The Ketone Signaling Cascade describes the complex series of molecular events initiated by the presence of ketone bodies, particularly beta-hydroxybutyrate (BHB), which extend far beyond their role as simple metabolic fuels. This cascade involves BHB acting as a powerful signaling molecule that influences numerous cellular processes, including gene expression, neurotransmitter function, and inflammatory pathway regulation. It represents a fundamental, protective metabolic switch.
Origin
This term is a relatively modern construct in metabolic research, emerging from the realization that ketones are not merely energy substrates but have significant pleiotropic effects on cell function. The ‘cascade’ analogy emphasizes the widespread, downstream effects initiated by this single molecule. It bridges the fields of bioenergetics, endocrinology, and neuroscience.
Mechanism
BHB triggers its effects by binding to specific G-protein coupled receptors, acting as an endogenous ligand, and by directly inhibiting histone deacetylases (HDACs), which is an epigenetic mechanism. Receptor binding can modulate satiety and energy expenditure, while HDAC inhibition promotes the transcription of genes related to antioxidant defense and longevity. This dual action allows the ketone cascade to simultaneously optimize cellular energy and enhance cellular resilience.
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