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Atypical Microglial Response to Biodiesel Exhaust in Healthy and Hypertensive Rats

机译:健康和高血压大鼠对生物柴油消耗的非典型小胶质细胞反应。

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摘要

Accumulating evidence suggests a deleterious role for urban air pollution in central nervous system (CNS) diseases and neurodevelopmental disorders. Microglia, the resident innate immune cells and sentinels in the brain, are a common source of neuroinflammation and are implicated in how air pollution may exert CNS effects. While renewable energy, such as soy-based biofuel, is of increasing public interest, there is little information on how soy biofuel may affect the brain. To address this, male spontaneously hypertensive rats (SHR) and normotensive Wistar Kyoto (WKY) rats were exposed to 100% Soy Biodiesel Exhaust (100SBDE; 0, 50, 150 and 500 μg/m3) by inhalation for 4 h/day for 4 weeks (5 days/week). IBA-1 staining of microglia in the substantia nigra revealed significant changes in morphology with 100SBDE exposure in rats from both genotypes, where the SHR were less sensitive. Further analysis failed to show consistent changes in pro-inflammatory cytokine expression, nitrated protein, and arginase1 expression in brain tissue from either rat strain exposed to 100SBDE. CX3CR1 and fractalkine mRNA expression were lower in the striatum of all 100SBDE exposed rats, but greater SBDE exposure was required for loss of fractalkine expression in the SHR. Together, these data support that month-long 100SBDE exposure impacts the basal ganglia with changes in microglia morphology, an impaired fractalkine axis, and an atypical activation response without traditional markers of M1 or M2 activation, where the SHR may be less sensitive to these effects.
机译:越来越多的证据表明,城市空气污染对中枢神经系统(CNS)疾病和神经发育障碍具有有害作用。小胶质细胞是大脑中固有的先天免疫细胞和前哨,是神经发炎的常见来源,与空气污染如何发挥中枢神经系统作用有关。尽管可再生能源(如大豆基生物燃料)日益受到公众关注,但有关大豆生物燃料如何影响大脑的信息很少。为了解决这个问题,雄性自发性高血压大鼠(SHR)和血压正常的Wistar Kyoto(WKY)大鼠暴露于100%大豆生物柴油排气(100SBDE; 0、50、150和500μg/ m 3 ),每天4小时吸气,持续4周(5天/周)。在两种基因型的大鼠中,黑质黑质的小胶质细胞的IBA-1染色显示在100SBDE暴露下,形态学上的显着变化,其中SHR敏感性较低。进一步的分析未能显示出暴露于100SBDE的任一大鼠品系的脑组织中促炎性细胞因子表达,硝化蛋白和精氨酸酶1表达的一致变化。在所有暴露于100SBDE的大鼠的纹状体中CX3CR1和fractalkine mRNA的表达均较低,但SHR中fractalkine表达的丧失需要更大的SBDE暴露。这些数据共同证明,长达一个月的100SBDE暴露会影响小神经胶质细胞形态,受损的碎裂碱轴和不典型的活化反应(无传统的M1或M2活化标志物),从而影响基底神经节,而SHR对这些作用的敏感性较低。

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