在高脂饮食-链脲佐菌素大鼠模型中,利拉鲁肽与普兰林肽通过影响PI3K/AKT/GSK-3β/TTBK通路和降低Tau过度磷酸化,保护大鼠免受认知功能损害。

IF 2.9 4区 医学 Q2 PHYSIOLOGY
Hoda M Moghazy, Nesreen G Abdelhaliem, Sherine Ahmed Mohammed, Asmaa Hassan, Amany Abdelrahman
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引用次数: 0

摘要

美国糖尿病协会指南(2021 年)确认了提高公众对糖尿病诱发认知障碍认识的重要性,强调了血糖控制不佳与认知障碍之间的联系。认知功能障碍的脑部特征性病变是神经纤维缠结(NFT)和淀粉样β沉积形成的老年斑,糖原合酶激酶3β(GSK3β)和高度同源激酶Tau微管蛋白激酶1(TTBK1)可在不同位点磷酸化Tau蛋白,这些酶的过度表达会使Tau蛋白产生广泛的磷酸化,使其不溶解,并促进NFT的形成,从而损害认知功能。本研究旨在探讨利拉鲁肽和普兰林肽在预防糖尿病引起的认知功能障碍方面的潜在作用,以及它们对2型糖尿病(T2D)大鼠模型中PI3K/AKT/GSK-3β/TTBK通路的影响。2型糖尿病大鼠通过高脂饮食诱导10周,然后注射单剂量链脲佐菌素(STZ);在高脂饮食的基础上,开始使用普兰林肽(200 μg/kg/天 sc)或利拉鲁肽(0.6 mg/kg/ 天 sc)治疗6周。研究结束时,通过新物体识别和T迷宫测试评估大鼠的认知功能。然后,将大鼠处死,对海马组织进行生化和组织学评估。结果表明,普拉林肽和利拉鲁肽都能有效控制糖尿病,防止记忆功能下降,并能增加PI3K/AKT的表达,同时降低GSK-3β/TTBK的表达;但利拉鲁肽显著减少Tau阳性细胞数量的效果优于普拉林肽。这项研究证实,普拉林肽和利拉鲁肽是很有前途的抗糖尿病药物,可通过不同的机制预防相关的认知障碍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Liraglutide versus pramlintide in protecting against cognitive function impairment through affecting PI3K/AKT/GSK-3β/TTBK1 pathway and decreasing Tau hyperphosphorylation in high-fat diet- streptozocin rat model.

Liraglutide versus pramlintide in protecting against cognitive function impairment through affecting PI3K/AKT/GSK-3β/TTBK1 pathway and decreasing Tau hyperphosphorylation in high-fat diet- streptozocin rat model.

The American Diabetes Association guidelines (2021) confirmed the importance of raising public awareness of diabetes-induced cognitive impairment, highlighting the links between poor glycemic control and cognitive impairment. The characteristic brain lesions of cognitive dysfunction are neurofibrillary tangles (NFT) and senile plaques formed of amyloid-β deposition, glycogen synthase kinase 3 beta (GSK3β), and highly homologous kinase tau tubulin kinase 1 (TTBK1) can phosphorylate Tau proteins at different sites, overexpression of these enzymes produces extensive phosphorylation of Tau proteins making them insoluble and enhance NFT formation, which impairs cognitive functions. The current study aimed to investigate the potential contribution of liraglutide and pramlintide in the prevention of diabetes-induced cognitive dysfunction and their effect on the PI3K/AKT/GSK-3β/TTBK1 pathway in type 2 diabetic (T2D) rat model. T2D was induced by administration of a high-fat diet for 10 weeks, then injection of a single dose of streptozotocin (STZ); treatment was started with either pramlintide (200 μg/kg/day sc) or liraglutide (0.6 mg/kg/day sc) for 6 weeks in addition to the HFD. At the end of the study, cognitive functions were assessed by novel object recognition and T-maze tests. Then, rats were sacrificed for biochemical and histological assessment of the hippocampal tissue. Both pramlintide and liraglutide treatment revealed equally adequate control of diabetes, prevented the decline in memory function, and increased PI3K/AKT expression while decreasing GSK-3β/TTBK1 expression; however, liraglutide significantly decreased the number of Tau positive cells better than pramlintide did. This study confirmed that pramlintide and liraglutide are promising antidiabetic medications that could prevent associated cognitive disorders in different mechanisms.

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来源期刊
CiteScore
8.80
自引率
2.20%
发文量
121
审稿时长
4-8 weeks
期刊介绍: Pflügers Archiv European Journal of Physiology publishes those results of original research that are seen as advancing the physiological sciences, especially those providing mechanistic insights into physiological functions at the molecular and cellular level, and clearly conveying a physiological message. Submissions are encouraged that deal with the evaluation of molecular and cellular mechanisms of disease, ideally resulting in translational research. Purely descriptive papers covering applied physiology or clinical papers will be excluded. Papers on methodological topics will be considered if they contribute to the development of novel tools for further investigation of (patho)physiological mechanisms.
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