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Pre-natal/juvenile chlorpyrifos exposure associated with immunotoxicity in adulthood in Swiss albino mice

机译:瑞士白化病小鼠的成年前/幼年毒死rif暴露与免疫毒性相关

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摘要

Chlorpyrifos (CPF) is a widely used agricultural organophosphorus insecticide (OP). Epidemiological studies have reported that children living in an OP contaminated environment, showed altered immune function. However, there is a paucity of experimental evidence for CPF-induced toxicity in the developmental phases of immune system. The current studies sought to ascertain the effect of CPF on the developing immune system of mice. Swiss albino dams were exposed orally with 0, 0.3, and 3.0 mg CPF/kg/day from GD12 to PND7, and then pups were directly dosed with CPF (by gavage) through PND42. One week after the final dose of CPF (i.e. on PND49), immunotoxicities in these offspring were assessed. These analyses revealed that there were increases in Foxp3 +CD25+CD4+ T-regulatory (Treg) cell frequency in the spleens of 3.0 mg CPF/kg/day-exposed female mice, but not in males. In contrast, the anti-sheep red blood cells IgM response was reduced in both genders. Moreover, splenic lymphoproliferative response to phytohemagglutinin (PHA), concanavalin A (ConA), and lipopolysaccharide (LPS), as well as interferon (IFN)-γ, tumor necrosis factor (TNF)-α, and interleukin (IL)-6 production following LPS stimulation decreased in mice of both sexes at higher CPF doses. Together, these findings suggest that developmental CPF exposure might cause immunosuppression in mice. Some of these outcomes might arise, in part, through a suppression of pro-inflammatory cytokine production and/or changes in the responsivity (specifically to mitogens) of lymphocytes in these hosts.
机译:毒死rif(CPF)是一种广泛使用的农业有机磷杀虫剂(OP)。流行病学研究报告说,生活在OP污染环境中的儿童表现出免疫功能改变。然而,在免疫系统的发育阶段,缺乏CPF诱导的毒性的实验证据。当前的研究试图确定CPF对小鼠免疫系统发育的影响。从GD12到PND7,瑞士白化病大坝每天口服0、0.3和3.0 mg CPF / kg / kg暴露,然后通过PND42向幼犬直接施用CPF(通过管饲法)。在最终剂量的CPF后一周(即在PND49上),评估了这些后代的免疫毒性。这些分析表明,在暴露于3.0 mg CPF / kg / day /日的雌性小鼠脾脏中,Foxp3 + CD25 + CD4 + T调节(Treg)细胞频率增加,而雄性小鼠则没有。相反,两种性别的抗绵羊红细胞IgM反应均降低。此外,对植物血凝素(PHA),伴刀豆球蛋白A(ConA)和脂多糖(LPS)以及脾脏(IFN)-γ,肿瘤坏死因子(TNF)-α和白介素(IL)-6产生的脾淋巴细胞增殖反应LPS刺激后,高CPF剂量的雌雄同体小鼠均降低。在一起,这些发现表明发育性CPF暴露可能会导致小鼠免疫抑制。这些结果中的某些可能部分是由于抑制这些宿主中促炎性细胞因子的产生和/或淋巴细胞的反应性(特别是对有丝分裂原的反应性)的改变而引起的。

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