Answer:
the correct answer is "when glucose is present, cAMP levels are high, so CAp is active and can bind to the activator"
Step-by-step explanation:
CAMP is synthesized from ATP by the enzyme adenylate cyclase which is located in the cell membrane. This enzyme is activated by Gα or Gα-activator subunit activators, belonging to protein G, and inhibited by agonists of adenylate cyclase G or Gi inhibitors, both coupled protein receptors. Hepatic adenylate cyclase responds more strongly to glucagon, whereas muscle adenylate responds more strongly to adrenaline.
The breakdown of cAMP to 5'-AMP is catalyzed by the enzyme phosphodiesterase.
that is why the cyclic amp is only present with an increase in ATP (adenosistriphosphate) and therefore with the presence of glucose in the blood (considering that the person does not present insulin disorders with respect to the assimilation of glucose)