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α2肾上腺素能受体介导的犬离体回结肠连接处氮能神经支配的调节

Alpha 2-adrenoceptor-mediated modulation of the nitrergic innervation of the canine isolated ileocolonic junction.

作者信息

Boeckxstaens G E, De Man J G, Pelckmans P A, Herman A G, Van Maercke Y M

机构信息

Division of Gastroenterology, Faculty of Medicine, University of Antwerp, Antwerpen-Wilrijk, Belgium.

出版信息

Br J Pharmacol. 1993 Aug;109(4):1079-84. doi: 10.1111/j.1476-5381.1993.tb13732.x.

Abstract
  1. The effects of specific alpha-adrenoceptor agonists and antagonists on electrically-evoked non-adrenergic non-cholinergic (NANC) relaxations, previously demonstrated as nitrergic, were investigated in isolated circular muscle strips of the canine ileocolonic junction. 2. During a substance P-induced contraction and in the presence of atropine and guanethidine, the specific alpha 1-adrenoceptor agonist, phenylephrine and antagonist, prazosin, as well as the specific alpha 2-adrenoceptor antagonist, yohimbine, had no effect on the NANC relaxations evoked by electrical field stimulation. In contrast, clonidine and the more specific alpha 2-adrenoceptor agonist, UK-14,304, significantly reduced the electrically-induced relaxations, preferentially those in response to low frequency stimulation. The inhibitory effect of UK-14,304 on these relaxations was antagonized by yohimbine. 3. During a noradrenaline-induced contraction, clonidine, but not UK-14,304 significantly augmented the relaxations to electrical stimulation. 4. The adrenoceptor agonists and antagonists used had no effect on concentration-response curves to NO or on the relaxation induced by nitroglycerin. 5. These results indicate that stimulation of prejunctional alpha 2-adrenoceptors inhibits the nitrergic NANC relaxations induced by field stimulation and thus suggest prejunctional regulation of nitric oxide release via alpha 2-adrenoceptors in the canine ileocolonic junction.
摘要
  1. 在犬回结肠连接处的离体环形肌条中,研究了特定α-肾上腺素能受体激动剂和拮抗剂对电诱发的非肾上腺素能非胆碱能(NANC)舒张的影响,此前已证明这种舒张是由一氧化氮介导的。2. 在P物质诱发的收缩过程中,且存在阿托品和胍乙啶的情况下,特定的α1-肾上腺素能受体激动剂去氧肾上腺素和拮抗剂哌唑嗪,以及特定的α2-肾上腺素能受体拮抗剂育亨宾,对电场刺激诱发的NANC舒张均无影响。相比之下,可乐定和更具特异性的α2-肾上腺素能受体激动剂UK-14,304显著降低了电诱发的舒张,尤其是对低频刺激的反应。UK-14,304对这些舒张的抑制作用可被育亨宾拮抗。3. 在去甲肾上腺素诱发的收缩过程中,可乐定而非UK-14,304显著增强了对电刺激的舒张反应。4. 所使用的肾上腺素能受体激动剂和拮抗剂对一氧化氮的浓度-反应曲线或硝酸甘油诱发的舒张均无影响。5. 这些结果表明,刺激节前α2-肾上腺素能受体会抑制电场刺激诱发的一氧化氮能NANC舒张,因此提示在犬回结肠连接处通过α2-肾上腺素能受体对一氧化氮释放进行节前调节。

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