Maladies Métaboliques, Institut de Recherches SERVIER Suresnes, France.
Front Endocrinol (Lausanne). 2012 Dec 21;3:160. doi: 10.3389/fendo.2012.00160. eCollection 2012.
The compound S38151 is a nanomolar antagonist that acts at the melanin-concentrating hormone receptor 1 (MCH(1)). S38151 is more stable than its purely peptide counterpart, essentially because of the blockade of its N-terminus. Therefore, its action on various models of obesity was studied. Acute intra-cerebroventricular (i.c.v.) administration of S38151 in wild-type rats counteracted the effect of the stable precursor of melanin-concentrating hormone (MCH), NEI-MCH, in a dose-dependent manner (from 0.5 to 50 nmol/kg). In genetically obese Zucker fa/fa rats, daily i.c.v. administration of S38151 induced dose-dependent (5, 10, and 20 nmol/kg) inhibition of food intake, water intake, and body weight gain, as well as increased motility (maximal effect observed at 20 nmol/kg). In Zucker fa/fa rats, intraperitoneal injection of S38151 (30 mg/kg) induced complete inhibition of food consumption within 1 h. Daily intraperitoneal injection of S38151 (10 and 30 mg/kg) into genetically obese ob/ob mice or diet-induced obese mice is able to limit body weight gain. Furthermore, S38151 administration (10 and 30 mg/kg) does not affect food intake, water intake, or body weight gain in MCHR1-deleted mice, demonstrating that its effects are linked to its interaction with MCH(1). These results validate MCH(1) as a target of interest in obesity. S38151 cannot progress to the clinical phase because it is still too poorly stable in vivo.
化合物 S38151 是一种对黑素浓缩激素受体 1(MCH(1))具有纳米摩尔亲和力的拮抗剂。S38151 比其纯肽对应物更稳定,这主要是因为其 N 端被封锁。因此,研究了它在各种肥胖模型中的作用。在野生型大鼠中,急性侧脑室(i.c.v.)给予 S38151 可剂量依赖性地拮抗黑素浓缩激素(MCH)稳定前体 NEI-MCH 的作用(0.5 至 50 nmol/kg)。在遗传性肥胖 Zucker fa/fa 大鼠中,每日 i.c.v.给予 S38151 可剂量依赖性地抑制(5、10 和 20 nmol/kg)食物摄入、水摄入和体重增加,并增加运动性(在 20 nmol/kg 时观察到最大效应)。在 Zucker fa/fa 大鼠中,S38151(30 mg/kg)腹腔注射可在 1 小时内完全抑制食物消耗。每日腹腔注射 S38151(10 和 30 mg/kg)到遗传性肥胖 ob/ob 小鼠或饮食诱导肥胖小鼠中,能够限制体重增加。此外,S38151 给药(10 和 30 mg/kg)不会影响 MCHR1 缺失小鼠的食物摄入、水摄入或体重增加,表明其作用与其与 MCH(1)的相互作用有关。这些结果验证了 MCH(1)作为肥胖治疗靶点的重要性。由于 S38151 在体内的稳定性仍然较差,因此它无法进入临床阶段。