Ellermann Melissa
Department of Biological Sciences, University of South Carolina, Columbia, SC, United States.
Adv Drug Alcohol Res. 2023 Dec 8;3:11359. doi: 10.3389/adar.2023.11359. eCollection 2023.
Bioactive lipids such as endocannabinoids serve as important modulators of host health and disease through their effects on various host functions including central metabolism, gut physiology, and immunity. Furthermore, changes to the gut microbiome caused by external factors such as diet or by disease development have been associated with altered endocannabinoid tone and disease outcomes. These observations suggest the existence of reciprocal relationships between host lipid signaling networks and bacterial populations that reside within the gut. Indeed, endocannabinoids and their congeners such as acylethanolamides have been recently shown to alter bacterial growth, functions, physiology, and behaviors, therefore introducing putative mechanisms by which these bioactive lipids directly modulate the gut microbiome. Moreover, these potential interactions add another layer of complexity to the regulation of host health and disease pathogenesis that may be mediated by endocannabinoids and their derivatives. This mini review will summarize recent literature that exemplifies how acylethanolamides and monoacylglycerols including endocannabinoids can impact bacterial populations and within the gut microbiome. We also highlight exciting preclinical studies that have engineered gut bacteria to synthesize host acylethanolamides or their precursors as potential strategies to treat diseases that are in part driven by aberrant lipid signaling, including obesity and inflammatory bowel diseases.
内源性大麻素等生物活性脂质通过对包括中枢代谢、肠道生理和免疫在内的各种宿主功能产生影响,从而成为宿主健康和疾病的重要调节因子。此外,饮食等外部因素或疾病发展所引起的肠道微生物群变化,已与内源性大麻素水平改变及疾病结局相关联。这些观察结果表明,宿主脂质信号网络与肠道内细菌群体之间存在相互关系。事实上,内源性大麻素及其同系物(如酰基乙醇酰胺)最近已被证明可改变细菌的生长、功能、生理和行为,从而引入了这些生物活性脂质直接调节肠道微生物群的假定机制。此外,这些潜在的相互作用为宿主健康和疾病发病机制的调节增加了另一层复杂性,而这可能由内源性大麻素及其衍生物介导。本综述将总结近期的文献,这些文献例证了酰基乙醇酰胺和包括内源性大麻素在内的单酰甘油如何影响肠道微生物群中的细菌群体。我们还重点介绍了令人兴奋的临床前研究,这些研究通过改造肠道细菌来合成宿主酰基乙醇酰胺或其前体,作为治疗部分由异常脂质信号驱动的疾病(包括肥胖症和炎症性肠病)的潜在策略。