Institute of Pharmacology, Shandong First Medical University and Shandong Academy of Medical Sciences, Taian, Shandong 271016, P.R. China.
The Second School of Clinical Medicine, Guangzhou University of Chinese Medicine, Guangzhou, Guangdong 510006, P.R. China.
Int J Neuropsychopharmacol. 2023 Jan 19;26(1):70-79. doi: 10.1093/ijnp/pyac060.
Alcohol abuse is 1 of the most significant public health problems in the world. Chronic, excessive alcohol consumption not only causes alcohol use disorder (AUD) but also changes the gut and lung microbiota, including bacterial and nonbacterial types. Both types of microbiota can release toxins, further damaging the gastrointestinal and respiratory tracts; causing inflammation; and impairing the functions of the liver, lung, and brain, which in turn deteriorate AUD. Phosphodiesterases (PDEs) are critical in the control of intracellular cyclic nucleotides, including cyclic adenosine monophosphate and cyclic guanosine monophosphate. Inhibition of certain host PDEs reduces alcohol consumption and attenuates alcohol-related impairment. These PDEs are also expressed in the microbiota and may play a role in controlling microbiota-associated inflammation. Here, we summarize the influences of alcohol on gut/lung bacterial and nonbacterial microbiota as well as on the gut-liver/brain/lung axis. We then discuss the relationship between gut and lung microbiota-mediated PDE signaling and AUD consequences in addition to highlighting PDEs as potential targets for treatment of AUD.
酗酒是世界上最重大的公共卫生问题之一。慢性、过量饮酒不仅会导致酒精使用障碍(AUD),还会改变肠道和肺部微生物群,包括细菌和非细菌类型。这两种类型的微生物群都可以释放毒素,进一步损害胃肠道和呼吸道;引起炎症;并损害肝脏、肺部和大脑的功能,进而使 AUD 恶化。磷酸二酯酶(PDEs)在控制细胞内环核苷酸(包括环腺苷酸和环鸟苷酸)中起着关键作用。抑制某些宿主 PDEs 可以减少酒精摄入量并减轻与酒精相关的损害。这些 PDEs也在微生物群中表达,可能在控制与微生物群相关的炎症中发挥作用。在这里,我们总结了酒精对肠道/肺部细菌和非细菌微生物群以及肠道-肝脏/大脑/肺部轴的影响。然后,我们讨论了肠道和肺部微生物群介导的 PDE 信号与 AUD 后果之间的关系,并强调 PDE 作为 AUD 治疗的潜在靶点。