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GLP-1 受体激动剂在慢性治疗后对皮质酮释放具有持续的刺激作用。

GLP-1 receptor agonists have a sustained stimulatory effect on corticosterone release after chronic treatment.

机构信息

1Department of Physiology,University of Tartu,Tartu,Estonia.

3Department of Dermatology;University of Tartu,Tartu,Estonia.

出版信息

Acta Neuropsychiatr. 2015 Feb;27(1):25-32. doi: 10.1017/neu.2014.36. Epub 2014 Dec 3.

Abstract

OBJECTIVE

Glucagon-like peptide 1 (GLP-1) receptor agonists are a new group of antidiabetic medications quickly gaining popularity. We aimed to examine behavioural and neuroendocrine changes following chronic treatment with GLP-1 receptor agonists in animal models.

METHODS

The effects of chronic treatment with GLP-1 receptor agonists were determined on behavioural parameters [anxiety level in the light-dark compartment test, the motor activity in automated activity cages, immobility in the forced swimming test (FST)] and on corticosterone release in mice. The possible antidepressant effect of chronic liraglutide treatment was also studied in Flinders Sensitive Line (FSL) rats, a genetic model of depression.

RESULTS

Two weeks of treatment with exenatide (10 µg/kg twice daily) or liraglutide (1200 µg/kg once daily) did not affect the anxiety level in a light-dark compartment test nor induce an antidepressant-like effect in the FST in mice. Moreover, chronic treatment with liraglutide had no effect on depression-related behaviour in FSL rats. Interestingly, hypolocomotion induced by the drugs in mice disappeared after chronic dosing. Both of the GLP-1 receptor agonists induced robust increases in corticosterone levels in mice under basal conditions as well as in the case of combination with swimming stress. Remarkably, exenatide was as potent a stimulator of corticosterone release after 2 weeks as after acute administration.

CONCLUSIONS

The increases in corticosterone release seen after acute exenatide or liraglutide treatment do not abate after 2 weeks of treatment demonstrating that tolerance does not develop towards this particular effect of GLP-1 agonists.

摘要

目的

胰高血糖素样肽 1(GLP-1)受体激动剂是一类新兴的抗糖尿病药物,正迅速普及。我们旨在研究 GLP-1 受体激动剂在动物模型中慢性治疗后的行为和神经内分泌变化。

方法

测定 GLP-1 受体激动剂慢性治疗对行为参数[明暗箱试验中的焦虑水平、自动活动笼中的运动活性、强迫游泳试验(FST)中的不动性]和小鼠皮质酮释放的影响。还在抑郁的遗传模型弗林德斯敏感系(FSL)大鼠中研究了慢性利拉鲁肽治疗的可能抗抑郁作用。

结果

艾塞那肽(10μg/kg,每日两次)或利拉鲁肽(1200μg/kg,每日一次)治疗 2 周均不影响明暗箱试验中的焦虑水平,也不诱导 FST 中的抗抑郁样作用。此外,利拉鲁肽慢性治疗对 FSL 大鼠的抑郁相关行为没有影响。有趣的是,药物引起的小鼠运动减少在慢性给药后消失。两种 GLP-1 受体激动剂均在基础条件下以及与游泳应激联合时,显著增加小鼠的皮质酮水平。值得注意的是,艾塞那肽在 2 周后作为皮质酮释放的刺激物与急性给药一样有效。

结论

急性艾塞那肽或利拉鲁肽治疗后观察到的皮质酮释放增加在 2 周治疗后并未减弱,表明对 GLP-1 激动剂的这种特殊作用不会产生耐受性。

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