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首页> 外文期刊>Japanese Journal of Pharmacology >Tachykinin-Induced Contractions in the Circular Muscle of Guinea Pig Ileumt
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Tachykinin-Induced Contractions in the Circular Muscle of Guinea Pig Ileumt

机译:速激肽诱导的豚鼠腹肌环形肌肉收缩

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References(30) Cited-By(4) Actions of substance P (SP, 10-9 to 10-6 M), neurokinin A (NKA, 10-9 to 10-6 M) and neurokinin B (NKB, 10-10 to 10-6 M) in the circular muscle of guinea pig ileum were investigated in segment and strip preparations, in which methacholine produced similar contractions. In the segment preparations, three tachykinins produced repeatedly occurring twitch-like contractions. Their efficacies were similar with the same maximal contractions, but their potencies were different (NKB > NKA = SP). Latency (38 sec) was observed before the initiation of contractions in response to NKA, but not to SP or NKB. Atropine (10-6 M) and tetrodotoxin (3×10-7M) did not affect NKA-induced contractions, but inhibited SP and NKB-induced contractions; the dose-response curves for SP and NKB were rightwardly shifted by atropine. The treatment with atropine brought out latency in the responses for NKB. In the strip preparations, SP did not substantially induce contractions, but NKA and NKB produced twitch-like contractions after latent periods of 28 and 36 sec, respectively. The efficacy of NKA was similar to that in segment preparations, while that of NKB was much lower in strip preparations. Unlike in segment preparations, atropine did not inhibit contractions induced by the two tachykinins in strip preparations. These results suggest that tachykinins induce contractions through myogenic and neurogenic mechanisms, the latter of which may be inoperative in strip preparations.
机译:参考文献(30)被引用的(4)物质P(SP,10-9至10-6 M),神经激肽A(NKA,10-9至10-6 M)和神经激肽B(NKB,10-10)的作用在段和条状制剂中研究了豚鼠回肠的环形肌肉中最大至10-6 M)的浓度,其中乙酰甲胆碱产生类似的收缩。在分段制剂中,三种速激肽产生反复发生的抽搐样收缩。在最大收缩相同的情况下,它们的功效相似,但功效不同(NKB> NKA = SP)。在响应NKA而不是SP或NKB收缩开始之前观察到延迟(38秒)。阿托品(10-6 M)和河豚毒素(3×10-7M)不会影响NKA引起的收缩,但会抑制SP和NKB引起的收缩。阿托品使SP和NKB的剂量反应曲线向右移动。阿托品的治疗使NKB的应答潜伏期延长。在试纸条中,SP基本上没有引起收缩,但是在潜伏期分别为28和36秒后,NKA和NKB产生了类似抽搐的收缩。 NKA的功效与节段制剂相似,而NKB的功效在条状制剂中要低得多。与分段制剂不同,阿托品不抑制条形制剂中两种速激肽诱导的收缩。这些结果表明速激肽通过肌源性和神经源性机制诱导收缩,后者在剥离制剂中可能无效。

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