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首页> 外文期刊>Experimental Eye Research >Protective effects and mechanism of tetramethylpyrazine against lens opacification induced by sodium selenite in rats.
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Protective effects and mechanism of tetramethylpyrazine against lens opacification induced by sodium selenite in rats.

机译:川methyl嗪对亚硒酸钠致大鼠晶状体混浊的保护作用及其机制。

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摘要

Tetramethylpyrazine (TMP), extracted from the Chinese herbal medicine Ligusticum wallichii franchat (chuan xiong in Chinese), is a potent anti-free radical and calcium antagonist. Correspondingly, two important hypotheses in the causation of cataracts are free radical toxicity and calcium ion overload. In this study we investigated the effect of TMP on lens opacification induced by sodium selenite in rats, addressing the potential of TMP eye drops to prevent and treat cataracts. Results showed that the extent of lens opacification in the untreated Normal Control group (NC group) was significantly less than that of selenite-injected untreated rats (MC group) on days 3, 5, 7 and 10 (p < 0.001), while TMP treated selenite-injected rats (TMP group) had less lens opacification than the MC group on days 3, 5, 7 and 10 (p < 0.05). Compared with the NC group, the MC group had significantly decreased activity of super-oxide dismutase (SOD), glutathione peroxidase (GSH-PX) and catalase (CAT) and significantly elevated malondialdehyde (MDA) and calcium ion content (p < 0.001). Compared with the MC group, the activity of (SOD), (GSH-PX) and (CAT) were significantly higher while (MDA) and calcium ion levels were significantly lower in the TMP group at all time points (p < 0.01). The findings demonstrate that the selenite-induced cataract rat models were successfully built and the TMP eye drops can delay lens opacification induced by sodium selenite in rats. The mechanism by which TMP preserves lens transparency from selenite treated animals is associated with the lenses' ability to maintain normal levels of activity of SOD, GSH-PX and CAT and normal concentrations of MDA and calcium ion.
机译:川methyl嗪(TMP)是一种有效的抗自由基和钙离子拮抗剂,它是从中草药川gust(Ligusticum wallichii franchat)中提取的。相应地,白内障病因的两个重要假设是自由基毒性和钙离子超负荷。在这项研究中,我们研究了TMP对亚硒酸钠诱导的大鼠晶状体混浊的影响,探讨了TMP滴眼液预防和治疗白内障的潜力。结果显示,未治疗的正常对照组(NC组)在第3、5、7和10天时晶状体混浊的程度明显小于注射亚硒酸盐的未治疗大鼠(MC组)(p <0.001),而TMP在第3、5、7和10天,治疗的亚硒酸盐注射大鼠(TMP组)的晶状体混浊比MC组少(p <0.05)。与NC组相比,MC组的超氧化物歧化酶(SOD),谷胱甘肽过氧化物酶(GSH-PX)和过氧化氢酶(CAT)的活性显着降低,丙二醛(MDA)和钙离子含量显着升高(p <0.001) 。与MC组相比,TMP组在所有时间点的(SOD),(GSH-PX)和(CAT)活性均显着升高,而(MDA)和钙离子水平则显着降低(p <0.01)。这些发现表明,成功建立了亚硒酸钠诱发的白内障大鼠模型,TMP滴眼液可以延缓亚硒酸钠诱发的大鼠晶状体混浊。 TMP保持亚硒酸盐处理过的动物的晶状体透明性的机制与晶状体保持SOD,GSH-PX和CAT正常活性水平以及MDA和钙离子正常浓度的能力有关。

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