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在树鼩乳头肌制备物中证明介导正性肌力作用的α-肾上腺素能受体:与豚鼠的比较。

Demonstration in Tupaia papillary muscle preparations of alpha-adrenoceptors mediating positive inotropic effects: comparison with guinea-pigs.

作者信息

Koga T, Shiraki Y, Sakai K

机构信息

Department of Pharmacology, Fujigotemba Research Laboratories, Chugai Pharmaceutical Co., Ltd., Shizuoka, Japan.

出版信息

Br J Pharmacol. 1989 Oct;98(2):552-6. doi: 10.1111/j.1476-5381.1989.tb12629.x.

DOI:10.1111/j.1476-5381.1989.tb12629.x
PMID:2573402
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1854701/
Abstract
  1. Positive inotropic responses to alpha- and beta-adrenoceptor agonists of isolated papillary muscles from the tree shrew (Tupaia), were compared with those from guinea-pigs. 2. In Tupaia, the concentration-response curve for phenylephrine, unlike that for isoprenaline, was not affected by pindolol in a concentration (10(-8) M) sufficient to block beta-adrenoceptor-mediated responses, but it was significantly shifted to the right by phentolamine (10(-6) M). In guinea-pig papillary muscles, however, the concentration-response curve for phenylephrine, like that for isoprenaline, was shifted to the right by pindolol (10(-8) M) but was unaltered by phentolamine (10(-6) M). Furthermore, when the mean concentrations of agonists inducing maximal positive inotropic responses were compared (relative to that of isoprenaline = 1.0), phenylephrine was found to be only slightly less potent (0.84 +/- 0.04; n = 5) in Tupaia and much less potent (0.33 +/- 0.06; n = 5) in the guinea-pig. 3. Although in Tupaia papillary muscles the increase in developed tension induced by a combination of phenylephrine and isoprenaline did not significantly differ from that by phenylephrine alone, it was approximately 3 times larger than that produced by phenylephrine alone in guinea-pigs. 4. These results indicate that in papillary muscles from Tupaia, unlike the guinea-pig, the positive inotropic effects of phenylephrine can be mediated by alpha-adrenoceptors.
摘要
  1. 将树鼩(笔尾树鼩属)分离乳头肌对α-和β-肾上腺素能受体激动剂的正性肌力反应与豚鼠的进行比较。2. 在树鼩中,去氧肾上腺素的浓度-反应曲线与异丙肾上腺素不同,在足以阻断β-肾上腺素能受体介导反应的浓度(10⁻⁸M)下,吲哚洛尔对其无影响,但酚妥拉明(10⁻⁶M)使其显著右移。然而,在豚鼠乳头肌中,去氧肾上腺素的浓度-反应曲线与异丙肾上腺素一样,被吲哚洛尔(10⁻⁸M)右移,但不受酚妥拉明(10⁻⁶M)影响。此外,当比较诱导最大正性肌力反应的激动剂平均浓度(相对于异丙肾上腺素 = 1.0)时,发现去氧肾上腺素在树鼩中的效力仅略低(0.84 ± 0.04;n = 5),而在豚鼠中效力低得多(0.33 ± 0.06;n = 5)。3. 虽然在树鼩乳头肌中,去氧肾上腺素和异丙肾上腺素联合诱导的张力增加与单独使用去氧肾上腺素时无显著差异,但在豚鼠中,该联合诱导的张力增加约为单独使用去氧肾上腺素时的3倍。4. 这些结果表明,与豚鼠不同,在树鼩乳头肌中,去氧肾上腺素的正性肌力作用可由α-肾上腺素能受体介导。

相似文献

1
Demonstration in Tupaia papillary muscle preparations of alpha-adrenoceptors mediating positive inotropic effects: comparison with guinea-pigs.在树鼩乳头肌制备物中证明介导正性肌力作用的α-肾上腺素能受体:与豚鼠的比较。
Br J Pharmacol. 1989 Oct;98(2):552-6. doi: 10.1111/j.1476-5381.1989.tb12629.x.
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本文引用的文献

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Phyletic position of tree shrews.树鼩的系统发育位置。
Science. 1966 Sep 23;153(3743):1550. doi: 10.1126/science.153.3743.1550-a.
2
Function of myocardial alpha-adrenoceptors.心肌α-肾上腺素能受体的功能。
Life Sci. 1982 Jul 12;31(2):101-12. doi: 10.1016/0024-3205(82)90421-0.
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Carcinogen-induced sarcoma in the primitive primate, Tupaia glis.致癌物诱发的原猴(树鼩)肉瘤
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Interactions between sympathomimetic amines and blocking agents on the rat ventricle strip.拟交感神经胺与阻断剂在大鼠心室肌条上的相互作用。
Arch Int Pharmacodyn Ther. 1966 Apr;160(2):379-89.
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Natural Herpesvirus hominis infection of tree shrews (Tupaia glis).树鼩(笔尾树鼩)的自然人类疱疹病毒感染
Lab Anim Sci. 1972 Aug;22(4):517-21.
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Positive inotropic effects of phenylephrine in the isolated rabbit papillary muscle mediated both by alpha- and beta-adrenoceptors.去氧肾上腺素对离体兔乳头肌的正性肌力作用是由α和β肾上腺素能受体介导的。
Naunyn Schmiedebergs Arch Pharmacol. 1974;284(2):133-48. doi: 10.1007/BF00501118.
9
Functional alpha-adrenoceptors in human atrial preparations in the presence of beta-receptor blockade.在β受体阻断情况下人心房组织中的功能性α肾上腺素能受体
Acta Physiol Scand. 1987 Nov;131(3):439-45. doi: 10.1111/j.1748-1716.1987.tb08259.x.
10
Characterization of the alpha-adrenoceptors mediating positive inotropy of rat left atria by use of selective agonists and antagonists.利用选择性激动剂和拮抗剂对介导大鼠左心房正性肌力作用的α-肾上腺素能受体进行表征。
Arch Int Pharmacodyn Ther. 1987 Feb;285(2):181-98.