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Long Answer Questions · Q30

Q.Explain in detail the mechanism of action of protein hormones and of steroid hormones on their target cells, bringing out clearly the differences between the two mechanisms.

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Protein and peptide hormones (e.g. GH, insulin, glucagon, PTH, and the catecholamines) are water-soluble and cannot cross the lipid plasma membrane. They bind a specific receptor on the outer cell surface, without entering the cell; this binding activates a G-protein and membrane enzyme (e.g. adenylate cyclase), generating a diffusible second messenger inside the cell (e.g. cyclic AMP), which activates an existing enzyme cascade, rapidly altering cell metabolism. Because this works through existing cellular machinery rather than new protein synthesis, the response begins within seconds to minutes but is relatively short-lived once the hormone is withdrawn, as the second-messenger signal is quickly broken down.

Steroid hormones (e.g. testosterone, estrogen, progesterone, cortisol, aldosterone) are lipid-soluble, sharing a cholesterol-derived structure that lets them diffuse directly across the plasma membrane without any membrane receptor. Once inside, a steroid hormone binds a receptor located in the cytoplasm or nucleus; the resulting hormone-receptor complex binds a specific DNA sequence (a hormone response element), acting as a transcription factor that switches a particular gene's transcription on or off, altering the amount of a specific protein the cell produces. Because this mechanism depends on new protein synthesis, the response takes longer to begin -- often hours -- but is far more sustained once established than the rapid, transient protein-hormone response. Thyroid hormone (T3/T4), though not a true steroid, is lipid-soluble enough to act by this same intracellular-receptor, gene-regulation mechanism rather than the membrane-receptor route.

[!ANSWER]

Protein/peptide hormones act via membrane receptor + second messenger (e.g. cAMP), fast and transient. Steroid hormones diffuse across the membrane, bind intracellular receptors, and directly regulate gene transcription, slower onset but longer-lasting.

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