Rourke Claire, Starr Kathryn R, Reavill Charlie, Fenwick Sue, Deadman Kim, Jones Declan N C
Psychiatry Centre of Excellence for Drug Discovery, GlaxoSmithKline plc, New Frontiers Science Park, Third Ave., CM19 5AW Harlow, Essex, UK.
Psychopharmacology (Berl). 2006 Jan;184(1):107-14. doi: 10.1007/s00213-005-0230-1. Epub 2005 Dec 7.
Hyperprolactinaemia is a common side effect of antipsychotic treatment and the clinical consequences associated with this, e.g. sexual dysfunction, can have a negative impact on patient compliance.
The aim of this study was to investigate the effect of the atypical antipsychotics olanzapine and risperidone on prolactin levels in rats using different treatment regimes and to compare these data with those reported clinically.
All experiments were carried out in male CD rats. In separate studies, the effects of acute, sub-chronic (7 days) and chronic (28 days) olanzapine and risperidone administration on prolactin levels were determined. Further studies investigated the time course of the prolactin response following olanzapine and risperidone treatment over 24 h.
Both drugs significantly increased prolactin levels in a similar manner following acute administration, in keeping with clinically reported data. However, this elevation was still present following sub-chronic and chronic treatment, contrasting with clinical data with respect to olanzapine but not risperidone. Over 24 h, olanzapine demonstrated a more transient elevation of prolactin levels, whereas risperidone caused a robust and persistent increase in prolactin up to 24 h post-dose, closely mimicking clinical results.
The present study has demonstrated that olanzapine and risperidone display similar effects on prolactin levels in the rat following acute and chronic administration but differ in their prolactin response over a 24-h period. In conclusion, prolactin levels in rats following atypical antipsychotic treatment may not be fully predictive of the clinical situation.
高催乳素血症是抗精神病药物治疗的常见副作用,与之相关的临床后果,如性功能障碍,会对患者的依从性产生负面影响。
本研究旨在使用不同治疗方案,研究非典型抗精神病药物奥氮平和利培酮对大鼠催乳素水平的影响,并将这些数据与临床报告的数据进行比较。
所有实验均在雄性CD大鼠中进行。在单独的研究中,测定了急性、亚慢性(7天)和慢性(28天)给予奥氮平和利培酮对催乳素水平的影响。进一步的研究调查了奥氮平和利培酮治疗24小时后催乳素反应的时间进程。
急性给药后,两种药物均以相似的方式显著提高了催乳素水平,这与临床报告的数据一致。然而,亚慢性和慢性治疗后这种升高仍然存在,这与奥氮平的临床数据不同,但与利培酮的临床数据相符。在24小时内,奥氮平使催乳素水平升高更为短暂,而利培酮在给药后24小时内导致催乳素强劲且持续升高,与临床结果非常相似。
本研究表明,奥氮平和利培酮在急性和慢性给药后对大鼠催乳素水平显示出相似的影响,但在24小时内它们的催乳素反应有所不同。总之,非典型抗精神病药物治疗后大鼠的催乳素水平可能无法完全预测临床情况。