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1
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本文引用的文献

1
Differentiation of receptor systems activated by sympathomimetic amines.拟交感胺激活的受体系统的分化
Nature. 1967 May 6;214(5088):597-8. doi: 10.1038/214597a0.
2
Membrane stabilization and cardiac effects of d,1-propranolol, d-propranolol and chlorpromazine.右旋-1-普萘洛尔、右旋普萘洛尔和氯丙嗪对膜的稳定作用及心脏效应。
Eur J Pharmacol. 1970;13(1):6-14. doi: 10.1016/0014-2999(70)90174-3.
3
Effects of chlorpromazine, d,l-propranolol, and d-propranolol in the isolated rat heart: modification of the response to isoprenaline and glucagon.氯丙嗪、消旋普萘洛尔和右旋普萘洛尔对离体大鼠心脏的作用:对异丙肾上腺素和胰高血糖素反应的改变
Eur J Pharmacol. 1971 Jul;15(2):164-70. doi: 10.1016/0014-2999(71)90168-3.
4
Circulatory changes following adrenalectomy in the rat.大鼠肾上腺切除术后的循环系统变化。
Cardiovasc Res. 1974 Mar;8(2):268-75. doi: 10.1093/cvr/8.2.268.
5
Central hypotensive effect of propranolol in the rabbit.普萘洛尔对家兔的中枢性降压作用。
Br J Pharmacol. 1973 Jun;48(2):343P.
6
Central alpha- and beta-adrenoceptors modifying arterial blood pressure and heart rate in conscious cats.中枢α和β肾上腺素能受体对清醒猫动脉血压和心率的调节作用
Br J Pharmacol. 1974 Jul;51(3):325-33. doi: 10.1111/j.1476-5381.1974.tb10666.x.
7
Effect of beta-adrenoceptor blocking compounds (propranolol, practolol and LB 46) on isoprenaline induced changes in regional blood flow in the rat.β-肾上腺素受体阻断化合物(普萘洛尔、普拉洛尔和LB 46)对异丙肾上腺素诱导的大鼠局部血流变化的影响。
Br J Pharmacol. 1971 Feb;41(2):171-6. doi: 10.1111/j.1476-5381.1971.tb08019.x.
8
Comparative chronotropic activity of beta-adrenoceptive antagonists.β-肾上腺素能拮抗剂的比较变时活性
Br J Pharmacol. 1970 Nov;40(3):373-81. doi: 10.1111/j.1476-5381.1970.tb10619.x.
9
Effect of acute and chronic treatment with practolol on cardiovascular responses in the pithed rat.心得宁急性和慢性给药对脊髓麻醉大鼠心血管反应的影响。
J Pharm Pharmacol. 1974 Oct;26(10):783-8. doi: 10.1111/j.2042-7158.1974.tb09174.x.
10
The actions of a new beta-adrenoceptor blocking drug, ICI 66082, on the rabbit papillary muscle and on the dog heart.一种新型β-肾上腺素能受体阻断药物ICI 66082对兔乳头肌和犬心脏的作用。
Br J Pharmacol. 1974 Jun;51(2):169-77. doi: 10.1111/j.1476-5381.1974.tb09644.x.

大鼠心血管系统中β-肾上腺素能受体的细分

The subdivision of beta-adrenoceptors in the cardiovascular system of the rat.

作者信息

Imms F J, Neame R L, Powis D A

出版信息

Br J Pharmacol. 1979 Nov;67(3):367-70. doi: 10.1111/j.1476-5381.1979.tb08689.x.

DOI:10.1111/j.1476-5381.1979.tb08689.x
PMID:227513
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2043960/
Abstract

1 The antagonism by the beta-adrenoceptor blocking drugs, propranolol (non-selective) and practolol (beta-selective), of the cardiovascular actions of isoprenaline has been investigated in the rat. 2 All doses of practolol (0.1, 1 and 3 mg/kg) blocked the cardio-accelerator action of isoprenaline but only the largest dose blocked the vasodilator effect. 3 All doses of propranolol (0.01, 0.03 and 0.1 mg/kg) blocked the vasodilator effect of isoprenaline but only the largest dose diminished the tachycardia. 4 It is concluded that in the rat, as in other species, beta-adrenoceptors may be subdivided into beta 1 (cardiac) and beta 2 (peripheral vascular) types.

摘要
  1. 已在大鼠中研究了β肾上腺素受体阻断药普萘洛尔(非选择性)和美托洛尔(β选择性)对异丙肾上腺素心血管作用的拮抗作用。2. 所有剂量的美托洛尔(0.1、1和3毫克/千克)均阻断了异丙肾上腺素的心脏加速作用,但只有最大剂量阻断了血管舒张作用。3. 所有剂量的普萘洛尔(0.01、0.03和0.1毫克/千克)均阻断了异丙肾上腺素的血管舒张作用,但只有最大剂量减轻了心动过速。4. 得出结论,在大鼠中,与其他物种一样,β肾上腺素受体可分为β1(心脏)和β2(外周血管)类型。