The Endocrine Pacreas Flashcards

1
Q

Role of digestive enzymes in pancreas

A

Proteases (trypsin & chymotrypsin)- trypsin cleaves trypsinogen & chymotrysinogen. Pancreatic lipase- digests triglycerides. Pancreatic amylase- digests starch to glucose.

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2
Q

What are the major cell types in islets?

A

Beta cells- insulin, Alpha cells- glucagon, Delta cells- somatostatin

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3
Q

Insulin vs glucagon.

A

Insulin dominates the fed state and acts to lower plasma glucose. Glucagon dominates in the fasted state and acts to raise plasma glucose.

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4
Q

Describe the structure of insulin.

A

51 amino acid peptide hormone that is made of 2 chains- the A and B chains are held together by 2 disulfide bonds.

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5
Q

Beta cell at rest vs insulin secretion

A

At rest- the Katp channel is open and the cell is at its resting membrane potential. Secretion- Katp channels close, less K+ leaves cell causing the cell to depolarise. Ca2+ channel opens and Ca2+ entry triggers exocytosis and insulin in secreted.

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6
Q

How does insulin exert its effect on cells?

A

Insulin binds to the insulin receptor, receptor auto-phosphorylation, recruitment and activation of signalling complexes at cell membrane. This has effects on metabolic pathways and glucose uptake.

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7
Q

What are the main target tissues insulin acts on?

A

Liver, skeletal muscle and adipose tissue

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8
Q

Describe the structure of glucagon.

A

A 29 amino acid peptide hormone with no disulfide bonds. It is a major catabolic hormone of the body that opposes the actions of insulin.

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9
Q

Hat does glucagon promote in the liver?

A

Glycogenolysis-breakdown of glycogen to glucose, gluconeogenesis- synthesis of glucose

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10
Q

Control of glucagon release.

A

Katp channels close in response to a fall in glucose concentration, depolarisation of cell membrane opens voltage-gated Ca2+ channels allowing influx of Ca2+ triggering exocytosis of glucagon from vesicles.

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11
Q

How does glucagon exert its effect on cells?

A

Binds to the glucagon receptor, G-protein activation, effector protein activation, 2nd messenger deformation. This has effects on metabolic pathways and gene expression.

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