O'Halloran K D, Perl E R
Department of Physiology, School of Medicine, University of North Carolina, Chapel Hill 27599-7545, USA.
Brain Res. 1997 Jun 13;759(2):233-40. doi: 10.1016/s0006-8993(97)00261-8.
The effects of partial division of the great auricular nerve of adult rabbits were evaluated on the responsiveness of cutaneous C-fiber polymodal nociceptors (CPMs) to sympathetic stimulation (SS), close-arterial injections of epinephrine (EPI) and other alpha-adrenergic agonists. In normal unanesthetized rabbits, the two ears were usually at the same temperature. Two to 4 weeks after partial nerve lesions, however, the operated ear was cooler by 1-3 degrees C in the majority of animals, suggestive of increased vasoconstriction and possible denervation supersensitivity. Neither SS nor EPI (50 ng) excited CPM units (n = 23) from intact anesthetized animals. In contrast, 14-27 days after partial nerve lesions, SS (8 out of 38 units) and EPI (12 out of 38 units) were excitatory for a class of CPMs. There was notable variability in the response of different units and of a given unit between first and second trials. Responses consisted of 1-22 impulses for SS and 1-23 impulses for EPI in the 60 s following a trial. Arterial occlusion did not activate responsive units, suggesting that the excitation was not caused by vascular or temperature changes. Selective alpha2-adrenoceptor blockade with yohimbine (0.6-1.0 mg/kg i.v.) or rauwolscine (1.0 mg/kg i.v.) reversibly antagonized the effects of SS and EPI. EPI-responsive units were also excited by norepinephrine (50 ng) and guanabenz (10 microg) but not by clonidine (3 microg) or B-HT 933 (3 microg). The results suggest that circulating EPI, acting via an alpha-adrenoceptor subtype, can play a part in the development and/or maintenance of aberrant pain syndromes such as causalgia and other sympathetically related dystrophies.
研究评估了成年兔耳大神经部分切断对皮肤C纤维多模式伤害感受器(CPM)对交感神经刺激(SS)、动脉内注射肾上腺素(EPI)及其他α-肾上腺素能激动剂反应性的影响。在正常未麻醉的兔子中,双耳温度通常相同。然而,部分神经损伤后2至4周,大多数动物的手术耳温度比未手术耳低1至3摄氏度,提示血管收缩增强及可能的去神经超敏反应。SS和EPI(50 ng)均不能兴奋完整麻醉动物的CPM单位(n = 23)。相反,部分神经损伤后14至27天,SS(38个单位中的8个)和EPI(38个单位中的12个)可兴奋一类CPM。不同单位以及同一单位在第一次和第二次试验中的反应存在显著差异。试验后60秒内,SS的反应为1至22个冲动,EPI的反应为1至23个冲动。动脉闭塞未激活反应性单位,提示兴奋并非由血管或温度变化引起。用育亨宾(0.6 - 1.0 mg/kg静脉注射)或罗芙辛(1.0 mg/kg静脉注射)进行选择性α2-肾上腺素能受体阻断可逆转SS和EPI的作用。EPI反应性单位也可被去甲肾上腺素(50 ng)和胍那苄(10 μg)兴奋,但不受可乐定(3 μg)或B-HT 933(3 μg)兴奋。结果表明,循环中的EPI通过一种α-肾上腺素能受体亚型发挥作用,可能参与灼痛和其他交感神经相关营养不良等异常疼痛综合征的发生和/或维持。