Miscellaneous Flashcards
what is tachyphylactic in terms of drug interactions?
acute decrease in response to a drug after initial/repeated administration
ex) nitrates, niacin, phenylephrine, LSD MDMA
how can Wilson disease lead to basal ganglia atrophy?
copper accumulates in the brain (basal ganglia)
how can nitroprusside cause cyanide toxicity
nitroprusside is metabolized in body to release nitric oxide and cyanide ions
how to treat cyanide toxicity
- sodium nitrite: promotes methemoglobin formation, which combines cyanide to form cyanmethemoglobin
- sodium thiosulfate: serves as sulfur donor to promote hepatic rhodanese-mediated conversion of cyanide to thiocyanate to be excreted in urine
- hydroxocobalamin: binds to cyanide ions and forms cyanocobalamin to be excreted in urine
osteocytes are connected to each other through
gap junctions
can sense mechanical stresses and send signals to modulate the activity of surface osteoblasts, so they help regulate bony remodeling
mechanism of action of colchicine
inhibits leukocyte migration and phagocytosis by blocking tubulin polymerization
used to treat acute gouty arthritis in those who can’t take NSAIDs (normally the first line treatment)
side effects: nausea and diarrhea
how does anterior dislocation of the humerus presents
flattening of the deltoid prominence, protrusion of the acromion, and anterior axillary fullness (due to humeral head’s movement into this location)
injured axillary nerve which innervates deltoid and teres minor muscles and provides sensory innervation of the skin overlying the lateral shoulder
1st pharyngeal pouch derivatives
middle ear cavity, eustachian tube, mastoid air cells
2nd pharyngeal pouch derivatives
epithelial lining of the palatine tonsil
3rd pharyngeal pouch derivatives
dorsal wings–> inferior parathyroids
ventral wings–> thymus
4th pharyngeal pouch derivatives
dorsal wings–> superior parathyroids
ventral wings–> ultimobranchial body, parafollicular (C) cells of thyroid
what is developmental field defect
multiple malformations that occur secondary to an embryonic disturbance in an adjoining group of cells
initial embryonic disturbance leads to multiple malformations by disrupting the development of adjacent tissues and structures within a particular region
what are caspases and what do they do?
proteolytic enzymes that cleave cellular proteins- activated by cytochrome c
apoptosis can occur through either intrinsic (mitochondria-mediated) pathway or the extrinsic (receptor-initiated) pathway
both pathways converge in the activation of caspases
lymph nodes of the lower extremities
divided into superficial lymphatic vessels (follow venous system) and the deep lymphatic vessels (follow the arterial system)
superficial divided into medial and lateral tracks
-medial track runs up the superficial inguinal lymph nodes, bypassing the popliteal nodes
lesions on the medial foot cause inguinal lymphadenopathy, whereas lateral lesions are more likely to cause lymphadenopathy in both the popliteal and inguinal areas
what is responsible for synthesizing cytosolic proteins
free ribosomes floating in the cytosol- translate proteins found found within the cytosol, nucleosol, peroxisome matrix, and nuclear-encoded mitochondrial proteins
the ribosomes on RER synthesizecell membrane proteins
homocystinuria-what is the cause and what happens to the individuals affected by this
cause by cystathionine synthase deficiency
affected individuals have marfanoid habitus, ectopia lentis, and developmental delay
many patients respond dramatically to pyridoxine (vitamin B6) supplementation
which are the stop codons
UAA, UAG, UGA
duchenne muscular dystrophy is caused by what type of mutation
frameshift mutations (most common) or nonsense mutations in the dystrophin gene that lead to the formation of truncated, defective protein
nonsense mutations introduce premature stop codons int he coding sequence of the mRNA
how is isoniazid metabolized
metabolized by acetylation
speed of which a patient is able to acetylate drugs depends on whether they are genetically “fast” or “slow” acetylators
what is tuberous sclerosis
autosomal dominant condition characterized by cortical tubers and subependymal hamartomas in the brain, with consequent seizures and cognitive disability, cardiac rhabdomyomas, facial angiofibromas, and leaf-shaped patches of skin lacking pigment (ask-leaf patches)
associated with renal angiomyolipoma (benign tumor composed of blood vessels (angio), smooth muscle (myo), and fat (lipoma)
amino acid binding site of tRNA
3’ CCA tail
aminoacyl tRNA synthetase is the enzyme responsible for “loading” the appropriate amino acid to the 3’ terminal hydroxyl group of the CCA tail