| Term 
 
        | classes of antimicrobials: |  | Definition 
 
        | antibacterials, antivirals, antifungals, antiprotozoals, antihelmenthics |  | 
        |  | 
        
        | Term 
 
        | prokaryote ribosome subunits: eukaryote ribosome subunits:
 |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | gram positive large ___ layer |  | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | Penicillin (a beta lactam- targets cell wall) (antibiotic)
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | glycopeptide (affects cell wall) (antibiotic)
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | cephalosporin -a beta lactam- affects cell wall (antibiotic)
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | cephalosporin- beta lactam- targets cell wall (antibiotic)
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | a polymyxin- affects cell membrane (antibiotic)
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | a mix of trimethoprim and sulfonamides =act on folic acid synthesis (antibiotic)
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | a quinolone -targets DNA (antibiotic)
 |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | a macrolide- targets protein synthesis (antibiotic)
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | an aminoglycoside- affects protein synthesis |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | affects protein synthesis |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | gram +ve cocci - a narrow spectrum antibiotic |  | 
        |  | 
        
        | Term 
 
        | tetracyclines- action on: |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | bacteriostatic: bacteriocidal:
 |  | Definition 
 
        | stops the bacteria from growing kill the bacteria
 |  | 
        |  | 
        
        | Term 
 
        | tetracyclines (bacteriostatic or cidal?) |  | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 
        | tetracycline + penicillin |  | Definition 
 
        | tetracycline inhibits penicillin |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | labile- destroyed in acid |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 
        | benzathine benzylpenicillin is a _____ penicillin |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | kidney excretion of penicillin delayed by: |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | cephalosporins is part of __ class: and has 4 classes:
 |  | Definition 
 
        | beta- lactam antibiotic 1st generation: gram+
 2nd gen: gram -ve, 3rd and 4th gen: broad
 |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 
        | difference between tetracyclines and aminoglycosides: |  | Definition 
 
        | tetracyclines: reversible, inhibit protein synthesis, bacteriostatic, broad spectrum, insoluble complex, variable, oral/topical, delayed bone growth, tooth discoloration aminoglycosides: irreversible, bactericidal, gram -ve, nephrotoxic, ototoxic
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | inhibit topoisomerase 2 broad spectrum
 |  | 
        |  | 
        
        | Term 
 
        | organs most likely to receive metastasis: |  | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 
        | while doing chemo monitor: |  | Definition 
 
        | CBC- liver and renal function |  | 
        |  | 
        
        | Term 
 
        | cell cycle specific antineoplastics: |  | Definition 
 
        | antimitotics, antimetabolites |  | 
        |  | 
        
        | Term 
 
        | antimetabolites structure: |  | Definition 
 
        | analogues of pyrimidines, purines |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | purine analogue- antimetabolite (antineoplastic) |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | pyrimidine analogue-antimetabolite -(antineoplastic) |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | pyrimidine analogue-antimetabolite -(antineoplastic) |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | antifolate (antineoplastic) |  | 
        |  | 
        
        | Term 
 
        | antimitotics target ___ phase of cell cycle: |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | 2 main types of antimitotics: |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | vincristine/vinblastine class: |  | Definition 
 
        | vinca alkaloids- antimitotics |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | prevent microtubules from forming |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | prevent separation of chromosomes (antimitotic) |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | nitrogen mustard- alkylating agent (antineoplastic) |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | nitrogen mustard- alkylating agent (antineoplastic) |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | nitrosoureas- alkylating agent |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | platinum based drugs -alkylating agent (also neurotoxic) -an antineoplastic |  | 
        |  | 
        
        | Term 
 
        | topoisomerase 1 topoisomerase 2:
 |  | Definition 
 
        | cuts and ligates ssDNA cuts and ligates both strands of DNA
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | topoisomerase 2 inhibitor (antineoplastic) |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | topoisomerase 2 (DNA gyrase) |  | 
        |  | 
        
        | Term 
 
        | actinomycin/ bleomycin class: |  | Definition 
 
        | antitumor antibiotics (antineoplastic) |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | antiestrogen (antineoplastic) |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | retinoids (VitA analogue) stimulate apoptosis (antineoplastic) |  | 
        |  | 
        
        | Term 
 
        | antiangiogenic agents action: |  | Definition 
 
        | interfere with neovascularization- interrupt tumour growth and spread |  | 
        |  | 
        
        | Term 
 
        | 2 pathways for metabolizing alochol: |  | Definition 
 
        | alcohol dehydrogenase- to acetaldehyde microsomal ethanol oxidizing system (when alcohol dehydrogenase is saturated)
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | inhibits aldehyde deghydrogenase |  | 
        |  | 
        
