Heinonen M V, Purhonen A K, Mäkelä K A, Herzig K H
Department of Biotechnology and Molecular Medicine, A. I. Virtanen Institute for Molecular Sciences, University of Kuopio, Kuopio, Finland.
Acta Physiol (Oxf). 2008 Apr;192(4):471-85. doi: 10.1111/j.1748-1716.2008.01836.x. Epub 2008 Feb 22.
Orexin A (OXA) and orexin B were originally isolated as hypothalamic peptides regulating sleep, wakefulness and feeding. However, growing evidence suggests that orexins have major functions also in the peripheral tissues. Central orexigenic pathways originating from medulla activate the hypothalamus-pituitary axis and can influence the sympathetic tone. Orexins and their receptors are widely dispersed throughout the intestine, where orexin receptors are regulated by the nutritional status, affect insulin secretion and intestinal motility. Although the primary source of the peptide has not been elucidated, OXA is detected in plasma and its level varies in response to the metabolic state. In this review, we focus on the current knowledge on peripheral functions of orexins and discuss possible endocrine, paracrine and neurocrine roles.
食欲素A(OXA)和食欲素B最初是作为调节睡眠、觉醒和进食的下丘脑肽被分离出来的。然而,越来越多的证据表明,食欲素在周围组织中也具有重要功能。源自延髓的中枢促食欲途径激活下丘脑-垂体轴,并可影响交感神经张力。食欲素及其受体广泛分布于整个肠道,在肠道中食欲素受体受营养状态调节,影响胰岛素分泌和肠道蠕动。尽管该肽的主要来源尚未阐明,但在血浆中可检测到OXA,其水平会随代谢状态而变化。在本综述中,我们聚焦于目前关于食欲素外周功能的知识,并讨论其可能的内分泌、旁分泌和神经分泌作用。