Pharmacology Flashcards
Why is the Oral dose sometimes higher than the IV dose?
Oral dose = first pass metabolism, less reaches circulation . IV = No first pass metabolism. NEVER ASSUME DOSE SAME FOR DIFFERENT ROUTES.
Why do we need to be careful in animals with hepatic dysfunction?
Hepatic dysfunction = less first pass metabolism when given orally therefore more absorbed into systemic circulation. IF DRUG HAS NARROW THERAPEUTIC INDEX = more significant. Drug may also PERSIST longer therefore decreased dosing interval.
Which routes avoid the first pass metabolism
ALL ROUTES APART FROM ORAL BY PASS FIRST PASS METABOLISM.
Does Rectal administration avoid first pass metabolism
Yes. e.g. diazepam.
Bladder infection why is first antibiotic given SC in consult room?
NO PHARMACOLOGIAL REASON. GIVE TABS
How is Volume of distribution calculated?
Total amount of drug given/ plasma concentration of drug
Larger volume of distribution =
The more it has gone in body compartments i.e. if LOW volume of distribution = restricted to plasma.
Which antibiotics are good at crossing the BBB
Fluoriquinalone, Metronidazole, Lincosamides, Clindamycin, Sulphonamides
Which antibiotics are bad at crossing the BBB
Penicillin (way too water based) Tetracyclines are theoretically good but actually bad as pumped straight back out again. Aminoglycosine (gentamycin) I.E. POOR FOR PROSTATE/BRAIN/EYE
Phase 1 metabolism occurs where?
Endoplasmic reticulum e.g. hydrolysis, reduction. Makes water soluble to be excreted. If still not water soluble enough goes into phase 2
Phase 2 metabolism occurs where?
Occurs if phase 1 doesn’t make water soluble enough. Occurs in microsomes or in the cytosol. Involves specific transfer enzymes e.g. glucaroninc acid. MARKED SPECIES DIFFERENCES
Phase 3 metabolism occurs where?
Across membranes. Active drug transport. e.g. P-glycoproetin
How does phase 2 differ in cats
Dogs metabolise like people. Cats very different. Cats have Limited acetylation. Glucaronidation relatively unaffected by hepatic disease
Pigs have no ___ conjugation
Pigs have no sulphate conjugation.
Which species drug pharmokinetics is relatively unaffected by hepatic disease
Cats, glucaronidation relatively unaffected by hepatic disease
Difference in drugs metabolism between sheep and goats
Goats have MUCH faster metabolism therefore increase dosing frequency.
Dogs/Cats. Which species has higher half life for Asprin
Cats on asprin have very prolonged half life c.f. dogs. Carprofen half life longer in cats than dogs. Metacam relatively similar
Which type of metabolism of paracetamol gives a toxic product in cats
Glucaronidation/ Sulphonation = NOT TOXIC METABOLITES BUT IN CATS, OXIDATATION = TOXIC METABOLITES (NAPQI binds to essential amino acids and results in cellular death)
Why is paracetamol toxic in cats
Glucaronidation major metabolic pathway in most species, cats have lower glucaronyl transferase level. Sulphation is major pathay in cat but limited capacity therefore drug oxidised leading to toxicity. NAPQI