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3 components of glycerophospholipids are
glycerol backbone, fatty acid chain at sn1/sn2 position, phospho-head group
what are the various phospho-head groups
choline, ethanolamine, serine, glycerol
cardiolipin is a
special glycerophospholipid which has shared glycerol as head group
glycerophospholipid synthesis by remodel pathway
head groups of PC, PS, PE can be interconverted into each other
glycerophospholipid synthesis by de novo pathway
the fatty acid chains can be switched between different glycerophospholipids by acyltransferase
3 components of sphingolipids
sphingosine backbone, fatty acid chain, head group
which sphingolipid has H as the head group
ceramide
which sphingolipid has phosphocholine as the head group
sphingomyelin
which sphingolipid has sugars as the head group
glycosphingolipids
what is gaucher disease an example of
a lysosome storage disease
what is deficient in gaucher disease
glucosidase
what is glucosidase
a lysosomal hydrolase that hydrolyzes glucosylceramide in ceramide
what effect does gaucher disease have on the body
it causes accumulation of glucosylceramide in lysosomes leading to gaucher disease due to deficiency in glucosidase
what are gangliosides
they are glycosphingolipids with a polysaccharide chain which contains sialic acid
what is the function of gangliosides
they polysaccharide chain of gangliosides can serve as receptor for bacterial proteins
what an example of polysaccharide chains of gangliosides serving as a receptor
where cholera toxin binds to ganglioside GM1
how are sphinoglipids metabolized
primarily degraded by lysosomes by lysosomal hydrolases
what does deficiency in lysosomal hydrolase activity result in
accumulation of precursor for the hydrolase in lysosomes causing lysosome storage diseases
what is the effect of folate deficiency on nucleotide biosynthesis
it decreases availability of carbon donors for IMP de novo synthesis OR inhibits folate recycling thus resulting in inhibition of conversion of dUMP to TMP
folate deficiency inhibits
de novo synthesis of both purine and pyrimidine nucleotides
what is the critical role of ribonucleotide reductase (RNR) in deoxyribonucleotide biosynthesis
RNR can reduce all ribonucleoside diphosphate (NDP) to deoxyribonucleoside diphosphate (dNDP)
what enzyme is the bridge linking RNA and DNA synthesis
ribonucleotide reductase (RNR)
what are risk factors for gout development
diet, tumor, renal disease, drug treatment, etc.
what drug is used for treatment of gout
allopurinol
how does allopurinol help treat gout
it inhibits xanthine oxidase causing decreased uric acid thus decreasing MSU crystal formation
what is the precursor for synthesis of all nucleotides both in de novo and salvage pathways
PRPP
what does overexpression of PRPP synthetase cause
it results in overproduction of purine nucleotides leading to hyperuricemia
what is gout arthritis mainly due to
the deposition of monosodium urate (MSU) crystals in the joints which induce inflammation and pain
what happens if monosodium urate (MSU) crystals is in the joints
it induces inflammation and pain
what is uric acid in salt form called
monosodium urate (MSU)
what are the 3 endogenous anti-coagulation systems
anti-thrombin, TFPI, protein C system
what is anti-thrombin activated by
heparin
what causes prolonged APTT
assess intrinsic pathway
what causes prolonged PT
assess extrinsic pathway
what causes prolonged TCT
assess final common pathway
what is the pharmacology of an antiplatelet drug
it blocks ADP receptor signaling, enhances cAMP signal by PDE inhibition, inhibit TXA2 production/action by aspirin, GPIIb-IIIa antagonists block platelet aggregation
what is the function of lipoprotein lipase (LPL)
convert chylomicron to its remnant; convert VLDL to its remnant = IDL
what is the remnant of VLDL
IDL
what is the function HTGL
converts VLDL remnant (known as IDL) into LDL
what are different types of lipoprotein
chylomicron, VLDL, HDL, IDL, LDL
what are the sources of chylomicron
in the intestine
what are sources of VLDL and HDL
in the liver
what are sources for IDL and LDL
derived from VLDL by lipase
which lipoprotein has the highest triglycerides
chylomicron
which lipoprotein has the highest cholesterol
LDL
what is structural role of apolipoproteins
needed for de novo synthesis
which lipoproteins are de novo synthesized
VLDL, HDL, chylomicron
which lipoproteins are dervied from VLDL
IDL and LDL
which apolipoprotein is used for chylomicron
Apo B48
which apolipoprotein is used for VLDL, IDL, and LDL
Apo B100
which apolipoprotein is used for HDL
Apo A
which lipoprotein receptor is regulated by intracellular cholesterol
LDLR
which lipoprotein receptor is not regulated by intracellular cholesterol
scavenger receptor
what is foam cell formation due to
the continuous uptake of oxidized LDL by scanvenger receptor
types of acyltransferase
LCAT and ACAT
what does LCAT do
in HDL it converts free cholesterol to cholesterol
what does ACAT do
inside the cells it converts free cholesterol to cholesterol and is then stored in lipid droplets
what are the structural components of a nucleotide
consist of base, pentose sugar, and phosphate at carbon 5
without a phosphate a nucleotide is considered a
nucleoside
which pathway preferred to synthesize purine nucleotides
salvage pathway due to recycling performed bases, and less energy cost
difference between de novo and salvage pathway for nucleotide biosynthesis
de novo builds nucleotide from beginning (from small precursor), salvage recycles components that already exist (from free nitrogenous base)
what 2 enzymes in thymine formation can be subject to drug targets
thymidylate synthase and dihydrofolate reductase
thymidylate synthase inhibitor
fluorocytosine convert to FdUMP → inhibits thymidylate synthase → TMP production
dihydrofolate reductase inhibitor
blocks folate recycling → prevents TMP production
what does blockade of thymine formation do
it inhibits DNA synthesis WITHOUT affecting ribonucleotide biosynthesis
what is unique biosynthesis pathway for TMP production
thymine formation
why can thymine formation pathway be a target for cancer treatment
due to cancer cells needing large amount of thymidine nucleotides in order to replicate their DNA rapidly
inhibiting thymidylate synthase causes
prevention of adequate TMP production thus interfereing with DNA synthesis
what drug inhibits dihydrofolate reductase (DHFR)
methotrexate
what drug inhibits thymidylate synthase
5-fluorouracil by FdUMP
what disease is due to deficiency of HGPRT
Lesch-Nyhan syndrome (X-linked recessive disorder)
what symptoms occur due to Lesch-Nyhan syndrome
hyperuricemia and gout arthritis
what does HGPRT deficiency cause
hypoxanthine not recycled to salvage pathway → accumulation of hypoxanthine → increase uric acid produced
upregulation of de novo purine synthesis → accumulation of hypoxanthine → increase uric acid produced