setup and operation of the hyperglycemic and hypoglycemic clamps in mouse for monitoring blood glucose and insulin release

Chirurgische installatie van hyperglykemische en hypoglykemische klemmen bij muizen

Glucose is an important source of energy for cells, and a lack of glucose can lead to a variety of symptoms and complications. In the event of low glucose (hypoglycemia, generally less than 70 mg/dL in fasting blood glucose level, but should not be determined by a single value1), the most common symptoms include weakness, confusion, sweating, and headache. It can also disrupt cerebral function and increase the risk of cardiovascular events and mortality2. Conversely, hyperglycemia is a medical condition in which the plasma glucose concentration exceeds normal levels (generally &#62; 126 mg/dL in fasting blood glucose level3). This can occur in individuals with diabetes who have either a deficit in insulin production or utilization. Hyperglycemia can lead to diabetic ketoacidosis, which occurs when the body cannot use glucose for energy but instead breaks down fatty acids for fuel. The hyperglycemic hyperosmolar state also increases mortality4. Long-term hyperglycemia can cause damage to blood vessels, nerves, and organs, leading to the development of several chronic complications such as cardiovascular disease, retinopathies, and kidney diseases. Thus, the blood glucose concentration must be maintained in a tight range between 100 mg/dL and 120 mg/dL.
Blood glucose is regulated by the balance between glucose input and output in a one-compartment model (Figure 1A). Glucose input includes absorbed glucose from food and glucose production from the liver, kidneys, and small intestine. Glucose output comprises glucose uptake in tissues and glucose disposal from the kidneys. Both the amount of glucose input and output are regulated by endocrine hormones. For example, glucagon, corticosterone, and catecholamines, known as counter-regulatory hormones, are released when blood glucose levels decrease5. They stimulate the breakdown of glycogen and the synthesis of glucose, mainly from the liver; these processes are known as glycogenolysis and gluconeogenesis, respectively. Hyperglycemia increases insulin release from pancreatic &#946;-cells and stimulates glucose uptake in the muscles, adipose tissues, and heart6,7,8,9. Exercise increases insulin-independent glucose uptake10. The sympathetic nervous system increases glucose uptake in muscles and brown adipose tissue6,11. To measure the ability to regulate glucose metabolism in peripheral tissues, researchers typically use the glucose tolerance test (GTT) and the insulin tolerance test (ITT) (Figure 1B,C). In GTT, two factors must be considered: insulin release and insulin sensitivity (Figure 1B). However, the glucose concentration curve during the 120 min test is different in each mouse, which may affect different amounts of hormone release. In ITT, blood glucose is regulated by both insulin sensitivity and the release of counter-regulatory hormones. Therefore, it is difficult to determine the precise meaning of glucose metabolism, insulin release, and insulin sensitivity in GTT and ITT, in situations where blood glucose levels are not constant.
To overcome these problems, it is desirable to keep blood glucose at a constant level (or &#34;clamp&#34;). In hyperglycemic clamp, glucose is infused into the bloodstream to raise blood glucose levels to a specific level and then maintained at that level for a period of time. The amount of infused glucose is adjusted based on measurements of blood glucose levels every 5-10 min to maintain a steady state. This technique is particularly useful for understanding the parameters of insulin secretion at a clamped glucose level. Hypoglycemic clamp is a method to maintain low blood glucose levels by infusing insulin. Glucose is infused at a variable rate to maintain a specific blood glucose level. If the mouse cannot recover from hypoglycemia, more glucose should be infused.
Although there are many advantages to performing hyperglycemic and hypoglycemic clamps, the surgical and experimental procedures are considered technically difficult. Thus, few research groups have been able to do them. We aimed to describe these methods for researchers with financial and workforce constraints to start these experiments at a lower budget.

Auteur in de schijnwerpers: onderzoek naar de bloedglucosehomeostase in de hersenen van muizen met behulp van een kosteneffectieve hyperglykemische en hypoglykemische klemtechniek

Hyperglykemische klem en hypoglykemische klem bij bewuste muizen

Our research investigates how our brain regulates the homeo status of blood glucose levels, and what kind of neurons, neuropeptides, and neuron circuits do that. Additionally, how does our memory of food, psychological stress, pain, and other somatic sensations affect it? It is difficult to assess glucose metabolism precisely.We must check in insulin sensitivity or resistance, insulin secretion and counter regulatory responses. We should also check which tissue changes glucose uptake and glucose production regarding insulin sensitivity or resistance. We believe that not only insulin sensitivity, but also insulin secretion and counter regulatory responses are all affecting normal blood glucose levels, even in healthy conditions.We are trying to understand the whole picture of glucose regulation by the brain. Our protocol is low cost and does not need a special and expensive device to create a clamp. It'll enable researchers to implement the use of the clamp easily and quickly.Because this protocol helps researchers to use the clamp very easily, we expect our protocol will encourage more research in the entire field of life sciences.

Installatie en werking van de hyperglykemische en hypoglykemische klemmen in muizen voor het bewaken van bloedglucose en insulineafgifte

Begin met het opzetten van het pompsysteem voor de hypoglykemische of hyperglykemische klemmen. Vul hiervoor twee Hamilton-spuiten met het insuline-infusaat en de 30%-glucoseoplossing. Sluit de gevulde spuiten aan op de twee lange slangen van de verlengbuis die bedoeld is voor glucose- en insuline-infusie.Nadat u de spuit aan de respectievelijke spuitpompen hebt bevestigd, vult u elke oplossing in de respectievelijke verlengslangen. Vul vervolgens zoutoplossing in de spuit van één milliliter en de verlengbuis voor het afnemen van bloed uit de slagader. Sluit vervolgens de verlengbuis voor infusie aan op de vooraf geïnstalleerde halsaderkatheter van de goed verdoofde muis.De verlengbuis voor het afnemen van bloed naar de katheter van de halsslagader van het dier. Gebruik cellofaantape om de buizen aan elkaar te bevestigen. Plaats de muis met de slangen in een leeg bekerglas van 500 milliliter met bodembedekking.Klem het bovenste uiteinde van de verlengbuis vast voor het afnemen van bloed terwijl u deze aansluit op een nieuwe spuit. Extraheer 50 microliter bloed, breng het over naar een buis van 1,5 milliliter en meet de bloedglucosespiegel. Voeg vervolgens 50 microliter zoutoplossing toe.Om bloed te verzamelen voor hormoonmetingen, neemt u nog eens 50 microliter bloed af en brengt u dit over naar een buis van 1,5 milliliter op ijs. Start na de bloedglucosemeting van nul minuten de insulinespuitpomp om de juiste hoeveelheid insuline toe te dienen. Blijf de bloedglucosespiegel meten en verander de glucose-infusiesnelheid elke 5 tot 10 minuten gedurende de 120 minuten durende controletijd totdat een stabiele toestand is bereikt.Volg voor de hyperglykemische klem de stappen die zijn gedemonstreerd voor de hypoglykemische klem, exclusief insuline-infusie en een aangepaste steady-state bloedglucosespiegel.

Research

JoVE Journal

Medicine

Setup and Operation of the Hyperglycemic and Hypoglycemic Clamps in Mouse for Monitoring Blood Glucose and Insulin Release

Hyperglycemic Clamp and Hypoglycemic Clamp in Conscious Mice

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Chirurgie om hypoglykemische en hyperglykemische klemslangen in muizen te implanteren