Carnosine-Based Reversal of Diabetes-Associated Cognitive Decline via Activation of the Akt/mTOR Pathway and Modulation of Autophagy in a Rat Model of Type 2 Diabetes Mellitus.

IF 2.2 4区 医学 Q3 CLINICAL NEUROLOGY
Rodgers Odhiambo Ndolo, Lu Yu, Yan Zhao, Jinying Lu, Gao Wang, Xinmin Zhao, Yi Ren, Jing Yang
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引用次数: 2

Abstract

Introduction: Carnosine can suppress secondary complications in diabetes and show robust neuroprotective activity against neurodegenerative diseases. Here, we report that carnosine ameliorates diabetes-associated cognitive decline in vivo through the modulation of autophagy.

Methods: A high-fat diet (HFD) and one intraperitoneal injection of 30 mg/kg streptozotocin (STZ) were used to induce type 2 diabetes mellitus in Sprague-Dawley rats. The rats were randomly divided into five groups: control (CON), HFD/STZ, and three intragastric carnosine treatment groups receiving low (100 mg/kg), medium (300 mg/kg), and high (900 mg/kg) doses over 12 weeks. Body weight, blood glucose levels, and cognitive function were continuously monitored. From excised rat hippocampi, we determined superoxide dismutase (SOD) activity and malondialdehyde (MDA) levels; carnosine concentration; protein expressions of Akt, mTOR and the autophagy markers LC3B and P62 and performed histopathological evaluations of the cornu ammonis 1 region.

Results: The HFD/STZ group showed increased blood glucose levels and decreased body weight compared to the CON group. However, there were no significant differences in body weight and blood glucose levels between carnosine-treated and -untreated HFD-STZ-induced diabetic rats. Diabetic animals showed obvious learning and memory impairments in the Morris water maze test compared to the CON group. Compared to those in the HFD/STZ group, carnosine increased SOD activity and decreased MDA levels, increased hippocampal carnosine concentration, increased p-Akt and p-mTOR expression, decreased LC3B and P62 expression, alleviated neuronal injuries, and improved cognitive performance in a dose-dependent manner.

Conclusion: Independent of any hyperglycemic effect, carnosine may improve mild cognitive impairments by mitigating oxidative stress, activating the Akt/mTOR pathway, and modulating autophagy in the hippocampus of type 2 diabetic rats.

在2型糖尿病大鼠模型中,肌肽通过激活Akt/mTOR通路和调节自噬逆转糖尿病相关认知衰退
肌肽可以抑制糖尿病的继发性并发症,并对神经退行性疾病显示出强大的神经保护活性。在这里,我们报告了肌肽通过调节自噬改善体内糖尿病相关的认知能力下降。方法:采用高脂饮食(HFD)和1次腹腔注射链脲佐菌素(STZ) 30 mg/kg诱导sd大鼠2型糖尿病。将大鼠随机分为5组:对照组(CON)、HFD/STZ组和3个胃内肌肽治疗组,分别给予低(100 mg/kg)、中(300 mg/kg)和高(900 mg/kg)治疗,持续12周。持续监测体重、血糖水平和认知功能。从切除的大鼠海马中,我们测定了超氧化物歧化酶(SOD)活性和丙二醛(MDA)水平;肌肽浓度;Akt、mTOR及自噬标志物LC3B、P62的蛋白表达,并对玉米氨1区进行组织病理学评价。结果:与CON组相比,HFD/STZ组血糖水平升高,体重下降。然而,肌肽处理和未处理的hfd - stz诱导的糖尿病大鼠的体重和血糖水平没有显著差异。与对照组相比,糖尿病动物在Morris水迷宫实验中表现出明显的学习和记忆障碍。与HFD/STZ组相比,肌肽增加SOD活性,降低MDA水平,增加海马肌肽浓度,增加p-Akt和p-mTOR表达,降低LC3B和P62表达,减轻神经元损伤,改善认知能力,呈剂量依赖性。结论:肌肽可能通过减轻2型糖尿病大鼠的氧化应激、激活Akt/mTOR通路和调节海马自噬来改善轻度认知障碍,而不受任何高血糖作用的影响。
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来源期刊
CiteScore
4.70
自引率
0.00%
发文量
46
审稿时长
2 months
期刊介绍: As a unique forum devoted exclusively to the study of cognitive dysfunction, ''Dementia and Geriatric Cognitive Disorders'' concentrates on Alzheimer’s and Parkinson’s disease, Huntington’s chorea and other neurodegenerative diseases. The journal draws from diverse related research disciplines such as psychogeriatrics, neuropsychology, clinical neurology, morphology, physiology, genetic molecular biology, pathology, biochemistry, immunology, pharmacology and pharmaceutics. Strong emphasis is placed on the publication of research findings from animal studies which are complemented by clinical and therapeutic experience to give an overall appreciation of the field.
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