Abstract |
The present study was designed to investigate the immunotoxicity of atrazine (ATZ) in male Balb/c mice. ATZ (175, 87.5, and 43.75 mg/kg bw/day) was administered by gavage method for 28 days. The following indexes were determined in various groups of mice: body and organ weight; antibody aggregation of serum hemolysin; proliferative response of splenocytes to ConA; delayed-type hypersensitivity (DTH); natural killer cell activity; clearance of neutral red and nitric oxide (NO) release from peritoneal macrophages; apostosis and necrosis of splenocytes and thymocytes; cytokine production; and serum lysozyme. Results showed that cell-mediated, humoral immunity, and non-specific immune function in the high-dose ATZ group were suppressed; NO release and interferon-γ(IFN-γ)/ interleukin-4 (IL-4) were also significantly decreased in the high-dose group. In the medium-dose group, the proliferation response and IFN-γ production was significantly decreased. In the low-dose group, the proliferation response was significantly decreased. Serum lysozyme was decreased in the ATZ-treated groups. The percentage of early apoptosis in thymocytes was increased significantly in high- and medium-dose ATZ groups. In conclusion, ATZ elicited an inhibitory effect on cell-mediated immunity, humoral immunity, and non-specific immune function of mice.
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Authors | Jin Y Chen, Yang Song, Li S Zhang |
Journal | Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes
(J Environ Sci Health B)
Vol. 48
Issue 8
Pg. 637-45
( 2013)
ISSN: 1532-4109 [Electronic] England |
PMID | 23638890
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Herbicides
- Interleukin-4
- Interferon-gamma
- Muramidase
- Atrazine
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Topics |
- Animals
- Apoptosis
(drug effects)
- Atrazine
(immunology, toxicity)
- Body Weight
(drug effects)
- Dose-Response Relationship, Drug
- Dose-Response Relationship, Immunologic
- Herbicides
(immunology, toxicity)
- Immunity, Humoral
(drug effects)
- Interferon-gamma
(metabolism)
- Interleukin-4
(metabolism)
- Macrophages, Peritoneal
(drug effects, immunology)
- Male
- Mice
- Mice, Inbred BALB C
- Muramidase
(blood)
- Necrosis
- Organ Size
(drug effects)
- Spleen
(drug effects, immunology, pathology)
- Thymocytes
(drug effects, pathology)
- Toxicity Tests, Acute
(methods)
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