The precise, hormonally-driven cascade of molecular events within adipocytes (fat cells) that leads to the breakdown of stored triglycerides into free fatty acids and glycerol, which are then released into the bloodstream for energy use. This sequence is a fundamental component of energy mobilization, particularly during fasting or prolonged exercise. Clinically, understanding this sequence is vital for strategies aimed at body fat reduction.
Origin
The concept is foundational to lipid biochemistry and endocrinology, originating from research that elucidated the role of hormones in fat metabolism. The term “sequence” highlights the ordered nature of the enzyme activation necessary for the catabolic process. Its clinical relevance is high in the context of weight management and understanding metabolic flexibility.
Mechanism
The sequence is initiated by the binding of lipolytic hormones, such as epinephrine, norepinephrine, or glucagon, to their receptors on the adipocyte surface, which activates adenylyl cyclase. This enzyme increases the intracellular concentration of cyclic AMP (cAMP), which in turn activates Protein Kinase A (PKA). PKA then phosphorylates and activates Hormone-Sensitive Lipase (HSL) and Perilipin, allowing HSL access to the stored triglycerides and initiating the breakdown process.
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