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P物质在豚鼠回肠纵行平滑肌中的作用机制:重新评估

Mechanism of action of substance P in guinea-pig ileum longitudinal smooth muscle: a re-evaluation.

作者信息

Hall J M, Morton I K

机构信息

Pharmacology Group, Biomedical Sciences Division, King's College, London.

出版信息

J Physiol. 1990 Dec;431:529-41. doi: 10.1113/jphysiol.1990.sp018345.

Abstract
  1. A proposed mechanism of contractile action of substance P in guinea-pig ileum longitudinal smooth muscle involving a decrease in membrane K+ permeability (PK) has been re-examined. 2. Potentiation of responses to substance P by the K+ channel blocker tetraethylammonium (TEA) was originally proposed as evidence for a mechanism of action of substance P involving a decrease in PK. Potentiation was confirmed; however this was found not to be specific to substance P since a similar potentiation of responses was seen with agonists not thought to act via a decrease in PK. 3. Antagonism of contractile responses to substance P by noradrenaline was similarly confirmed. However, this antagonism was found to represent a non-specific functional interaction through the inhibitory actions of beta-adrenoceptors rather than the proposed specific interaction with an increase in PK by noradrenaline which is normally alpha 1-adrenoceptor mediated. 4. Experiments were made measuring 86Rb efflux, in depolarized guinea-pig ileum longitudinal smooth muscle, to estimate PK. These studies confirmed a reported decrease in PK with TEA, but failed to detect the previously reported decrease with substance P. 5. These results, although not disproving a suggested mechanism of direct contractile action of substance P in guinea-pig ileum longitudinal smooth muscle involving a decrease in PK, do throw doubt on either the evidence, or its interpretation, as proposed by the original authors in support of such a mechanism.
摘要
  1. 对一种关于P物质在豚鼠回肠纵行平滑肌中收缩作用的机制进行了重新研究,该机制涉及膜钾离子通透性(PK)降低。2. 钾离子通道阻滞剂四乙铵(TEA)对P物质反应的增强作用最初被提出作为P物质作用机制的证据,该机制涉及PK降低。这种增强作用得到了证实;然而,发现这并非P物质所特有的,因为在那些被认为并非通过降低PK起作用的激动剂作用下也观察到了类似的反应增强。3. 去甲肾上腺素对P物质收缩反应的拮抗作用同样得到了证实。然而,发现这种拮抗作用代表了一种通过β肾上腺素能受体的抑制作用产生的非特异性功能相互作用,而非所提出的去甲肾上腺素通过增加PK产生的特异性相互作用,后者通常由α1肾上腺素能受体介导。4. 在去极化的豚鼠回肠纵行平滑肌中进行了测量86Rb外流的实验,以估计PK。这些研究证实了TEA会导致PK降低的报道,但未能检测到先前报道的P物质导致的PK降低。5. 这些结果虽然没有否定P物质在豚鼠回肠纵行平滑肌中通过降低PK产生直接收缩作用这一推测机制,但确实对原始作者为支持这种机制而提出的证据或其解释产生了怀疑。

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