluor 488 donkey anti-rabbit</td>
			<td>ThermoFisher Scientific</td>
			<td>A-21206</td>
			<td></td>
		</tr>
		<tr>
			<td>Anti-Fluorescent Gold (rabbit polyclonal)</td>
			<td>Millipore</td>
			<td>AB153-I</td>
			<td></td>
		</tr>
		<tr>
			<td>Bottle Top Vacuum Filter, 500 mL, 0.22 &#956;m, PES, Sterile</td>
			<td>NEST</td>
			<td>121921LA01</td>
			<td></td>
		</tr>
		<tr>
			<td>CaCl2&#160;</td>
			<td>Sigma-Aldrich</td>
			<td>C1016</td>
			<td>ACSF: 0.14 g/L</td>
		</tr>
		<tr>
			<td>Chlorhexidine scrub 2%</td>
			<td>Phoenix</td>
			<td>NDC 57319-611-09</td>
			<td></td>
		</tr>
		<tr>
			<td>Chlorhexidine solution</td>
			<td>Phoenix</td>
			<td>NDC 57319-599-09</td>
			<td></td>
		</tr>
		<tr>
			<td>Commercial dummy</td>
			<td>RWD Life Science</td>
			<td>62004</td>
			<td>Single_OD 0.20 mm/ M3.5/G = 0.5 mm</td>
		</tr>
		<tr>
			<td>Commercial guide cannul</td>
			<td>RWD Life Science</td>
			<td>62104</td>
			<td>Single_OD 0.41 mm-27G/ M3.5/C = 2.5 mm&#160;</td>
		</tr>
		<tr>
			<td>Commercial injector</td>
			<td>RWD Life Science</td>
			<td>62204</td>
			<td>Single_OD 0.21 mm-33G/ Mates with M3.5/C = 3.5 mm/G = 0.5 mm</td>
		</tr>
		<tr>
			<td>D-(+)-Glucose</td>
			<td>Sigma-Aldrich</td>
			<td>G8270</td>
			<td>ACSF: 0.61 g/L</td>
		</tr>
		<tr>
			<td>Dental acrylic</td>
			<td>HYGENIC</td>
			<td>n/a</td>
			<td></td>
		</tr>
		<tr>
			<td>Fixing screws</td>
			<td>RWD Life Science</td>
			<td>62521</td>
			<td></td>
		</tr>
		<tr>
			<td>Fluoroshield mounting medium with DAPI</td>
			<td>Abcam</td>
			<td>AB104139</td>
			<td></td>
		</tr>
		<tr>
			<td>Horse serum</td>
			<td>ThermoFisher Scientific</td>
			<td>16050130</td>
			<td></td>
		</tr>
		<tr>
			<td>Insulin syringes</td>
			<td>BBraun</td>
			<td>XG-LBB-9151133S-1BX</td>
			<td>1 mL</td>
		</tr>
		<tr>
			<td>Isoflurane&#160;</td>
			<td>Panion &#38; BF biotech</td>
			<td>DG-4900-250D</td>
			<td></td>
		</tr>
		<tr>
			<td>KCl&#160;</td>
			<td>Sigma-Aldrich</td>
			<td>P3911</td>
			<td>ACSF: 0.19 g/L</td>
		</tr>
		<tr>
			<td>Ketoprofen&#160;</td>
			<td>Swiss Pharmaceutical</td>
			<td>n/a</td>
			<td></td>
		</tr>
		<tr>
			<td>Lidocaine&#160;</td>
			<td>AstraZeneca</td>
			<td>n/a</td>
			<td></td>
		</tr>
		<tr>
			<td>Low melting point agarose</td>
			<td>Invitrogen</td>
			<td>16520</td>
			<td></td>
		</tr>
		<tr>
			<td>MgCl2&#160;</td>
			<td>Sigma-Aldrich</td>
			<td>M8266</td>
			<td>ACSF: 0.19 g/L</td>
		</tr>
		<tr>
			<td>Microscope cover slips</td>
			<td>MARIENFELD</td>
			<td>101242</td>
			<td></td>
		</tr>
		<tr>
			<td>Microscope slides</td>
			<td>ThermoFisher Scientific</td>
			<td>4951PLUS-001E</td>
			<td></td>
		</tr>
		<tr>
			<td>Mineral oil light, white NF</td>
			<td>Macron Fine Chemicals</td>
			<td>MA-6358-04</td>
			<td></td>
		</tr>
		<tr>
			<td>NaCl&#160;</td>
			<td>Sigma-Aldrich</td>
			<td>S9888</td>
			<td>ACSF: 7.46 g/L</td>
		</tr>
		<tr>
			<td>NaH2PO4&#160;</td>
			<td>Sigma-Aldrich</td>
			<td>S8282</td>
			<td>ACSF: 0.18 g/L</td>
		</tr>
		<tr>
			<td>NaHCO3&#160;</td>
			<td>Sigma-Aldrich</td>
			<td>S5761</td>
			<td>ACSF: 1.76 g/L</td>
		</tr>
		<tr>
			<td>n-butyl cyanoacrylate adhesive (tissue adhesive glue)</td>
			<td>3M</td>
			<td>1469SB</td>
			<td>3M Vetbond</td>
		</tr>
		<tr>
			<td>Neural tracer&#160;</td>
			<td>Santa Cruz</td>
			<td>SC-358883</td>
			<td>FluoroGold</td>
		</tr>
		<tr>
			<td>Paraformaldehyde</td>
			<td>Sigma-Aldrich</td>
			<td>P6148</td>
			<td></td>
		</tr>
		<tr>
			<td>Polyethylene tube</td>
