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BRL 35135,一种强效且选择性的非典型β-肾上腺素能受体激动剂。

BRL 35135, a potent and selective atypical beta-adrenoceptor agonist.

作者信息

Cawthorne M A, Sennitt M V, Arch J R, Smith S A

机构信息

Diabetes Programme, SmithKline Beecham Pharmaceuticals, Great Burgh, Epsom, Surrey, UK.

出版信息

Am J Clin Nutr. 1992 Jan;55(1 Suppl):252S-257S. doi: 10.1093/ajcn/55.1.252s.

Abstract

BRL 35135, via its active deesterified metabolite BRL 37344, is a potent example of a new group of beta-adrenoceptor agonists that stimulate selectively a novel beta adrenoceptor that was originally shown to be present in brown adipose tissue in rodents. BRL 35135 produces a dose-related increase in energy expenditure in rodents and, in genetically obese (ob/ob) mice, a dose of 0.5 mg.kg-1.d-1 has significant antiobesity activity. This weight loss is entirely due to loss of fat; muscle protein is preserved. In studies in nonobese men, BRL 35135 (0.1 mg/kg) increased both resting metabolic rate and the thermic response to a glucose load. BRL 35135 is effective in improving glucose tolerance in genetically obese (ob/ob) mice and obese Zucker (fa/fa) rats at doses that have no significant antiobesity activity. The improved glucose tolerance is the result of significant improvement in insulin sensitivity. In 10-d studies in obese and diabetic patients, BRL 35135 produced improvements in glucose tolerance and insulin sensitivity.

摘要

BRL 35135通过其活性去酯化代谢物BRL 37344,成为一类新型β-肾上腺素能受体激动剂的有力代表,这类激动剂能选择性地刺激一种新的β肾上腺素能受体,该受体最初在啮齿动物的棕色脂肪组织中被发现。BRL 35135能使啮齿动物的能量消耗呈剂量依赖性增加,在遗传性肥胖(ob/ob)小鼠中,0.5毫克·千克-1·天-1的剂量具有显著的抗肥胖活性。这种体重减轻完全是由于脂肪减少;肌肉蛋白得以保留。在对非肥胖男性的研究中,BRL 35135(0.1毫克/千克)提高了静息代谢率以及对葡萄糖负荷的热反应。BRL 35135在对遗传性肥胖(ob/ob)小鼠和肥胖Zucker(fa/fa)大鼠进行的研究中,在不具有显著抗肥胖活性的剂量下,能有效改善葡萄糖耐量。葡萄糖耐量的改善是胰岛素敏感性显著提高的结果。在对肥胖和糖尿病患者进行的为期10天的研究中,BRL 35135改善了葡萄糖耐量和胰岛素敏感性。

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