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The effect of chlorhexidine on blood cells
Author(s) -
Gabler Walter L.,
Roberts Daniel,
Harold William
Publication year - 1987
Publication title -
journal of periodontal research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.31
H-Index - 83
eISSN - 1600-0765
pISSN - 0022-3484
DOI - 10.1111/j.1600-0765.1987.tb01555.x
Subject(s) - degranulation , chlorhexidine , chemistry , antimicrobial , activator (genetics) , chemotaxis , pharmacology , cytotoxic t cell , microbiology and biotechnology , biochemistry , in vitro , medicine , biology , receptor , dentistry , organic chemistry
Chlorhexidine was cytotoxic to both neutrophils and red blood cells over a narrow concentration range of 0.01 to 0.02% drug. Serum provided significant protection against the cytotoxic effects of the antimicrobial agent. At a concentration of 0.01%, chlorhexidine acted as a potent activator of the neutrophil's oxidative burst, stimulating the cells to produce oxygen radicals such as super‐oxide (O −2 ). Chlorhexidine ranging from 10 −4 to 10 −2 caused spontaneous degranulation of neutrophils. If neutrophils were pretreated with chlorhexidine and then activated by the chemoattractant tripeptide FMLP, chlorhexidine inhibited the induced Of generation and degranulation. If, on the other hand, neutrophils were activated with phorbol myristate acetate (PMA) following chlorhexidine treatment, the antimicrobial agent enhanced both O −2 synthesis and degranulation. It appears that the responsiveness of chlorhexidinetreated neutrophils to subsequent activators is dependent upon the nature of the activator.