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Molecular Interplay of Oxidative Stress and Gut Microbiome in Aging

  • Ahamed Basha Abdul Bari,
  • Madhan Krishnan,
  • Shyamaladevi Babu

摘要

Oxidative stress results from an imbalance between reactive oxygen species production and the capacity of the organism to counteract them. These species are reactive substances that may deteriorate lipids, proteins, and DNA, which causes cellular malfunction and acts as etiological factors for various age-related disorders, including aging. The gut microbiota contains trillions of microorganisms, including bacteria, protozoa, viruses, and fungi, as well as their combined genetic material, that are present in the gastrointestinal tract. These microbiomes can also influence oxidative stress through their metabolic activities. As we age, the gut microbiome undergoes changes in composition and diversity, which can alter its metabolic activities and contribute to oxidative stress through mechanisms like production of reactive oxygen species, and modulation of antioxidant defences. For example, certain gut bacteria can produce reactive oxygen species as a byproduct of their metabolism, while others can generate antioxidants that neutralise them. The balance between reactive oxygen species-producing and antioxidant-producing bacteria can shift as we age, leading to increased oxidative stress. In addition, the gut microbiome can influence the host’s antioxidant defence system by producing short-chain fatty acids and other metabolites that can modulate gene expression and signalling pathways. One of the short-chain fatty acids, butyrate, can result in an increase in the production of antioxidant enzymes such as catalase and superoxide dismutase and reduce oxidative stress in the gut and other organs. Additionally, available literature also indicates that oxidative stress can affect the gut microbiome by changing its structure and functionality through the immune response, which in turn influences the aging process. Oxidative byproducts can damage bacterial membranes, DNA, and proteins, leading to microbial cell death and dysbiosis. Dysbiosis, on the other hand, might increase oxidative stress by lowering the production of short-chain fatty acids and other antioxidant metabolites. Overall, the molecular interaction between oxidative stress and the gut microbiome in aging is intricate and complicated. Further research is required to understand the mechanisms underlying these interactions and identify strategies to promote a healthy gut microbiome and reduce oxidative stress in the aging process.