The IGF-1 Synthesis Pathway describes the specific biochemical cascade responsible for the creation and release of Insulin-like Growth Factor 1, a crucial anabolic peptide hormone. This pathway is predominantly initiated by Growth Hormone (GH) signaling in the liver, where GH binds to its receptors on hepatocytes. IGF-1 acts as the primary mediator of many of GH’s growth-promoting and metabolic effects throughout the body. Understanding the steps of this pathway is vital for diagnosing growth disorders and for optimizing anabolic drive in adult health and longevity protocols.
Origin
This concept is foundational to molecular endocrinology, established with the discovery of somatomedins, which were later identified as IGFs, in the mid-20th century. The term “pathway” refers to the sequential series of molecular reactions and enzyme-catalyzed steps that lead to the final product. The hepatic IGF-1 axis has been a central focus of research due to its pivotal role in regulating systemic growth, metabolism, and cellular proliferation.
Mechanism
The pathway begins when circulating Growth Hormone binds to its receptor on the liver cell surface, initiating intracellular signaling, primarily through the JAK/STAT cascade. This signal activates gene transcription, leading to the synthesis of the IGF-1 precursor protein. The precursor is then cleaved and processed into the mature IGF-1 peptide, which is subsequently secreted into the bloodstream, often bound to binding proteins (IGFBPs). The mature IGF-1 then acts on target tissues via its own specific receptor, mediating anabolic and anti-catabolic effects.
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