首页> 外文期刊>Environmental toxicology and pharmacology >Effects of the food additives sodium acid pyrophosphate, sodium acetate, and citric acid on hemato-immunological pathological biomarkers in rats: Relation to PPAR-α, PPAR-γ and tnfα signaling pathway
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Effects of the food additives sodium acid pyrophosphate, sodium acetate, and citric acid on hemato-immunological pathological biomarkers in rats: Relation to PPAR-α, PPAR-γ and tnfα signaling pathway

机译:食品添加剂焦磷酸钠,乙酸钠和柠檬酸对大鼠血液免疫病理生物标志物的影响:与PPAR-α,PPAR-γ和tnfα信号通路的关系

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The food additives sodium acid pyrophosphate (SAPP), sodium acetate (SA), and citric acid (CA) were evaluated for their hemato-immunotoxic effects. Forty adult Sprague-Dawley rats were distributed into four groups and were orally administered water, SAPP (12.6 mg/kg), CA (180 mg/kg), or SA (13.5 mg /kg) daily for 90 days. Erythrogram and leukogram profiles were evaluated. The levels of lysozyme, nitric oxide, immunoglobulin, and phagocytic activity were measured. Histologic and immunohistochemical evaluations of splenic tissues were performed. Changes in the mRNA expression levels of peroxisome proliferator-activated receptor alpha and gamma (PPAR alpha and PPAR-gamma), and tumor necrosis factor alpha (TNF-alpha) genes were assessed. A significant leukopenic condition was observed with SAPP, while CA induced marked leukocytosis, and SA showed a lymphocytosis condition. Both the innate and humoral parameters were significantly depressed. Various pathological lesions were observed, including diffuse hyperplasia of the red pulp, depletion of the white pulp, and capsular and parenchymal fibrosis. A marked decrease in CD3 T-lymphocyte and CD20 B-lymphocyte immunolabeling in rats treated with SAPP and SA was evident. Marked downregulation of PPAR-alpha and PPAR-gamma together with upregulation of TNF-a was recorded. These results indicate that high doses of SAPP, SA and CA exert hematotoxic and immunotoxic effects with long-term exposure.
机译:评价了食品添加剂焦磷酸钠(SAPP),乙酸钠(SA)和柠檬酸(CA)的血液免疫毒性作用。将40只成年Sprague-Dawley大鼠分为四组,每天口服水,SAPP(12.6 mg / kg),CA(180 mg / kg)或SA(13.5 mg / kg),持续90天。评估了红描图和白细胞图谱。测量了溶菌酶,一氧化氮,免疫球蛋白和吞噬活性的水平。进行脾组织的组织学和免疫组织化学评估。评估了过氧化物酶体增殖物激活受体α和γ(PPARα和PPAR-γ)和肿瘤坏死因子α(TNF-α)基因的mRNA表达水平的变化。 SAPP观察到明显的白细胞减少症,而CA引起明显的白细胞增多,SA则显示淋巴细胞增多。先天和体液参数均显着降低。观察到各种病理性病变,包括红色牙髓的弥漫性增生,白色牙髓的耗竭以及荚膜和实质纤维化。在用SAPP和SA处理的大鼠中,CD3 T淋巴细胞和CD20 B淋巴细胞免疫标记明显降低。记录到PPAR-α和PPAR-γ明显下调以及TNF-α上调。这些结果表明,高剂量的SAPP,SA和CA具有长期暴露的血液毒性和免疫毒性作用。

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