Department of Biotechnology, Bharathidasan University, Trichy, 620024, India.
Neurochem Res. 2011 Aug;36(8):1344-52. doi: 10.1007/s11064-011-0449-7. Epub 2011 Apr 7.
The present study is aimed to evaluate the putative neuroprotective effect of quercetin on PCB induced impairment of dopaminergic receptor mRNA expression in cerebral cortex of adult male Wistar rats. Group I (control) received only vehicle (corn oil; 0.1 ml/kg bwt) intraperitoneally (i.p); Group II Aroclor 1254 at a dose of 2 mg/kg bwt/day (i.p); Group III (Aroclor 1254-exposed (i.p), quercetin treated gavage (50 mg/kg bwt/day); Group IV received quercetin alone (gavage). 24 h after the 30th day treatment rats were euthanized. From each rat cerebral cortex tissues was collected and analyzed for mean activities of creatine kinase, acetylcholine esterase, Na(+)/K(+), Ca(2+) and Mg(2+)ATPases, Hydrogen peroxide generation, protein carbonyl content and lipid peroxidation levels. The fates of the mRNA expression of dopaminergic receptors, Cacna1d on all the groups were studied by RT-PCR. Results evidenced that significant reduction of neurodegeneration in PCBs exposed rats treated with quercetin was ascertained suggesting, quercetin treatment precludes against PCB induced oxidative stress and protects dopaminergic receptor dysfunction in rat cerebral cortex.
本研究旨在评估槲皮素对多氯联苯(PCBs)诱导的成年雄性 Wistar 大鼠大脑皮质多巴胺受体 mRNA 表达损伤的潜在神经保护作用。第 I 组(对照组)仅接受腹腔内注射玉米油(0.1ml/kg 体重);第 II 组接受 Aroclor 1254 (2mg/kg 体重/天,腹腔内注射);第 III 组(Aroclor 1254 暴露组,腹腔内注射槲皮素 50mg/kg 体重/天);第 IV 组单独接受槲皮素(灌胃)。第 30 天治疗后 24 小时处死大鼠。从每只大鼠的大脑皮质组织中收集并分析肌酸激酶、乙酰胆碱酯酶、Na(+)/K(+)、Ca(2+)和 Mg(2+)ATP 酶的平均活性、过氧化氢生成、蛋白羰基含量和脂质过氧化水平。通过 RT-PCR 研究了所有组多巴胺能受体、Cacna1d 的 mRNA 表达的命运。结果表明,用槲皮素治疗暴露于多氯联苯的大鼠的神经退行性变显著减少,表明槲皮素治疗可以防止多氯联苯引起的氧化应激,并保护大鼠大脑皮质中的多巴胺能受体功能障碍。