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Evaluation of ICI D7114, a putative stimulant of brown adipocytes, on histamine-contracted guinea-pig ileum.ICI D7114(一种推测的棕色脂肪细胞刺激剂)对组胺收缩的豚鼠回肠的作用评估。
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Atypical beta-adrenoceptor on brown adipocytes as target for anti-obesity drugs.棕色脂肪细胞上的非典型β-肾上腺素能受体作为抗肥胖药物的靶点。
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The pharmacology of a beta 2-selective adrenoceptor antagonist (ICI 118,551).一种β2 选择性肾上腺素能受体拮抗剂(ICI 118,551)的药理学
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Responses to norepinephrine resistant to inhibition by alpha and beta adrenoceptor antagonists.对α和β肾上腺素能受体拮抗剂抑制作用具有抗性的去甲肾上腺素反应。
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ICI-215001(一种假定的β3肾上腺素能受体激动剂)的β1和β2肾上腺素能受体拮抗剂活性。

Beta 1- and beta 2-adrenoceptor antagonist activities of ICI-215001, a putative beta 3-adrenoceptor agonist.

作者信息

Tesfamariam B, Allen G T

机构信息

Department of Pharmacology, Bristol-Myers Squibb Research Institute, Princeton, New Jersey 08543.

出版信息

Br J Pharmacol. 1994 May;112(1):55-8. doi: 10.1111/j.1476-5381.1994.tb13028.x.

DOI:10.1111/j.1476-5381.1994.tb13028.x
PMID:7913381
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1910297/
Abstract
  1. The present study was undertaken to characterize the beta 3-adrenoceptor agonist activity of ICI-215001 and to determine whether it exhibits additional activities on beta 1- and beta 2-adrenoceptors in isolated spontaneously beating atrium, trachea and ileum of guinea-pig. 2. In guinea-pig atrium, isoprenaline, a non-selective beta-adrenoceptor agonist, caused concentration-dependent, positive chronotropic effects that were inhibited by atenolol, a selective beta 1-antagonist. ICI-215001 also competitively antagonized the increase in heart rate caused by isoprenaline. 3. ICI-215001 exhibited low intrinsic activity at increasing the beating rate of atrium and no activity on resting or induced tone of tracheal strips. 4. In strips of guinea-pig trachea, contracted submaximally with carbachol, isoprenaline, caused concentration-dependent relaxations. Both ICI-118551, a selective beta 2-adrenoceptor antagonist, and ICI-215001 competitively inhibited the relaxations caused by isoprenaline. 5. In isolated strips of guinea-pig ileum longitudinal smooth muscle contracted with histamine, isoprenaline and ICI-215001 caused relaxations which were inhibited by alprenolol, a beta-adrenoceptor antagonist with modest affinity for beta 3-adrenoceptors, but were resistant to ICI-118551 and atenolol. 6. These results indicate that ICI-215001 exhibits beta 3-adrenoceptor agonist activity as demonstrated by relaxations mediated via atypical beta-adrenoceptors in the longitudinal smooth muscle of guinea-pig ileum. Further, the studies demonstrate that ICI-215001 can act as an antagonist at beta 1- and beta 2-adrenoceptors in situations where its intrinsic agonist activity is low.
摘要
  1. 本研究旨在表征ICI - 215001的β3 - 肾上腺素能受体激动剂活性,并确定其在豚鼠离体自发搏动的心房、气管和回肠中对β1 - 和β2 - 肾上腺素能受体是否表现出额外活性。2. 在豚鼠心房中,非选择性β - 肾上腺素能受体激动剂异丙肾上腺素引起浓度依赖性的正性变时效应,该效应被选择性β1 - 拮抗剂阿替洛尔抑制。ICI - 215001也竞争性拮抗异丙肾上腺素引起的心率增加。3. ICI - 215001在增加心房搏动率方面表现出低内在活性,对气管条的静息或诱导张力无活性作用。4. 在豚鼠气管条中,用卡巴胆碱使其亚最大收缩,异丙肾上腺素引起浓度依赖性舒张。选择性β2 - 肾上腺素能受体拮抗剂ICI - 118551和ICI - 215001均竞争性抑制异丙肾上腺素引起得舒张。5. 在豚鼠回肠纵行平滑肌条中,用组胺使其收缩,异丙肾上腺素和ICI - 215001引起舒张,该舒张被对β3 - 肾上腺素能受体亲和力适中的β - 肾上腺素能受体拮抗剂阿普洛尔抑制,但对ICI - 118551和阿替洛尔有抗性。6. 这些结果表明,ICI - 215001表现出β3 - 肾上腺素能受体激动剂活性,如在豚鼠回肠纵行平滑肌中通过非典型β - 肾上腺素能受体介导的舒张所证明。此外,研究表明,在其内在激动剂活性较低的情况下,ICI - 215001可作为β1 - 和β2 - 肾上腺素能受体的拮抗剂。