NSAID GIT ulceration occurs because they reduce synthesis of GI prostaglandins (which inhibit gastric acid secretion and protective mucus production)
NSAIDs cause nephrotoxicity by unopposed constriction of the afferent arteriole and decreased renal perfusion. (normally mediated by prostaglandins)
NSAIDs cause coagulation effects (haemotoxicities) as they inhibit thromboxane which activated platelets
alpha-2 receptors are found presynaptically in the CNS to inhibit noradrenaline release, and postsynaptically in the vascular smooth muscle to cause vasoconstriction
GCPRs have an inner carboxy terminus and an outer amino terminus . adrenoreceptors are a type of g coupled receptor
classes of veterinary analgesics are opioids, NSAIDs, alpha-2 agonists and NMDA antagonists
opioids inhibit adenylate cyclase via GPCRs, reducing cAMP production. they also promote K+ channel opening (out) to hyperpolarise cells and prevent Ca2+ entry so neurotransmitters cannot be released
benzodiazepines potentiate GABA mediated inhibition- decrease excitability of neurons by ca2+ influx. Cells are hyperpolarised
cephalosporins are time dependent antibiotics which inhibit penicillin binding proteins and disrupt cross-linkage of glycopeptide in bacterial cell wall (prevent cell wall formation / lyse cell walls)
buprenorphine lasts 6-8 hours
methadone lasts 4-6 hours
benzimadoles and imidazothiaznes are used against GI nematodes in cattle
affinity is the tendecy of a drug to bind to its receptor
efficacy is how good a drug is at eliciting a response
aminoglycosides bind to the 30s ribosome unit. causes non-functional proteins
tetracyclines bind to the 30s ribosome subunit - bacteriostatic by preventing amino acid formation
macrolides are bacteriostatic, bind to 50s ribosome subunit and prevent RNA translocation
lincosamides are bacteriostatic - bind to 50s subunit and form truncated bacterial proteins
chloramphenicol bind irreversibly yo 50s subunit and blocks peptidyl transferase
computed radiography used a photostimulable phosphor storage layer, read by a laser reader
indirect digital radiography uses a photocathode. direct digital radiography uses a selenium plate
radiographic quality is based on exposure (too long = motion blur), mAs (too much burns out detail), collimation, patient positioning
osteophytosis is new bone formation at a joint surface when it is perceived as unstable. joint space appears reduced. often a secondary change to osteoarthritis
enthesiophytosis is bone formation at ligament or tendon attachments . includes spondylosus deformens (ossification of vertebral end plates)
food producing animal cascade use requires maximum residue limits, special withdrawal periods, be on the table of allowed substances
addition of clavulanate to a penicillin makes them more beta-lactamase resistant
aminoglycosides have poor GI absorption, poor penetration, excreted in the kidney unchanged
fluoroquinolones are broad spectrum, high oral availability, good csf penetration, metabolised in the liver and excreted by the kidneys
penicillins target the cell wall - bactericidal
macrolides target 30s protein synthesis - bacteriostatic
PGF2a can be used in cattle to synchronise oestrus, induce myometrial contraction, and to abort preganancy
the main mechanism of veterinary antifungals are binding to ergosterol to prevent cell wall formation
establishment of steady state means drug concentration in the central compartment is constant and prevents fluctuation (consistent therapeutic effect)
atropine is a muscarinic antagonist used as a premed, some analgesia, and used to raise hr in a crashing patient who still has some rhythm
ester-linked LAs have shorter duration than amide-linked LAs. they are metabolised by tissue and plasma esterases and have poor tissue penetration
prolonged use of exogenous corticosteroids can cause iatrogenic cushing's disease, pituitary gland atrophy, PU/PD, increased liver enzymes, pot belly
the four full mu opioids are morphine, fentanyl, pethidine and methadone
anaesthetised animals need minimum 200ml per kg per minute
alfaxolone is a neuroactive steroid which is a GABA agonist