Author: Paltrinieri, Saverio; Cazzaniga, Stefania; Da Cunha, Nazarè Pinto; Giordano, Alessia
Title: Electrophoretic fractionation of creatine kinase isoenzymes and macroenzymes in clinically healthy dogs and cats and preliminary evaluation in central neurologic disease Cord-id: w6qfzpi4 Document date: 2010_8_2
ID: w6qfzpi4
Snippet: Background: Information about the electrophoretic distribution of CKâ€MM, CKâ€MB, and CKâ€BB, serum creatine kinase (CK) isoenzymes that are indicators of skeletal muscle, cardiac muscle, and brain lesions, respectively, and CK macroenzymes (macroâ€CK1 and macroâ€CK2) in dogs and cats with and without central neurologic disease is scant and equivocal. Objectives: The objectives of this study were to describe the electrophoretic distribution of CK isoenzymes and macroenzymes in healthy dogs
Document: Background: Information about the electrophoretic distribution of CKâ€MM, CKâ€MB, and CKâ€BB, serum creatine kinase (CK) isoenzymes that are indicators of skeletal muscle, cardiac muscle, and brain lesions, respectively, and CK macroenzymes (macroâ€CK1 and macroâ€CK2) in dogs and cats with and without central neurologic disease is scant and equivocal. Objectives: The objectives of this study were to describe the electrophoretic distribution of CK isoenzymes and macroenzymes in healthy dogs and cats and to provide a preliminary assessment of the utility of CK enzymatic electrophoresis in dogs and cats with central neurologic disease. Methods: Electrophoretic separation of serum CK isoenzymes and macroenzymes was performed on freezeâ€thawed serum samples from 20 healthy dogs and 3 dogs with central neurologic disease and from 14 healthy cats and 6 cats with neurologic feline infectious peritonitis (FIP). Electrophoretic separation was also performed on supernatants of homogenized brain, skeletal muscle, and cardiac muscle from both species, to assess the tissue distribution of isoenyzmes in dogs and cats. Results: CKâ€MM was the predominant isoenzyme in the serum of healthy dogs and cats, followed by macroâ€CK2 and CKâ€BB in dogs and by both macroenzymes in cats. In dogs, CKâ€MB was essentially absent from both serum and homogenized hearts. CKâ€BB increased in dogs with neurologic disease. In cats, CKâ€BB was essentially absent from serum, but was present in brain homogenates. Two of 6 cats with FIP had increased macroâ€CK1 and increased CKâ€BB activity. Conclusions: This study identified the electophoretic distribution of CK isoenzymes and macroenzymes of dogs and cats and provided encouraging data about the possible use of CKâ€BB as a biomarker for canine neurologic disorders, but not for FIP.
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