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Plasma-based approach to measure target engagement for liver-targeting stearoyl-CoA desaturase 1 inhibitors

机译:基于血浆的方法可测量针对肝脏的硬脂酰辅酶A去饱和酶1抑制剂的靶标参与度

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摘要

A positive correlation between stearoyl-CoA desaturase (SCD)1 expression and metabolic diseases has been reported in rodents and humans. These findings indicate that SCD1 is a promising therapeutic target for the chronic treatment of diabetes and dyslipidemia. The SCD1 enzyme is expressed at high levels in several human tissues and is required for the biosynthesis of monounsaturated fatty acids, which are involved in many biological processes. Liver-targeted SCD inhibitors were designed to pharmacologically manipulate SCD1 activity in the liver to avoid adverse events due to systemic inhibition. This article describes the development of a plasma-based SCD assay to assess the level of SCD inhibition, which is defined in this article as target engagement. Essentially, animals are dosed with an exogenous deuterated tracer (d7-stearic acid) as substrate, and the converted d7-oleic acid product is measured to monitor SCD1 inhibition. This study reveals that this plasma-based assay correlates with liver SCD1 inhibition and can thus have clinical utility.
机译:据报道,啮齿动物和人类中,硬脂酰辅酶A去饱和酶(SCD)1表达与代谢性疾病呈正相关。这些发现表明SCD1是糖尿病和血脂异常的慢性治疗的有希望的治疗靶标。 SCD1酶在几种人体组织中高表达,是生物合成单不饱和脂肪酸所必需的。设计针对肝脏的SCD抑制剂可通过药理作用控制肝脏中的SCD1活性,以避免由于全身性抑制而引起的不良事件。本文介绍了基于血浆的SCD分析方法的开发,以评估SCD抑制水平,本文将其定义为靶标参与。基本上,给动物服用外源性氘代示踪剂(d7-硬脂酸)作为底物,并测量转化的d7-油酸产物以监测SCD1抑制。这项研究表明,这种基于血浆的测定与肝脏SCD1抑制有关,因此可以具有临床实用性。

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