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肽类及其他物质在血管自主神经和感觉神经元共同传递中的作用。

Roles of peptides and other substances in cotransmission from vascular autonomic and sensory neurons.

作者信息

Morris J L, Gibbins I L, Kadowitz P J, Herzog H, Kreulen D L, Toda N, Claing A

机构信息

Department of Anatomy and Histology, School of Medicine, Flinders University of South Australia, Adelaide.

出版信息

Can J Physiol Pharmacol. 1995 May;73(5):521-32. doi: 10.1139/y95-067.

Abstract

Blood vessels may be innervated by up to three major classes of neurons: sympathetic vasoconstrictor neurons; sympathetic or parasympathetic vasodilator neurons; and peripheral fibres of small diameter sensory neurons, which can mediate vasodilation. Most vascular neurons utilise multiple transmitters, including neuropeptides and small nonpeptides such as ATP or nitric oxide, often in addition to noradrenaline or acetylcholine. Subpopulations of each major class of vascular neurons innervating different vascular segments may contain different combinations of neurotransmitters. Furthermore, the same population of neurons can release different cotransmitters in response to different patterns of stimulation. In general, peptides mediate slower and more long lasting changes in vascular resistance than do nonpeptides. Thus, autonomic and sensory neurons are well adapted to produce qualitatively different vascular effects in response to different types of afferent input. The major challenge for the future is to develop new antagonists for many of the substances colocalised in vascular neurons, particularly neuropeptides. These agents will allow us to precisely determine the relative roles of multiple cotransmitters, and are likely to provide therapeutic agents that can be targeted to specific regions of the vasculature.

摘要

血管可能受多达三类主要神经元支配

交感缩血管神经元;交感或副交感舒血管神经元;以及小直径感觉神经元的外周纤维,它们可介导血管舒张。大多数血管神经元利用多种递质,包括神经肽和小的非肽类物质,如三磷酸腺苷(ATP)或一氧化氮,通常除了去甲肾上腺素或乙酰胆碱之外还会利用这些物质。支配不同血管节段的每一类主要血管神经元的亚群可能含有不同的神经递质组合。此外,同一群神经元可根据不同的刺激模式释放不同的共递质。一般来说,与非肽类物质相比,肽类物质介导的血管阻力变化更缓慢且持续时间更长。因此,自主神经和感觉神经元能够很好地适应,根据不同类型的传入输入产生性质不同的血管效应。未来的主要挑战是为许多共定位在血管神经元中的物质,特别是神经肽,开发新的拮抗剂。这些药物将使我们能够精确确定多种共递质的相对作用,并可能提供可靶向血管系统特定区域的治疗药物。

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