Answer:
A. Inhibition of glycogen synthesis.
B. Activation of PKA, which turns on glycogen degradation.
C. Activation of adenylate cyclase and an increase in cAMP levels.
E. Net glucose export.
Step-by-step explanation:
The process begins in the islets of Langerhans, where glucagon is released when the concentration of glucose in the bloodstream falls too low. It reaches the hepatocytes, connects with a membranous receptor, which activates the Gs protein. Since it activates the adenylate cyclase, cAMP is generated and kinase A is activated, whose catalytic subunits phosphorylate two cytosolic enzymes: phosphorylase kinase and glycogen synthase. The phosphorylase kinase activates and phosphorylates another enzyme, the glycogen phosphorylase, which degrades glycogen, releasing glucose-1-P. In contrast, glycogen synthase is inhibited and stops synthesizing glycogen from glucose molecules.
After an isomerization to glucose-6-P, an enzyme located in the SER membrane, glucose 6-phosphatase, transforms glucose 6-P into glucose, which leaves the hepatocyte.