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.

Creatine kinase isoenzymes in healthy newborn foals and preliminary evaluation in septic and in asphyctic animals / L. Giori; S. Panzani; E. Tagliabue; A. Giordano; C. Castagnetti; M.C. Veronesi; S. Paltrinieri. - In: VETERINARY CLINICAL PATHOLOGY. - ISSN 0275-6382. - STAMPA. - 40:4(2011), pp. 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
Creatine kinase isoenzymes in healthy newborn foals and preliminary evaluation in septic and in asphyctic animals / L. Giori; S. Panzani; E. Tagliabue; A. Giordano; C. Castagnetti; M.C. Veronesi; S. Paltrinieri. - In: VETERINARY CLINICAL PATHOLOGY. - ISSN 0275-6382. - STAMPA. - 40:4(2011), pp. 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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