Department of Endocrinology, First Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Shanghai Key Laboratory for Molecular Imaging, Shanghai University of Medicine and Health Sciences, Shanghai, China,
Obes Facts. 2021;14(1):10-20. doi: 10.1159/000509956. Epub 2020 Dec 18.
To investigate the relationship of central and peripheral ghrelin during an exendin-4 (Ex-4) intervention to feeding in obese type 2 diabetic rodents.
Animal models of diet-induced obesity (DIO) and type 2 diabetes were developed using male Sprague-Dawley rats fed with a high-fat diet and induced into DIO-streptozotocin diabetic rats. Ex-4 or the glucagon-like peptide-1 (GLP-1) receptor agonist exendin fragment-[9-39] (Ex-9) was intracerebroventricularly (ICV) administered. Multivariate linear regression analysis was performed to investigate potential predictors of food intake after Ex-4 administration.
ICV administration of Ex-4 significantly inhibited feeding and decreased weight, plasma active ghrelin, hypothalamic ghrelin, and gastric ghrelin levels. The changes in hypothalamic ghrelin and plasma ghrelin could predict the amount of 8-h average food intake. Central preadministration of Ex-9 followed by treatment with Ex-4 could inhibit the decrease in feeding at 0.5, 2, and 8 h. It could also inhibit the decrease in hypothalamic ghrelin at 0.5, 2, and 8 h, as well as in plasma and gastric ghrelin at 2 and 8 h.
In a GLP-1 receptor-dependent manner, central and peripheral ghrelin play a vital role in the inhibition of feeding by Ex-4 administration. Hypothalamic ghrelin, but not plasma ghrelin, may be involved in central Ex-4 inhibition of feeding in the very early feeding period.
探讨外源性胰高血糖素样肽-4(Ex-4)干预肥胖 2 型糖尿病大鼠摄食时,中枢和外周胃饥饿素之间的关系。
采用高脂饮食喂养雄性 Sprague-Dawley 大鼠建立饮食诱导肥胖(DIO)和 2 型糖尿病动物模型,并用链脲佐菌素诱导 DIO 糖尿病大鼠。通过脑室内(ICV)给予 Ex-4 或胰高血糖素样肽-1(GLP-1)受体激动剂 Exendin Fragment-[9-39](Ex-9)。采用多元线性回归分析,研究 Ex-4 给药后摄食量的潜在预测因素。
脑室内给予 Ex-4 可显著抑制摄食,并降低体重、血浆活性胃饥饿素、下丘脑胃饥饿素和胃饥饿素水平。下丘脑胃饥饿素和血浆胃饥饿素的变化可预测 8 小时平均摄食量。预先给予 Ex-9 后再给予 Ex-4 可抑制 0.5、2 和 8 小时时摄食的减少。还可以抑制 0.5、2 和 8 小时时下丘脑胃饥饿素的减少,以及 2 和 8 小时时血浆和胃饥饿素的减少。
以 GLP-1 受体依赖的方式,中枢和外周胃饥饿素在 Ex-4 给药抑制摄食中发挥重要作用。在非常早期的摄食阶段,可能是下丘脑胃饥饿素而不是血浆胃饥饿素参与了 Ex-4 对摄食的中枢抑制作用。