Endo Flashcards

1
Q

aspart

A
Short acting insulin 
Type 1 DM, type 2 DM,
GDM (postprandial glucose
control).
Binds insulin receptor (tyrosine
kinase activity).
Liver: increase glucose stored as
glycogen.
Muscle: increase glycogen, protein
synthesis; increase K+ uptake.
Fat: increase TG storage.
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2
Q

glulisine

A
Short acting insulin 
Type 1 DM, type 2 DM,
GDM (postprandial glucose
control).
Binds insulin receptor (tyrosine
kinase activity).
Liver: increase glucose stored as
glycogen.
Muscle: increase glycogen, protein
synthesis; increase K+ uptake.
Fat: increase TG storage.
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3
Q

tolbutamide

A
Sulfonylurea 
Stimulate release of
endogenous insulin in
type 2 DM. Require some
islet function, so useless in
type 1 DM.
Close K+ channel in β cell
membrane > cell depolarizes
> insulin release via increased Ca2+
influx.
Risk of hypoglycemia increased in renal
failure, weight gain.
First generation: disulfiram-like
effects.
Second generation:
hypoglycemia.
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4
Q

chlorpropamide,

A
1st gen Sulfonylurea 
Stimulate release of
endogenous insulin in
type 2 DM. Require some
islet function, so useless in
type 1 DM.
Close K+ channel in β cell
membrane > cell depolarizes
> insulin release via increased Ca2+
influx.
Risk of hypoglycemia increased in renal
failure, weight gain.
First generation: disulfiram-like
effects.
Second generation:
hypoglycemia.
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5
Q

glipizide,

A
Sulfonylurea 
Stimulate release of
endogenous insulin in
type 2 DM. Require some
islet function, so useless in
type 1 DM.
Close K+ channel in β cell
membrane > cell depolarizes
> insulin release via increased Ca2+
influx.
Risk of hypoglycemia increased in renal
failure, weight gain.
First generation: disulfiram-like
effects.
Second generation:
hypoglycemia.
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6
Q

repaglinide

A
meglitinide 
Used as monotherapy in
type 2 DM or combined with
metformin.
Stimulate postprandial
insulin release by binding
to K+ channels on β cell
membranes (site differs from
sulfonylureas).
Hypoglycemia (increased risk with
renal failure), weight gain
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