2010
DOI: 10.1016/j.fct.2010.03.036
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Immunotoxicity of paraquat after subacute exposure to mice

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Cited by 46 publications
(51 citation statements)
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“…The results of this study also suggested that PRQ at higher concentrations can deplete immune functions, but it can alter immune responses towards the proinflammatory profiles at lower concentrations. However, another study held in BALB/C mice revealed suppression of cellular as well as humoral immunity at dose 1 mg/kg given intraperitoneally for 21 days but no change at dose 0,01 mg/kg (Riahi et al, 2010). Thus, the outcomes of the effects of PRQ on immunity are route of exposure-and timingdependent since slight discrepancies are evident between these two studies.…”
Section: Discussionmentioning
confidence: 89%
“…The results of this study also suggested that PRQ at higher concentrations can deplete immune functions, but it can alter immune responses towards the proinflammatory profiles at lower concentrations. However, another study held in BALB/C mice revealed suppression of cellular as well as humoral immunity at dose 1 mg/kg given intraperitoneally for 21 days but no change at dose 0,01 mg/kg (Riahi et al, 2010). Thus, the outcomes of the effects of PRQ on immunity are route of exposure-and timingdependent since slight discrepancies are evident between these two studies.…”
Section: Discussionmentioning
confidence: 89%
“…Interestingly, carnosol, at doses of 2.4 and 4 mg/kg/day, was able to inhibit acquired immunity higher than cyclophosphamide, which is a known potent immunosuppressant. A significant decrease in DTH and HA may suggest a direct effect on the activation and differentiation of the T and B lymphocytes, respectively (14). Acquired immunity includes two arms: the effector B-cell arm and effector Tcell arm, which act together to destroy non-self.…”
Section: Discussionmentioning
confidence: 99%
“…on Day 15), mice (n ¼ 6/group) were euthanized by cervical dislocation and the spleen of each was aseptically removed and weighed. Thereafter, single cell suspensions were prepared in RPMI 1640 medium using standard protocols (Riahi et al, 2010). Specifically, each spleen was placed into a small petri dish including 10 ml RPMI 1640 media supplemented with 10% fetal bovine serum (FBS), 100 U penicillin/ml, 100 mg streptomycin/ml and 2 mM L-glutamine (all Gibco, Paisley, UK).…”
Section: Measurement Of Spleen Weight and Cellularitymentioning
confidence: 99%
“…A minimum of 10 000 events/sample was acquired for each sample. The absolute number of each cell type in each spleen was determined by multiplying the differential ratio of the subtypes by the total spleen cell contents (Riahi et al, 2010). Levels of T-lymphocyte subsets and CD19 cells in the splenocyte suspensions were separately determined.…”
Section: Spleen Cell Subtypingmentioning
confidence: 99%