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Factors influencing fluoxetine-induced sexual dysfunction in female rats

机译:影响氟西汀致雌性大鼠性功能障碍的因素

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Treatment with selective serotonin reuptake inhibitors, such as fluoxetine, produces sexual side effects with low sexual desire being the most prevalent effect in females. In few studies have preclinical models for such antidepressant-induced sexual dysfunction been fruitful. In the current manuscript, the effects of fluoxetine on multiple measures of female sexual motivation and sexual receptivity were examined. Ovariectomized, Fischer rats were primed with 10 μg estradiol benzoate and 500 μg progesterone. Partner preference, active investigation of the male, and measures of sexual behavior were examined after injection with 15 mg/kg fluoxetine. Factors (pretesting for sexual behavior, size of the test arena, non-contact time with a male) that differ among experiments designed to study antidepressant-induced female rat sexual dysfunction were studied.The male preference ratio was not affected by fluoxetine treatment but active investigation of the male was reduced; lordosis behavior was inhibited and pretesting for sexual receptivity amplified fluoxetine's inhibition; size of the testing arena or non-contact experience with the male had no effect. Regardless of test condition, when given the opportunity to escape from the male, fluoxetine-treated females displayed escape behavior. Measures of male preference and active investigation, but not lordosis behavior, appeared to be affected by fluoxetine's impact on activity. The collective data provided a behavioral profile of fluoxetine-induced sexual dysfunction. These findings reinforce the value of multiple measures when attempting to model antidepressant-induced female sexual dysfunction.
机译:用选择性5-羟色胺再摄取抑制剂(例如氟西汀)进行治疗会产生性副作用,而性欲低下是女性中最普遍的作用。在极少的研究中,针对此类抗抑郁药诱发的性功能障碍的临床前模型卓有成效。在当前的手稿中,检查了氟西汀对女性性动机和性接受能力的多种测量的影响。去卵巢的Fischer大鼠用10μg雌二醇苯甲酸酯和500μg孕酮灌注。注射15 mg / kg氟西汀后检查伴侣的偏好,对男性的积极调查以及性行为的度量。研究了抗抑郁药诱发的雌性大鼠性功能障碍的实验中不同的因素(性行为的预测试,试验场的大小,与雄性的非接触时间)不同。雄性偏爱率不受氟西汀治疗的影响,但活跃减少了对男性的调查;脊柱前凸行为受到抑制,性接受能力的预先测试增强了氟西汀的抑制作用;测试场地的大小或与男性的非接触经验都没有影响。无论测试条件如何,当给予从男性逃脱的机会时,氟西汀治疗的女性都表现出逃逸行为。氟西汀对活动的影响似乎影响了男性偏爱和积极调查的措施,但不影响脊柱前凸行为。收集的数据提供了氟西汀诱导的性功能障碍的行为特征。这些发现增强了在尝试为抗抑郁药诱发的女性性功能障碍建模时采取多种措施的价值。

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