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食欲肽、食欲肽受体拮抗剂与心血管中枢调控

Orexin, orexin receptor antagonists and central cardiovascular control.

机构信息

Blood Pressure, Brain and Behavior Laboratory, School of Medical Sciences, University of New South Wales Sydney, NSW, Australia.

出版信息

Front Neurosci. 2013 Dec 30;7:257. doi: 10.3389/fnins.2013.00257.

Abstract

Orexin makes an important contribution to the regulation of cardiovascular function. When injected centrally under anesthesia, orexin increases blood pressure, heart rate and sympathetic nerve activity. This is consistent with the location of orexin neurons in the hypothalamus and the distribution of orexin terminals in the central autonomic network. Thus, the two orexin receptors, Ox1R and Ox2R, which have partly overlapping distributions in the brain, are expressed in the sympathetic preganglionic neurons (SPN) of the thoracic cord as well as in regions such as the pressor area of the rostral ventrolateral medulla (RVLM). Both Ox1R and Ox2R appear to contribute to the cardiovascular effects of orexin, although Ox1R is probably more important. Blockade of orexin receptors reduces the cardiovascular response to certain stressors, especially psychogenic stressors such as novelty, aggressive conspecifics and induced panic. Blockade of orexin receptors also reduces basal blood pressure and heart rate in spontaneous hypertensive rats, a model of essential hypertension. Thus, there is a link between psychogenic stress, orexin and elevated blood pressure. The use of dual orexin receptor antagonists (DORAs) and selective orexin receptor antagonists (SORAs) may be beneficial in the treatment of certain forms of hypertension.

摘要

食欲素对心血管功能的调节起着重要作用。在麻醉状态下中枢注射时,食欲素会升高血压、心率和交感神经活性。这与下丘脑食欲素神经元的位置以及中枢自主神经网络中食欲素末端的分布一致。因此,两种食欲素受体 Ox1R 和 Ox2R 在大脑中有部分重叠的分布,它们在胸段交感节前神经元(SPN)以及诸如延髓头端腹外侧区(RVLM)的加压区中表达。Ox1R 和 Ox2R 似乎都对食欲素的心血管作用有贡献,尽管 Ox1R 可能更为重要。食欲素受体阻断剂可降低对某些应激源(尤其是新奇、攻击性同种动物和诱发恐慌等心理应激源)的心血管反应。食欲素受体阻断剂还可降低自发性高血压大鼠(一种原发性高血压模型)的基础血压和心率。因此,心理应激、食欲素和血压升高之间存在关联。双重食欲素受体拮抗剂(DORAs)和选择性食欲素受体拮抗剂(SORAs)的应用可能有益于某些类型高血压的治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7801/3874580/b0af55a922f0/fnins-07-00257-g0001.jpg

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