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食欲素能/下丘脑泌素能系统的功能。

Functions of the orexinergic/hypocretinergic system.

作者信息

Kukkonen Jyrki P, Holmqvist Tomas, Ammoun Sylwia, Akerman Karl E O

机构信息

Laboratory of Cell Physiology, Department of Neuroscience, Division of Physiology, Uppsala University, Biomedical Center, SE-75123 Uppsala, Sweden.

出版信息

Am J Physiol Cell Physiol. 2002 Dec;283(6):C1567-91. doi: 10.1152/ajpcell.00055.2002.

Abstract

Orexin A and orexin B are hypothalamic peptides that act on their targets via two G protein-coupled receptors (OX1 and OX2 receptors). In the central nervous system, the cell bodies producing orexins are localized in a narrow region within the lateral hypothalamus and project mainly to regions involved in feeding, sleep, and autonomic functions. Via putative pre- and postsynaptic effects, orexins increase synaptic activity in these regions. In isolated neurons and cells expressing recombinant receptors orexins cause Ca2+ elevation, which is mainly dependent on influx. The activity of orexinergic cells appears to be controlled by feeding- and sleep-related signals via a variety of neurotransmitters/hormones from the brain and other tissues. Orexins and orexin receptors are also found outside the central nervous system, particularly in organs involved in feeding and energy metabolism, e.g., gastrointestinal tract, pancreas, and adrenal gland. In the present review we focus on the physiological properties of the cells that secrete or respond to orexins.

摘要

食欲素A和食欲素B是下丘脑肽,它们通过两种G蛋白偶联受体(OX1和OX2受体)作用于其靶标。在中枢神经系统中,产生食欲素的细胞体位于下丘脑外侧的一个狭窄区域,并主要投射到参与进食、睡眠和自主功能的区域。通过假定的突触前和突触后效应,食欲素增加这些区域的突触活动。在表达重组受体的分离神经元和细胞中,食欲素会导致Ca2+升高,这主要依赖于内流。食欲素能细胞的活性似乎受到来自大脑和其他组织的多种神经递质/激素的进食和睡眠相关信号的控制。在中枢神经系统之外也发现了食欲素和食欲素受体,特别是在参与进食和能量代谢的器官中,如胃肠道、胰腺和肾上腺。在本综述中,我们重点关注分泌食欲素或对食欲素作出反应的细胞的生理特性。

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