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首页> 外文期刊>Pharmacology, Biochemistry and Behavior >I. Antidepressants and sexual behavior: Weekly ketamine injections increase sexual behavior initially in female and male rats
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I. Antidepressants and sexual behavior: Weekly ketamine injections increase sexual behavior initially in female and male rats

机译:I.抗抑郁药和性行为:每周氯胺酮注射,最初在女性和雄性大鼠中增加性行为

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The present study characterized the effects of weekly ketamine injections on sexual behavior and anxiety in female and male rats, using a dosing protocol that mimics human therapeutic treatment for depression. In Experiment 1A, ketamine (10 mg/kg, i.p.) or saline was injected once per week for four consecutive weeks. The partner preference paradigm was used to measure sexual motivation 30 min after each weekly injection. Briefly, subjects were first given a 10-min test during which they could choose to spend time in the vicinity of a sexually receptive female stimulus or a sexually experienced male stimulus, however physical contact was restricted (no-contact). Immediately after, subjects were given unrestricted access to the stimulus animals (contact). After a washout period, subjects received four additional weekly injections of ketamine or saline, and then were tested for anxiety-like behavior on the elevated plus maze (EPM) after the last injection (Experiment 1B). For Experiment 2, similar procedures were used to test the effects of weekly ketamine injections on sexual motivation (Experiment 2A) and anxiety (Experiment 2B) in male subjects. In female subjects, ketamine increased sexual motivation as measured by greater time spent with the male stimulus, decreased likelihood of leaving after receiving mounts, and shorter return latencies after receiving intromissions, when compared to saline controls. In male subjects, ketamine shortened latency to first mount and first intromission, as well as increased time spent with the female stimulus. Very little anxiety was observed in either group (ketamine or saline) of female or male subjects when tested on the EPM. In conclusion, even after four weeks of ketamine exposure, sexual dysfunction did not emerge in either females or males. In contrast, ketamine increased sexual motivation in both females and males, with an initial robust response. However, as both groups gained sexual experience, the impact of ketamine diminished.
机译:本研究采用类似人类抑郁症治疗的给药方案,研究每周注射氯胺酮对雌性和雄性大鼠性行为和焦虑的影响。在实验1A中,每周注射一次氯胺酮(10mg/kg,i.p.)或生理盐水,连续四周。在每周注射30分钟后,使用伴侣偏好范式测量性动机。简单地说,受试者首先接受10分钟的测试,在此期间,他们可以选择在性接受的女性刺激或性经历的男性刺激附近度过时间,但身体接触受到限制(没有接触)。紧接着,受试者被允许不受限制地接触刺激动物(接触)。在一段洗出期后,受试者每周额外注射四次氯胺酮或生理盐水,然后在最后一次注射后在高架+迷宫(EPM)上测试焦虑样行为(实验1B)。对于实验2,使用类似的程序测试每周注射氯胺酮对男性受试者的性动机(实验2A)和焦虑(实验2B)的影响。与生理盐水对照组相比,在女性受试者中,氯胺酮增加了性动机,其测量方法是:与男性刺激物一起花费的时间更长,接受坐骑后离开的可能性降低,接受导入后的返回潜伏期更短。在男性受试者中,氯胺酮缩短了第一次坐骑和第一次插入的潜伏期,并增加了与女性刺激物相处的时间。在EPM测试中,观察到两组(氯胺酮或生理盐水)的女性或男性受试者几乎没有焦虑。总之,即使在氯胺酮暴露四周后,女性或男性都没有出现性功能障碍。相比之下,氯胺酮增加了女性和男性的性动机,最初反应强烈。然而,随着这两组人都有了性经验,氯胺酮的影响就减弱了。

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