Microbial metabolite signaling describes the extensive and crucial biochemical communication network mediated by small molecules produced by the gut microbiota, which act as signaling messengers to host cells and tissues. These metabolites, including short-chain fatty acids, bile acid derivatives, and various neurotransmitter precursors, influence host physiology far beyond the gastrointestinal tract, affecting immune response, energy metabolism, and neuroendocrine function. Understanding this signaling is paramount for optimizing hormonal health and metabolic resilience.
Origin
‘Microbial’ refers to the microbiota, the community of microorganisms in the gut. ‘Metabolite’ denotes the small molecules produced during metabolism. ‘Signaling’ refers to the process of transmitting information between cells. This field emerged from the recognition that the gut microbiome is essentially a vast, distributed endocrine organ, profoundly influencing the host’s systemic biology.
Mechanism
The mechanism involves the absorption of these microbial-derived molecules into the bloodstream, where they interact with specific host receptors, such as G-protein coupled receptors (GPRs) on enteroendocrine cells, or directly modulate enzyme activity and gene expression in distant organs like the liver, brain, and adipose tissue. For example, short-chain fatty acids can modulate epigenetic mechanisms in immune cells, while certain secondary bile acids can influence thyroid hormone metabolism. This continuous cross-talk integrates gut ecology with the host’s entire endocrine regulatory network.
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