Astaxanthin attenuates glucose-induced liver injury in largemouth bass: role of p38MAPK and PI3K/Akt signaling pathways.

IF 6.1 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Cell and Bioscience Pub Date : 2024-09-19 DOI:10.1186/s13578-024-01304-7
Zhihong Liao, Xuanshu He, Anqi Chen, Jian Zhong, Sihan Lin, Yucai Guo, Xin Cui, Baoyang Chen, Wei Zhao, Jin Niu
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Abstract

Background: Astaxanthin (ASX) has been documented to exert beneficial influence on various processes in fish. Largemouth bass (Micropterus salmoides) serves as a common model for studying glucose-induced liver disease, making it imperative to investigate the regulatory mechanisms underlying its liver health.

Methods: Largemouth bass were fed with a control diet (CON), a high carbohydrate diet (HC), or a HC diet supplemented astaxanthin (HCA) for 8-weeks, followed by the glucose tolerance test (GTT). Primary hepatocytes were treated with low glucose and high glucose combined with different concentrations of astaxanthin for 48 h. The histopathology, enzymology, transcriptomics, molecular biology and cell biology were combined to investigate the mechanism of liver injury.

Results: This study provides evidence for the protective effects of ASX against growth performance reduction and hepatic liver injure in largemouth bass fed HC diet. In GTT, HCA diet exhibited an improvement in glucose tolerance following glucose loading. Although HCA diet did not restore the expression of insulin resistance-related genes in livers at different time during the GTT, the addition of ASX in the long-term HC diet did improve the insulin resistance pathway by regulating the PTP1B/PI3K/Akt signaling pathway. Hepatic transcriptome analyses showed that ASX plays an essential role in the modulation of glucose homeostasis in response to treated with HC diet. In in vitro study, ASX treatment resulted in an exaltation in cell viability and a reduction in the rate of cell apoptosis and reactive oxygen species (ROS). Additionally, astaxanthin was observed to improve apoptosis induced by high-glucose via p38MAPK/bcl-2/caspase-3 signaling pathway.

Conclusions: Astaxanthin exhibited a protective effect against apoptosis by regulating p38MAPK/bcl-2/caspase-3 pathway, and ameliorated insulin resistance by activating the PTP1B/PI3K/Akt pathway. This study elucidated the mechanism of astaxanthin in the liver injury of largemouth bass from a new perspective and provided a new target for the treatment of insulin resistance.

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虾青素可减轻葡萄糖诱导的大口鲈鱼肝损伤:p38MAPK 和 PI3K/Akt 信号通路的作用。
背景:据记载,虾青素(ASX)对鱼类的各种过程产生有益影响。大口鲈鱼(Micropterus salmoides)是研究葡萄糖诱导肝病的常见模型,因此研究其肝脏健康的调节机制势在必行:方法:用对照饮食(CON)、高碳水化合物饮食(HC)或添加虾青素(HCA)的高碳水化合物饮食喂养大口鲈鱼 8 周,然后进行葡萄糖耐量试验(GTT)。原代肝细胞经低糖和高糖联合不同浓度虾青素处理48小时后,结合组织病理学、酶学、转录组学、分子生物学和细胞生物学研究肝损伤的机制:本研究证明了虾青素对大嘴鲈生长性能下降和肝损伤的保护作用。在 GTT 中,HCA 日粮在葡萄糖负荷后显示出葡萄糖耐量的改善。虽然在 GTT 期间的不同时间段,HCA 日粮并不能恢复肝脏中胰岛素抵抗相关基因的表达,但在长期 HC 日粮中添加 ASX 可通过调节 PTP1B/PI3K/Akt 信号通路来改善胰岛素抵抗通路。肝脏转录组分析表明,ASX在HC饮食治疗后的葡萄糖稳态调节中发挥了重要作用。在体外研究中,ASX处理可提高细胞活力,降低细胞凋亡率和活性氧(ROS)。此外,还观察到虾青素通过p38MAPK/bcl-2/caspase-3信号通路改善了高葡萄糖诱导的细胞凋亡:结论:虾青素通过调节p38MAPK/bcl-2/caspase-3通路对细胞凋亡具有保护作用,并通过激活PTP1B/PI3K/Akt通路改善胰岛素抵抗。该研究从一个新的角度阐明了虾青素在大口鲈肝损伤中的作用机制,为治疗胰岛素抵抗提供了一个新的靶点。
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来源期刊
Cell and Bioscience
Cell and Bioscience BIOCHEMISTRY & MOLECULAR BIOLOGY-
CiteScore
10.70
自引率
0.00%
发文量
187
审稿时长
>12 weeks
期刊介绍: Cell and Bioscience, the official journal of the Society of Chinese Bioscientists in America, is an open access, peer-reviewed journal that encompasses all areas of life science research.
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