Department of Biochemistry and Nutrition, CSIR-Central Food Technological Research Institute (CFTRI) Mysore-570020, India.
Prog Neuropsychopharmacol Biol Psychiatry. 2013 Jan 10;40:83-92. doi: 10.1016/j.pnpbp.2012.08.018. Epub 2012 Aug 31.
While the beneficial effects of fish oil (FO) supplements on the central nervous system function are well established, few findings have led to the hypothesis that long term n-3 polyunsaturated fatty acid (n-3 PUFA) supplements at higher doses render the membranes more susceptible to lipid peroxidation. Hence recent studies suggest the use of dietary antioxidants as adjuncts with n-3 fatty acids to effectively improve the clinical outcome in neurological disorders. In the present investigation, we examined the hypothesis, if enrichment of FO with quercetin (a natural flavonoid) can provide a higher degree of neuroprotection and tested the same in a 3-nitropropionic acid (NPA) rat model. Growing male rats administered with NPA (25 mg/kg bw/d, i.p. 4 days) were provided either with FO (2 mL/kg bw), or Q (25mg/kg bw) or FO+Q for 14 days. NPA elicited marked oxidative stress in brain (striatum and cerebellum) as evidenced by significantly enhanced ROS, malondialdehyde, protein carbonyls and nitric oxide levels. Although varying degree of protection was evident among FO or Q groups, complete normalization of oxidative markers ensued only among FO+Q rats. Further, FO+Q combination completely normalized the elevated acetylcholinesterase activity and protected against NPA-induced mitochondrial dysfunctions. NPA induced depletion of dopamine levels was restored among all groups. Interestingly, NPA induced motor deficits were significantly improved among FO+Q rats. However, further studies are necessary to understand the mechanism/s by which FO enrichment with Q provides higher degree of protection. Nevertheless, our findings clearly suggest that the use of natural phytochemicals with moderate doses of FO may provide better neuroprotection and higher therapeutic advantage in the prevention or treatment of neurodegenerative diseases like Huntington's disease.
虽然鱼油(FO)补充剂对中枢神经系统功能的有益影响已得到充分证实,但很少有研究结果提出假设,即长期高剂量的 n-3 多不饱和脂肪酸(n-3 PUFA)补充剂会使膜更容易发生脂质过氧化。因此,最近的研究表明,使用膳食抗氧化剂作为 n-3 脂肪酸的辅助剂,可有效改善神经退行性疾病的临床预后。在本研究中,我们检验了这样一个假设,即如果 FO 中添加槲皮素(一种天然类黄酮)是否可以提供更高程度的神经保护,并在 3-硝基丙酸(NPA)大鼠模型中对此进行了测试。给予 NPA(25mg/kg bw/d,腹腔注射 4 天)的雄性大鼠提供 FO(2mL/kg bw)、Q(25mg/kg bw)或 FO+Q 14 天。NPA 在大脑(纹状体和小脑)中引起明显的氧化应激,表现为 ROS、丙二醛、蛋白质羰基和一氧化氮水平显著升高。虽然 FO 或 Q 组表现出不同程度的保护作用,但只有在 FO+Q 组中才完全使氧化标志物正常化。此外,FO+Q 联合用药完全使乙酰胆碱酯酶活性升高得到纠正,并保护免受 NPA 引起的线粒体功能障碍。所有组的多巴胺水平降低均得到恢复。有趣的是,NPA 诱导的运动缺陷在 FO+Q 大鼠中得到显著改善。然而,需要进一步研究来了解 FO 与 Q 结合提供更高程度保护的机制。尽管如此,我们的研究结果清楚地表明,使用适量 FO 与天然植物化学物质的联合用药可能提供更好的神经保护作用,并在预防或治疗亨廷顿病等神经退行性疾病方面具有更高的治疗优势。