        | Term 
 
        | alcohol metabolism follow __ kinetics: |  | Definition 
 
        | 0 order kinetics- enzyme can be saturated |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | glutamate receptor -upregulated in alcoholics=greater withdrawal
 |  | 
        |  | 
        
        | Term 
 
        | Wernickes encephalopathy: S&S, cause
 |  | Definition 
 
        | ataxia (loss of coordination), confusion, short term memory loss -not enough Thiamine (B1)
 |  | 
        |  | 
        
        | Term 
 
        | Korsakoff's psychosis: 6 features:
 cause
 |  | Definition 
 
        | anterograde amnesia (can't create new memories), severe memory loss, confabulation, meager content in conversation, lack of insight, apathy -deficiency of thiamine (B1)
 |  | 
        |  | 
        
        | Term 
 
        | naltrexone class and use: |  | Definition 
 
        | long lasting opioid receptor antagonist -decrease desire for alcohol (for alcoholism)
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | NMDA receptor antagonist, GABAa receptor activator |  | 
        |  | 
        
        | Term 
 
        | withdrawal symptoms (from ethanol) |  | Definition 
 
        | excitability of the CNS: tremors (delirium tremens-hallucinations) irritability, anxiety, increased heart rate, convulsions, coma, possible death |  | 
        |  | 
        
        | Term 
 
        | characteristics of alcohol withdrawal mild
 moderate
 severe (delirium tremens)
 |  | Definition 
 
        | mild- BP >150/90, temp >37.7 moderate- BP> 150-200/100-140, temp 37.7-38.3
 severe: BP>200/140, temp>38.3
 |  | 
        |  | 
        
        | Term 
 
        | sedative therapy for alcohol withdrawal: |  | Definition 
 
        | benzodiazepines, barbituates |  | 
        |  | 
        
        | Term 
 
        | ethanol may be given for treatment: |  | Definition 
 
        | with ethylene glycol or methyl alcohol intoxication -has greater affinity for ADH |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | growth restriction, craniofacial dysmorophology, CNS dysfunction |  | 
        |  | 
        
        | Term 
 
        | diagnostic terms for FAS: |  | Definition 
 
        | alcohol related neurodevelopmental disorder- no facial features, no growth restriction partial fetal alcohol syndrome- 2 facial features
 FAS- all 3 diagnostic features
 |  | 
        |  | 
        
        | Term 
 
        | depression may be associated with these neurotransmitters: |  | Definition 
 
        | serotonin, dopamine, norepinephrine |  | 
        |  | 
        
        | Term 
 
        | SSRIs start working in about |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | neurotrophic hypothesis of depression: |  | Definition 
 
        | fewer dendritic sprouts and branching |  | 
        |  | 
        
        | Term 
 
        | 3 types of pharmacological treatment for depression: |  | Definition 
 
        | block NT reuptake: SSRIs, SNRIs, tricyclics block neuronal metabolism=increase amount released (MAOIs)
 increase neurotransmitter released (presynaptic autoreceptor blockade)
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | NT feedback on the receptor, inhibits more release of neurotransmitter ex. mirtazepine blocks autoreceptor
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | SNRI antidepressant- inhibits both serotonin and norepinephrine reuptake |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | may become too elevated -generally when you use multiple drugs that increase serotonin ex. MAOIs +SSRIs
 -increased body temp, mental changes, coma, death
 |  | 
        |  | 
        
        | Term 
 
        | different SSRIs have different: |  | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | P450 enzyme- may cause other drug toxicity |  | 
        |  | 
        
        | Term 
 
        | abrupt withdrawal of SSRI symptoms: |  | Definition 
 
        | anxiety, agitation, insomnia, confusion, diarrhea, sweating, vomiting, impaired coordination |  | 
        |  | 
        
        | Term 
 
        | tricyclic antidepressants adverse effects: |  | Definition 
 
        | due to collateral receptor effects: (they aren't selective!)
 -anticholinergic- delirium, dry mouth, urinary retention, impaired sweating
 -antihistaminergic-sedation
 -block alpha 1 adrenergic receptors:orthostatic hypotension, ECG effects, arrythmias, seizures
 |  | 
        |  | 
        
        | Term 
 
        | MAOIs increase storage and release of : |  | Definition 
 
        | NE, serotonin (5HT), dopamine, and epinephrine |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | reversible (safer if taken after meals), irreversible |  | 
        |  | 
        
        | Term 
 
        | adverse effects of MAOIs: |  | Definition 
 
        | hypo or hypertension -cheese effect- tyramine is an indirect sympathomimetic- (releases norepinephrine= hypertensive crisis!
 |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 
        | 2 step process to treating mania: |  | Definition 
 
