Laboratory of Toxicology (LATOX), Department of Analysis, Pharmacy Faculty, Federal University of Rio Grande do Sul, Porto Alegre, RS, Brazil.
Specialized Faculty in the Health Area of Rio Grande do Sul (FASURGS), Passo Fundo, RS, Brazil.
BMC Pharmacol Toxicol. 2019 Dec 19;20(Suppl 1):75. doi: 10.1186/s40360-019-0355-1.
Gasoline is a complex mixture of saturated and unsaturated hydrocarbons, in which aromatic compounds, such as BTX (benzene, toluene, and xylene) feature as the main constituents. Simultaneous exposure to these aromatic hydrocarbons causes a significant impact on benzene toxicity. In order to detect early alterations caused in gasoline station attendants exposed to BTX compounds, immunological, inflammatory, and oxidative stress biomarkers were evaluated.
A total of 66 male subjects participated in this study. The gasoline station attendants (GSA) group consisted of 38 gasoline station attendants from Rio Grande do Sul, Brazil. The non-exposed group consisted of 28 subjects who were non-smokers and who had no history of occupational exposure. Environmental and biological monitoring of BTX exposure was performed using blood and urine.
The GSA group showed increased BTX concentrations in relation to the non-exposed group (p < 0.001). The GSA group showed elevated protein carbonyl (PCO) levels and pro-inflammatory cytokines, decreased expression of CD80 and CD86 in monocytes, and reduced glutathione S-transferase (GST) activity compared to the non-exposed group (p < 0.05). BTX levels and trans,trans-muconic acid levels were positively correlated with pro-inflammatory cytokines and negatively correlated with interleukin-10 contents (p < 0.001). Increased levels of pro-inflammatory cytokines were accompanied by increased PCO contents and decreased GST activity (p < 0.001). Furthermore, according to the multiple linear regression analysis, benzene exposure was the only factor that significantly contributed to the increased pro-inflammatory cytokines (p < 0.05).
Taken together, these findings show the influence of exposure to BTX compounds, especially benzene, on the immunological, inflammatory, and oxidative stress biomarkers evaluated. Furthermore, the data suggest the relationship among the evaluated biomarkers of effect, which could contribute to providing early signs of damage to biomolecules in subjects occupationally exposed to BTX compounds.
汽油是一种由饱和和不饱和烃组成的复杂混合物,其中芳香族化合物,如 BTX(苯、甲苯和二甲苯)是主要成分。同时接触这些芳香族碳氢化合物会对苯毒性产生重大影响。为了检测接触 BTX 化合物的加油站工作人员早期出现的变化,评估了免疫、炎症和氧化应激生物标志物。
共有 66 名男性参与了这项研究。加油站工作人员(GSA)组由来自巴西南里奥格兰德州的 38 名加油站工作人员组成。非暴露组由 28 名非吸烟者和无职业暴露史的受试者组成。使用血液和尿液对 BTX 暴露进行环境和生物监测。
与非暴露组相比,GSA 组的 BTX 浓度升高(p<0.001)。GSA 组的蛋白羰基(PCO)水平升高,促炎细胞因子升高,单核细胞中 CD80 和 CD86 的表达降低,谷胱甘肽 S-转移酶(GST)活性降低(p<0.05)。BTX 水平和反式,反式-粘康酸水平与促炎细胞因子呈正相关,与白细胞介素-10 含量呈负相关(p<0.001)。促炎细胞因子水平升高伴随着 PCO 含量升高和 GST 活性降低(p<0.001)。此外,根据多元线性回归分析,苯暴露是唯一显著导致促炎细胞因子增加的因素(p<0.05)。
综上所述,这些发现表明接触 BTX 化合物(特别是苯)对所评估的免疫、炎症和氧化应激生物标志物的影响。此外,数据表明了所评估的效应生物标志物之间的关系,这可能有助于为接触 BTX 化合物的职业暴露者的生物分子早期损伤提供迹象。