Glycogen Degradation

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These flashcards cover key concepts related to glycogen degradation processes, enzymes involved, hormonal regulation, and physiological considerations.

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34 Terms

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Glycogen

A branched polymer of glucose residues used as a key energy source.

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Glycogenolysis

The process of breaking down glycogen into glucose.

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Glycogen phosphorylase

The key regulatory enzyme that cleaves glycogen to release glucose 1-phosphate.

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Phosphorylase regulation

Controlled by allosteric interactions and reversible phosphorylation.

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Allosteric effectors

Molecules that bind to an enzyme and alter its activity without changing the enzyme's concentration.

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Epinephrine

A hormone that stimulates glycogen breakdown primarily in muscle.

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Glucagon

A hormone that signals the need for glycogen breakdown, primarily affecting the liver.

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Phosphorolysis

The cleavage of a bond by the addition of orthophosphate.

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Enzymatic activities in glycogen breakdown

Includes glycogen phosphorylase, transferase, and debranching enzyme.

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Debranching enzyme

An enzyme that hydrolyzes the bonds at branch points in glycogen.

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Glucose 6-phosphate

An important metabolic intermediate derived from glucose 1-phosphate.

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Phosphoglucomutase

An enzyme that converts glucose 1-phosphate into glucose 6-phosphate.

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Liver vs. muscle glycogen

Liver glycogen is used to maintain blood glucose levels, while muscle glycogen serves immediate energy needs.

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Glycogen granules

Small structures in the cytoplasm where glycogen is stored.

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High gain system

A mechanism by which a small stimulus can lead to a large response in glycogen breakdown.

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Type I muscle fibers

Slow-twitch fibers that primarily use fatty acids for energy and have low glycogen amounts.

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Type IIb muscle fibers

Fast-twitch fibers that predominantly use glycogen for quick energy release.

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Feedback inhibition

A process where an end product inhibits an earlier step in the pathway.

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Isozymes

Enzymes that catalyze the same reaction but are different in structure and regulation.

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Hungry state

Condition when glucagon is released due to low blood glucose levels.

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Nocturnal fast

Period when the liver releases glucose to maintain brain function overnight.

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Creatine phosphate

A high-energy compound used to quickly regenerate ATP in muscle cells.

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McArdle’s disease

A glycogen storage disease caused by a deficiency in skeletal muscle glycogen phosphorylase.

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Hers disease

A glycogen storage disorder caused by a deficiency in liver glycogen phosphorylase.

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Calmodulin

A calcium-binding protein that plays a regulatory role in phosphorylase kinase activation.

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Phosphorylation

The addition of a phosphoryl group to a molecule, often regulating enzyme activity.

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Signal transduction cascade

A series of molecular events initiated by the binding of a signal molecule to a receptor.

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cAMP

A second messenger that activates protein kinase A in response to hormones.

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Glycogen saturation

The level of glycogen stored in muscle and liver relative to their capacity.

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Glycolytic enzymes

Enzymes involved in the breakdown of glucose to produce energy quickly.

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Phosphate release

The process of cleaving a phosphoryl group to generate free glucose from glucose 6-phosphate.

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Muscle contraction

The process requiring energy from glucose, particularly during intense exercise.

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Glycogen homeostasis

The balance of glycogen synthesis and breakdown to regulate glucose levels in the body.

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Epinephrine signal response

The process by which epinephrine binding to receptors leads to glycogen mobilization.