        | reduce mood to normal-antipsychotic med 2) stabilize mood within normal range
 |  | 
        |  | 
        
        | Term 
 
        | depressive phase of bipolar disorder: |  | Definition 
 
        | doesnt respond to SSRIs, much more difficult to treat -mood stabilizers effective
 |  | 
        |  | 
        
        | Term 
 
        | Lithium used for: adverse effects:
 |  | Definition 
 
        | mood stabilizer- used to be main treatment for bipolar disorders -replaces sodium modulates electrical activity but has many adverse effects: tremors, seizures, coma, polyuria (kidney), hypothyroidism
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | anticonvlusant and mood stabilizer for bipolar |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | anticonvulsant and mood stabilizer for bipolar |  | 
        |  | 
        
        | Term 
 
        | classes of medication for anxiety and sleep disorders: and an example of each
 |  | Definition 
 
        | barbituates -no longer used though ex. phenobarbitol benzodiazepines (diazepam)
 -Buspirone
 -Z drugs (Zoplicone, Zaleplon, Zolpidem)
 -SSRIs
 |  | 
        |  | 
        
        | Term 
 
        | excitatory neurotransmitter: |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | inhibitory neurotransmitter: |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | Benzodiazepines action and 2 types
 |  | Definition 
 
        | promote GABA BZ1 receptors-inhibit CNS systems specific to sleep/wakefulness
 BZ2 receptors-inhibit CNS systems for anxiety, cognition, seizure threshold, respiration
 |  | 
        |  | 
        
        | Term 
 
        | benzodiazepines used for: |  | Definition 
 
        | anxiolytics, sedatives, anticonvulsant, muscle relaxant |  | 
        |  | 
        
        | Term 
 
        | adverse effects of benzodiazepines: |  | Definition 
 
        | sedation, ataxia, impair cognition and memory, resp depression (but not very much) |  | 
        |  | 
        
        | Term 
 
        | benzodiazepines interact with: |  | Definition 
 
        | alcohol, OTC cough meds (anticholinergics) |  | 
        |  | 
        
        | Term 
 
        | 3 classes of benzodiazepines: |  | Definition 
 
        | short, intermediate and long acting short acting used as hynotic
 |  | 
        |  | 
        
        | Term 
 
        | would we use a long acting benzodiazepine as a hypnotic? |  | Definition 
 
        | no! 1st order kinetics- the drug would still be there when they wake up instead use long acting for anxiety (ex. diazepam)
 |  | 
        |  | 
        
        | Term 
 
        | short acting benzodiazepines have ______ withdrawal effects |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | tolerance develops to the ____ component of benzodiazepines: |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | withdrawal symptoms of benzodiazepines: |  | Definition 
 
        | anxiety, agitation, insomnia, panic withdraw slowly!
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Serotonin 1a receptor agonist- anxiolytic -little tolerance or withdrawal
 |  | 
        |  | 
        
        | Term 
 
        | increase dietary tryptophan (turkey) has what effect? |  | Definition 
 
        | increases serotonin -anxiolytic |  | 
        |  | 
        
        | Term 
 
        | Z drugs for hynotics action: advantages:
 |  | Definition 
 
        | rapid onset, short half life, no withdrawal, little tolerance -enhance GABA at BZ1 receptors - just sleep (not resp depression, relaxation..)
 |  | 
        |  | 
        
        | Term 
 
        | benzodiazepines used with caution in: |  | Definition 
 
        | elderly, resp illness, people with potential for suicide |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | generalized (involve entire CNS) and partial |  | 
        |  | 
        
        | Term 
 
        | characteristics of generalized seizure: |  | Definition 
 
        | loss of consciousness, motor involvement: tonic, clonic (spasms of contraction/relaxation), atonic, recovery (postictal period)- takes mins to hours |  | 
        |  | 
        
        | Term 
 
        | characteristics of partial seizures: |  | Definition 
 
        | involve focal cortical areas may involve motor disturbances, changed behaviour,
 simple partial: NOT loss of consciousness
 complex partial: impaired consciousness
 |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | anticonvulsant -increase GABA activity, block Na channel electrical activity
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | anticonvulsant -increase GABA activity
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | anticonvulsant -blocks glutamate receptors
 |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | anticonvulsant -esp for tonic clonic |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | benzodiazepine- all benzodiazepines have anticonvulsant activity |  | 
        |  | 
        
        | Term 
 
        | treatment of choice for status epilecticus: |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | adverse effects of anticonvulsants: |  | Definition 
 