			<td>RWD Life Science</td>
			<td>62329</td>
			<td>OD 1.50, I.D 0.50 mm and OD 1.09, I.D 0.38 mm</td>
		</tr>
		<tr>
			<td>Puralube Vet (eye) Ointment</td>
			<td>Dechra&#160;</td>
			<td>12920060</td>
			<td></td>
		</tr>
		<tr>
			<td>Sodium acetate&#160;</td>
			<td>Sigma-Aldrich</td>
			<td>S2889</td>
			<td>SCFAs: 13.5 mM</td>
		</tr>
		<tr>
			<td>Sodium azide&#160;</td>
			<td>Sigma-Aldrich</td>
			<td>S2002</td>
			<td></td>
		</tr>
		<tr>
			<td>Sodium butyrate&#160;</td>
			<td>Sigma-Aldrich</td>
			<td>B5887</td>
			<td>SCFAs: 8 mM</td>
		</tr>
		<tr>
			<td>Sodium propionate&#160;</td>
			<td>Sigma-Aldrich</td>
			<td>P1880</td>
			<td>SCFAs: 5.18 mM</td>
		</tr>
		<tr>
			<td>Stainless guide cannula</td>
			<td>Chun Ta stainless steel enterprise CO., LTD.</td>
			<td>n/a</td>
			<td>OD 0.63 mm; Local vendor</td>
		</tr>
		<tr>
			<td>Stainless injector</td>
			<td>Chun Ta stainless steel enterprise CO., LTD.</td>
			<td>n/a</td>
			<td>OD 0.3 mm; dummy is made from injector; local vendor</td>
		</tr>
		<tr>
			<td>Superglue</td>
			<td>Krazy Glue</td>
			<td>KG94548R</td>
			<td></td>
		</tr>
		<tr>
			<td>Triton X-100</td>
			<td>Merck</td>
			<td>1.08603.1000</td>
			<td></td>
		</tr>
		<tr>
			<td>Equipment</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Cannula holder</td>
			<td>RWD Life Science</td>
			<td>B485-68217</td>
			<td></td>
		</tr>
		<tr>
			<td>Ceiling camera</td>
			<td>FOSCAM</td>
			<td>R2</td>
			<td></td>
		</tr>
		<tr>
			<td>Digital stereotaxic instruments</td>
			<td>Stoelting</td>
			<td>51730D</td>
			<td></td>
		</tr>
		<tr>
			<td>Dissecting microscope</td>
			<td>INNOVIEW</td>
			<td>SEM-HT/TW</td>
			<td></td>
		</tr>
		<tr>
			<td>Glass Bead Sterilizer</td>
			<td>RWD Life Science</td>
			<td>RS1501</td>
			<td></td>
		</tr>
		<tr>
			<td>Heating pad</td>
			<td>Stoelting</td>
			<td>53800M</td>
			<td></td>
		</tr>
		<tr>
			<td>Leica microscope&#160;</td>
			<td>Leica</td>
			<td>DM2500</td>
			<td></td>
		</tr>
		<tr>
			<td>Micro Dissecting Forceps</td>
			<td>ROBOZ</td>
			<td>RS-5136</td>
			<td>Serrated, Slight Curve; Extra Delicate; 0.5mm Tip Width; 4&#34; Length&#160;</td>
		</tr>
		<tr>
			<td>Micro Dissecting Scissors</td>
			<td>ROBOZ</td>
			<td>RS-5918</td>
			<td>4.5&#34; Angled Sharp</td>
		</tr>
		<tr>
			<td>Microinjection controller</td>
			<td>World Precision Instruments (WPI)</td>
			<td>MICRO2T</td>
			<td>SMARTouch Controller</td>
		</tr>
		<tr>
			<td>Microinjection syringe pump</td>
			<td>World Precision Instruments (WPI)</td>
			<td>UMP3T-1</td>
			<td>UltraMicroPump3&#160;&#160;</td>
		</tr>
		<tr>
			<td>Microliter syringe</td>
			<td>Hamilton</td>
			<td>80014</td>
			<td>10 &#181;L</td>
		</tr>
		<tr>
			<td>Optical Fiber Cold Light with double Fiber</td>
			<td>Step</td>
			<td>LGY-150</td>
			<td>Local vendor</td>
		</tr>
		<tr>
			<td>Pet trimmer</td>
			<td>WAHL</td>
			<td>09962-2018</td>
			<td></td>
		</tr>
		<tr>
			<td>Vaporiser for Isoflurane</td>
			<td>Step</td>
			<td>AS-01</td>
			<td>Local vendor</td>
		</tr>
		<tr>
			<td>Vibratome</td>
			<td>Leica</td>
			<td>VT1000S</td>
			<td></td>
		</tr>
		<tr>
			<td>Software</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Animal behavior video tracking software</td>
			<td>Noldus</td>
			<td>EthoVision</td>
			<td>Version: 15.0.1416</td>
		</tr>
		<tr>
			<td>Leica Application Suite X software</td>
			<td>Leica</td>
			<td>LASX</td>
			<td>Version: 3.7.2.22383</td>
		</tr>
	</tbody>
</table>

