endocrine pancreas Flashcards

1
Q

embryological origin of the pancreas

A

foregut outpouching. its located behind the stomach

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2
Q

functions of the pancreas

A

endocrine (1%)=hormone production from islets of langerhans. secrete into blood stream so have blood supply close by.
exocrine = produces digestive enzymes which are released into the duodenum + alkaline secretions. all secreted into ducts

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3
Q

important hormones secreted by the pancreas

A

insulin - beta cells
glucagon - alpha cells
somatostatin - delta cells
ghrelin (hunger) - e cells
gastrin - G cells (stimulates gastric acid secretion)
pancreatic polypeptide - PP cells (regulator of all pancreatic secretions)
vasoactive intestinal peptide - VIP

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4
Q

location of alpha and beta cells

A

alpha found at periphery and beat found in centre

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5
Q

actions of insulin

A

increased glucose after feeding = absorption of glucose in liver, adipose and skeletal muscle
leads to carb, lipid and protein anabolism

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6
Q

actions of glucagon

A

fasting - low glucose. release of glucose from liver and adipose. catabolism of mainly carbs and lipids

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7
Q

why is it important to keep blood glucose levels tightly regulated

A

brain uses glucose really fast and relies on it being steady because its v sensitive to osmolarity e.g increased glucose will cause water t be drawn out of cells - don’t want brain cells shrinking

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8
Q

normal, after meal and threshold levels of glucose

A

normal= 3.3-6mmol
after meal = 7-8mmol
renal threshol= 10mmol- if exceeds this then see glucose in urine

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9
Q

general structure of glucose and insulin

A

water soluble
v short half life (5 min)
interact with cell surface receptors
receptor with hormone bound can be inactivated by internalisation

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10
Q

specific structure of insulin

A

rigid structure

beat chain and alpha chain linked by disulphide bonds and C peptide ( which also helps to prevent vascular damage)

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11
Q

describe insulin synthesis

A
  1. pre-proinslun translation, signal cleavage and proinsulin folding in rER,
  2. proinsulin transported to golgi
  3. proinsulin cleaved to produce insulin and c peptide
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12
Q

describe insulin regulation

A

glucose enters cell when concs are high
converted to ATP
K+ channels sense high TAP causing them to close = DEPOLARISATION
depolarisation causes opening of Ca2+ channels
ca2+ enters and influx causes vesicles containing insulin to fuse and exit via exocytosis

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13
Q

actions of insulin

A

Increasss glucose uptake into target cells
increases glycogen synthesis
inhibits break down of fatty acids

in muscle - increases AA uptake = more protein synthesis
in adipose - increases storage of triglycerides
in liver- increases glycogen synthesis and inhibits break down of AA

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14
Q

insulin receptor structure

A

receptor is a dimer - 2 identical subunits spanning the membrane. 2 subunits are alpha chain and 1 beta chain connected by single disulphide bond. alpha on exterior of cell and beta on interior. makes more sense if look at pic

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15
Q

action of glucagon

A

glycogenolysis
glucogeneisis
- increases glycogen break down in liver
- synthesis of glucose from AA
- stimulates lipolysis to increase plasma fatty acids

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16
Q

synthesis of glucagon

A

synthesised in RER, transported to Golgi where its cleaved and packaged and marginated below plasma membrane until called upon

17
Q

structure of glucagon

A

v flexible

7 polypeptide chain and no disulphide bridges

18
Q

effect of high glucagon on diabetes

A

makes diabetes worse. release more glucose = high glucose

19
Q

effect of low glucagon

A

contributes to hypoglycaemia

20
Q

diagnosis of diabetes

A

venous plasma glucose levels.
if fasting > 7mmol = diabetes
random >11mmol = diabetes
also glucose in urine, this cannot be used as a diagnosis though