PHARMACOLOGY Flashcards

1
Q

what drug class is glicazide?

A

a sulphonylurea

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2
Q

what drug class is repaglinide?

A

a meglitinide

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3
Q

what is the mechanism of action for glicazide and repaglinide?

A

they antagonise the sulphonylurea type-1 receptor in the beta cells of the pancreas which prevents potassium ions from exiting the cell when intracellular ATP levels are low so we get depolarisation of the membrane potential which induces exocytosis of insulin

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4
Q

what is glucagon’s mechanism of action?

A

an agonist at glucagon receptors (GR) in the liver. Activation of these receptors
sets up a second mes
senger cascade involving cAMP, PKA, PPK and finally activation of glycogen
phosphorylase. This promotes the metabolism of glycogen into glucose which is then released into
the bloodstream

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5
Q

what is insulin’s mechanism of action?

A

Acts via the insulin receptor (IR) to control a vast range of processes in
almost all metabolically active cells in the body.
The main
effects are the absorption of glucose into metabolising tissues and the subsequent promotion of
glycolysis (converting glucose into useable energy (ATP) and storing of glucose for futu
re use as
glycogen (glycogenesis)

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6
Q

what is the effect of metformin?

A

to decrease conversion of glycogen to glucose (and subsequent release into blood) by
inhibition of the enzyme glycogen phosphorylase. It also affects insulin sensitivity, thus increasing
glucose uptake and utilisation in metabolising tissue

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7
Q

what drug class is octreotide?

A

a somatostatin analogue

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8
Q

what is the mechanism of octreotide?

A

Agonist of somatostatin receptors (SSTR) throughout the body. Affects a wide
range of biochemical
processes (thus long side
-effect list) but most potent at inhibiting INSULIN and GLUCAGON release.

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9
Q

what drug class is Pancreatin?

A

a thiazolidinedione

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10
Q

what is pancreatin mechanism of action?

A

An agonist at peroxisome proliferator-activated receptor gamma nuclear receptor (PPAR). Reduces
insulin resistance in metabolically active tissues (i.e. increases glucose absorption, storage and
conversion into ATP) and prevents glucose release from the liver.

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11
Q

What drug class is acarbose?

A

an alpha glucosidase inhibitor

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12
Q

what is acarbose’s mechanism of action?

A

Alpha glucosidase is present in the gut and is essential for breaking
down complex carbohydrates (i.e. starch) into glucose.
Thus, less glucose is released into the hepatic
portal vein following a meal

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13
Q

what drug class is liraglutide and exenatide?

A

GLP1R agonists

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14
Q

what are liraglutide and exenatides mechanisms of action?

A

GLP1 is released by intestinal endocrine cells
following ingestion of food. Has a synergistic set of effects on binding to the receptor including
promoting insulin release from pancreatic beta cell
s and reducing glucagon release from alpha cells

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15
Q

what drug class is sitagliptin?

A

a gliptin drug. antagonist of DPP-4

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16
Q

what is the function of DPP-4?

A

found in the liver and kidney and is involved in the breakdown of GLP-1

17
Q

what is DPP-4s mechanism of action?

A

it prevents GLP-1 being broken down and so boosts insulin levels

18
Q

what drug class is ipragliflozin?

A

a gliphlozin drug/ a sodium-glucose transport protein 2 antagonist

19
Q

what is the mechanism of ipragliflozin’s action?

A

SGLT2 is present in kidney (proximal
convoluted tubule) and is essential for reabsorption of glucose filtered through the glomeruli.
Blockade of this transporter protein increases glucose excretion into urine and thus
reduces blood
glucose concentration