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参与肛门内括约肌神经支配的不同抑制性介质的药理学鉴定。

Pharmacological identification of different inhibitory mediators involved in the innervation of the internal anal sphincter.

作者信息

Tøttrup A, Knudsen M A, Hanberg Sørensen F, Glavind E B

机构信息

Dept. of Surgical Research, University Hospital of Aarhus, Denmark.

出版信息

Br J Pharmacol. 1995 May;115(1):158-62. doi: 10.1111/j.1476-5381.1995.tb16333.x.

Abstract
  1. Inhibitory non-adrenergic, non-cholinergic (NANC) responses were studied in isolated strips from the rabbit internal anal sphincter. 2. In the presence of atropine and guanethidine, transmural field stimulation induced frequency-dependent relaxations that reached a plateau at frequencies > or = 4 Hz. 3. These relaxations were inhibited by apamin (10(-6) M) and by N omega-nitro-L-arginine (L-NOARG, 10(-4) M). With these two substances in combination, relaxations were still seen in response to field stimulation, but only at frequencies > 2 Hz. 4. In the presence of both apamin (10(-6) M) and L-NOARG (10(-4) M), responses at high frequencies consisted of a fast relaxation followed by a slow return to prestimulus tension level. alpha-Chrymotrypsin hastens the return of tension to prestimulus level after high frequency stimulation. 5. Zinc-protoporphyrin IX, an inhibitor of haeme oxygenase, had a significant inhibitory effect on relaxations induced by transmural field stimulation. It was found, however, that responses to sodium nitroprusside and to isoprenaline (both 10(-9)-10(-4) M) were reduced comparably, indicating that the effect of zinc-protoporphyrin IX was unspecific. 6. It is concluded that pharmacological analysis allows identification of at least three distinguishable components of the inhibitory NANC innervation of the rabbit internal anal sphincter. The study does not allow conclusions about the role of carbon monoxide, a recently proposed mediator of NANC responses in opossum internal anal sphincter.
摘要
  1. 对兔内括约肌分离条带中的抑制性非肾上腺素能、非胆碱能(NANC)反应进行了研究。2. 在阿托品和胍乙啶存在的情况下,经壁场刺激诱导出频率依赖性舒张,在频率≥4 Hz时达到平台期。3. 这些舒张反应被蜂毒明肽(10⁻⁶ M)和Nⁿ-硝基-L-精氨酸(L-NOARG,10⁻⁴ M)抑制。当这两种物质联合使用时,对场刺激仍有舒张反应,但仅在频率>2 Hz时出现。4. 在蜂毒明肽(10⁻⁶ M)和L-NOARG(10⁻⁴ M)均存在的情况下,高频反应包括快速舒张,随后缓慢恢复到刺激前的张力水平。α-糜蛋白酶可加速高频刺激后张力恢复到刺激前水平。5. 血红素加氧酶抑制剂锌原卟啉IX对经壁场刺激诱导的舒张有显著抑制作用。然而,发现对硝普钠和异丙肾上腺素(均为10⁻⁹ - 10⁻⁴ M)的反应也有类似程度的降低,表明锌原卟啉IX的作用是非特异性的。6. 得出结论,药理学分析可鉴定出兔内括约肌抑制性NANC神经支配中至少三种可区分的成分。该研究无法得出关于一氧化碳作用的结论,一氧化碳是最近提出的负鼠内括约肌NANC反应的介质。

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本文引用的文献

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Carbon monoxide: a putative neural messenger.一氧化碳:一种假定的神经信使。
Science. 1993 Jan 15;259(5093):381-4. doi: 10.1126/science.7678352.

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