        | GI, CNS- sedation, tremor, ataxia, hepatic, hematologic- transient leukopenia, aplastic anemia, weight gain, immune system, hypersensitivity reactions -induce CYP P450 enzymes -need to increase dose of some drugs
 |  | 
        |  | 
        
        | Term 
 
        | Stevens Johnson syndrome: |  | Definition 
 
        | skin hypersensitivity reaction with anticonvulsants |  | 
        |  | 
        
        | Term 
 
        | toxic epidermal necrolysis: |  | Definition 
 
        | skin hypersensitivity reaction with anticonvulsants where top 2 layers of skin separate |  | 
        |  | 
        
        | Term 
 
        | valproate, carbamazepine, phenytoin can induce: |  | Definition 
 
        | neural tube defects if taken in pregnancy -so need folate supplementation!
 -transient VitK deficiency -neonatal clotting disorders, supplmentation with VitK
 |  | 
        |  | 
        
        | Term 
 
        | Phenytoin in pregancy can cause: |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | GI problems with anticonvulsants can be avoided with: |  | Definition 
 
        | divided doses, administer with meals |  | 
        |  | 
        
        | Term 
 
        | target of non narcotic analgesics: |  | Definition 
 
        | Cyclooxygenase enzyme (COX): converts arachidonic acid to prostaglandins |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | widespread -homeostatic functions- GI, renal, platelet, macrophage differentiation |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | selective COX 2 inhibitor |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | irreversible inhibition of COX 1 and COX 2 (non selective): decrease prostaglandins and thromboxanes -analgesic, antipyretic, anti-platelet, at high dose- antiinflammatory |  | 
        |  | 
        
        | Term 
 
        | 2 pathways through which ASA inhibits pain: |  | Definition 
 
        | peripheral action- in the area of pain central action- whole pain pathway
 |  | 
        |  | 
        
        | Term 
 
        | mechanism for decreased fever with ASA: |  | Definition 
 
        | inhibit prostaglandin synthesis: reset temp center in hypothalamus |  | 
        |  | 
        
        | Term 
 
        | high dose of ASA needed for: |  | Definition 
 
        | inflammation- Rheumatoid fever, rheumatoid arthritis, gout |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | bleeding, tinnitus, GIT, asthma, metabolic acidosis- then resp alkalosis, nephritis, Reyes syndrome |  | 
        |  | 
        
        | Term 
 
        | acute aspirin toxicity signs: |  | Definition 
 
        | vomiting, abdominal pain, tinnitus, hypoglycemia, hypokalemia, hyperthermia, hyperventilation.. coma, death= cardiovascular collapse |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | no antidote, stabilize airway, give potassium, restore pH, glucose, charcoal? gastric lavage? dialysis? |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | inhibit COX enzyme -no inflammatory or antiplatelet
 |  | 
        |  | 
        
        | Term 
 
        | adverse effects of acetominophen: |  | Definition 
 
        | liver and renal damage long term large doses |  | 
        |  | 
        
        | Term 
 
        | antidote to acetaminophen toxicity: |  | Definition 
 
        | N-acetylcysteine -source of glutathione which decreases NAPQI (liver damage) |  | 
        |  | 
        
        | Term 
 
        | COX 2 inhibitors risks of: |  | Definition 
 
        | thrombosis, CV morbidity/mortality |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | endogenous (endorphins, enkephalins, dynorphins) plant alkaloids (morphine, codeine, thebaine)
 semisynthetic (diamorphine, hydromorphone)
 synthetic (pethidine, methadone, fentanyl)
 |  | 
        |  | 
        
        | Term 
 
        | ligand opioid receptor complex: and subtypes:
 |  | Definition 
 
        | G protein coupled receptors: delta, kappa and mu -all found in the CNS
 |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | mixed opioid agonist/antagonist agonist action: analgesia
 -can induce withdrawal if already taking opioids
 |  | 
        |  | 
        
        | Term 
 
        | opioids act as analgesics by: |  | Definition 
 
        | decreased presynaptic release of transmitters mobilized in pain impulse -block postynaptic effects
 inhibitory pathways-pain block, decreased emotional rxn to pain
 |  | 
        |  | 
        
        | Term 
 
        | treatment of opioid dependance: |  | Definition 
 
        | methadone, buprenorphine -similar effects as opioids |  | 
        |  | 
        
        | Term 
 
        | S&S of acute opioid toxicity: |  | Definition 
 
        | pinpoint pupils, hypoventilation, hypotension, flacid muscles late signs: severe resp depression, CV depression, seizures, coma
 |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 
        | most addictive drugs increase: except:
 |  | Definition 
 
        | dopamine except novelty drugs- hallucinogens or substances which reduce anxiety
 |  | 
        |  | 
        
