Ma Jingjing, Liu Yuanyuan, Hu Junya, Liu Xingjing, Xia Yin, Xia Wenqing, Shen Ziyang, Kong Xiaocen, Wu Xia, Mao Li, Li Qian
Department of Endocrinology, Nanjing First Hospital, Nanjing Medical University, 68 Changle Road, Qinhuai District, Nanjing, 21006, China.
Department of Endocrinology, The Affifiliated Huaian No. 1 People's Hospital of Nanjing Medical University, Huai'an, 223300, China.
Endocrine. 2025 Feb;87(2):486-497. doi: 10.1007/s12020-024-04013-w. Epub 2024 Sep 2.
High-fat diet (HFD) currently is reported that in connection with cognitive impairment. Tirzepatide is a novel dual receptor agonist for glycemic control. But whether Tirzepatide exerts a protective effect in HFD-related cognitive impairment remains to be explore.
During the study, the cognitive dysfunction mice model induced by HFD were established. The expressions synapse-associated protein and other target proteins were detected. The oxidative stress parameters, levels of inflammatory cytokine were also detected.
Our findings proved that Tirzepatide administration attenuates high fat diet-related cognitive impairment. Tirzepatide administration suppresses microglia activation, alleviates oxidative stress as well as suppressed the expression of NLRP3 in HFD mice by up-regulating SIRT3 expression. In conclusion, Tirzepatide attenuates HFD-induced cognitive impairment through reducing oxidative stress and neuroinflammation via SIRT3-NLRP3 signaling.
This study suggest that Tirzepatide has neuroprotective effects in HFD-related cognitive dysfunction mice model, which provides a promising treatment of HFD-related cognitive impairment.
目前有报道称高脂饮食(HFD)与认知障碍有关。替尔泊肽是一种用于血糖控制的新型双受体激动剂。但替尔泊肽在HFD相关认知障碍中是否发挥保护作用仍有待探索。
在研究过程中,建立了由HFD诱导的认知功能障碍小鼠模型。检测突触相关蛋白和其他靶蛋白的表达。还检测了氧化应激参数、炎性细胞因子水平。
我们的研究结果证明,给予替尔泊肽可减轻高脂饮食相关的认知障碍。给予替尔泊肽可抑制小胶质细胞活化,减轻氧化应激,并通过上调SIRT3表达抑制HFD小鼠中NLRP3的表达。总之,替尔泊肽通过SIRT3-NLRP3信号通路减轻氧化应激和神经炎症,从而减轻HFD诱导的认知障碍。
本研究表明,替尔泊肽在HFD相关认知功能障碍小鼠模型中具有神经保护作用,为HFD相关认知障碍提供了一种有前景的治疗方法