Lushchak Volodymyr I
Department of Biochemistry and Biotechnology, Vasyl Stefanyk Precarpathian National University, Ivano-Frankivsk, 57 Shevchenko Str., 76018 Ivano-Frankivsk, Ukraine.
Research and Development University, Ivano-Frankivsk, 13a Shota Rustaveli Str., 76018 Ivano-Frankivsk, Ukraine.
Biomolecules. 2025 Aug 11;15(8):1151. doi: 10.3390/biom15081151.
Digestion was once viewed as a host-driven process, dependent on salivary, gastric, pancreatic, and intestinal enzymes to break down macronutrients. However, new insights into the gut microbiota have redefined this view, highlighting digestion as a cooperative effort between host and microbial enzymes. Host enzymes initiate nutrient breakdown, while microbial enzymes, especially in the colon, extend this process by fermenting resistant polysaccharides, modifying bile acids, and transforming phytochemicals and xenobiotics into bioactive compounds. These microbial actions produce metabolites like short-chain fatty acids, which influence gut barrier function, immune regulation, and metabolism. I propose two frameworks to describe this interaction: the "duet," emphasizing sequential enzymatic cooperation, and the "orchestra," reflecting a spatially and temporally coordinated system with host-microbiota feedback. Disruption of this symbiosis, through antibiotics, inflammation, diet, or aging, leads to dysbiosis, impaired digestion, and contributes to metabolic, neurologic, cardiovascular, and inflammatory diseases. Recognizing digestion as a dynamic, integrated system opens new paths for therapies and nutrition. These include enzyme-targeted prebiotics, probiotics, postbiotics, and personalized diets. Embracing this systems-level perspective enables innovative diagnostics and treatments, aiming to restore enzymatic balance and improve digestive and systemic health.
消化曾被视为一个由宿主驱动的过程,依赖唾液、胃、胰腺和肠道中的酶来分解大量营养素。然而,对肠道微生物群的新见解重新定义了这一观点,强调消化是宿主酶与微生物酶共同作用的结果。宿主酶启动营养物质的分解,而微生物酶,尤其是在结肠中的微生物酶,则通过发酵抗性多糖、修饰胆汁酸以及将植物化学物质和外源性物质转化为生物活性化合物来扩展这一过程。这些微生物作用产生短链脂肪酸等代谢产物,它们会影响肠道屏障功能、免疫调节和新陈代谢。我提出了两个框架来描述这种相互作用:“二重奏”,强调酶的顺序合作;“管弦乐队”,反映一个具有宿主-微生物群反馈的时空协调系统。通过抗生素、炎症、饮食或衰老破坏这种共生关系会导致生态失调、消化功能受损,并引发代谢、神经、心血管和炎症性疾病。将消化视为一个动态的、综合的系统为治疗和营养开辟了新途径。这些途径包括针对酶的益生元、益生菌、后生元以及个性化饮食。接受这种系统层面的观点能够实现创新的诊断和治疗,旨在恢复酶的平衡并改善消化和全身健康。