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High-Fat Diet-Induced Alterations in the Feeding Suppression of Low-Dose Nisoxetine a Selective Norepinephrine Reuptake Inhibitor

机译:高脂饮食诱导的低剂量尼索西汀(一种选择性去甲肾上腺素再摄取抑制剂)的摄食抑制作用

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摘要

Central noradrenergic pathways are involved in feeding and cardiovascular control, physiological processes altered by obesity. The present studies determined how high-fat feeding and body weight gain alter the sensitivity to the feeding suppression and neural activation to a selective norepinephrine reuptake inhibitor, nisoxetine. Acute administration of nisoxetine (saline: 0, 3, 10, and 30 mg/kg; IP) resulted in a dose-dependent reduction in the 24 h refeeding response in male Sprague Dawley rats maintained on standard chow. In a similar fashion, nisoxetine resulted in reductions in blood pressure and a compensatory increase in heart rate. From these studies, the 3 mg/kg dose was subthreshold. In a separate experiment, however, 10 wk exposure to a high-fat diet (60% fat) resulted in weight gain and significant feeding suppression following administration of nisoxetine (3 mg/kg) compared with animals fed a control diet (10% fat). Nisoxetine (3 mg/kg) also resulted in greater neural activation, as measured by c-Fos immunohistochemistry, in the arcuate nucleus of the hypothalamus in animals exposed to the high-fat diet. Such data indicate acute nisoxetine doses that suppress food intake can impact cardiovascular measures. It also suggests that the feeding suppression to a low-dose nisoxetine is enhanced as a result of high-fat diet and weight gain.
机译:中枢去甲肾上腺素能途径参与进食和心血管控制,肥胖会改变生理过程。本研究确定了高脂喂养和体重增加如何改变对选择性去甲肾上腺素再摄取抑制剂尼西汀的喂养抑制和神经激活的敏感性。尼索西汀的急性给药(生理盐水:0、3、10和30μmg/ kg; IP)导致维持标准饲料的雄性Sprague Dawley大鼠的24μh补饲反应呈剂量依赖性降低。尼索西汀以类似的方式导致血压降低和心率代偿性增加。从这些研究中,3?mg / kg剂量是低于阈值的。然而,在一个单独的实验中,与饲喂对照饮食(10%脂肪)的动物相比,服用尼索西汀(3毫克/千克)后,高脂饮食(60%脂肪)10周暴露导致体重增加和显着的摄食抑制作用)。通过c-Fos免疫组织化学测定,在高脂饮食的动物的下丘脑弓状核中,尼索西汀(3毫克/千克)还导致更大的神经活化。这些数据表明抑制食物摄入的急性尼索西汀剂量可能会影响心血管指标。这也表明,由于高脂饮食和体重增加,对低剂量尼西汀的摄食抑制作用得到增强。

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