Arch J R, Ainsworth A T
Am J Clin Nutr. 1983 Oct;38(4):549-58. doi: 10.1093/ajcn/38.4.549.
The effects of a novel compound, BRL 26830A, on energy balance in normal and obese mice have been investigated. BRL 26830A reduced body weight or weight gain in genetically (ob/ob), goldthioglucose, and cafeteria diet obese mice and genetically obese (fa/fa) Zucker rats. Weight reduction was due to reduced body lipid content. BRL 26830A caused little or no reduction in food intake in these animals but it increased metabolic rate and in genetically obese mice this thermic effect was increased by repeat dosing. BRL 26830A did not reduce body weight gain in the lean counterparts of the genetically obese animals. Its thermic effect was smaller in the lean than the genetically obese mice and it caused an increase in food intake in the lean mice. The thermic effect of BRL 26830A was inhibited by dl- but not d-propranolol. BRL 26830A largely overcame the depression in metabolic rate caused by fasting.
已对一种新型化合物BRL 26830A对正常小鼠和肥胖小鼠能量平衡的影响进行了研究。BRL 26830A可减轻遗传性(ob/ob)、金硫葡萄糖诱导型和自助餐饮食诱导型肥胖小鼠以及遗传性肥胖(fa/fa) Zucker大鼠的体重或体重增加。体重减轻是由于体内脂质含量减少。BRL 26830A在这些动物中几乎不会减少或不会减少食物摄入量,但它会提高代谢率,并且在遗传性肥胖小鼠中,重复给药会增强这种产热效应。BRL 26830A不会减轻遗传性肥胖动物的瘦型对照动物的体重增加。其在瘦型小鼠中的产热效应比遗传性肥胖小鼠小,并且它会导致瘦型小鼠的食物摄入量增加。BRL 26830A的产热效应受到dl-普萘洛尔而非d-普萘洛尔的抑制。BRL 26830A在很大程度上克服了禁食引起的代谢率降低。