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猫、狗和北美负鼠(弗吉尼亚负鼠)食管黏膜肌层的药理学研究。

A pharmacological study of oesophageal muscularis mucosae from the cat, dog and American opossum (Didelphis virginiana).

作者信息

Christensen J, Percy W H

出版信息

Br J Pharmacol. 1984 Oct;83(2):329-36. doi: 10.1111/j.1476-5381.1984.tb16492.x.

Abstract

Strips of muscularis mucosae from the oesophagi of cat, dog and opossum have been studied to determine their responses to drugs to electrical field stimulation. All tissues were contracted by acetylcholine, histamine and, with the exception of strips of muscularis mucosae from the opossum proximal oesophagus, noradrenaline. The effects of acetylcholine and histamine were competitively antagonized by atropine (50 nM) and mepyramine (50 nM) and were abolished by atropine (1 microM) and mepyramine (1 microM) respectively. Contractile responses to noradrenaline were competitively antagonized by phentolamine (50 nM) but were converted to propranolol (50 nM)-sensitive relaxations by phentolamine (1 microM). Relaxations were abolished by propranolol (1 microM). Cholecystokinin octapeptide, gastrin 1 and vasoactive intestinal polypeptide were ineffective on any of the tissues examined. Substance P caused contractions in tissue from all three species. These effects were atropine and tetrodotoxin insensitive. All tissues gave atropine (50 nM)- and tetrodotoxin (100 nM)-sensitive contractions in response to electrical field stimulation. Contractions were not followed by relaxations and spontaneous mechanical activity was not suppressed between periods of stimulation. No evidence was obtained for the presence of non-adrenergic, non-cholinergic inhibitory innervation of the oesophageal muscularis mucosae in any species. During electrical field stimulation noradrenaline always reduced the amplitude of evoked contractions and, with the exception of tissue from proximal opossum oesophagus, increased resting tension. In opossum distal oesophageal muscularis mucosae, the effects of noradrenaline during electrical field stimulation were abolished by a 30 min pretreatment of the tissue with phentolamine (1 microM) and propranolol (1 microM). To Achieve this in all other tissues, it was also necessary to use yohimbine (1 microM). 7 In all tissues where noradrenaline caused a phentolamine (1 microM)-and propranolol (1 microM)- resistant depression of electrically evoked responses, clonidine produced a yohimbine (1 microM)- sensitive depression. 8 Evidence was obtained for the presence of excitatory alpha 1-and inhibitory alpha 2- and beta-adrenoceptors. Inter-species differences in their distribution are discussed.

摘要

对猫、狗和负鼠食管的黏膜肌层条带进行了研究,以确定它们对电场刺激药物的反应。所有组织对乙酰胆碱、组胺均有收缩反应,除负鼠近端食管的黏膜肌层条带外,对去甲肾上腺素也有收缩反应。乙酰胆碱和组胺的作用分别被阿托品(50 nM)和甲氧苄二胺(50 nM)竞争性拮抗,分别被阿托品(1 μM)和甲氧苄二胺(1 μM)消除。对去甲肾上腺素的收缩反应被酚妥拉明(50 nM)竞争性拮抗,但被酚妥拉明(1 μM)转化为对普萘洛尔(50 nM)敏感的舒张反应。普萘洛尔(1 μM)可消除舒张反应。八肽胆囊收缩素、胃泌素1和血管活性肠肽对所检查的任何组织均无作用。P物质使所有三个物种的组织产生收缩。这些作用对阿托品和河豚毒素不敏感。所有组织对电场刺激均产生对阿托品(50 nM)和河豚毒素(100 nM)敏感的收缩反应。收缩后无舒张反应,刺激期间自发机械活动未被抑制。未获得任何物种食管黏膜肌层存在非肾上腺素能、非胆碱能抑制性神经支配的证据。在电场刺激期间,去甲肾上腺素总是降低诱发收缩的幅度,除负鼠近端食管组织外,还增加静息张力。在负鼠远端食管黏膜肌层,电场刺激期间去甲肾上腺素的作用可通过用酚妥拉明(1 μM)和普萘洛尔(1 μM)对组织进行30分钟预处理而消除。在所有其他组织中要达到这一点,还需要使用育亨宾(1 μM)。7在所有去甲肾上腺素导致对酚妥拉明(1 μM)和普萘洛尔(1 μM)耐药的电诱发反应抑制的组织中,可乐定产生对育亨宾(1 μM)敏感的抑制作用。8获得了兴奋性α1受体、抑制性α2受体和β肾上腺素能受体存在的证据。讨论了它们分布的种间差异。

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1
Drug responses of human fetal esophagus.人类胎儿食管的药物反应。
Am J Physiol. 1957 Oct;191(1):37-9. doi: 10.1152/ajplegacy.1957.191.1.37.
2
The muscularis mucosae of the oesophagus of the cat, rabbit and rat.猫、兔和大鼠食管的黏膜肌层。
J Physiol. 1955 Oct 28;130(1):123-30. doi: 10.1113/jphysiol.1955.sp005398.
3
The muscularis mucosae of the human stomach.人类胃的黏膜肌层。
J Physiol. 1953 May 28;120(3):365-72. doi: 10.1113/jphysiol.1953.sp004900.

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