Page 1352 - Problem-Based Feline Medicine
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1344  PART 16  DRUGS


          continued

            Metronidazole       Disorientation.
                                Ataxia.
                                Seizures.
                                Blindness.
            Opioids: morphine   Inconsistent sedation.
            derivatives (excluding  Increased risk of excitation.
            meperidine [pethidine],
            butorphanol and
            buprenorphine)
            Organophosphates    Acute toxicity – hypersalivation, vomiting, diarrhea, muscle tremors.
                                Chronic or delayed toxicity – paresis or paralysis which may or may not be
                                reversible.
            Potassium bromide   Depression.
                                Severe coughing.
            Tetracyclines       Hepatic lipidosis.
                                Increased ALT activity.
                                Ptyalism.
                                Anorexia.
            Thiacetarsamide     Drug fever.
                                Respiratory distress.
                                Fulminant pulmonary edema.



                                                        Most differences between dogs and cats in drug dispo-
           INTRODUCTION
                                                        sition relate to  differences in Phase II metabolism,
                                                        although deficiencies in Phase I metabolism may be
          SPECIAL CONSIDERATIONS RELATED                involved in some drug toxicities in cats including chlo-
          TO DRUG USE IN CATS                           ramphenicol toxicity.
                                                        During Phase II metabolism, parent drugs or Phase
          Why are cats different?
                                                        I metabolites are bound (conjugated) to large molecules
          There are some important differences in drug disposi-  such as glucuronide, glutathione, sulfate and acetyl
          tion between dogs and cats that can have a profound  groups, and amino acids (e.g. glycine and taurine)
          influence on dosing recommendations for cats.  resulting in a water-soluble, inactive compound.
          The majority of the difference in drug disposition
          between cats and dogs  relates to differences in drug  FELINE DRUG METABOLISM
          metabolism.
                                                        Cats are deficient in some glucuronyl transferases
                                                        which are important for glucuronidation.
          DRUG METABOLISM – GENERAL                      ● Drugs that are excreted as glucuronide conjugates
                                                           in other species such as aspirin, benzoic acid, acet-
          Water-soluble drugs can be excreted in urine without
                                                           aminophen (paracetamol) and hexachlorophene
          being metabolized.
                                                           may have a prolonged half-life in cats.
          Drugs that are  lipid soluble must be  converted to  ● Increased half-life  increases the risk of toxicity
          water-soluble metabolites that can be excreted, usu-  due to drug accumulation.
          ally by the kidney.
                                                        Not all drugs that are glucuronidated are a problem in
          Drug metabolism occurs in the liver in two phases (I  cats.  Cats are only deficient in certain families of
          and II).                                      glucuronyl transferases.
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