        | Term 
 
        | drugs with ____ half life are more prone to tolerance |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | mechanism of tolerance development: |  | Definition 
 
        | decrease the rate of elimination (metabolic tolerance), cellular activity decreases b/c the drug is doing the work for it ie. endogenous system is downregulated |  | 
        |  | 
        
        | Term 
 
        | develop tolerance to ____ effects of benzodiazepines but not ___ effects |  | Definition 
 
        | sedating but not to antianxiety |  | 
        |  | 
        
        | Term 
 
        | cross tolerance occurs with heroin and ___ and benzodiazepines and ____
 |  | Definition 
 
        | methadone and heroin 
 benzodiazepines and alcohol
 |  | 
        |  | 
        
        | Term 
 
        | types of oral hypoglycemics: |  | Definition 
 
        | sulfonylureas, meglitinides, biguanides, thiazolidinediones (TZDs), alpha glucosidase inhibitors |  | 
        |  | 
        
        | Term 
 
        | requirement for sulfonylureas: |  | Definition 
 
        | functioning liver and kidney |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | stimulate insulin secretion by B cell -inhibit K channels on B-cell causing depolarization: calcium entry: insulin release
 -increase insulin receptor sensitivity
 |  | 
        |  | 
        
        | Term 
 
        | drugs that increase hypoglycemic effects: |  | Definition 
 
        | NSAIDs, coumarins, alcohol, MAO inhibitors, some antibacterials, microsomal enzyme inhibitors |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 
        | drugs that mask the symptoms of hypoglycemia: |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | classes of sulfonylureas: |  | Definition 
 
        | 1st, 2nd and 3rd generation |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | 1st generation sulfonylurea -short acting
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | 1st generation sulfonylurea -LOONNGG acting
 -risk of hypoglycemia!
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | 2nd generation sulfonylurea -short acting (6-10 hours)
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | 2nd generation sulfonylurea -intermediate acting
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | 2nd generation sulfonylurea intermediate acting
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | 3rd generation sulfonylurea -long acting
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | meglitinides, sulfonylureas |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | decrease gluconeogenesis in the liver increase glucose uptake by skeletal muscle -for obese patients
 -do not cause hypoglycemia
 side effects: anorexia, nausea, diarrhea, lactic acidosis, contraindicated in renal disease
 |  | 
        |  | 
        
        | Term 
 
        | meglitinides characteristics: |  | Definition 
 
        | short acting, similar to sulfonylureas -can be combined with metformin
 -side effects: hypoglycemia
 |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 
        | thiazolidinedione mechanism: |  | Definition 
 
        | activate transcription regulator that improves glucose uptake by skeletal muscles, decrease hepatic glucose production, modulate lipogenesis in adipocytes |  | 
        |  | 
        
        | Term 
 
        | side effects of thiazolidinedione: |  | Definition 
 
        | Congestive heart failure, myocardial ischemia, liver injury |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 
        | alpha glucosidase inhibitors action: |  | Definition 
 
        | inhibit alpha glucosidase in intestine- dont absorb as many carbs -control post prandial glucose levels not controlled adequately by diet and sulfonylureas
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | alpha glucosidase inhibitor |  | 
        |  | 
        
        | Term 
 
        | glucagon like peptide 1 agonists: |  | Definition 
 
        | insulin secretagogues- slow down gastric emptying rates |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | GLP-1 (glucagon like peptide) |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | decrease postmeal glucagon release -adjunct to type 1 and 2 treatment
 |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | exocrine-pancreatic enzymes endocrine- alpha- glucagon
 beta-insulin
 delta- somatostatin
 PP(F) -secrete pancreatic polypeptide
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | gluconeogenesis, glycogenolysis, lipolysis (increase blood sugar) |  | 
        |  | 
        
        | Term 
 
        | glucose enters cells through: |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | fasting plasma glucose normal (in mg/dL) |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | normal 2 hours post meal glucose level (mg/dL): |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | diabetes mellitus can be induced by this drug: |  | Definition 
 
        | thiazide diuretics, steroid therapy |  | 
        |  | 
        
        | Term 
 
        | infection that can cause diabetes: |  | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | intermediate acting -reasonably soluble zinc preparation
 |  | 
        |  | 
        
        | Term 
 
        | crystalline insulin type: |  | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | long acting insulin -poorly soluble zinc preparation
 |  | 
        |  | 
        
        | Term 
 
        | complications of injecting insulin at the same place every time |  | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | was a promising inhaled insulin product |  | 
        |  | 
        
