Qs2 Flashcards
(103 cards)
Pyruvate kinase deficiency (glycolysis final enzyme)
Unable to maintain Na/K ATPase
Hemolytic anemia
RBC swelling/lysis
Hemiballismus is caused by lesion to what part of the basal ganglia?
What kind of stroke?
Subthalamic nucleus
Lacunar stroke
Open angle glaucoma
Risk factors
Presentation
More common; Bilateral
Over 40, black diabetes
Asx early; reduced peripheral vision later
Acute angle-closure glaucoma
Risk factors
Presentation
Emergency
Abrupt onset of pain, nausea, colored halos, rainbows around light
Red teary eye, hazy cornea, mid dilated pupil (not reactive to light, firm to palpation
Retroperitoneal Abdominal Structures
A DUCK PEAR
Adrenal Glands Duodenum (2,3,4 parts) Ureters Colon (descending and ascending) Kidney Pancreas Esophagus Aorta Rectum
De novo pyrimidine synthesis RLS
CPS2
De novo purine synthesis RLS
glutamine PRPP amidotransferase
Glycolysis RLS
PFK1
Gluconeogenesis RLS
Fructose 1,6 bisphosphatase
Glycogen synthesis RLS
Glycogen synthase
Glycogenolysis RLS
Glycogen phosphorylase
TCA cycle RLS
Icocitrate dehydrogenase
HMP shunt RLS
glucose 6 phosphate dehydrogenase
Which cytokines inhibit Th1 cells?
IL-10
Flow of aqueous humor
- Formed in capillary bed of cilliary body
- Secreted into posterior chamber
- Flows between lens and iris diaphragm
- Into anterior chamber
- Reabsorbed by canal of schlemm
MOA of metoclopromide
Antagonist at dopamine 2 receptor
Serotonin agonist
Increase contractility in the GI tract
Landmark for pudendal nerve block
Ischial spine
RLS of carbohydrate digestion
Oligosaccharide hydrolases (intestinal brush border)
Vitamin deficiency from Hartnup disease
Tryptophan -> Niacin (B3) defciency -> pellagra
Pyruvate dehydrogenase complex cofactors
TLC for nobody
Thiamine (B1, pyrophosphate, TPP) Lipoic Acid Coenzyme A FAD (B2 riboflavin) NAD (B3 niacin)
Why are alanine and glutamine levels high in blood?
They are good carriers of N
What happens in transamination?
Transfer of an amino group from an AA to a-ketoglutarate –> forming glutamate
Deaminated AA –> ketoacid (like pyruvate)
How are aminotransferases named?
Named by donor of amino group
Alanine aminotransferase converts alanine to pyruvate, forming glutamate
What is required by all aminotransferases (besides substrates)?
Pyridoxal phosphate (B6 derivative)