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Glycogen Metabolism

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Total cards: 9•Content version: v4•Public deck•Updated: 8/1/2026

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#1
Front (Question)

Def of glycogenesis

Back (Answer)

Process of glycogen formation from glucose

#2
Front (Question)

Location of glycogenesis

Back (Answer)

Cytosol of liver and muscles

#3
Front (Question)

Importance of glycogenesis

Back (Answer)

Storage of excess glucose to use it later at time of requirement

#4
Front (Question)

Steps of glycogenesis

Back (Answer)

Glycogen synthase is the rate limiting enzyme

#5
Front (Question)

Def of glycogenolysis

Back (Answer)

Breakdown of glycogen into glucose in liver during fasting and G6p in muscles during exercise

#6
Front (Question)

Steps of glycogenolysis

Back (Answer)

Glycogen phophorylase is the rate limiting enzyme

#7
Front (Question)

Regulation of glycogenolysis and glycogenesis

Back (Answer)

Because of the importance of maintaining blood glucose levels, the synthesis and degra- dation of its glycogen storage form are tightly regulated. In the liver, glycogenesis accelerates during well fed state whereas glycogenolysis accelerates during fasting. In skeletal muscle, gly- cogenolysis occurs during active exercise, and glycogenesis begins at rest. Regulation of glycogen synthesis and degradation is accomplished on two levels. First, glycogen synthase and glycogen phosphorylase are hormonally regulated to meet the needs of the body as a whole (Covalent modification). Second, the pathways of glycogen synthesis and degradation are allosterically con- trolled to meet the needs of a particular tissue. (Allosteric modification). Glycogen synthase is activated by insulin ( glut 2) in liver Inhibited by epinephrine and glucagon It is activated in muscle by insulin ( glut 4) and inhibited by epinephrine Glycogen phosphorylase is activated in liver by epinephrine and glucagon and inhibited by insulin It is activated in muscle by epinephrine ca and AMP and inhibited by insulin and ATP

#8
Front (Question)

Glycogen storage disease

Back (Answer)

It is genetic characteristized by accumulation of glycogen 1- von gierke : deficiency in glucose 6 phosphatase results in severe hypoglycemia , lactic acidosis, hepatomegaly , hyperlipidimia, hyper uracimia and doll like facies 2- mcardle : deficiency in muscle glycogen phosphorylase results in cramps and weakness in muscle 3- hers : deficiency in hepatic glycogen phosphorylase results in fasting hypoglycemia , hepatomegaly and cirrhosis

#9
Front (Question)

Substrate for glycogenesis

Back (Answer)

1, In liver: • Blood glucose. • Other hexoses: fructose and galactose. • Non-carbohydrate sources: glycerol and lactate. These are converted first to glucose, then to glycogen. • In muscles: Blood glucose only.