        | Term 
 
        | components of general anesthesia: |  | Definition 
 
        | analgesia, amnesia, areflexia, relaxation, hypnosis |  | 
        |  | 
        
        | Term 
 
        | general anesthesia mechanism of action: |  | Definition 
 
        | depression of CNS, depression of Reticular Activating System, lipid matrix expansion, GABA mediated inhibition, glutamate antagonist |  | 
        |  | 
        
        | Term 
 
        | phases of general anesthetic: |  | Definition 
 
        | induction, maintenance, emergence |  | 
        |  | 
        
        | Term 
 
        | Primary route of elimination of general anesthetic drugs: 2ndary:
 |  | Definition 
 
        | lungs some liver metabolism
 |  | 
        |  | 
        
        | Term 
 
        | halothane metabolism yields: |  | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | degrades into nephrotoxic compound |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | minimum alveolar concentration- to prevent 50% of subjects from responding to painful surgical stimulus high MAC: low potency
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | incomplete anesthetic because low potency in order to put 50% of patients to sleep need 104%- not possible
 -minimal hypotension and resp depression
 -increases volume of air-filled spaces
 |  | 
        |  | 
        
        | Term 
 
        | volatile anesthetics: properties examples
 |  | Definition 
 
        | liquid at room temp, produce unconsciousness and analgesia, decrease blood pressure, depress respirations desflurane, sevofluranes, isoflurane, halothane
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | exposure to volatile anesthetics -hypermetabolic state, hypercalcemia, skeletal muscle rigidity, tachy, acidosis
 treatment: dantrolene, 100% oxygen
 |  | 
        |  | 
        
        | Term 
 
        | intravenous general anesthetics: properties
 examples
 |  | Definition 
 
        | thiopental, etomidate, propofol, ketamine] properties: rapid onset, short duration, rapid recovery, abscence of side effects
 |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | hypotension, tachy, apnea, NV, decrease in ICP |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | intravenous -rapid offset because rapid liver metabolism
 -hypotension, apnea, prevent NV
 -michael jackson
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | intravenous general anesthetics -block Norep uptake
 -not change in BP, HR, cause apnea, NV, adrenocortical suppression
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | hypertension, tachy, analgesia, increased ICP, dysphoria good for hemodynamic compromise
 |  | 
        |  | 
        
        | Term 
 
        | chemical structure of local anesthetics: |  | Definition 
 
        | amino esters, amino amides |  | 
        |  | 
        
        | Term 
 
        | local anesthetics mechanism: |  | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 
        | allergy more common with: (local anesthetic) |  | Definition 
 
        | amino esters (cocaine, tetracaine, procaine) |  | 
        |  | 
        
        | Term 
 
        | local anesthetics potency correlates with: |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | gonadal hormones made from: |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | most abundant: progestin
 estrogen
 androgen
 |  | Definition 
 
        | progesterone estradiol
 testosterone
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | progestin- inhibits estrogen effects |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | estrone, estradiol, estriol |  | 
        |  | 
        
        | Term 
 
        | after ovulation: estrogen
 LH
 progesterone:
 |  | Definition 
 
        | estrogen drops rapidly LH increases
 progesterone increases- to support pregnancy
 |  | 
        |  | 
        
        | Term 
 
        | natural estrogen: semisynthetic estrogen
 synthetic estrogen:
 |  | Definition 
 
        | estradiol estradiol valerate, ethinyl estradiol
 mestranol, stilboestrol
 |  | 
        |  | 
        
        | Term 
 
        | estrogen transport in body by: |  | Definition 
 
        | albumin, sex steroid binding globulin |  | 
        |  | 
        
        | Term 
 
        | metabolism of estrogens: excretion:
 |  | Definition 
 
        | liver, synthetic estrogens less prone to degradation excretion by kidneys
 |  | 
        |  | 
        
        | Term 
 
        | hypothalamic estrogen pathway: |  | Definition 
 
        | signal to hypothalamus, GNRH goes to anterior pituitary, makes FSH, LH, stimulate estrogen in ovaries |  | 
        |  | 
        
        | Term 
 
        | indications for estrogen: |  | Definition 
 
        | contraception, replacement for menopause, female hypogonadism, menstrual disorders, acne, prostatic cancer |  | 
        |  | 
        
        | Term 
 
        | hyperestrogenemia in males can be caused by: |  | Definition 
 
        | liver disease and hyperactivity of the zona reticularis |  | 
        |  | 
        
        | Term 
 
        | in females, hyperestrogenemia can cause: |  | Definition 
 
        | endometrial carcinoma breast cancer
 cervical cancer
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | antiestrogen, increases FSH, treatment of infertility |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 
        | medroxyprogesterone, norethindrone, norgestrel: |  | Definition 
 
