首页   按字顺浏览 期刊浏览 卷期浏览 Alteration of humoral and cellular immunity in manganese chloride‐treated mice
Alteration of humoral and cellular immunity in manganese chloride‐treated mice

 

作者: B. Srisuchart,   M. J. Taylor,   R. P. Sharma,  

 

期刊: Journal of Toxicology and Environmental Health  (Taylor Available online 1987)
卷期: Volume 22, issue 1  

页码: 91-99

 

ISSN:0098-4108

 

年代: 1987

 

DOI:10.1080/15287398709531053

 

出版商: Taylor & Francis Group

 

数据来源: Taylor

 

摘要:

Immunological effects of manganese chloride (MnCl2) were determined in male CD‐1 mice injected (ip) daily with MnCl2(0, 1, 3, or 10 mg/kg) for 4 wk. Liver and spleen weights increased in the 10‐mg/kg MnCl2treatment group. The weights of thymus, kidney, and adrenal glands were not affected by MnCl2treatment. No significant differences in peripheral erythrocyte or leukocyte counts were observed; however, packed cell volumes decreased in the medium‐ and high‐dose groups. Manganese treatment significantly increased the uptake of [3H]thymidine (3H‐TdR) by cultured splenic cells. The lymphoproliferative responses to phytohemagglutinin (PHA) and concanavalin A (Con A) increased at all levels of MnCl2exposure. No differences in the responses to lipopolysaccharide (LPS) were observed. Mixed lymphocyte responses increased significantly with exposure to 10 mg MnCl2/kg. Another immunological alteration induced by MnCl2was a dose‐dependent immunosuppressive effect on the development of antibody‐forming cells. The production of anti‐sheep red blood cell antibody (α‐SRBC) nearly ceased following exposure to 10 mg MnCl2/kg. This effect was apparently reversible, as the number of plaque‐forming cells in the 10‐mg/kg treatment group increased after MnCl2treatment had been halted for 2 wk. The a‐SRBC titer also decreased significantly in the 10‐mg/kg treatment group, corresponding to the reduction of antibody‐producing cells. MnCl2treatment was immunomodulatory in male CD‐1 mice,asindicated by the increase in mitogen and mixed lymphocyte responses and decrease in antibody production.

 

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