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胃饥饿素对小鼠胃平滑肌和后肢骨骼肌影响的实验研究

Experimental study on the effects of ghrelin on gastric smooth muscle and posterior limb skeletal muscle in mice.

作者信息

Wang Ping, Yu Cunbo, Li Yibing, Zhang Xiaoxiao, Yao Xueli, Zhang Yingjian

机构信息

College of Basic Medicine and Forensic Medicine, Henan University of Science and Technology, Luoyang, Henan, China.

Department of Gastroenterology, The First Affiliated Hospital, College of Clinical Medicine, Henan University of Science and Technology, Luoyang, Henan, China.

出版信息

Front Med (Lausanne). 2025 Jul 28;12:1631707. doi: 10.3389/fmed.2025.1631707. eCollection 2025.

Abstract

INTRODUCTION

This study aims to systematically explore the regulatory effects of ghrelin on hindlimb skeletal muscle function and gastrointestinal smooth muscle in mice. The objective is to elucidate the improvement effects of ghrelin on functional constipation through regulating skeletal muscle function and gastrointestinal motility, providing new theoretical support for the prevention and treatment of functional constipation.

METHODS

Dexamethasone-induced cell models and tail suspension-induced mouse models were employed to analyze the regulatory effect of ghrelin on the PI3K-Akt-mTORC1 signaling pathway. Additionally, a loperamide-induced constipation mouse model was used to evaluate the effects of ghrelin on fecal output, gastric motility, and smooth muscle activity. Experimental techniques included Western blotting, enzyme-linked immunosorbent assay (ELISA), histopathological staining, phenol red assay, and quantitative analyses of Ca and ATP to comprehensively assess the impact of ghrelin on muscle atrophy and gastrointestinal function.

RESULTS

The results showed that, , ghrelin significantly upregulated the expression of p-AKT and reduced the levels of p-Foxo3a, effectively alleviating muscle atrophy. , the muscle condition of mice was improved and the expression of atrophy-related proteins (MAFbx and MuRF1) decreased, promoting the functional recovery of hindlimb muscles. In constipated mice, ghrelin increased fecal water content and defecation frequency, and accelerated gastric emptying, findings consistent with elevated ghrelin levels in serum and tissue. Moreover, ghrelin promoted calcium ion influx and ATP production in gastric smooth muscle cells, thereby enhancing gastrointestinal motility.

DISCUSSION

In conclusion, ghrelin effectively alleviates muscle atrophy by activating the PI3K-Akt-mTORC1 signaling pathway, and improves gastrointestinal motility by enhancing smooth muscle activity. These findings highlight ghrelin's potential as an effective therapy for functional constipation.

摘要

引言

本研究旨在系统探讨胃饥饿素对小鼠后肢骨骼肌功能和胃肠平滑肌的调节作用。目的是阐明胃饥饿素通过调节骨骼肌功能和胃肠蠕动对功能性便秘的改善作用,为功能性便秘的防治提供新的理论支持。

方法

采用地塞米松诱导的细胞模型和尾悬吊诱导的小鼠模型分析胃饥饿素对PI3K-Akt-mTORC1信号通路的调节作用。此外,使用洛哌丁胺诱导的便秘小鼠模型评估胃饥饿素对粪便排出量、胃动力和平滑肌活性的影响。实验技术包括蛋白质免疫印迹法、酶联免疫吸附测定(ELISA)、组织病理学染色、酚红试验以及钙和三磷酸腺苷(ATP)的定量分析,以全面评估胃饥饿素对肌肉萎缩和胃肠功能的影响。

结果

结果显示,胃饥饿素显著上调p-AKT的表达并降低p-Foxo3a的水平,有效减轻肌肉萎缩。此外,小鼠的肌肉状况得到改善,萎缩相关蛋白(MAFbx和MuRF1)的表达降低,促进了后肢肌肉的功能恢复。在便秘小鼠中,胃饥饿素增加粪便含水量和排便频率,并加速胃排空,这些结果与血清和组织中胃饥饿素水平升高一致。此外,胃饥饿素促进胃平滑肌细胞中钙离子内流和ATP生成,从而增强胃肠蠕动。

讨论

总之,胃饥饿素通过激活PI3K-Akt-mTORC1信号通路有效减轻肌肉萎缩,并通过增强平滑肌活性改善胃肠蠕动。这些发现突出了胃饥饿素作为功能性便秘有效治疗方法的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e059/12336119/413b8f8aa581/fmed-12-1631707-g001.jpg

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