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32 Cards in this Set

  • Front
  • Back
What is the major source of fuel oxidation in the cel?
TCA cycle, citric acid cycle, or the krebs cycle
In which organelle do the key reaction of the TCA cycle and the electron transport chain occur? How many ATP are produce by malate electron transfer? FADH?
Mitochondria
Malate 2.5
G3-P 1.5
What does isocitrate dehydrogenase do? What does ADP do to the rate? NADH?
Converts isocitrate to alpha-ketoglutarate
high ADP - no energy increases rate
high NADH - Slows it down b/c reaction requires NAD+
What does citrate synthase do?
It makes citrate using acetyl coA
What does alpha - ketoglutarate dehydrogenase do?
It produces succinyl CoA from alpha ketoglutarate
What does Pyruvate dehydrogenase do?
Changes pyruvate into Acetyl CoA
What is the rate limiting enzyme of the TCA cycle?
isocitrate dehydrogenase
What is the rate limiting enzyme of glycolysis?
Phosphofructokinase-1
What does excise do?
Removes calcium
What does FAD do?
Accepts single electrons through binding with 1 e- and a H+
What does NAD do? What does it balance? can FAD do this?
Accepts a pair of electrons as the hydride (H-) ion
Balances energy metabolism no
What does CoA do?
High energy bond that allow citrate to be formed, or GTP
What does lipoate do?
Accepts the acyl portion of the alpha keto acid, and the acyl group is then transferred to CoASH, and transfers electrons to FAD which then forms NADH
What is arsenic poisoning
Arsenite binds the sulfhydryl group of lipoate and prevents alpha keto acid dehydrogenase activity (acceptance of the acyl group) may inhibit enzymes of glycolysis
What feeds the citric acid cycle?
Intermediates for synthesis purposes:
1. Citrate. 2. alpha ketoglutarate
3. succinyl CoA 4. Malate 5. Oxaloacetate
Acetyl CoA
1. Fatty acid synthesis
2. Amino Acid synthesis & neurotransmitter
3. Heme synthesis 4. Gluconeogenesis
5. Amino acid synthesis
What converts pyruvate into oxaloacetate?
pyruvate carboxylase
How does fructose enter into metabolism?
It is phosphorylated, broken, and benters as glyceraldehyde which becomes pyruvate
Benign fructosuria?
Accumulation of fructose in urine due to the a defficiency of fructokinase
What can uridine diphosphate galactose become?
IF UDP is removed and glucose is added, what does it become?
Glycoproteins, glycolipids, proteoglycans
Lactose
What is galactosemia?
Hereditary disorder preventing the metabolism of galactose into glucose metabolites, defect in galactose 1-phosphate. Leads to galactose 1-P accumulation, deplete phospate in liver leading to liver failure and mental retardation
What is UDP-glucouronate good for?
Increasing the soluble of things through adding negative charges
Which cell is bilirubin from, if there is an issue what are clinical signs?
Red blood cell
yellowing of the skin and white of eyes
What does ADH do in ethanol metabolism? ADH - alcohol dehydrogenase
Converts ethanol to acetaldehyde
What does aldehyde dehydrogenase do?
Converts acetaldehyde to acetate which is then made into acetyl coA in the muscles
MEOS - microsomal ethanol oxidizing system does what? using what?
Changes ethanol to acetaldehyde (most ethanol goes through ADH/ALDH) with cytochrome p450 oxidizers
What starts ethanol metabolism, what begins secondarily?
alcohol dehydrogenase
then MEOS
Acute effects of ethanol?
damage to mitochondria by high levels of acetaldehyde and free radicals. leads to fatty liver, ketoacidosis, lactic acidosis, hypoglycemia
Alcohol induced hepatitis
inflamed liver from acetaldehyde and fre radicals
Fatty liver
inhibition of FA oxidation, stimulation of TAG synthesis
Fibrosis and cirrhosis
Chronic diffuse damage leads to scarring and loss of blood flow, function, and hepatic failure
What does chronic ethanol consumption do to CYP2E1 transcription?
up regulate it
What 2 things cause majority of problems associated with chronic drinking?
Abundance of acetaldehyde an ROS - toxic radicals