At high doses, what type of receptor agonist activity does dopamine exhibit?

Explore the USMLE Step 3 Drug MOA Test. Use flashcards and multiple-choice questions, each with hints and explanations. Ace your exam with confidence!

Dopamine, at high doses, primarily exhibits agonist activity at both α1 and α2 adrenergic receptors. This pharmacological action contributes to multiple physiological effects, including vasoconstriction and increased vascular resistance, which can be particularly relevant during situations such as shock or severe heart failure where elevated systemic vascular resistance is required.

At lower doses, dopamine predominantly stimulates D1 receptors, leading to renal vasodilation and increased renal blood flow, which can be beneficial in certain clinical scenarios. As the dose increases, however, the drug's effects shift due to the engagement of adrenergic receptors. Ultimately, at high concentrations, dopamine's action becomes more focused on α receptor stimulation, specifically enhancing vasoconstriction through α1 receptor activation while also affecting α2 receptors that can modulate neurotransmitter release and further influence the sympathetic nervous system.

This nuanced understanding of dopamine's dose-dependent receptor affinity is crucial in clinical practice and helps guide its use in different therapeutic contexts.

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