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大鼠胃底抑制性传递中的一氧化氮能与嘌呤能相互作用。

Nitrergic and purinergic interplay in inhibitory transmission in rat gastric fundus.

作者信息

Vetri T, Bonvissuto F, Marino A, Postorino A

机构信息

Dipartimento di Biologia cellulare e dello Sviluppo, Laboratorio di Fisiologia Generale, Università degli Studi di Palermo, Viale delle Scienze, Parco D'Orleans II, Palermo, Italy.

出版信息

Auton Autacoid Pharmacol. 2007 Jul;27(3):151-7. doi: 10.1111/j.1474-8673.2007.00406.x.

Abstract

1 This study was undertaken to analyse the involvement of ATP in non-adrenergic non- cholinergic (NANC) relaxation and possible interplay between nitrergic and purinergic systems in rat gastric fundus. 2 Experiments were performed in vitro on strips of longitudinal muscle from rat gastric fundus, recording the mechanical activity as changes in isometric force. In addition, NO release induced by different experimental conditions was assayed. 3 Under NANC conditions in serotonin-precontracted strips, electrical field stimulation (EFS) elicited a tetrodotoxin (TTX)-sensitive relaxation accompanied by nitric oxide (NO) release. This effect was antagonized by pretreatment with the NO synthase antagonist Nomega-nitro-L-arginine (L-NA) or by desensitization of purinergic receptors. Purinergic desensitization was also able to further antagonize the residual EFS-induced relaxation remaining after L-NA treatment. Exogenously applied NO [delivered as sodium nitroprusside (SNP)] or ATP (and related purines) induced concentration-dependent, TTX-insensitive relaxant responses. ATP also induced the release of NO. A reduction in the responses to ATP was observed in the presence of L-NA. In contrast, SNP-induced relaxation remained unchanged after desensitization of purinergic receptors. Finally, apamin, a blocker of the small conductance Ca2+ -dependent K+ channels, reduced the amplitude of the muscular relaxation evoked by either EFS, ATP or SNP. 4 In conclusion, this study provides evidence that in rat gastric fundus, ATP is one of the inhibitory transmitters released from NANC intramural neurones acting directly on the muscle, through receptors coupled to apamin-sensitive Ca2+ -dependent K+ channels and, indirectly, through the stimulation of NO production.

摘要

1 本研究旨在分析三磷酸腺苷(ATP)在大鼠胃底非肾上腺素能非胆碱能(NANC)舒张中的作用,以及一氧化氮能和嘌呤能系统之间可能的相互作用。2 实验在体外对大鼠胃底纵行肌条进行,记录等长力变化作为机械活动。此外,还检测了不同实验条件下诱导的一氧化氮(NO)释放。3 在5-羟色胺预收缩条带的NANC条件下,电场刺激(EFS)引起对河豚毒素(TTX)敏感的舒张,并伴有一氧化氮(NO)释放。这种效应可被一氧化氮合酶拮抗剂Nω-硝基-L-精氨酸(L-NA)预处理或嘌呤能受体脱敏所拮抗。嘌呤能脱敏也能够进一步拮抗L-NA处理后残留的EFS诱导的舒张。外源性应用的NO [以硝普钠(SNP)形式提供] 或ATP(及相关嘌呤)诱导浓度依赖性、对TTX不敏感的舒张反应。ATP还诱导NO释放。在存在L-NA的情况下,观察到对ATP的反应降低。相反,嘌呤能受体脱敏后,SNP诱导的舒张保持不变。最后,小电导钙依赖性钾通道阻滞剂蜂毒明肽降低了EFS、ATP或SNP引起的肌肉舒张幅度。4 总之,本研究提供了证据表明,在大鼠胃底,ATP是NANC壁内神经元释放的抑制性递质之一,它通过与蜂毒明肽敏感的钙依赖性钾通道偶联的受体直接作用于肌肉,并通过刺激NO生成间接发挥作用。

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