Parm Question
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Wondering if someone might enlighten me, I am preparing for an interview and have a couple pharm questions I can't seem to find answers to yet.
1) When dopamine stimulates D1 receptors in the renal vasculature it causes vasodilation, however the mechanism of Increasing cAMP and intracellular calcium is the exact same as say stimulating B1 receptors in the heart that leads to increased intracellular calcium, and therefore an increased contraction. To clarify, my question is why does increased intracellular calcium (after D1 receptor stimulation) in the renal arteries cause vasodialtion instead of vasoconstriction like other areas of the body when calcium is increased intracellularly?
2)Are D2 receptors stimulated the same time D1 receptors are and just counteract D1? (D1 stimulates adenlyly cyclase, D2 inhibits adenylyl cyclase correct?)
Any help is appreciated, thanks.