BCHEM LE6 (2025) Flashcards
- Conversion of purines to uric acid in humans are mediated by the following enzymes except?
A. Deaminase
B. Uricase
C. Phosphorylase
D. Oxidase
B. Uricase
- Failure of this transporter is a major factor in human hyperuricemia?
A. URAT1
B. GLUT9
C. ABCG2
D. SLC22
C. ABCG2
- Urate transport disorders can cause hyperuricemia in the majority of gout patients by which mechanism?
A. Increase renal urate secretion
B. Increase renal urate reabsorption
C. Reduced renal excretion
D. Reduced renal reabsorption
C. Reduced renal excretion
- Deficiency in enzymes involved in the Salvage pathway of purines lead to accumulation of?
(0/1 Point)
A. HGPRT
B. PRPP
C. Hypoxanthine
D. Adenine
C. Hypoxanthine
- Most relevant pathway which also offers significant perspectives for pharmacologic approach of hyperuricemia?
A. ADA
B. mdN
C. XDH
D. XOR
D. XOR
- Key enzymes in the synthesis of pyrimidines?
A. CPSI
B. DHODH
C. IMPDH
D. ADSS
B. DHODH
- Increase in purine nucleotide levels is sufficient to induce expression of this cell surface glycoprotein in cancer cells?
A. MICA
B. NKG2D
C. M-CSF
D. TLR
A. MICA
- Downregulation of nucleotide metabolic pathways as true anticancer mechanism are brought about by?
A. Mutant P53
B. Mitogen-activated protein kinase
C. Ribonucleotide reductase regulatory subunit
D. Oncogen induced senescence
D. Oncogen induced senescence
- Oncogenes and tumor suppressor genes are key regulatory molecules in?
A. Salvage pathway nucleotide synthesis
B. De novo nucleotide synthesis
C. Both
D. None
B. De novo nucleotide synthesis
- Expression of this nucleotide inhibits antitumor immune response?
A. Guanosine
B. Thymine
C. Adenosine
D. Cytosine
D. Cytosine
- Which of the following has an
adenine-containing nucleotide in its structure?
A. PRPP
B. Coenzyme A
C. Carbamoyl phosphate
D. SAM
D. SAM
- Delivery of cholesterol to liver and other tissues by plasma lipoproteins leads to a reduction in de novo cholesterol synthesis and decrease in the synthesis of:
a. LDL receptors
b. HDL receptors
c. VLDL receptors
d. triacylglycerol receptors
a. LDL receptors
- Which of the following is true?
a. Spherical lipoprotein particles have a hydrophilic core of triacylglycerols
b. Lipoproteins have cholesteryl esters surrounded by a phospholipid layer associated with cholesterol and lipids.
c. As the lipid-to-protein ratio decreases, particles becomes larger
d. As the lipid-to-protein ratio decreases, particles becomes more dense
d. As the lipid-to-protein ratio decreases, particles becomes more dense
`
- This nucleotide activates protein kinases during glycogen breakdown:
A. ATP
B. GTP
C. Cyclic GMP
D. Cyclic AMP
D. Cyclic AMP
- Chylomicrons transports dietary triacylglycerol to muscles and dietary cholesterol to liver.
They are formed and secreted by :
a.liver
b.intestinal mucosa
c. kidneys
d,pancreas
b.intestinal mucosa
- It is activated by high-density lipoproteins to form cholesteryl esters:
a. LCAT
b. apo-C
c. apo-E
d.HMGCO-A
a. LCAT
- Major structural protein for HDL1:
a. apo-A-1
b. apo-B-48
c. apo-E
d. apo-B-100
e. apo-A-1
- The only structural protein in LDL that contains another apoprotein domain plus the LDL receptor recognition domain permitting binding to LDL receptors:
a. apo-A-1
b. apo- B-48
c. apo-E
d. apo-B-100
d. apo-B-100
`
- Which of the following is not true of free cholesterol in the cytosol?
a. Activates ACAT
b.Suppresses HMG CoA reductase; decreases de novo synthesis of cholesterol
c. Suppresses further LDL receptor synthesis; decreases further uptake of LDL
d. Mediates esterification of receptors removed from peripheral tissues by HDL.
d. Mediates esterification of receptors removed from peripheral tissues by HDL.
- Most common hyperlipoproteinemia where there is Increased triacylglycerol beginning at puberty with increased incidence of coronary artery disease and peripheral vascular disease:
a. Type I
b. Type II
c.Type III
d. Type IV
d. Type IV
`
- Most commonly a familial hypertriglyceridemia with exacerbating factors particularly common in alcoholics and individuals with diabetic ketoacidosis:
a. Type I
b. Type III
c.Type V
d. Type VI
c.Type V
- Which of the following is true about plasma lipoproteins?
a. They are held together by covalent bonds.
b. They are composed of a neutral lipid core surrounded by esterified cholesterol.
c. They have varied protein to lipid ratio.
d. The principal lipid carried by lipoprotein particles are chylomicrons.
c. They have varied protein to lipid ratio.
