Evaluation of the potential immunotoxicity of chlorinated drinking water in mice

Recent epidemiological studies have reported associations between the consumption of chlorinated drinking water and various types of human cancer; in addition, exposure to chlorine (Cl −) in drinking water has been reported to suppress certain immune functions in laboratory animals. The current stud...

Full description

Saved in:
Bibliographic Details
Published inToxicology (Amsterdam) Vol. 125; no. 1; pp. 53 - 58
Main Authors French, Alexandra S, Copeland, Carey B, Andrews, Debbie L, Wiliams, Wanda C, Riddle, Marie M, W. Luebke, Robert
Format Journal Article
LanguageEnglish
Published Shannon Elsevier Ireland Ltd 16.01.1998
Amsterdam Elsevier Science
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Recent epidemiological studies have reported associations between the consumption of chlorinated drinking water and various types of human cancer; in addition, exposure to chlorine (Cl −) in drinking water has been reported to suppress certain immune functions in laboratory animals. The current studies were conducted to extend our knowledge of the effects of drinking water exposure to Cl −. Female C57BL/6 mice were administered hyperchlorinated drinking water (7.5, 15, or 30 ppm Cl −) for 2 weeks prior to sacrifice for evaluation of spleen and thymus weights, the plaque-forming cell (PFC) response, hemagglutination (HA) titer, and lymphocyte proliferation (LP). Significant reductions in organ weights and immune response were observed in the positive control groups (i.e. dexamethasone- or cyclophosphamide-exposed mice). No consistent differences were observed between the Cl −-exposed animals and vehicle control mice for the evaluated parameters. Thus, under the conditions of these experiments, 2 weeks of exposure to hyperchlorinated drinking water had no apparent adverse effects on immune function.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ObjectType-Article-1
ObjectType-Feature-2
ISSN:0300-483X
1879-3185
DOI:10.1016/S0300-483X(97)00163-7