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首页> 外文期刊>Pharmacology, Biochemistry and Behavior >Reduction of fat and protein intakes but not carbohydrate intake following acute and chronic fluoxetine in female rats.
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Reduction of fat and protein intakes but not carbohydrate intake following acute and chronic fluoxetine in female rats.

机译:雌性大鼠急性和慢性氟西汀治疗后减少脂肪和蛋白质的摄入,但不减少碳水化合物的摄入。

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Fluoxetine hydrochloride, a selective serotonin reuptake inhibitor, leads to reductions in food intake and body weight and is under investigation as a possible treatment for obesity. Additionally, it has been suggested that fluoxetine administration could lead to a selective suppression in carbohydrate consumption. Because women more often than men seek weight reduction treatment, the present study examined the acute and chronic effects of fluoxetine on food intake, macronutrient selection, body weight, estrous cycle, and motor activity in female rats. Female Long-Evans rats were provided with separate sources of protein, fat and carbohydrate, and nutrient intakes were recorded following single (5.0, 10.0, and 20.0 mg/kg, IP) and chronic daily (10 mg/kg for 28 days) injections of fluoxetine. Acute and chronic administration of fluoxetine significantly reduced total caloric intake when compared to vehicle treatment. Moreover, fluoxetine significantly suppressed fat and protein intakes, but not carbohydrate intake following both acute and chronic drug administration. Animals chronically treated with fluoxetine gained significantly less weight than animals treated with vehicle. Chronic fluoxetine treatment did not significantly alter estrous cycle. However, in both fluoxetine- and vehicle-treated animals, total caloric intake, and carbohydrate and protein intakes were reduced and fat intake was increased when estrogen levels were high. Fluoxetine significantly reduced motor activity up to 4 h postinjection, and increased motor activity 24 h postinjection.
机译:盐酸氟西汀是一种选择性的5-羟色胺再摄取抑制剂,可减少食物摄入和减轻体重,目前正在研究作为肥胖症的一种可能治疗方法。另外,已经建议氟西汀的施用可以导致碳水化合物消耗的选择性抑制。因为女性比男性更多地寻求减重治疗,所以本研究研究了氟西汀对雌性大鼠食物摄入,大量营养选择,体重,发情周期和运动活动的急性和慢性影响。向Long-Evans雌性大鼠提供单独的蛋白质,脂肪和碳水化合物来源,并在单次(5.0、10.0和20.0 mg / kg,IP)和慢性每天(10 mg / kg连续28天)注射后记录营养摄入氟西汀。与赋形剂治疗相比,氟西汀的急性和慢性给药显着降低了总热量摄入。此外,氟西汀在急性和慢性给药后均显着抑制了脂肪和蛋白质的摄入,但没有抑制碳水化合物的摄入。长期用氟西汀治疗的动物的体重显着少于用赋形剂治疗的动物。慢性氟西汀治疗并未显着改变发情周期。但是,在氟西汀和媒介物处理的动物中,雌激素水平高时,总热量摄入以及碳水化合物和蛋白质摄入减少,脂肪摄入增加。氟西汀可在注射后4小时内显着降低运动活动,并在注射后24小时内增加运动活动。

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