- Which of the following proteins are the major carriers of triacylglycerols?
a. VLDL and LDL
b. chylomicrons and VLDL
c. chylomicrons and LDL
d. VLDL and HDL
b. chylomicrons and VLDL
- Transporter of lipid that is lowest in density but largest in size. It contains the highest percentage of lipid and the smallest of protein:
a. Chylomicron
b. VLDL
c. LDL
d. HDL
a. Chylomicron
`
- As the lipid-to-protein ratio decreases, particles become smaller and more dense in the following order:
a. chylomicron > HDL> VLDL > LDL
b chylomicron > VLDL > LDL > HDL.
c. HDL>LDL>VLDL > chylomicron
d. HDL>LDL>VLDL > chylomicron
b chylomicron > VLDL > LDL > HDL.
- This apolipoprotein antagonizes ApoE &
is known to inhibit lipoprotein lipase.
(0/1 Point)
A, apoB
B. apoB
C. apo C-IIl
D. apo C-II
D. apo C-II
- Site of action of hormone sensitive lipase that degrades stored triacylglycerols activated by cAMP-dependent protein kinase:
A. stomach
B. pancreas
C. adipocytes
D. liver
C. adipocytes
- Nascent triglyceride-rich very low density lipoproteins are secreted from the :
A. intestinal mucosal cells
B. liver
C. stomach
D. pancreas
B. liver
- The initiating step in the modification of apoB involves which process?
A. Peroxidation of polyunsaturated fatty acids in the LDL lipids.
B. Regulation of modified LDL taken up by macrophages
C. Acetylation of apolipoprotein B
D. Oxidation of circulating macrophages with low levels of scavenger receptor activity.
A. Peroxidation of polyunsaturated fatty acids in the LDL lipids.
- After addition of carbohydrate residues in the Golgi apparatus, chylomicrons are released into the cells through:
a. exocytosis
b. reverse pinocytosis
c. reverse endocytosis
d. pinocytosis
d. pinocytosis
- This transfers cholesterol from HDL to VLDL and triacylglycerols from VLDL to HDL
a. Lipoprotein lipase (LPL)
b. Cholesteryl Ester Transfer Protein(CETP)
c. Hepatic Lipase (HPL)
d. CURL
b. Cholesteryl Ester Transfer Protein(CETP)
- Familial hypercholesterolemia is usually secondary to a deficiency in:
a. apoCII
b. apoB48
c. apoB100
d. apoCIII
a. apoCII
- Which of the following best describes the role of the cholesterol ester transfer protein?
a.It converts cholesterol from LDL to cholesterol esters
b.It exchanges cholesterol esters from HDL to other lipoproteins
c.It acts as a ligand for hepatic receptors of LDL
d.It is the major protein of VLDL
b.It exchanges cholesterol esters from HDL to other lipoproteins
- Which of the following comprises Metabolic Syndrome?
A. elevated HDL, hypertension, elevated blood sugar, obesity
B. elevated LDL, hypertension, elevated blood sugar, obesity
C. elevated HDL, hypertension, elevated triglycerides, obesity
D. elevated LDL, hypotension, elevated blood sugar, obesity
B. elevated LDL, hypertension, elevated blood sugar, obesity
- Which makes up 15% of the white matter of the brain?
A. sulfogalactocerebrosides
B. sulfoglucocerebrosides
C. triacylglycerols
D. ganglioside GM1
A. sulfogalactocerebrosides
- Which of the sphingolopids has no glycerol backbone?
A. cardiolipin
B. plasmalogen
C. lecithin
D. sphingomyelin
D. sphingomyelin
- Which phospholipid serves as the precursor for the generation of IP3 and 1,2 DAG?
A. phosphatidyl choline
B. phosphatidyl inositol
C. phosphatidyl serine
D. phosphatidyl ethanolamine
B. phosphatidyl inositol
- Which ganglioside serves as the receptor for cholera toxin in the intestinal cells?
A. GM2
B. GM1
C. GM3
D. GM4
B. GM1
- Which intermediate is shared both for the synthesis of phospholipids and triacylglycerols?
A. 1,2 diacyglycerol
B. cholesterol
C. HMGCoA
D. glycerol 3 PO4
A. 1,2 diacyglycerol
- A 3 year old child was brought to the medical center and found to have hepatosplenomegaly, with ataxia, dysarthria, dysphagia, dystonia sometime going into gelastic cataplexy with laughing, supranuclear gaze, dementia and sometimes seizures. What is the nature of the disease?
A. Guacher’s
B. Niemann Pick’s
C. Krabbe’s
D. Tay Sach’s
B. Niemann Pick’s