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用甲氯芬那酸处理的豚鼠胃环形肌中参与对儿茶酚胺机械反应的受体。

Receptors involved in mechanical responses to catecholamines in the circular muscle of guinea-pig stomach treated with meclofenamate.

作者信息

Syed M M, Parekh A B, Tomita T

机构信息

Department of Physiology, School of Medicine, Nagoya University, Japan.

出版信息

Br J Pharmacol. 1990 Dec;101(4):809-14. doi: 10.1111/j.1476-5381.1990.tb14162.x.

DOI:10.1111/j.1476-5381.1990.tb14162.x
PMID:1982230
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1917864/
Abstract
  1. In circular muscle strips of the fundus and corpus of guinea-pig stomach, mechanical responses to catecholamines were studied mainly in the presence of a prostaglandin biosynthesis inhibitor, meclofenamate. 2. Normal preparations developed considerable muscle tone, and adrenaline (10-100 microM) in the presence of 3-5 microM propranolol produced a multiphasic response, generally consisting of transient relaxation and contraction, followed by slow relaxation and then contraction. Responses to phenylephrine were similar to those of adrenaline. 3. Meclofenamate (0.3 microM) nearly abolished the muscle tone and under this condition, both adrenaline and phenylephrine produced a simple contraction. This response was strongly inhibited by prazosin, but only weakly by yohimbine. 4. When muscle tone was maintained by prostaglandin E2 (10 nM) in the presence of meclofenamate, phenylephrine (30 microM) produced transient relaxation followed by slow contraction in most preparations. These were strongly inhibited by prazosin. Adrenaline produced a similar response, but the relaxation was only partially reduced by prazosin. The remaining relaxation was more dominant in the middle fundic region and this was considered to be mediated through beta-adrenoceptors. 5. It is concluded that in the circular muscle of the fundic region of guinea-pig stomach, endogenous prostaglandins are involved in maintaining muscle tone and in modifying the response to catecholamines and that both contraction and relaxation are mediated by alpha 1-adrenoceptors.
摘要
  1. 在豚鼠胃底和胃体的环形肌条中,主要在存在前列腺素生物合成抑制剂甲氯芬那酸的情况下研究了对儿茶酚胺的机械反应。2. 正常标本产生相当大的肌张力,在存在3 - 5 microM普萘洛尔的情况下,肾上腺素(10 - 100 microM)产生多相反应,通常包括短暂的松弛和收缩,随后是缓慢的松弛,然后是收缩。对去氧肾上腺素的反应与肾上腺素相似。3. 甲氯芬那酸(0.3 microM)几乎消除了肌张力,在这种情况下,肾上腺素和去氧肾上腺素都产生简单的收缩。这种反应被哌唑嗪强烈抑制,但仅被育亨宾微弱抑制。4. 当在甲氯芬那酸存在下用前列腺素E2(10 nM)维持肌张力时,在大多数标本中,去氧肾上腺素(30 microM)产生短暂的松弛,随后是缓慢的收缩。这些被哌唑嗪强烈抑制。肾上腺素产生类似的反应,但哌唑嗪仅部分降低了松弛。其余的松弛在胃底中部区域更占优势,这被认为是通过β - 肾上腺素能受体介导的。5. 得出结论,在豚鼠胃底区域的环形肌中,内源性前列腺素参与维持肌张力并改变对儿茶酚胺的反应,并且收缩和松弛均由α1 - 肾上腺素能受体介导。

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本文引用的文献

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Benzamide action at alpha 2-adrenoceptors modifies catecholamine-induced contraction and relaxation of circular smooth muscle from guinea-pig stomach.苯甲酰胺作用于α2 - 肾上腺素能受体可改变儿茶酚胺诱导的豚鼠胃环形平滑肌的收缩和舒张。
Naunyn Schmiedebergs Arch Pharmacol. 1982 Apr;319(1):8-11. doi: 10.1007/BF00491470.
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