Sharpe M, Clements A, Hawton K, Young A H, Sargent P, Cowen P J
University Department of Psychiatry, Warneford and Littlemore Hospitals, Oxford, UK.
J Affect Disord. 1996 Nov 4;41(1):71-6. doi: 10.1016/0165-0327(96)00075-4.
We studied the endocrine and subjective responses that followed acute administration of the 5-HT1A receptor agonist buspirone (0.5 mg/kg orally) in 11 male patients with chronic fatigue syndrome (CFS) and a group of matched healthy controls. Patients with CFS had significantly higher plasma prolactin concentrations and experienced more nausea in response to buspirone than did controls. However, the growth hormone response to buspirone did not distinguish CFS patients from controls. Our data question whether the enhancement of buspirone-induced prolactin release in CFS is a consequence of increased sensitivity of post-synaptic 5-HT1A receptors. It is possible that the increased prolactin response to buspirone in CFS could reflect changes in dopamine function.
我们研究了11名慢性疲劳综合征(CFS)男性患者和一组匹配的健康对照者在急性口服5-HT1A受体激动剂丁螺环酮(0.5mg/kg)后出现的内分泌及主观反应。与对照组相比,CFS患者对丁螺环酮的反应表现为血浆催乳素浓度显著升高且恶心感更强。然而,丁螺环酮引起的生长激素反应并未区分出CFS患者和对照组。我们的数据对CFS中丁螺环酮诱导的催乳素释放增强是否是突触后5-HT1A受体敏感性增加的结果提出了质疑。CFS患者对丁螺环酮的催乳素反应增加可能反映了多巴胺功能的变化。