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人离体小肠:纵行肌对场刺激和外源性神经肽的运动反应。

Human isolated small intestine: motor responses of the longitudinal muscle to field stimulation and exogenous neuropeptides.

作者信息

Maggi C A, Patacchini R, Santicioli P, Giuliani S, Turini D, Barbanti G, Beneforti P, Misuri D, Meli A

机构信息

Pharmacology Department, A. Menarini Pharmaceuticals, Florence, Italy.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1989 Apr;339(4):415-23. doi: 10.1007/BF00736056.

Abstract

(1) Longitudinal muscle strips from the human small intestine (jejunum/ileum) responded to electrical field stimulation (1-50 Hz) with frequency-related primary contractions which were largely atropine- (3 microM) sensitive. When the tone was raised by addition of galanin (0.3-1 microM), prostaglandin (PG) E2 (1-10 microM) or neurokinin A (NKA, 0.1 microM), a frequency-related relaxation was evident which was potentiated by atropine. All the responses to field stimulation were abolished by tetrodotoxin (1 microM), thus indicating their neural origin. (2) The atropine-sensitive primary contraction to field stimulation was virtually abolished by omega conotoxin fraction GVIA (CTX, 0.1-0.3 microM) while the relaxations were CTX-resistant. The field stimulation-induced relaxations, which were observed in the presence of atropine and guanethidine (3 microM), were also unaffected by apamin (0.1 microM). (3) NKA and substance P (SP) produced a concentration- (1 nM-1 microM for both peptides) related contraction, NKA being about 53 times more potent than SP. [Pro9]SP sulphone and [MePhe7]-NKB, selective agonists of the NK-1 and NK-3 receptor, respectively, were barely effective. On the other hand, [beta Ala8]NKA(4-10), a selective NK-2 receptor agonist, had a potent contractile activity, similar to that of NKA. (4) Galanin (1 nM-1 microM) produced an atropine- and tetrodotoxin-resistant concentration-related contraction of longitudinal muscle of human isolated small intestine. The response to galanin did not show any sign of fading and was particularly suitable to study the evoked relaxations.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

(1) 取自人小肠(空肠/回肠)的纵行肌条对电场刺激(1 - 50赫兹)产生与频率相关的原发性收缩反应,这种反应在很大程度上对阿托品(3微摩尔)敏感。当通过添加甘丙肽(0.3 - 1微摩尔)、前列腺素(PG)E2(1 - 10微摩尔)或神经激肽A(NKA,0.1微摩尔)来提高张力时,明显出现与频率相关的舒张,且阿托品可增强这种舒张。对电场刺激的所有反应都被河豚毒素(1微摩尔)消除,这表明它们起源于神经。(2) 对电场刺激的阿托品敏感的原发性收缩几乎被ω - 芋螺毒素GVIA组分(CTX,0.1 - 0.3微摩尔)消除,而舒张对CTX有抗性。在阿托品和胍乙啶(3微摩尔)存在的情况下观察到的电场刺激诱导的舒张,也不受蜂毒明肽(0.1微摩尔)影响。(3) NKA和P物质(SP)产生浓度(两种肽均为1纳摩尔 - 1微摩尔)相关的收缩,NKA的效力约为SP的53倍。[Pro9]SP砜和[MePhe7]-NKB分别是NK - 1和NK - 3受体的选择性激动剂,几乎没有效果。另一方面,[βAla8]NKA(4 - 10),一种选择性NK - 2受体激动剂,具有强大的收缩活性,与NKA相似。(4) 甘丙肽(1纳摩尔 - 1微摩尔)对人离体小肠纵行肌产生与浓度相关的、对阿托品和河豚毒素有抗性的收缩。对甘丙肽的反应没有任何衰减迹象,特别适合研究诱发的舒张。(摘要截断于250字)

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