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瘦素:缺氧鱼类食欲不振的线索。

Leptin: clue to poor appetite in oxygen-starved fish.

机构信息

Department of Biology and Chemistry, City University of Hong Kong, Kowloon, Hong Kong Special Administrative Region, People's Republic of China.

出版信息

Mol Cell Endocrinol. 2010 May 5;319(1-2):143-6. doi: 10.1016/j.mce.2010.01.018. Epub 2010 Jan 18.

Abstract

Hypoxia is the most widespread deleterious consequence of eutrophication and has become a major cause of fishery decline. One feature of chronic exposure to hypoxia in fish is inhibition of feeding. In this study, we investigated if the gene that encodes the appetite-suppressing hormone leptin is regulated by hypoxia in zebrafish (Danio rerio). Exposure of adult zebrafish to hypoxic conditions (1+/-0.2 mg O(2) L(-1)) for 4 and 10 days significantly increased leptin-a (zlep-a) mRNA levels in the liver. To evaluate the role of hypoxia-inducible factor 1 (HIF-1) in regulating zlep-a expression, zebrafish embryos were exposed to cobalt chloride (CoCl(2), a HIF-1 inducer) and overexpressed with HIF-1alpha mRNA. Both CoCl(2) treatment and HIF-1alpha overexpression markedly increased zlep-a expression in developing embryos, indicating the possible involvement of HIF-1 in zlep-a regulation. In vivo promoter analysis indicated that zlep-a promoter activity is found in the muscle fibers of zebrafish embryos and enhanced by CoCl(2). This is the first report to show that leptin gene expression in fish is regulated by hypoxia possibly via the involvement of HIF-1.

摘要

缺氧是富营养化最广泛的有害后果,已成为渔业衰退的主要原因之一。鱼类慢性缺氧的一个特征是摄食抑制。在这项研究中,我们研究了编码食欲抑制激素瘦素的基因是否受斑马鱼(Danio rerio)缺氧的调节。将成年斑马鱼暴露于缺氧条件(1+/-0.2 mg O2 L-1)4 和 10 天,可显著增加肝脏中瘦素-a(zlep-a)mRNA 水平。为了评估缺氧诱导因子 1(HIF-1)在调节 zlep-a 表达中的作用,将斑马鱼胚胎暴露于氯化钴(CoCl2,HIF-1 诱导剂)并过表达 HIF-1alpha mRNA。CoCl2 处理和 HIF-1alpha 过表达均可显著增加发育中胚胎的 zlep-a 表达,表明 HIF-1 可能参与了 zlep-a 的调节。体内启动子分析表明,zlep-a 启动子活性存在于斑马鱼胚胎的肌肉纤维中,并可被 CoCl2 增强。这是第一项表明鱼类瘦素基因表达受缺氧调节的报告,可能通过 HIF-1 的参与。

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