intracerebroventricular delivery of gut-derived microbial metabolites in freely moving mice

The impact of gut microbiota and their metabolites on host physiology and behavior has been extensively investigated in this decade. Numerous studies have revealed that gut microbiota-derived metabolites modulate brain-mediated physiological functions through intricate gut-brain pathways in the host. Short-chain fatty acids (SCFAs) are the major bacteria-derived metabolites produced during dietary fiber fermentation by the gut microbiome. Secreted SCFAs from the gut can act at multiple sites in the periphery, affecting the immune, endocrine, and neural responses due to the vast distribution of SCFAs receptors. Therefore, it is challenging to differentiate the central and peripheral effects of SCFAs through oral and intraperitoneal administration of SCFAs. This paper presents a video-based method to interrogate the functional role of SCFAs in the brain via a guide cannula in freely moving mice. The amount and type of SCFAs in the brain can be adjusted by controlling the infusion volume and rate. This method can provide scientists with a way to appreciate the role of gut-derived metabolites in the brain.

The mouse was infused with SCFAs 1 week after recovery from the guide cannula implantation to evaluate locomotor activity in a novel cage. The mouse was placed in a novel cage and infused with 2,100 nL of SCFAs or ACSF in the first 5 min (delivery rate of 7 nL/s) into the brain through the commercial guide cannula implanted in the lateral ventricle of the brain. The locomotor activity in a novel cage was recorded for an additional 30 min after infusion. No difference was observed in the locomotor activity in the novel ca...

Watch this Scientific Journal Video about Intracerebroventricular Delivery of Gut-Derived Microbial Metabolites in Freely Moving Mice at JoVE.com

Intracerebroventricular Delivery of Gut-Derived Microbial Metabolites in Freely Moving Mice

Gut-derived microbial metabolites have multifaceted effects leading to complex behavior in animals. We aim to provide a step-by-step method to delineate the effects of gut-derived microbial metabolites in the brain via intracerebroventricular delivery via a guide cannula.

The impact of gut microbiota and their metabolites on host physiology and behavior has been extensively investigated in this decade. Numerous studies have ...

