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Repeated finasteride administration induces depression-like behavior in adult male rats

机译:重复的聚亚磷酸酯给药诱导成年雄性大鼠的抑郁状行为

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The enzyme 5 alpha-Reductase (5 alpha-R) catalyzes the formation of dihydrotestosterone, which is involved in male pattern hair loss and benign prostatic hyperplasia. Finasteride inhibits 5 alpha-R and is used to treat both these conditions. Several clinical studies show that chronic finasteride treatment induces persistent depression, suicidal thoughts, and cognitive impairment. The neural mechanisms underlying these effects of finasteride are not known and it is imperative that an animal model that mimics the clinical neuropsychiatric effects of finasteride is developed. Accordingly, we evaluated the behavioral effects of acute and repeated finasteride administration. Two months old male Wistar rats were administered with either vehicle (hydroxypropyl-beta-cyclodextrin) or different doses of finasteride, subcutaneously, either acutely (30 min or 2 h) or for 1, 3, and 6 days (one dose per day). Behavioral despair and motivational behavior were evaluated in the forced swim test (FST) and splash test, respectively. FST and splash test were video-recorded and analyzed offline. Finasteride did not show any effects in the acute, one day or three days studies in the FST. However, repeated finasteride administration for 6 days significantly increased the immobility time. In the splash test, finasteride (100 mg/kg) administration increased the latency to groom and decreased the grooming duration implying lack of motivation in the three-day study. In the six-day study, latency to groom was significantly increased by the 100 mg/Kg dose. Further, a significant dose dependent decrease in the grooming duration was observed. In summary, our results indicate that repeated finasteride administration induces depression-like behavior in rats. This study provides the evidence that an animal model of finasteride-induced depression is feasible to investigate the cellular and molecular mechanisms, and the pharmacology underlying the neuropsychiatric effects of finasteride. Further, these results provide insights into the potential involvement of neurosteroids in depression and will lead to the development of novel therapeutics for its treatment.
机译:酶5α-还原酶(5α-R)催化Dihydrottorons的形成,其参与男性图案脱发和良性前列腺增生。聚光酰亚胺抑制5α-R并用于治疗这些条件。几项临床研究表明,慢性三甾胺治疗诱导持续抑郁,自杀思想和认知障碍。内亚偶联物的这些效果的神经机制尚不清楚,并且势在必行的是,模拟临床神经精神效应的临床神经精神效应是开发的。因此,我们评估了急性和重复的三甾胺给药的行为效应。用载体(羟丙基 - β-环糊精)或不同剂量的小甾体,皮下,急性(30分钟或2小时)或1,3和6天(每天一次剂量)给予两个月的雄性Wistar大鼠。在强制游泳试验(FST)和飞溅试验中评估了行为绝望和动机行为。 FST和Splash测试是视频录制和分析的离线。美亚斯蒂德没有在FST中的一天或三天的研究中显示任何效果。然而,重复的三甾胺给药6天显着增加了不可动行时间。在飞溅试验中,三甾胺(100 mg / kg)给药增加了新郎的潜伏期,并降低了缺乏三天研究中缺乏动机的美容持续时间。在六天的研究中,100 mg / kg剂量的新郎潜伏期显着增加。此外,观察到修饰持续时间的显着剂量依赖性降低。总之,我们的结果表明,重复的三甾胺给药诱导大鼠抑郁样行为。本研究提供了一种证据表明,致细胞内诱导的抑郁症的动物模型是可以研究细胞和分子机制的可行性,以及多亚匹克的神经精神效应的药理学。此外,这些结果提供了洞察神经活体在抑郁症中的潜在参与,并将导致新的治疗方法的发展。

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