利莫那班的安魂曲:大麻素CB1受体拮抗剂在秋季后的治疗潜力

Taryn Bosquez-Berger, G. Szanda, A. Straiker
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引用次数: 0

摘要

内源性大麻素系统遍布整个中枢神经系统和身体,它影响许多重要的生理过程。人们对靶向大麻素受体在治疗上有益的期望很高;制药公司迅速抓住大麻素的食欲和代谢作用,开发了一种治疗减肥的药物。唉,一流的大麻素1型受体(CB1R)拮抗剂利莫那班的经历是药物开发危险的经典警示故事,利莫那班的失势对那些寻求CB1R拮抗剂治疗的人造成了打击。利莫那班在商业上最具吸引力的应用现在已经部分地被具有不同作用机制和更大效果的药物所掩盖。然而,阻断CB1受体会引起有趣的代谢效应,其中一些似乎发生在中枢神经系统之外。此外,近年来大麻的法律地位发生了惊人的变化,伴随着“所有大麻”的流行。这些变化与新的药理学策略和勤奋的药物化学相结合,可能还会看到该领域在某种程度上实现其早期的承诺。在这里,我们回顾利莫那班的故事,以及一些在秋天之后仍然有希望的治疗利基和策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Requiem for Rimonabant: Therapeutic Potential for Cannabinoid CB1 Receptor Antagonists after the Fall
The endocannabinoid system is found throughout the CNS and the body where it impacts many important physiological processes. Expectations were high that targeting cannabinoid receptors would prove therapeutically beneficial; pharmaceutical companies quickly seized on the appetitive and metabolic effects of cannabinoids to develop a drug for the treatment of weight loss. Alas, the experience with first-in-class cannabinoid type-1 receptor (CB1R) antagonist rimonabant is a now-classic cautionary tale of the perils of drug development and the outcome of rimonabant’s fall from grace dealt a blow to those pursuing therapies involving CB1R antagonists. And this most commercially compelling application of rimonabant has now been partially eclipsed by drugs with different mechanisms of action and greater effect. Still, blocking CB1 receptors causes intriguing metabolic effects, some of which appear to occur outside the CNS. Moreover, recent years have seen a startling change in the legal status of cannabis, accompanied by a popular embrace of ‘all things cannabis’. These changes combined with new pharmacological strategies and diligent medicinal chemistry may yet see the field to some measure of fulfillment of its early promise. Here, we review the story of rimonabant and some of the therapeutic niches and strategies that still hold promise after the fall.
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