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Adrenergic beta-receptors are GPCRs divided into three main subtypes (β1, β2, β3) that mediate critical cardiovascular, metabolic, and respiratory functions by transducing catecholamine signals into cellular responses through cAMP-dependent pathways. Their pharmacological modulation is central to treatment strategies across several major diseases.
Agonists stimulate adenylyl cyclase via G_s protein activation, increasing cAMP levels and activating PKA. Antagonists block the receptor, preventing catecholamine binding and downstream signaling.
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