        | 1st generation synthetic progestins |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | 2nd gen progestins synthetic) |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | 3rd gen synthetic progestin -least androgenic effect
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | 3rd gen synthetic progestin |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | 3rd gen synthetic progestin |  | 
        |  | 
        
        | Term 
 
        | progestins therapeutic indications: |  | Definition 
 
        | dysmenorrhea, endometriosis, endometrial carcinoma, contraception (egg cant implant), hormone replacement |  | 
        |  | 
        
        | Term 
 
        | mifepristone class: mechanism:
 used for:
 |  | Definition 
 
        | antiprogestin -competitive inhibition of progesterone
 used for abortion
 |  | 
        |  | 
        
        | Term 
 
        | types of oral contraceptives: |  | Definition 
 
        | monophasic, biphasic, triphasic |  | 
        |  | 
        
        | Term 
 
        | estrogen progesterone combination oral contraceptives mechanism: |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | low dose progestin oral contraceptive mechanism: |  | Definition 
 
        | thicken cervical secretions, inhibit implantation, suppress ovulation by acting on FSH/LH |  | 
        |  | 
        
        | Term 
 
        | adverse effects of oral contraception: |  | Definition 
 
        | edema, HTN, vascular disorders-thromboembolic, coronary artery/ Cerebrovascular, headache, depression, postpill amenorrhea |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | injected every three months- Oral contraceptive |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | inserted ropes under skin for oral contraceptive, last 3-5 years |  | 
        |  | 
        
        | Term 
 
        | hormone replacement therapy for menopause: |  | Definition 
 
        | LOW doses of estrogen reduce symtpoms osteoporosis, flushing ,headache, genital tract atrophy, CV disease -may be cmovined with progestin to reduce risk of endometrial carcinoma
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | testosterone, dihydrotestosteron,e androstenedione, dehydroepiandrosterone |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 
        | therapeutic indications of androgens: |  | Definition 
 
        | hormone replacement, anemia, breast cancer, anabolic agents (for protein loss) |  | 
        |  | 
        
        | Term 
 
        | types of male hypogonadism: |  | Definition 
 
        | primary testicular failure secondary:hypothalamic pituitary disease
 |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 
        | androgen suppressors used to treat: |  | Definition 
 
        | prostate carcinoma, endometriosis |  | 
        |  | 
        
        | Term 
 
        | androgen receptor inhibitors used to treat: |  | Definition 
 
        | prostate carcinoma, hirsutism and virilization in women, precocious puberty in boys |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | inhibitis androgen receptors |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | male oral contraceptive -inhibit sperm production
 adverse effects: irreversibility, hypokalemia
 |  | 
        |  | 
        
        | Term 
 
        | base of all the adrenal steroids: |  | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | androstenedione (both genders make both male and female sex hormones) |  | 
        |  | 
        
        | Term 
 
        | modified sympathetic ganglion: |  | Definition 
 
        | epinephrine and norepinephrine go straight to the blood -doesnt act on postganglionic factors |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | increase mental alertness, metabolic rate, increased HR,BP,RR, contractility, pupil dilation |  | 
        |  | 
        
        | Term 
 
        | 3 regions of adrenal cortex: |  | Definition 
 
        | zona glomerulosa (secrete mineralocorticoids), zona fasciculata (glucocorticoids), zona reticularis (sex hormones) |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | increase Na and water in body decrease K, increase blood volume, BP
 |  | 
        |  | 
        
        | Term 
 
        | what regulates the release of glucocorticoids? |  | Definition 
 
        | Corticotropin releasing hormone (by hypothalamus) adrenocorticotropic releasing hormone (by pituitary)
 glucocorticoids (-ve feedback)
 |  | 
        |  | 
        
        | Term 
 
        | effects of glucocorticoids: |  | Definition 
 
        | gluconeogenesis (glucose from noncarb sources), decrease glucose uptake by cells, increase protein metabolism, redistribute fat to face and trunk, anti-inflammatory, immunosuppressive, increase RBCs, Na/water retention, osteoporosis, ulceration GI, mood changes |  | 
        |  | 
        
        | Term 
 
        | therapeutic use of glucocorticoids: |  | Definition 
 
        | asthma, adrenal hypofunction, allergic reaction, autoimmune-RA, systemic lupus erythmotosis, organ transplant, leukemia, inflammotory conditions |  | 
        |  | 
        
        | Term 
 
        | administration of glucocorticoids: |  | Definition 
 
        | IM, topical, inhalation, oral, injection remember equivalent concentrations: a small amount of dexamethasone=large amount of cortisone
 |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | hyperfunction of zona glomerulosa |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | hyperfunction of zona fasciculata |  | 
        |  | 
        
