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