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ω-芋螺毒素GVIA(一种N型电压敏感性钙通道的肽类调节剂)对哺乳动物平滑肌中传出神经和感觉神经激活所产生的运动反应的影响。

The effect of omega conotoxin GVIA, a peptide modulator of the N-type voltage sensitive calcium channels, on motor responses produced by activation of efferent and sensory nerves in mammalian smooth muscle.

作者信息

Maggi C A, Patacchini R, Santicioli P, Lippe I T, Giuliani S, Geppetti P, Del Bianco E, Selleri S, Meli A

机构信息

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

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1988 Aug;338(2):107-13. doi: 10.1007/BF00174856.

Abstract
  1. The effect of omega-conotoxin (CTX) GVIA, a peptide which blocks neuronal calcium channels, were investigated on nerve-mediated motor responses in a variety of isolated smooth muscle preparations from rats and guinea-pigs. 2. In the rat or guinea-pig isolated vas deferens CTX (1 nM-1 microM) produced a concentration and time-related inhibition of the response to field stimulation, while the responses to KCl, noradrenaline or adenosine triphosphate were unaffected. In the presence of CTX a series of tetrodotoxin-resistant contractions could be elicited by field stimulation by increasing pulse width and/or voltage. 3. In the rat or guinea-pig isolated urinary bladder, CTX produced a concentration and time-dependent inhibition of twitch responses to field stimulation without affecting the response to exogenous acetylcholine. In the rat bladder the maximal effect did not exceed 25% inhibition while a much larger fraction of the response (about 70%) was inhibited in the guinea-pig bladder. The CTX-resistant response was abolished, in both tissues, by tetrodotoxin. 4. The effects of CTX in the rat bladder were also studied with a whole range of frequencies of field stimulation (0.1-50 Hz). Maximal inhibition was observed toward contractions elicited at frequencies of 2-5 Hz. At low frequencies the inhibitory effects of CTX and atropine were almost additive while at high frequencies of stimulation a large component of the atropine-sensitive response was CTX-resistant. 5. In the rat isolated proximal duodenum, field stimulation in the presence of atropine and guanethidine produced a primary relaxation followed by a rebound contraction.(ABSTRACT TRUNCATED AT 250 WORDS)
摘要
  1. 研究了ω-芋螺毒素(CTX)GVIA(一种可阻断神经元钙通道的肽)对大鼠和豚鼠多种离体平滑肌制剂中神经介导的运动反应的影响。2. 在大鼠或豚鼠离体输精管中,CTX(1 nM - 1 μM)对场刺激反应产生浓度和时间依赖性抑制,而对氯化钾、去甲肾上腺素或三磷酸腺苷的反应不受影响。在CTX存在下,通过增加脉冲宽度和/或电压,场刺激可引发一系列对河豚毒素不敏感的收缩。3. 在大鼠或豚鼠离体膀胱中,CTX对场刺激引起的抽搐反应产生浓度和时间依赖性抑制,而不影响对外源性乙酰胆碱的反应。在大鼠膀胱中,最大抑制作用不超过25%,而在豚鼠膀胱中,反应的更大比例(约70%)受到抑制。在两种组织中,河豚毒素均可消除对CTX不敏感的反应。4. 还研究了CTX在大鼠膀胱中对一系列不同频率场刺激(0.1 - 50 Hz)的影响。观察到对2 - 5 Hz频率引起的收缩有最大抑制作用。在低频时,CTX和阿托品的抑制作用几乎是相加的,而在高频刺激时,阿托品敏感反应的很大一部分对CTX不敏感。5. 在大鼠离体十二指肠近端,在阿托品和胍乙啶存在下进行场刺激,会先出现一次原发性松弛,随后出现反弹收缩。(摘要截断于250字)

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