Istituto di Biologia e Biotecnologia Agraria, Consiglio Nazionale delle Ricerche, Pisa, Italy.
Dipartimento di Scienze della Salute, Università di Firenze, Firenze, Italy.
Front Endocrinol (Lausanne). 2023 Apr 5;14:1135157. doi: 10.3389/fendo.2023.1135157. eCollection 2023.
A vast literature strongly suggests that the endocannabinoid (eCB) system and related bioactive lipids (the paracannabinoid system) contribute to numerous physiological processes and are involved in pathological conditions such as obesity, type 2 diabetes, and intestinal inflammation. The gut paracannabinoid system exerts a prominent role in gut physiology as it affects motility, permeability, and inflammatory responses. Another important player in the regulation of host metabolism is the intestinal microbiota, as microorganisms are indispensable to protect the intestine against exogenous pathogens and potentially harmful resident microorganisms. In turn, the composition of the microbiota is regulated by intestinal immune responses. The intestinal microbial community plays a fundamental role in the development of the innate immune system and is essential in shaping adaptive immunity. The active interplay between microbiota and paracannabinoids is beginning to appear as potent regulatory system of the gastrointestinal homeostasis. In this context, oleoylethanolamide (OEA), a key component of the physiological systems involved in the regulation of dietary fat consumption, energy homeostasis, intestinal motility, and a key factor in modulating eating behavior, is a less studied lipid mediator. In the small intestine namely duodenum and jejunum, levels of OEA change according to the nutrient status as they decrease during food deprivation and increase upon refeeding. Recently, we and others showed that OEA treatment in rodents protects against inflammatory events and changes the intestinal microbiota composition. In this review, we briefly define the role of OEA and of the gut microbiota in intestinal homeostasis and recapitulate recent findings suggesting an interplay between OEA and the intestinal microorganisms.
大量文献强烈表明,内源性大麻素(eCB)系统和相关生物活性脂质(拟大麻素系统)有助于许多生理过程,并参与肥胖、2 型糖尿病和肠道炎症等病理状况。肠道拟大麻素系统在肠道生理学中发挥着重要作用,因为它影响运动、通透性和炎症反应。调节宿主代谢的另一个重要因素是肠道微生物群,因为微生物对于保护肠道免受外源性病原体和潜在有害常驻微生物的侵害是不可或缺的。反过来,微生物群的组成受肠道免疫反应的调节。肠道微生物群落在先天免疫系统的发育中起着基础性作用,对于塑造适应性免疫也是必不可少的。微生物群和拟大麻素之间的积极相互作用开始显现为胃肠道稳态的有效调节系统。在这种情况下,油酰乙醇胺(OEA)是参与调节膳食脂肪消耗、能量平衡、肠道运动以及调节进食行为的关键因素之一,是一种研究较少的脂质介质。在小肠,即十二指肠和空肠,OEA 的水平根据营养状况而变化,在禁食期间减少,在再喂养时增加。最近,我们和其他人的研究表明,OEA 治疗可保护啮齿动物免受炎症事件的影响,并改变肠道微生物群的组成。在这篇综述中,我们简要地定义了 OEA 和肠道微生物群在肠道稳态中的作用,并回顾了最近的研究结果,这些结果表明 OEA 与肠道微生物之间存在相互作用。