Koss M C, Kawarai M, Ito T
Department of Pharmacology, University of Oklahoma Health Sciences Center, Oklahoma.
J Pharmacol Exp Ther. 1991 Mar;256(3):1126-31.
The present study was designed to assess the relative contribution of postjunctional alpha-1 and alpha-2 adrenoceptors in neurally evoked cutaneous vasoconstrictor responses in anesthetized cats. Preganglionic stimulation of the thoracic sympathetic nerve trunk produced an intensity-related decrease of digital skin blood flow as measured by laser-Doppler flowmetry. Sympathetic-cholinergic sudomotor (electrodermal) responses were recorded simultaneously as an additional index of neuronal activation. Vasoconstrictor responses were not altered by pretreatment with i.v. propranolol (1 mg/kg) or atropine (1 mg/kg) and were refractory to low doses (2 mg/kg) of hexamethonium. As expected, atropine abolished evoked skin potential responses which were also sensitive only to higher doses (20 mg/kg) of hexamethonium. Pretreatment with either phentolamine (1 mg/kg i.v.), yohimbine (0.5 mg/kg i.v.) or prazosin (0.3 mg/kg i.v.) produced significant reduction of sympathetic vasoconstriction with blockade by phentolamine and yohimbine being far greater than that seen with prazosin. In animals previously given prazosin (0.3 mg/kg), subsequent administration of yohimbine (0.5 mg/kg) almost totally blocked the remaining evoked cutaneous vasoconstriction. These results demonstrate that both alpha-1 and alpha-2 adrenoceptors are present in the cutaneous bed of the cat with the predominant effect mediated by innervated alpha-2 adrenoceptors.
本研究旨在评估麻醉猫神经诱发的皮肤血管收缩反应中,接头后α-1和α-2肾上腺素能受体的相对作用。通过激光多普勒血流仪测量,对胸交感神经干进行节前刺激会使指端皮肤血流量出现与刺激强度相关的减少。同时记录交感胆碱能发汗运动(皮肤电)反应,作为神经元激活的额外指标。静脉注射普萘洛尔(1mg/kg)或阿托品(1mg/kg)预处理不会改变血管收缩反应,且对低剂量(2mg/kg)六甲铵不敏感。正如预期的那样,阿托品消除了诱发的皮肤电位反应,该反应也仅对较高剂量(20mg/kg)的六甲铵敏感。酚妥拉明(1mg/kg静脉注射)、育亨宾(0.5mg/kg静脉注射)或哌唑嗪(0.3mg/kg静脉注射)预处理均能显著降低交感神经血管收缩,酚妥拉明和育亨宾的阻断作用远大于哌唑嗪。在先前给予哌唑嗪(0.3mg/kg)的动物中,随后给予育亨宾(0.5mg/kg)几乎完全阻断了剩余的诱发皮肤血管收缩。这些结果表明,猫的皮肤床中同时存在α-1和α-2肾上腺素能受体,其主要作用由支配的α-2肾上腺素能受体介导。