Hudzik T J, McMillan D E
Department of Pharmacology and Toxicology, University of Arkansas for Medical Sciences.
J Pharmacol Exp Ther. 1994 Mar;268(3):1335-42.
Preclinical assays used to screen for antidepressant activity have traditionally been limited in their ability to selectively detect antidepressants. In the present study, we assessed the effects of antidepressant and non-antidepressant drugs on response-duration differentiation responding as a potential screen for antidepressant activity. Under this schedule, rats were trained to hold a lever in the down position for a duration greater than 1 sec but not more than 1.3 sec. The effects of the monoamine oxidase inhibitor tranylcypromine, the tricyclics imipramine and amitriptyline, and the atypical antidepressants trazadone and bupropion, as well as haloperidol, chlorpromazine, scopolamine and diazepam were studied. The antidepressant drugs selectively produced increases in the mean response durations. The non-antidepressant drugs produced much shorter mean response durations, although diazepam and chlorpromazine also increased the proportion of response durations that were greater than 1.3 sec. The order of potency of the antidepressants for increasing mean response durations corresponded well with their clinical potencies, suggesting that response-duration differentiation may be useful in screening for antidepressant activity.
传统上,用于筛选抗抑郁活性的临床前试验在选择性检测抗抑郁药的能力方面存在局限性。在本研究中,我们评估了抗抑郁药和非抗抑郁药对作为抗抑郁活性潜在筛选指标的反应持续时间分化的影响。在此实验安排下,训练大鼠将杠杆保持在向下位置的持续时间大于1秒但不超过1.3秒。研究了单胺氧化酶抑制剂反苯环丙胺、三环类药物丙咪嗪和阿米替林、非典型抗抑郁药曲唑酮和安非他酮,以及氟哌啶醇、氯丙嗪、东莨菪碱和地西泮的作用。抗抑郁药选择性地使平均反应持续时间增加。非抗抑郁药产生的平均反应持续时间要短得多,尽管地西泮和氯丙嗪也增加了反应持续时间大于1.3秒的比例。抗抑郁药增加平均反应持续时间的效力顺序与其临床效力相当吻合,这表明反应持续时间分化可能有助于筛选抗抑郁活性。