Flavahan N A, Cooke J P, Shepherd J T, Vanhoutte P M
J Pharmacol Exp Ther. 1987 May;241(2):361-5.
Experiments were performed in order to characterize the post-junctional alpha adrenoceptors that mediate contraction in arteries of human limbs. Blood vessels were obtained from patients undergoing amputation of an extremity for reasons other than vascular disease. Proximal (dorsalis pedis and arcuate arteries of the foot, superficial palmer arch of the hand) and distal (digital arteries of the foot and hand) blood vessels were studied from each limb. The blood vessels were removed within 60 min of amputation and were suspended for isometric tension recording in modified Krebs-Ringer bicarbonate solution. In proximal and distal arteries, alpha-1 adrenergic blockade with prazosin produced a nonparallel shift in the concentration-effect curve to high compared to low concentrations of the agonist. In contrast, alpha-2 adrenergic blockade with rauwolscine was more effective against responses evoked by low concentrations of norepinephrine. This suggests that the alpha-2 adrenergic component of the response to norepinephrine is a low-maximum effect compared to the alpha-1 adrenergic component. Prazosin was less potent and rauwolscine more potent in distal arteries, compared to proximal arteries which might indicate an increased alpha-2 adrenergic response in distal arteries. The selective alpha-1 adrenergic agonist, phenylephrine, produced similar responses in proximal and distal arteries. However, the selective alpha-2 adrenergic agonist, B-HT 920, caused greater contractile responses in distal arteries compared to proximal arteries. The results suggest that alpha-1 and alpha-2 adrenoceptors are present on the vascular smooth muscle of arteries of human limbs, and that alpha-2 adrenoceptors are more prominent on distal arteries. This may be related to an increased contribution of the distal arteries to thermoregulation.
进行实验以表征介导人肢体动脉收缩的节后α肾上腺素能受体。血管取自因血管疾病以外的原因接受肢体截肢的患者。从每个肢体研究近端(足背动脉和足弓动脉、手掌浅弓)和远端(足和手的指动脉)血管。在截肢后60分钟内取出血管,并将其悬挂在改良的克雷布斯-林格碳酸氢盐溶液中进行等长张力记录。在近端和远端动脉中,与低浓度激动剂相比,哌唑嗪对α-1肾上腺素能的阻断使浓度-效应曲线向高浓度方向发生非平行移动。相比之下,育亨宾对α-2肾上腺素能的阻断对低浓度去甲肾上腺素诱发的反应更有效。这表明与α-1肾上腺素能成分相比,去甲肾上腺素反应中的α-2肾上腺素能成分是一种低最大效应。与近端动脉相比,哌唑嗪在远端动脉中的效力较低,育亨宾在远端动脉中的效力较高,这可能表明远端动脉中α-2肾上腺素能反应增加。选择性α-1肾上腺素能激动剂去氧肾上腺素在近端和远端动脉中产生相似的反应。然而,选择性α-2肾上腺素能激动剂B-HT 920在远端动脉中比在近端动脉中引起更大的收缩反应。结果表明,α-1和α-2肾上腺素能受体存在于人肢体动脉的血管平滑肌上,并且α-2肾上腺素能受体在远端动脉上更为突出。这可能与远端动脉对体温调节的贡献增加有关。