Department of Veterinary and Animal Sciences, University of Copenhagen, Copenhagen, Denmark.
Global Drug Discovery, Novo Nordisk A/S, Måløv, Denmark.
Sci Rep. 2021 Mar 16;11(1):5983. doi: 10.1038/s41598-021-84758-w.
The potentially fatal cardiovascular effects of hypoglycaemia are not well understood and large animal models of the counter-regulatory responses and cardiovascular consequences of insulin-induced hypoglycaemia are needed to understand the mechanisms in humans. The aim of this study was to develop a human-like minipig model of hypoglycaemia including healthy and diabetic pigs to investigate endocrine, electrocardiographic and platelet effects. Hypoglycaemia was induced using a hyperinsulinaemic, hypoglycaemic clamp and an insulin bolus protocol. Plasma glucose, glucagon, C-peptide, insulin, epinephrine and platelet aggregation responses were measured before, during and after hypoglycaemia. Continuous electrocardiographic recordings were obtained. Hypoglycaemia at a plasma glucose concentration of 0.8-1.0 mM in the clamp induced 25-fold increase in epinephrine and sixfold and threefold increase in glucagon for healthy and diabetic pigs, respectively. The hypoglycaemic clamp induced QTc-interval prolongation and increase in cardiac arrhythmias. In the bolus approach, the non-diabetic group reached plasma glucose target of 1.5 mM and QTc-interval was prolonged after insulin injection, but before glucose nadir. The diabetic group did not reach hypoglycaemic target, but still demonstrated QTc-interval prolongation. These results demonstrate effects of hyperinsulinaemic hypoglycaemia closely resembling human physiology, indicating the minipig as a translational animal model of counter-regulatory endocrine and myocardial effects of hypoglycaemia.
低血糖对心血管的潜在致命影响尚未被充分了解,因此需要建立大型动物模型来研究胰岛素诱导的低血糖时的代偿反应和心血管后果,以了解人类的相关机制。本研究旨在建立一种类似人类的小型猪低血糖模型,包括健康猪和糖尿病猪,以研究内分泌、心电图和血小板的影响。低血糖通过高胰岛素-低血糖钳夹和胰岛素推注方案来诱导。在低血糖发生前后测量血浆葡萄糖、胰高血糖素、C 肽、胰岛素、肾上腺素和血小板聚集反应。连续进行心电图记录。在钳夹试验中,健康猪和糖尿病猪的血糖浓度分别降至 0.8-1.0mM 时,肾上腺素分别增加了 25 倍和 6 倍、3 倍。低血糖钳夹导致 QTc 间期延长和心律失常增加。在推注方法中,非糖尿病组的血糖目标达到 1.5mM,胰岛素注射后 QTc 间期延长,但在血糖最低值之前。糖尿病组未达到低血糖目标,但仍表现出 QTc 间期延长。这些结果表明,高胰岛素诱导的低血糖对心血管的影响与人类生理学非常相似,表明小型猪是研究低血糖时代偿性内分泌和心肌效应的转化动物模型。