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The question ID is Q Id 1367 (351594).
It basically wants you to distinguish between the different receptors that norepi works on (alpha1, alpha2, and beta1) and the downstream effects (cAMP, DAG, IP3).
My question: According to the question, you would give norepi to someone who is hypotensive (that makes sense), but how do we distinguish between the Gq receptor and Gs receptor.
I know alpha1 is Gq, increasing IP3, and that beta1 receptor would increase vascular smooth muscle contractility (which would increase blood pressure, solving hypotension, right?)
Also, alpha1 is Gs, increasing cAMP, and that alpha1 receptor would increase contracility (which would increase blood pressure, solving hypotension, right?)
So, now back to the uworld question, there were two choices, one said increased IP3 and one said increased cAMP, how to tell the difference between the two?
It basically wants you to distinguish between the different receptors that norepi works on (alpha1, alpha2, and beta1) and the downstream effects (cAMP, DAG, IP3).
My question: According to the question, you would give norepi to someone who is hypotensive (that makes sense), but how do we distinguish between the Gq receptor and Gs receptor.
I know alpha1 is Gq, increasing IP3, and that beta1 receptor would increase vascular smooth muscle contractility (which would increase blood pressure, solving hypotension, right?)
Also, alpha1 is Gs, increasing cAMP, and that alpha1 receptor would increase contracility (which would increase blood pressure, solving hypotension, right?)
So, now back to the uworld question, there were two choices, one said increased IP3 and one said increased cAMP, how to tell the difference between the two?