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34 Cards in this Set
- Front
- Back
LIPOLYSIS:
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Fats:
• Synthesis in cytoplasm • Breakdown in mitochondria |
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Fatty Acid =>AcetylCoA + PropionylCoA
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Activator: Glucagon
Inhibitor: MalonylCoA enzyme is CAT 1 |
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Citrate Shuttle
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FA transport out of the mitochondria
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Carnitine Shuttle
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FA transport into the mitochondria
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Citrate Shuttle:
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• Feeds Acetyl CoA into fatty acid synthesis
• Citrate moves out to the cytoplasm via the citrate shuttle |
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Carnitine Shuttle: what is it used for, commited step, deficiency
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Used for long chain fatty acids
Phosphorilation is the committed step • Carnitine Deficiency: low energy state, fat build up in the cytoplasm |
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βeta-Oxidation:
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The process where fatty acids are broken down to form Acetyl-CoA as an entry into the Kreb cycle.
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what happens when you loose fat? how many atp do you produce?
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=> Oh HOT!"
1) Oxidation:7 NADH => 21ATP 2) Hydration 3) Oxidation: 7 FADH2=> 14 ATP 4) Thiolysis: 8 AcCoA => 96 ATP |
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cost how many atp to get back 131
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Costs 15 ATP, get back 131 ATP
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Ratio is about 9:1 what does this mean?
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that is why there are 9 calorie per gram of fat
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how can we store fat without gaining weight?
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Fat repels water, thus able to store a lot of fat without excess water weight
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Which layer of the abdomen has the worst wound healing?
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Adipose because it is always repelling water and has least amount of blood supply
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describe how ketones are made?
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1) AcCoA + AcCoA⇨ AcetoAcetylCoA
2) AcetoAcetylCoA + AcCoA⇨ HMG-CoA 3) HMG-CoA ⇨AcCoA +AcetoAcetate 4) AcetoAcetate ⇨ Acetone 5) AcetoAcetate⇨beta-OH Butyrate |
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the rate limiting enzyme for ketogenesis
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HMG-CoA synthase
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what is measure on a dipstick for ketones
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Acetone is the only one able to be measured on a dipstick
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beta-OH Butyrate
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• Uses NADH cofactor
• crosses BBB • hydroxy group-is less polar than a ketone group |
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Glycogen: Glycogenolysis vs. Glycogenesis: why is the liver big?
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1 gram of Glycogen carries 2-3 grams of water
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how does glycogen maintain blood sugar levels?
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Glycogen= branched glucose polymer, maintains blood glucose levels
•α1,4 glycosidic bonds • α1,6 branches (every 10 residues) |
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lnsulin=>effects on glycogen
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glycogen synthesis
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epinephrine = >effects on glycogen
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glycogen breakdown
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G-6P=>Glycogen (enzyme)
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Glycogen synthase
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Glycogen =>Glucose (liver) or Lactate (muscle)
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Glycogen phosphorylase
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Von Gierke
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G6Pase deficiency ''von Gierke's Guts enGorged"
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Cori's
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Debranching enzyme deficiency "Cori is a short name"
Short branches of glycogen |
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Anderson's
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Branching enzyme deficiency "Anderson is a long branching name"
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McArdel's disease
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muscle phosphorylase deficiency, muscle cramps during excercise, rhabdomyolisis
"McArdels muscles got messed up" |
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pentose Phosphate Pathway:
Ribose-5P's job: |
Nucleotide synthesis
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NADPH's job
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FA synthesis, RBC membrane repair, kill bacteria
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PPP: G-6P⇨A⇨Ribose-5P + NADPH⇨B⇨F-6P + G-3P
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A:G-6PD
B: transketolase |
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G-6PD: Glucose 6 Phosphate Dehydrogenase: RLE, activator and inhibitor
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• Rate limiting enzyme for Pentose Pathway
• Activator: Glucose-6P Phosphate • Inhibitor: Ribose-5 phosphate |
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G-6PD Deficiency: NADPH levels, ethnicity, MCC of what crisis, Drugs that oxidize RBC's, Peripheral smear
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• ⇩NADPH: hemolytic anemia, infection,
• More common in Mediteranians (protects them from-malaria), • MCC of hemolytic crisis is 1. infection, 2. drugs, • Drugs that oxidize RBC's: Sulfa drugs, Anti malarials, Metronidazole, INH, • Peripheral smear: heinz bodies |
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NADPH: when is it used?
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• Fatty acid Synthesis
• DNA synthesis • RBC repair used by Glutathion |
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Sources of NADPH:
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• 90% fom pentose phosphate Pathway
• 10% from OAA-converted to Pyruvate |
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Ribose-5 Phosphate: function and deficiency
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nucleotide synthesis, Forms DNA for cellular division, Deficiency leads to poor wound healing
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