        | Term 
 
        | congenital adrenal hyperplasia: |  | Definition 
 
        | hyperfunction of zona reticularis |  | 
        |  | 
        
        | Term 
 
        | primary addisons disease: secondary:
 |  | Definition 
 
        | -primary: adrenal gland disorder: autoimmune, TB, infections -secondary: pituitary gland disorder: inadequate secretion of ACTH, sudden withdrawal of prolonged steroid therapy, destruction of pituitary gland
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | weight loss, hypotension, fatigue, mental depression, addisonian crisis-severe hypotension-shock treatment: hydrocortisone if cortisol deficient, fludrocortisone if aldosterone deficient
 |  | 
        |  | 
        
        | Term 
 
        | Conn's syndrome: causes:
 s&S:
 |  | Definition 
 
        | hyperfunction of fasciculata: increased aldosterone secretion in absence of RAS
 cause: adrenal hyperplasia, adrenal tumors
 s&s: HTN, hypokalemia, decreased renin, alkalosis
 |  | 
        |  | 
        
        | Term 
 
        | cushings syndrome: causes:
 |  | Definition 
 
        | increase in glucocorticoids -iatrogenic (excess steroid therapy)
 or spontaneous (adrenal hyperplasia, adrenal tumours, excess pituitary ACTH syndrome, ectopic tumor- secretes ACTH
 |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | obesity, myopathy, HTN, hyperglycemia, infections, osteoporosis |  | 
        |  | 
        
        | Term 
 
        | congenital adrenal hyperplasia caused by: results in:
 |  | Definition 
 
        | congenital metabolic disorder- most common: 21-hydroxylase deficient -increase adrenal androgens, decrease cortisol and aldosterone
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | herbal drug -sedative and hypnotic -bad if mixed with alcohol!
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | contains hypericin, inhibit uptake of serotonin and norep -treat depression
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | herbal -contains kava lactones: anti-anxiety
 -but potentiates other CNS drugs
 -additive response with other antidepressants -should not be used!
 |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | analgesic, antipyretic, anti-inflammatory, inhibit platelet aggregation (low dose) -gastric irritation, tinnitus, reyes
 |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | analgesic, antipyretic, not antiinflammatory, inhibits COX 1 and 2 overdose: fatal hepatic necrosis
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | analgesic, antipyretic, antiinflammtory |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | analgesic, antipyretic, may use as antiinflammatory |  | 
        |  | 
        
        | Term 
 
        | Cold preparations include: |  | Definition 
 
        | antihistamines -may alleviate symptoms if there is an allergic reaction
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | alpha agonists ex. phenylephrine -cause decongestion because of vasoconstriction -may alter BP
 |  | 
        |  | 
        
        | Term 
 
        | cough suppressants: (antitussives) |  | Definition 
 
        | codeine or dextromethorphan -suppress cough centre in medulla |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | lower phlegm -glyceryl guaiacolate
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | H1 antagonist but tolerance develops
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | absorbed by ozone sunburn, tans, cancer
 UVA- photosensitivity
 |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | min erythema dose protected/min erythema dose unprotected |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | laxative- stimulate intestinal muscle to increase contractions -increase secretion of water into intestine
 |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | laxative-forms a gel in water |  | 
        |  | 
        
        | Term 
 
        | dioctyl sodium sulfosuccinate (colace) |  | Definition 
 
        | laxative -emollient: surface active agent |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | antidiarrheal -synthetic opioid that does not enter CNS |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | claimed to be effective against cancer -from the bottom of the sea
 |  | 
        |  | 
        
        | Term 
 
        | 2 major groups of antiasthma agents: |  | Definition 
 
        | bronchodilators, anti-inflammatory agents |  | 
        |  | 
        
        | Term 
 
        | 3 types of bronchodilators |  | Definition 
 
        | sympathomimetics (B2 and alpha adrenoreceptor antagonists), anticholinergics, xanthines |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | decrease muscarinic receptors |  | 
        |  | 
        
        | Term 
 
        | ipratropium bromide class: |  | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | caffeine, theophylline, theobromine |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | xanthine -anti-asthma drug but many side effects
 (aminophylline) -decrease phosphodiesterases, decrease cAMP hydrolysis, cAMP accumulates, relaxation of bronchial smooth muscles
 |  | 
        |  | 
        
        | Term 
 
        | theophylline side effects: |  | Definition 
 
        | dysrhythmias, convlusions, nausea |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | glucocorticoids mast cell stabilizers
 leukotriene receptor antagonists
 methotrexate
 |  | 
        |  | 
        
        | Term 
 
        | nedocromil, cromolyn sodium: |  | Definition 
 | 
        |  |