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Effects of periadolescent fluoxetine and paroxetine on elevated plus-maze, acoustic startle, and swimming immobility in rats while on and off-drug

机译:青春期氟西汀和帕罗西汀对服用和停用药物时大鼠正迷宫升高,听觉惊吓和游泳不动的影响

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Rationale Whether selective serotonin reuptake inhibitors (SSRIs) exposure during adolescent brain development causes lasting effects remains unresolved. Objective Assess the effects of fluoxetine and paroxetine 60 days after adolescent exposure compared with when on-drug. Methods Male Sprague-Dawley littermates (41 litters) were gavaged on postnatal days 33-53 with fluoxetine (3 or 10 mg/kg/day), paroxetine (3, 10 or, 17 mg/kg/day), or water; half were tested while on-drug (21 litters) and half after 60 days off-drug (20 litters). Results The highest dose of the drugs reduced body weight gain during treatment that rebounded 1 week post-treatment. On-drug, no significant group differences were found on elevated plus maze time-in-open, zone entries, or latency to first open entry; however, the high dose of paroxetine significantly reduced head-dips (N = 20/group). No significant effects were found on-drug for acoustic startle response/prepulse inhibition (ASR/PPI) although a trend (p Conclusions The data provide no evidence that fluoxetine or paroxetine have long-term adverse effects on the behaviors measured here after adolescent to young adult exposure.
机译:基本原理青春期大脑发育过程中选择性5-羟色胺再摄取抑制剂(SSRIs)暴露是否会产生持久影响仍未得到解决。目的评估与药物治疗相比,青少年暴露后60天氟西汀和帕罗西汀的疗效。方法在出生后第33-53天,用氟西汀(3或10 mg / kg / day),帕罗西汀(3、10或17 mg / kg / day)或水对雄性Sprague-Dawley同窝仔(41窝)进行管饲。一半在服药时进行了测试(21胎),一半在服药60天后进行了测试(20胎)。结果最高剂量的药物降低了治疗后1周反弹的体重增加。药物方面,在高架迷宫开启时间,区域进入或首次开启进入的延迟方面,没有发现显着的群体差异;然而,高剂量的帕罗西汀可显着减少头昏(N = 20 /组)。尽管有趋势(p结论),但未发现药物对声音惊吓反应/脉冲抑制(ASR / PPI)有显着影响(结论)该数据没有提供证据表明氟西汀或帕罗西汀对青少年至青年后的行为有长期不良影响。成人接触。

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