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Combined effects of oleoyl-estrone and a beta(3)-adrenergic agonist (CL316,243) on lipid stores of diet-induced overweight male Wistar rats

机译:油酰基雌酮和β(3)-肾上腺素能激动剂(CL316,243)对饮食诱导的超重雄性Wistar大鼠脂质存储的联合作用

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Oleoyl-estrone (OE) decreases appetite, induces adipose tissue wasting and resets the ponderostat setting, sparing glucose and protein. The beta(3)-adrenergic agonists increase energy expenditure and lipolysis. We studied the combination of both treatments to enhance fat mobilization. Overweight male rats received oral OE for 10 days; they were compared with controls and rats receiving a beta(3)-adrenergic agonist, CL316,243 (B3A); another group received both OE and B3A. Serum 3-hydroxybutyrate, NEFA, triacylglycerols and glucose showed only slight changes in all groups vs. controls; OE-treated rats showed lower cholesterol. OE decreased food intake and B3A increased energy expenditure. OE rats lost about 15%, B3A 24%, and those receiving both compounds lost 39% of their initial total body energy. In all cases, most of this energy imbalance was accounted for by the loss of body lipid. The combined treatment of OE and B3A reduced food intake, nevertheless maintaining a high energy expenditure. The combination of a beta(3)-adrenergic agonist with OE may help compensate the short-lived effects of the agonist and enhance the lipid mobilization action of OE. The eventual combination of both compounds should be explored as a way to obtain faster and more effective ways to treat obesity. (c) 2005 Elsevier Inc. All rights reserved.
机译:油酰-雌酮(OE)会降低食欲,引起脂肪组织消瘦,并使定型稳压器恢复原状,并保留葡萄糖和蛋白质。 β(3)-肾上腺素能激动剂增加能量消耗和脂解作用。我们研究了两种治疗方法的组合以增强脂肪动员。超重雄性大鼠口服OE持续10天;将它们与对照组和接受β(3)-肾上腺素能激动剂CL316,243(B3A)的大鼠进行比较;另一组同时接受了OE和B3A。与对照组相比,所有组的血清3-羟基丁酸酯,NEFA,三酰甘油和葡萄糖仅显示出轻微变化。 OE处理的大鼠显示出较低的胆固醇。 OE减少食物摄入,B3A增加能量消耗。 OE大鼠损失约15%,B3A损失24%,而同时接受这两种化合物的大鼠则损失其初始全身能量的39%。在所有情况下,这种能量失衡的大部分是由体内脂质的损失引起的。 OE和B3A的组合处理减少了食物摄入,但仍保持了高能量消耗。 β(3)-肾上腺素能激动剂与OE的组合可帮助补偿激动剂的短暂作用并增强OE的脂质动员作用。两种化合物的最终组合应作为一种获得更快,更有效的肥胖治疗方法进行研究。 (c)2005 Elsevier Inc.保留所有权利。

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