WorksheetsDr. Gupta endocrine exam 2 pptx part 2
Total questions: 62
Worksheet time: 2hrs 4mins
Which of the following is adverse reaction for insulin products?
Hypoglycemia
allergic reaction (IgE mediated)
Lipodystrophy
Hyperglycemia
Which of the following is true when insulin products cause hypoglycemia?
-Release of epinephrine, glucagon, cortisol
-These hormones try to compensate
Sweating, hunger, palpitations, tremor, anxiety
-May lead to convulsions & coma
Lipodystrophy: Common when same injection site utilized. Loss of fat may impact insulin absorption from that site
True
False
Analog of human ______ with additional amino acids and substitutions for aqueous stability.
Ready to use aqueous product for treatment of severe _______ via SC injection in both pediatric and adult diabetic patients
Glucagon, Hypoglycemia
Insulin, Hypoglycemia
Insulin, Hyperglycemia
Glucagon, Hyperglycemia
______, insulin and glucagon work together in inter-related fashion to maintain normal world glucose
Amylin
GLP-1 agonist
DPP4Is
SGLT2
Group of gastric hormones stimulating insulin release are commonly called as___________
Incretins
Glucagon
Secretin
Gastrin
What is the role of incretins (GLP-1) in insulin and glucagon?
Increase insulin
& Decrease glucagon
Decrease insulin
& Increase glucagon
Increase insulin
Decrease glucagon
What is the role of incretins (GIP) in insulin and glucagon?
In
Increase glucagon
Increase insulin & Decrease glucagon
Decrease insulin
•Isolated from the saliva of the Gila Monster
•39 a.a. polypeptide (53% same AA as GLP-1)
•t1/2 = 2-4 hours
•Bid or Q7d
Exenatide (Byetta)
Liraglutide (Victoza)
Dulaglutide (Trulicity)
Semaglutide ( Ozempic)
Anti-diabetic Drugs: Peptides
GLP-1 Agonists
Natide + Glutide
Gliptins
Glinides
Gliflozins
•Fatty acid molecule at one position of the GLP-1
•t1/2 = 11-15 hours
•Once daily
Liraglutide (Victoza)
Exenatide (Byetta)
Dulaglutide (Trulicity)
Semaglutide (Ozempic)
•GLP-1 analog with amino acid substitution
•t1/2 = 4days
•Q7d
Dulglutide (trulicity)
Semaglutide (Ozempic)
Exenatide (Byetta)
Liraglutide (Victoza)
•GLP-1 analog with stearic diacid substitution at Lys26 for t1/2 & introduction of amino α-aminobutyric at position 8 acid for DPP4-stability
•t1/2 = ~ 1 week
•Q7d
Semaglutide (Ozempic)
Dulaglutide (Trulicity)
Liraglutide (Victoza)
Exenatide (Byetta)
What are the adverse effects of GLP-1 Agonist?
Fullness
Nausea/vomiting
GERD
decreased appetite
increased appetite
Which of the following GLP-1 agonist is fused to a fatty molecule to increase it’s half life?
Duraglutide
Detemir
Liraglutide
Pramlintide
Which of the following are Non-peptides (orally) antidiabetic drugs?
DPP4Is
Sulfonyl ureas
Biguanides
Insulin
GLP-1
What is the role of the DPP4Is drugs?
• Increases endogenous incretin levels
•Decreases plasma glucose
•Increases plasma glucose
• Decreases endogenous incretin levels
What are the adverse effects of DPP4Is ?
Nausea
Nasopharyngitis
Dizziness
Weight gain
Which oral antidiabetic drug DPP-4 inhibitors is highly metabolized?
Saxagliptin
Sitagliptin
Linagliptin
Alogliptin
Which group in oral antidiabetic drugs DPP-4 inhibitors is mainly responsible for longer DOA?
-CN
-C=O
-NH2
Following functional group in Saxagliptin is responsible for its pseudoirreversible nature
Hydroxyl
Amine of β–amino acid
Peptide/amide (-CO-NH)
Cyano
What is the difference between first-generation and second-generation oral (antidiabetic drugs sulfonylureas)?
•First Generation-Small substitution
•Second Generation-Bulky substitution
•Second Generation-Small substitution
•First Generation-Bulky substitution
Bulkier substituents on ___ increase molecular affinity for SUR1 receptors and cause β cells to ________.
R1, secrete insulin
R2, secrete insulin
R1, secrete glucagon
R2, secrete insulin
The first-generation sulfonylurea oral antidiabetic drugs are less potent and have a higher chance of hypoglycemia.
True
False
Sulfonylureas inhibit ______ clearance of insulin
hepatic
renal
intestinal
What is the mechanism of sulfonylureas?
1. Bind to SUR1 subunit of K+/ATP channel
2. SUR1 = Sulfonylurea receptor
3. Inhibit K+ conductance
4. Promote depolarization
5. Ca2+ influx -> Insulin release
1. Bind to SUR1 subunit of Ca++/ATP channel
2. SUR1 = Sulfonylurea receptor
3. Inhibit K+ conductance
4. Promote depolarization
5. K+ influx -> Insulin release
1. Bind to SUR1 subunit of K+/ATP channel
2. SUR1 = Sulfonylurea receptor
3. Inhibit Ca++ conductance
4. Promote depolarization
5. Ca2+ influx -> Insulin release
What are the adverse effects of Sulfonylureas ?
Weight gain
Cause sun sensitivity
Hypoglycemia
Which of the following drug can produce much longer hypoglycemic side effect as seen with SUs and therefore contraindicated in elderly?
