Abstract
To clarify the mechanism of cytotoxicity induced by captopril (Cp), interactions between tissue protein and Cp were studied by the enzyme-linked immunosorbent assay (ELISA) method. The amide-linked adducts [hemocyanin from keyhole limpet-Cp adduct (KLH-Cp) and poly-l-Lys-Cp adduct (pLys-Cp)] using carbodiimide, and a disulfide-linked adduct [ovalbumin-Cp adduct (OVA-Cp)] were prepared. To determine the formation of the protein-Cp adduct, rabbit antisera against KLH-Cp was employed. The immunoreactivities with pLys-Cp and OVA-Cp against anti KLH-Cp sera were elevated when compared with the unmodified protein. With the inhibition ELISA, this antisera was useful for detecting the Cp disulfide-linked conjugate. In kidney cytosol, a high level of immunoreactivity was observed. Plasma and liver cytosol reactivities were similar, and ∼40% against kidney cytosol. Thus, a method for the detection of the Cp-protein adduct using ELISA has been established. Formation of the Cp-protein adduct was observed in rat plasma and in liver and kidney cytosol. These findings suggest the possibility that the formation of Cp-protein adduct is partially related to cytotoxicity in liver.
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Received: 7 May 1997 / Accepted: 2 October 1997
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Narazaki, R., Watanabe, H., Maruyama, T. et al. An immunological method for the detection of captopril-protein conjugate. Arch Toxicol 72, 203–206 (1998). https://doi.org/10.1007/s002040050489
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DOI: https://doi.org/10.1007/s002040050489