Background: Information about the possible role of serum activity of creatine kinase (CK) isoenzymes as a biomarker for septicemia and asphyxia in newborn foals is not available. Objectives: To evaluate the activity of CK isoenzymes in healthy newborns and in septicemic or asphyctic foals. Methods: Electrophoretic separation of CK isoenzymes (CK-MM, CK-MB, CK-BB) and macroenzymes (Macro-CKI and Macro-CK2) was performed on sera from healthy foals sampled 30 minutes after birth, at 3, 12, 24 hours, and daily until day 7. Sera from 9 septicemic and 5 asphyctic foals were also examined at admission and during the follow up. The results were compared with those of age-matched controls. For both healthy and sick foals, differences among the sequential time samplings were also assessed. Results: In healthy foals, total CK activity significantly increased in the first day then decreased on day 2. CK-BB is the main isoenzyme at birth and up to day 7, except at 3 and 12 hours, when CK-MM is the prevalent isoenzyme. CK-MB and macroenzymes are negligible. Compared with age-matched controls, asphyctic foals have increased CK-MM activity, whereas electrophoretic changes in septicemic foals are variable and generally mild. During the follow up, isoenzyme activities normalized in both groups of sick foals. Conclusions: The proportions and activities of the different isoenzymes vary with age, with CK-BB being the main serum isoenzyme in most samplings. Thus it is important to compare the results of sick foals with those of age-matched controls. This comparison reveals severe CK-MM increases in asphyctic foals and variable changes in septicemic foals.

L. Giori, S. Panzani, E. Tagliabue, A. Giordano, C. Castagnetti, M.C. Veronesi, et al. (2011). Creatine kinase isoenzymes in healthy newborn foals and preliminary evaluation in septic and in asphyctic animals. VETERINARY CLINICAL PATHOLOGY, 40(4), 578-578 [10.1111/j.1939-165X.2011.00348.x].

Creatine kinase isoenzymes in healthy newborn foals and preliminary evaluation in septic and in asphyctic animals

CASTAGNETTI, CAROLINA;
2011

Abstract

Background: Information about the possible role of serum activity of creatine kinase (CK) isoenzymes as a biomarker for septicemia and asphyxia in newborn foals is not available. Objectives: To evaluate the activity of CK isoenzymes in healthy newborns and in septicemic or asphyctic foals. Methods: Electrophoretic separation of CK isoenzymes (CK-MM, CK-MB, CK-BB) and macroenzymes (Macro-CKI and Macro-CK2) was performed on sera from healthy foals sampled 30 minutes after birth, at 3, 12, 24 hours, and daily until day 7. Sera from 9 septicemic and 5 asphyctic foals were also examined at admission and during the follow up. The results were compared with those of age-matched controls. For both healthy and sick foals, differences among the sequential time samplings were also assessed. Results: In healthy foals, total CK activity significantly increased in the first day then decreased on day 2. CK-BB is the main isoenzyme at birth and up to day 7, except at 3 and 12 hours, when CK-MM is the prevalent isoenzyme. CK-MB and macroenzymes are negligible. Compared with age-matched controls, asphyctic foals have increased CK-MM activity, whereas electrophoretic changes in septicemic foals are variable and generally mild. During the follow up, isoenzyme activities normalized in both groups of sick foals. Conclusions: The proportions and activities of the different isoenzymes vary with age, with CK-BB being the main serum isoenzyme in most samplings. Thus it is important to compare the results of sick foals with those of age-matched controls. This comparison reveals severe CK-MM increases in asphyctic foals and variable changes in septicemic foals.
2011
L. Giori, S. Panzani, E. Tagliabue, A. Giordano, C. Castagnetti, M.C. Veronesi, et al. (2011). Creatine kinase isoenzymes in healthy newborn foals and preliminary evaluation in septic and in asphyctic animals. VETERINARY CLINICAL PATHOLOGY, 40(4), 578-578 [10.1111/j.1939-165X.2011.00348.x].
L. Giori; S. Panzani; E. Tagliabue; A. Giordano; C. Castagnetti; M.C. Veronesi; S. Paltrinieri
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/212436
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