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去大脑大鼠心脏α1 - 肾上腺素能受体激活后的正性变时反应。

Positive chronotropic responses to cardiac alpha 1-adrenoreceptor activation in the pithed rat.

作者信息

Tung L H, Rand M J, Louis W J

出版信息

J Auton Pharmacol. 1986 Dec;6(4):285-90. doi: 10.1111/j.1474-8673.1986.tb00655.x.

Abstract

Adrenaline (0.1-10 micrograms/kg), noradrenaline (0.1-10 micrograms/kg) and phenylephrine (1-100 micrograms/kg) acted on both cardiac alpha 1- and beta-adrenoreceptors to induce positive chronotropic responses in the pithed rat. When beta-adrenoreceptors were blocked by propranolol (1 mg/kg), the residual chronotropic responses were due to activation of alpha 1-adrenoreceptors since they were significantly reduced by prazosin (10-100 micrograms/kg). Methoxamine (10-300 micrograms/kg) acted solely on cardiac alpha 1-adrenoreceptors to induce positive chronotropic responses which were abolished by prazosin (10-100 micrograms/kg) alone, as has been demonstrated previously for amidephrine. The rank order of potency for eliciting the positive chronotropic response to alpha 1-adrenoreceptor activation was adrenaline greater than noradrenaline greater than phenylephrine greater than methoxamine. The positive chronotropic responses to adrenaline (3-10 micrograms/kg), noradrenaline (3-10 micrograms/kg) and phenylephrine (30-100 micrograms/kg) produced by activating alpha 1-adrenoreceptors had a slower time course than did the chronotropic responses produced by activation of beta-adrenoreceptors.

摘要

肾上腺素(0.1 - 10微克/千克)、去甲肾上腺素(0.1 - 10微克/千克)和去氧肾上腺素(1 - 100微克/千克)作用于去大脑大鼠心脏的α1和β肾上腺素能受体,诱导正性变时反应。当β肾上腺素能受体被普萘洛尔(1毫克/千克)阻断时,残余的变时反应归因于α1肾上腺素能受体的激活,因为它们被哌唑嗪(10 - 100微克/千克)显著降低。甲氧明(10 - 300微克/千克)仅作用于心脏α1肾上腺素能受体以诱导正性变时反应,单独使用哌唑嗪(10 - 100微克/千克)即可消除该反应,正如先前对酰胺福林所证明的那样。引发对α1肾上腺素能受体激活的正性变时反应的效力顺序为肾上腺素>去甲肾上腺素>去氧肾上腺素>甲氧明。激活α1肾上腺素能受体产生的对肾上腺素(3 - 10微克/千克)、去甲肾上腺素(3 - 10微克/千克)和去氧肾上腺素(30 - 100微克/千克)的正性变时反应的时相比激活β肾上腺素能受体产生的变时反应更慢。

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