Inactivation of creatine kinase by Adriamycin during interaction with horseradish peroxidase.

Abstract:

:Oxidative damage of creatine kinase (CK) induced by Adriamycin((R)) (ADM) with peroxidase was investigated using horseradish peroxidase (HRP). ADM oxidatively inactivated CK during its interaction with HRP in the presence of H(2)O(2) (HRP-H(2)O(2)). The red color of ADM was lost during oxidation by HRP-H(2)O(2). Adding catalase stopped the color change of ADM induced by HRP-H(2)O(2), indicating that ADM was oxidized by HRP complex I or II. CK was inactivated readily, even when it was added to the reaction mixture containing colorless ADM. Some sulfhydryl groups of CK, which have an important role in its enzyme activity, were very sensitive to ADM activated by HRP-H(2)O(2), suggesting that inactivation of CK is due to oxidation of SH groups at the active center. Presumably, oxidative ADM quinone is involved dominantly in the inactivation of CK. Among the anthracycline drugs tested in this study, only ADM and epirubicin caused inactivation of CK and alcohol dehydrogenase and loss of the red color during oxidation by HRP-H(2)O(2).

journal_name

Biochem Pharmacol

journal_title

Biochemical pharmacology

authors

Miura T,Muraoka S,Fujimoto Y

doi

10.1016/s0006-2952(00)00303-8

subject

Has Abstract

pub_date

2000-07-01 00:00:00

pages

95-9

issue

1

eissn

0006-2952

issn

1873-2968

pii

S0006295200003038

journal_volume

60

pub_type

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