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Hepatic glucose metabolism refers to the collection of biochemical pathways and regulatory mechanisms by which the **liver maintains blood glucose homeostasis**. This includes four main processes: glycolysis, gluconeogenesis, glycogenolysis, and glycogenesis. The liver acts both as a producer and consumer of glucose depending on physiological needs—exporting it during fasting via gluconeogenesis and glycogenolysis, and importing/storing it after meals through glycolysis and glycogenesis[1][2][3]. These processes are tightly regulated by hormones such as insulin and glucagon[1][2], with additional modulation by signaling molecules like cAMP, AMP/ATP ratio, citrate, alanine[3], endocannabinoids[4], transcription factors[6], among others. Dysregulation is central to diseases such as diabetes mellitus—where increased hepatic gluconeogenesis contributes to hyperglycemia—and other metabolic disorders[5]. While many drugs act on specific enzymes or receptors involved in these pathways (e.g., glucokinase activators), "hepatic glucose metabolism" itself is not a single molecular entity or canonical therapeutic target but rather an umbrella term describing integrated liver functions essential for systemic energy balance.
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