The metabolites released by gut microbiota produce complex effects on the host. This protocol presents a method to interrogate the role of gut metabolites in the mouse brain and behavior. This technique provides a precise, meticulous, and validated method to deliver gut metabolites into a brain in freely moving mice.We provide a comprehensive and physiological best methodology for insight into gut brain axis research. Place the mouse onto the stereotaxic frame and fix the mouse incisors on the incisor bar in the stereotaxic incisor holder. Cover the nose with the nose cone mask.Then evaluate the nociception of the mouse via the top pinch reflex, and ensure a constant breathing rate before incising the surgical site. Once trimmed fur on the head is removed by the adhesive tape, subcutaneously inject the analgesic ketoprofen to relieve pain and apply eye ointment. Next, fix the head by inserting the pointed ear bar in the ear canal.Tighten the nose clamp on the incisor holder and press the head gently to ensure that the head is fixed. Use 3 alternating scrubs of chlorhexidine swab to disinfect the scalp. Now, use dissecting scalpel to make an incision of less than one centimeter in the scalp in an anterior posterior manner.After opening the incision, wipe the skull with a cotton swab held by micro dissecting forceps. Based on the stereotaxic coordinates, identify and label the position of the right lateral ventricle as described in the manuscript. Next, drill a hole through the skull at the labeled site using a stereotaxic drill, and later, drill two to four more holes in the skull.Wipe the skull with lidocaine cotton swab and mount 2 to 4 stainless screws on the holes. Place the commercial guide cannula on the stereotaxic cannula holder and disinfect with the glass speed sterilizer at 150 degrees Celsius. Then, move the stereotaxic cannula holder to the hole drilled for the lateral ventricle and slowly insert the commercial guide cannula into the hole until the desired depth is attained.Now apply 10 microliters of n-Butyl cyanoacrylate adhesive to fix the commercial guide cannula in the drilled hole and wait for 3 to 4 minutes. Release the commercial guide cannula gently from the stereotaxic cannula holder and apply dental acrylic to the incised scalp to fix the commercial guide cannula and wait for at least 5 minutes. Implant the commercial dummy into the commercial guide cannula.Then, place the mouse into a new cage with a heating pad underneath for recovery from anesthesia and continuously observe until the mouse fully awakens. Mount the microliter syringe, containing 10 microliters of distilled water, on the microinjection pump. Using an insulin syringe, fill the polyethylene tube with distilled water and connect the microliter syringe to the hanging polyethylene tube.Turn on the microinjection controller and press display all channels to access the command screen. Next, press configuration and set volume target to 9, 800 nanoliters with delivery rate of 100 nanoliters per second. Then press direction to switch to the infuse mode and press run to infuse 9, 800 nanoliters of distilled water from the polyethylene tube connected to the microliter syringe.Now, place the injector into a vial containing the mineral oil, press configuration and set the volume target to 3, 000 nanoliters with delivery rate to 100 nanoliters per second. For withdrawing 3, 000 nanoliters of mineral oil, press direction to switch to the withdraw mode and then press run. Disassemble the polyethylene tube from the microliter syringe needle.To spit out 3, 000 nanoliters of distilled water from the microliter syringe needle, press direction to switch to the infuse mode and press run. Then insert the microliter syringe back into the polyethylene tube. Place the injector into a vial containing SCFAs.Press configuration and set volume target to 9, 500 nanoliters with delivery rate to 100 nanoliters per second. Withdraw 9, 500 nanoliters of SCFAs by pressing direction to switch to the withdraw mode and press run. Label the oil SCFAs phase to validate whether the SCFAs are successfully infused.Press configuration and set the desired volume target with delivery rate to 7 nanoliters per second. Press direction to switch to the infuse mode. Press run to infuse the microliter syringe forward until the liquid comes out at the front end of the commercial injector before inserting the injector into the cannula for SCFAs injection.After anesthetizing the mouse, insert the commercial injector into the commercial guide cannula. Once the mouse is recovered from anesthesia, place it in a novel cage and allow it to explore for 35 minutes freely. Infuse SCFAs using a delivery rate of 7 nanoliters per second for a target volume of 2, 100 nanoliters in the first 5 minutes.Then press direction to the infuse mode and press run. After behavioral testing, remove the commercial injector from the commercial guide cannula. Infuse 2, 100 nanoliters of the neutral tracer with the delivery rate of 7 nanoliters per second to verify the infusion site.Image the fluorescent signal in the infusion site using a fluorescence microscope. Both ACSF and SCFAs-infused mice traveled in a novel cage for a total of 35 minutes. No difference was observed in the locomotor activity in the novel cage between infusion of SCFAs and ACSF.The fluorescent dye was detected in the lateral ventricle and the surrounding regions of the mouse brain when infused with a commercial guide cannula. Similarly, infusion through the stainless steel guide cannula leads to the detection of signals in the lateral ventricle and the surrounding regions of the mouse brain. Combining this procedure with circuit based neural technologies will allow scientists to gain insight into the circuit based control of the brain and behavior contributed by gut metabolites.This technique paves the way for the researchers to explore the role of microbiota and metabolites in the intricate gut brain axis.

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Neuroscience

2.9K ビュー.  National Cheng Kung University. 腸内細菌叢によって放出される代謝産物は、宿主に複雑な影響を及ぼします。このプロトコルは、マウスの脳と行動における腸代謝物の役割を調べる方法を提示します。この技術は、自由に動くマウスの脳に腸代謝物を送達するための正確で綿密で検証された方法を提供します。私たちは、腸の脳軸研究への洞察のための包括的かつ生理学的な最良の方法論を提供?...