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Nesfatin-1作为爬行动物黄斑半叶趾虎体内葡萄糖稳态的关键调节因子。

Nesfatin-1 as a crucial mediator of glucose homeostasis in the reptile, Hemidactylus flaviviridis.

作者信息

Dotania Krittika, Tripathy Mamta, Rai Umesh

机构信息

Department of Zoology, University of Delhi, Delhi, 110007, India.

University of Jammu, Jammu and Kashmir, 180006, India.

出版信息

Sci Rep. 2024 Dec 30;14(1):31565. doi: 10.1038/s41598-024-74371-y.

Abstract

Nesfatin-1 is a crucial regulator of energy homeostasis in mammals and fishes, however, its metabolic role remains completely unexplored in amphibians, reptiles, and birds. Therefore, present study elucidates role of nesfatin-1 in glucose homeostasis in wall lizard wherein fasting stimulated hepatic nucb2/nesfatin-1, glycogen phosphorylase (glyp), phosphoenolpyruvate carboxykinase (pepck), and fructose 1,6-bisphosphatase (fbp), while feeding upregulated pancreatic nucb2/nesfatin-1 and insulin, suggesting towards tissue-specific dual role of nesfatin-1 in glucoregulation. The glycogenolytic/gluconeogenic role of nesfatin-1 was further confirmed by an increase in media glucose levels along with heightened hepatic pepck and fbp expression and concomitant decline in liver glycogen content in nesfatin-1-treated liver of wall lizard. Moreover, treatment with nesfatin-1 stimulated insulin expression in pancreas while insulin downregulated pancreatic nucb2/nesfatin-1. Further, prolonged fasting induced elevated nucb2/nesfatin-1, and lipolytic markers, adipose triglyceride lipase (atgl) and monoglyceride lipase (mgl) in adipose tissue implicate nesfatin-1 in lipolysis which is substantiated by nesfatin-1-mediated direct upregulation of atgl and mgl. Our study provides the first comprehensive overview of tissue-dependent role of nesfatin-1 in regulating energy homeostasis in a reptile.

摘要

Nesfatin-1是哺乳动物和鱼类能量稳态的关键调节因子,然而,其在两栖动物、爬行动物和鸟类中的代谢作用仍完全未被探索。因此,本研究阐明了nesfatin-1在壁蜥葡萄糖稳态中的作用,其中禁食刺激肝脏中的nucb2/nesfatin-1、糖原磷酸化酶(glyp)、磷酸烯醇丙酮酸羧激酶(pepck)和果糖1,6-二磷酸酶(fbp),而进食则上调胰腺中的nucb2/nesfatin-1和胰岛素,这表明nesfatin-1在葡萄糖调节中具有组织特异性双重作用。nesfatin-1的糖原分解/糖异生作用通过壁蜥nesfatin-1处理的肝脏中培养基葡萄糖水平的升高、肝脏pepck和fbp表达的增强以及肝脏糖原含量的相应下降得到进一步证实。此外,nesfatin-1处理刺激胰腺中胰岛素的表达,而胰岛素则下调胰腺中的nucb2/nesfatin-1。此外,长期禁食诱导脂肪组织中nucb2/nesfatin-1以及脂解标志物脂肪甘油三酯脂肪酶(atgl)和甘油单酯脂肪酶(mgl)升高,这表明nesfatin-1参与脂解作用,nesfatin-1介导的atgl和mgl的直接上调证实了这一点。我们的研究首次全面概述了nesfatin-1在调节爬行动物能量稳态中的组织依赖性作用。

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