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斯普拉格-道利大鼠气道中感觉神经和神经肽介导的舒张反应。

Sensory nerve- and neuropeptide-mediated relaxation responses in airways of Sprague-Dawley rats.

作者信息

Szarek J L, Stewart N L, Spurlock B, Schneider C

机构信息

Marshall University School of Medicine, Department of Pharmacology, Huntington, West Virginia 25704-9388, USA.

出版信息

J Appl Physiol (1985). 1995 May;78(5):1679-87. doi: 10.1152/jappl.1995.78.5.1679.

Abstract

We examined the role of sensory nerves in mediating nonadrenergic inhibitory responses in airway segments isolated from male Sprague-Dawley rats. In the presence of adrenergic blockade, capsaicin (Cap; 1 microM) elicited marked relaxation responses in isolated bronchi precontracted with bethanechol (Beth). Cap-induced inhibitory responses were unaffected by tetrodotoxin (TTX), were attenuated by incubation of the airway with indomethacin (Indo), phosphoramidon, or RP-67580, but were abolished by previous exposure of the airway to Cap and by denuding the epithelium. Substance P (SP; 1 microM), neurokinins A and B (1 microM), and calcitonin gene-related peptide (0.1 microM) relaxed Beth-contracted airway segments to a similar extent. The SP-induced responses were unaffected by adrenergic blockade or by pretreatment with either TTX, phosphoramidon, or Cap, but were attenuated by RP-67580 and abolished by Indo and by denuding the epithelium. In anesthetized mechanically ventilated rats, Cap (50 and 100 micrograms/kg i.v.) elicited a dose-dependent reversal of the increase in lung resistance induced by an infusion of Beth. The Cap-induced bronchodilation was unaffected by pretreatment with propranolol alone or in combination with hexamethonium. SP (44 nmol/kg iv) also evoked bronchodilatory responses in intact animals, which were unaffected by propranolol and hexamethonium but were abolished by treatment of the animals with Indo. Electrical-field stimulation (EFS) evoked nonadrenergic noncholinergic relaxation responses in contracted airway segments. These EFS-induced inhibitory responses were markedly attenuated by treatment of the airway segment with TTX, Cap, or RP-67580. We conclude that neuropeptides released from Cap-sensitive sensory nerves have potent inhibitory effects in rat airways that are mediated, in part, by activation of neurokonin NK1 receptors on epithelium and subsequent release of an inhibitory prostaglandin(s).

摘要

我们研究了感觉神经在介导从雄性Sprague-Dawley大鼠分离的气道节段中非肾上腺素能抑制反应中的作用。在存在肾上腺素能阻断的情况下,辣椒素(Cap;1微摩尔)在与氨甲酰甲胆碱(Beth)预收缩的离体支气管中引发明显的舒张反应。Cap诱导的抑制反应不受河豚毒素(TTX)影响,在用吲哚美辛(Indo)、磷酰胺或RP-67580孵育气道后减弱,但在气道预先暴露于Cap并去除上皮后被消除。P物质(SP;1微摩尔)、神经激肽A和B(1微摩尔)以及降钙素基因相关肽(0.1微摩尔)使Beth收缩的气道节段舒张程度相似。SP诱导的反应不受肾上腺素能阻断或用TTX、磷酰胺或Cap预处理的影响,但被RP-67580减弱,并被Indo和去除上皮消除。在麻醉的机械通气大鼠中,Cap(静脉注射50和100微克/千克)引起由输注Beth诱导的肺阻力增加的剂量依赖性逆转。Cap诱导的支气管舒张不受单独用普萘洛尔或与六甲铵联合预处理的影响。SP(静脉注射44纳摩尔/千克)在完整动物中也引起支气管舒张反应,不受普萘洛尔和六甲铵影响,但在用Indo处理动物后被消除。电场刺激(EFS)在收缩的气道节段中引发非肾上腺素能非胆碱能舒张反应。这些EFS诱导的抑制反应在用TTX、Cap或RP-67580处理气道节段后明显减弱。我们得出结论,从对Cap敏感的感觉神经释放的神经肽在大鼠气道中具有强大的抑制作用,部分是通过上皮上神经激肽NK1受体的激活以及随后抑制性前列腺素的释放介导的。

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