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[自主神经系统与前列腺生理学。α-肾上腺素能系统的特异性]

[Autonomic nervous system and prostatic physiology. Specific features of the alpha-adrenergic system].

作者信息

Mottet N, Costa P, Bali J P

机构信息

Service d'Urologie, CHU Gaston Doumergue, Nîmes, France.

出版信息

Prog Urol. 1999 Feb;9(1):26-36.

PMID:10212950
Abstract

A better understanding of the rich autonomic innervation of the prostate allows more effective treatment of voiding disorders secondary to benign prostatic hyperplasia. The glandular contingent possesses mainly cholinergic innervation (M2 muscarinic receptors). Smooth muscle cells are richly supplied with alpha and beta catecholaminergic receptors, involved in muscle contraction and muscle relaxation, respectively, but they may also be involved in growth. These alpha receptors, divided into 2 families (alpha 1 and alpha 2), belong to the family of G protein-coupled seven membrane-spanning helix receptors. The genes, followed by the recombinant proteins of 3 subtypes of alpha 1 receptors have been described: alpha 1-a, -b, -d. In the prostate, these receptors are predominantly located in the stroma, mainly in the centroprostatic region. The mRNA present mainly code for the alpha 1a subtype. The use of specific agonists and antagonists shows that these receptors control smooth muscle contraction according to a mechanism initially considered to be of the alpha 1a type. However, their low affinity for prazosin and the development of new alpha 1 blocking agents is in favour of the involvement of a different functional subtype: alpha 1L. This difference could be explained by a different conformation of the receptor or by different coupling mechanisms. The subtype involved in prostatic smooth muscle contraction has yet to be characterized.

摘要

对前列腺丰富的自主神经支配有更深入的了解,有助于更有效地治疗良性前列腺增生继发的排尿障碍。腺性部分主要具有胆碱能神经支配(M2毒蕈碱受体)。平滑肌细胞富含α和β肾上腺素能受体,分别参与肌肉收缩和肌肉舒张,但它们也可能参与生长。这些α受体分为2个家族(α1和α2),属于G蛋白偶联的七跨膜螺旋受体家族。已经描述了α1受体3个亚型的基因及其重组蛋白:α1-a、-b、-d。在前列腺中,这些受体主要位于基质中,主要在前列腺中央区域。存在的mRNA主要编码α1a亚型。使用特异性激动剂和拮抗剂表明,这些受体根据最初被认为是α1a型的机制控制平滑肌收缩。然而,它们对哌唑嗪的低亲和力以及新的α1阻滞剂的出现支持了一种不同功能亚型α1L的参与。这种差异可以通过受体的不同构象或不同的偶联机制来解释。参与前列腺平滑肌收缩的亚型尚未得到明确鉴定。

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