Chlorpropamide
Glipizide
Glyburide
Glimepiride
What are true about Substituted Benzoic Acids or ‘Glinides’ ?
Non sulfonylurea hypoglycemic agent
Structural and functional similarity to SUs
Less problematic hypoglycemia
sulfonamide
Different binding site than SUs
Which of the following drug is the most potent?
Chlorpropamide
Glipizide
Glyburide
Glimepiride
Acetohexamide
What classes of antidiabetic drugs can cause hypoglycemia?
Insulin
Amylin
SUs
Glinidines
•Bind to the peroxisome proliferator-activated receptor (PPAR-γ) receptors in fat cells and making the cells more responsive to insulin (aka insulin sensitizers)
Thiazolidinediones (Glitazones)
Sulfonyl Ureas (SUs)
SGLT2 inhibitors (Gliflozins)
Biguanides
Which of the following drugs are Thiazolidinediones?
Rosiglitazone (Avandia)
Pioglitazone (Actos)
Glimepiride (Amaryl)
Glipizide (Glucotrol)
____________ antidiabetic agent that lowers blood glucose by improving target cell response to insulin, without increasing pancreatic insulin secretion. It has a mechanism of action that is dependent on the presence of insulin for activity.
Thiazolidinedione
Biguanides
Sulfonylureas
DPP4Is
What are the adverse effects of Thiazolidinedione?
Increase in liver transaminases
Decrease in liver transaminases
Weight gain
Fluid retention and edema
lose weight
Reabsorbs 10% of glucose in kidneys
SGLT1
SGLT2
Reabsorbs 90% of glucose in kidneys-Important target
SGLT2
SGLT1
Which of the following drugs are Substituted Benzoic Acids?
Repaglinidine (Prandin)
Nateglinide (Starlix)
Metformin (Glucophage)
Glimepiride (Amaril)
Which of the following drugs are DPP4Is?
Sitagliptin (Januvia)
Alogliptin (Nesine)
Repaglinide (Prandin)
Nateglinide (Starlix)
Which of the following drugs are SGLT2 INHIBITORS?
Canagliflozin (Invokana)
Dapagliflozin (Farxiga)
Glimepiride (Amaryl)
Empagliflozin (Jardiance)
SGLT2 inhibitors (gliflozins) have a _____________.
low risk of hypoglycemia
High risk of hypoglycemia
What drug is the combination with sitagliptin (Steglujan®) and metformin (Segluromet®) ?
Ertugliflozin (Steglatro)
Canagliflozin (Invokana)
Dapafliflozin (Farxiga)
Which of the following drugs is biguanide?
Metformin (Glucophage)
Glipizide (Glucotrol)
Glyburide (Micronaze)
Which of the following is true about Buguanides?
Highly polar, basic drug
Almost 100% eliminated by kidneys
Eliminated by active tubular secretion (OCT)
Almost 60% eliminated by kidneys
What are the role of Biguanides?
Insulin sensitizer
No effect on insulin levels
Not hypoglycemic
can cause hypoglycemic
What are the mechanisms of action of biguanides by the liver?
decrease gluconeogenesis
decrease glycogenolysis
increase gluconeogenesis
increase glycogenolysis
What are the mechanisms of action of biguanides by the Muscle?
increase glucose uptake
decrease lipolysis
decrease gluconeogenesis
decrease glycogenolysis
What are the mechanisms of action of biguanides by the Fat?
increase glucose uptake
decrease lipolysis
decrease glucose uptake
decrease gluconeogenesis
What are the adverse effects of Biguanides?
nausea, diarrhea
lactic acidosis
dizziness
__________releases glucose from larger carbohydrates
α-Glucosidase
Biguanides
GLP-1 Agonist
Amylin Agonists
Which of the following are true about of Acarbose (Precose) ?
•-O- replaced with –NH-
•Sugar ring changed to cyclohexene
•Highly absorbed
•Not absorbed as such
•Drug excreted in feces (51%)
Which of the following are true about of Miglitol (Glyse)t ?
•Sugar monomer like structure
•Highly absorbed
•Excreted unchanged in urine
•Drug excreted in feces (51%)
Which of the following drugs are α-Glucosidase Inhibitors?
Acarbose (Precose)
Miglitol (Glyset)
Glimepiride (Amaryl)
Glipizide (Glucotrol)
A patient on alpha-glucosidase inhibitor is experiencing hypoglycemia. What should be given?
Fruit juice
Glucose tab
Lactose
What classes of antidiabetic drugs not cause hypoglycemia?
GLP-1 agonists
Metformin
•SGLT2 inhibitors
•Alpha-glucosidase inhibitors
Thiazolidinedione
What oral anti-diabetic drugs cause weight loss?
Amylin
GLP-1 agonist
Metformin
DPP4 inhibitor
What oral anti-diabetic drugs cause weight neutral?
Metformin
DPP4 INHIBITORS
Sulfonylureas
Meglinitides
What oral anti-diabetic drugs cause weight gain?
Sulfonylureas
Meglinitides
Thiazolidinedione
Metformin
Miglitol is an example of
α–glucosidase inhibitor
DPP-4 inhibitor
Amylin Analogue
GLP-1 agonist
Metformin belongs to which of the following class of anti-diabetics?
Buguanides
Sulfonylureas
Glitazone
Gliptins
Which of the following statements is not applicable to metformin?
Insulin sensitizer
Not hypoglycemic
Can cause weight gain
No effect on insulin levels
Which of the following is true about Hexamer?
long term stability
storage form in body
can not storage form in body
low term stability
