Uworld Part 3 Flashcards
what side effect of dopamine is central?
does carbidopa increase or decrease?
how to avoid?
anxiety and agitation is central effects.
carbidopa can increase thru increasing central availability by inhibiting peripheral conversion
decrease dose
use atypical antipsychotics like cloazpine
what can carbidopa help you avoid
peripheral effects of dopamine
- postural hypotension
- hot flashes
- tachyarrhthmias
- Nausea and vomiting
RNA polymerase I function
form ribosomal components
RNA polymerase II function
mRNA
snRNA
micro RNAa
RNA polymerase III fxn
tRNA
Component of 60S ribosomal subunit
selectivity for CCB
Verapamil most on heart
Nifedipine most on peripheral vasculature
Diltiazem in between
SE of verapamil
constipation
gingival hyperplasia
bradycardia
first/second/third degree AV nodal block
most acid labile piconravirus
rhinovirus
most acid stable piconravirus
enteroviruses
most common species for aspiration pneumoniae
fusobacterium
peptostreptoccus
bacteroides
16S rRNA fxn
complementary and binds to Shine Delgarno sequence in all prokarotic mRNA 10 bases upstream of AUG start.
mRNA and 30S ribosomal subunit bind, an initiator tRNA binds to AUG, the 50S ribosomal subunit joins and protein synth begins
23s rRNA
found in 50S, faciltates peptide bond formation in protein translation
isoniazid function
req. conversion to active compound by mycobacterial enzyme catalase-peroxidase
inhibits mycolic acid synthesis
rifampin function
imhibits DNA dependent RNA synthesis
50S antibiotics
chloramphenicol
clindamycin
linezolid
macrolides (erythromycin/azithromycin/clarithroycin)
30S antibiotics
tetracycline
doxycycline
aminoglycosides (gentamicin, streptomycin and others)
beta blocker function in thyrotoxicosis
Block increased sensitivity to catecholamines via thyroid hormone mediated upregulation of beta-adrenergic receptor expression
Decrease peripheral conversion of T4 to T3 by inhibiting iodothyronine deiodinase
G6PD genetic
X linked recessive
Hereditary spherocytosis genetic
autosomal dominant
vitamin D-resistant rickets genetic
x-linked dominant inheritance
oxidative phosphorylation mutations tend to be
mitochondrial diseases
autosomal dominant diseases
ADPKD FAP Familial hypercholesterolemia Hereditary hemorrhagic telangietasia Heredtiary spherocytosis Huntington disease Marfan syndrome MEN Neurofibromatosis 1 Neurofibromatosis 2 Tuberous sclerosis Von Hippel Lindau disease
autosomal recessive diseases
Albinism ARPKD Cystic fibrosis Glycogen storage diseases hemochromatosis Kartagener syndrome Mucopolysaccharidoses (except hunter syndrome) Phenylketouria Sickle cell anemia Sphingolipidoses (except Fabry disease) Thalessemias Wilson disease
xlinked recessive disorders
Be Wise, Fool’s GOLD Heeds Silly HOpe
Bruton agammaglobulinemia Wiskott-Aldrich syndrome Fabry disease G6PD deficiency Ocular albinism Lesch-Nyhan syndrome Duchenne (and Becker) muscular dystrophy Hunter Syndrome Hemophilia A and B Ornithine transcarbamylase deficiency
Trinucleotide repeat expansion diseases and the trinucleotide repeats are
Huntington disease (CAG)
Myotonic dystrophy (CTG)
Friedreich ataxia (GAA)
Fragile X syndrome (CGG)
where does digestion of triglycerides occur
duodenum
where does absorption of triglycerides occur
jejunum
hemosiderin laden macrophages in pulmonary alveoli indicates
chronic elevation of pulmonary capillary hydrostatic pressures which is usually the result of left sided heart failure.
how to differentiate b/w lipofuscin or hemosiderin
prussian blue stain, detects intracellular iron, colorless potassium ferrocyanide converted by iron to blue black ferric ferrocyanide.
left ventricular leads in biventricular pacemakers courses through
coronary sinus residing in the atrioventricular groove on the posterior aspect of the heart.
vitiligo is caused by
loss of epidermal melanocytes