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利拉鲁肽通过 NRF2 信号通路减轻 Zucker 糖尿病 fatty 大鼠肝糖脂毒性诱导的肝细胞凋亡。

Liraglutide reduces hepatic glucolipotoxicity‑induced liver cell apoptosis through NRF2 signaling in Zucker diabetic fatty rats.

机构信息

The MOH Key Laboratory of Geriatrics, Beijing Hospital, National Center of Gerontology, Beijing 100730, P.R. China.

Department of Encephalopathy, Medical Department of Chinese Medicine, Shandong University of Traditional Chinese Medicine, Jinan, Shandong 250355, P.R. China.

出版信息

Mol Med Rep. 2018 Jun;17(6):8316-8324. doi: 10.3892/mmr.2018.8919. Epub 2018 Apr 23.

DOI:10.3892/mmr.2018.8919
PMID:29693190
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5984007/
Abstract

The primary aim of the present study was to evaluate the effects of liraglutide on glucolipotoxicity‑induced liver cell apoptosis and the underlying mechanisms in Zucker diabetic fatty (ZDF) rats. The results revealed that liraglutide significantly decreased the body weight, hyperglycemia and hyperlipidemia of ZDF rats relative to those of Zucker lean (ZL) rats (P<0.05). Furthermore, the reduced liver cell apoptosis was observed in the ZDF rats following 6 weeks of liraglutide therapy. These data validated the beneficial effects of liraglutide on diabetic and obese ZDF rats. In addition, novel data was obtained that demonstrated that liraglutide treatment increased the expression of the antioxidant transcription factor nuclear factor‑erythroid 2‑related factor 2 (NRF2), as well as the transcription of downstream target genes, including nicotinamide adenine dinucleotide phosphate quinone dehydrogenase 1 and heme oxygenase‑1 (P<0.05). Additionally, serum and hepatic GSH and SOD levels increased following liraglutide therapy (P<0.05). Hence, it was proposed that liraglutide may enhance the antioxidant activity of liver cells by activating the NRF2 signaling pathway, thereby reducing liver cell apoptosis induced by glucolipotoxicity in ZDF rats, which may shed light on the application of liraglutide in the treatment of diabetes‑ and obesity‑induced liver injury.

摘要

本研究的主要目的在于评估利拉鲁肽对糖脂毒性诱导的肝实质细胞凋亡的影响及其在 Zucker 糖尿病肥胖(ZDF)大鼠中的作用机制。结果显示,与 Zucker 正常(ZL)大鼠相比,利拉鲁肽显著降低了 ZDF 大鼠的体重、高血糖和高血脂(P<0.05)。此外,经过 6 周的利拉鲁肽治疗后,ZDF 大鼠的肝实质细胞凋亡减少。这些数据验证了利拉鲁肽对糖尿病和肥胖 ZDF 大鼠的有益作用。此外,还获得了新的数据,表明利拉鲁肽治疗增加了抗氧化转录因子核因子-红细胞 2 相关因子 2(NRF2)的表达,以及下游靶基因的转录,包括烟酰胺腺嘌呤二核苷酸磷酸醌脱氢酶 1 和血红素加氧酶-1(P<0.05)。此外,利拉鲁肽治疗后血清和肝 GSH 和 SOD 水平增加(P<0.05)。因此,提出利拉鲁肽可能通过激活 NRF2 信号通路增强肝实质细胞的抗氧化活性,从而减少 ZDF 大鼠糖脂毒性诱导的肝实质细胞凋亡,这可能为利拉鲁肽在治疗糖尿病和肥胖相关肝损伤中的应用提供思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9993/5984007/e1cd01501bb1/MMR-17-06-8316-g04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9993/5984007/8ce0012a3dc7/MMR-17-06-8316-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9993/5984007/927ed7c3ae3e/MMR-17-06-8316-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9993/5984007/6dde9a41d31d/MMR-17-06-8316-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9993/5984007/e1cd01501bb1/MMR-17-06-8316-g04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9993/5984007/8ce0012a3dc7/MMR-17-06-8316-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9993/5984007/927ed7c3ae3e/MMR-17-06-8316-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9993/5984007/6dde9a41d31d/MMR-17-06-8316-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9993/5984007/e1cd01501bb1/MMR-17-06-8316-g04.jpg

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2
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Sci Rep. 2017 Aug 14;7(1):8008. doi: 10.1038/s41598-017-06712-z.
3
Liraglutide improves liver microvascular dysfunction in cirrhosis: Evidence from translational studies.
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Nutrients. 2023 Mar 17;15(6):1456. doi: 10.3390/nu15061456.
4
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Mediators Inflamm. 2023 Jan 29;2023:8974960. doi: 10.1155/2023/8974960. eCollection 2023.
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7
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