Department of Pharmaceutics, School of Pharmacy, University of Washington, Seattle, WA 98195, United States.
Department of Pharmaceutics, School of Pharmacy, University of Washington, Seattle, WA 98195, United States.
Pharmacol Ther. 2024 Apr;256:108605. doi: 10.1016/j.pharmthera.2024.108605. Epub 2024 Feb 16.
Microbial metabolites have emerged as key players in the interplay between diet, the gut microbiome, and host health. Two major classes, short-chain fatty acids (SCFAs) and tryptophan (Trp) metabolites, are recognized to regulate inflammatory, immune, and metabolic responses within the host. Given that many human diseases are associated with dysbiosis of the gut microbiome and consequent reductions in microbial metabolite production, the administration of these metabolites represents a direct, multi-targeted treatment. While a multitude of preclinical studies showcase the therapeutic potential of both SCFAs and Trp metabolites, they often rely on high doses and frequent dosing regimens to achieve systemic effects, thereby constraining their clinical applicability. To address these limitations, a variety of pharmaceutical formulations approaches that enable targeted, delayed, and/or sustained microbial metabolite delivery have been developed. These approaches, including enteric encapsulations, esterification to dietary fiber, prodrugs, and nanoformulations, pave the way for the next generation of microbial metabolite-based therapeutics. In this review, we first provide an overview of the roles of microbial metabolites in maintaining host homeostasis and outline how compromised metabolite production contributes to the pathogenesis of inflammatory, metabolic, autoimmune, allergic, infectious, and cancerous diseases. Additionally, we explore the therapeutic potential of metabolites in these disease contexts. Then, we provide a comprehensive and up-to-date review of the pharmaceutical strategies that have been employed to enhance the therapeutic efficacy of microbial metabolites, with a focus on SCFAs and Trp metabolites.
微生物代谢产物已成为饮食、肠道微生物组和宿主健康之间相互作用的关键因素。两类主要的代谢产物,短链脂肪酸 (SCFA) 和色氨酸 (Trp) 代谢产物,被认为可以调节宿主的炎症、免疫和代谢反应。鉴于许多人类疾病都与肠道微生物组的失调以及微生物代谢产物产生的相应减少有关,因此这些代谢产物的给药代表了一种直接的、多靶点的治疗方法。虽然大量的临床前研究展示了 SCFA 和 Trp 代谢产物的治疗潜力,但它们通常依赖于高剂量和频繁的给药方案来实现全身效应,从而限制了它们的临床适用性。为了解决这些限制,已经开发了各种能够实现靶向、延迟和/或持续微生物代谢产物递送的药物制剂方法。这些方法包括肠内包封、酯化到膳食纤维、前药和纳米制剂,为下一代基于微生物代谢产物的治疗方法铺平了道路。在这篇综述中,我们首先概述了微生物代谢产物在维持宿主内稳态中的作用,并概述了代谢产物产生受损如何导致炎症、代谢、自身免疫、过敏、感染和癌症等疾病的发病机制。此外,我们还探讨了代谢产物在这些疾病背景下的治疗潜力。然后,我们全面而最新地综述了用于增强微生物代谢产物治疗效果的药物策略,重点关注 SCFA 和 Trp 代谢产物。