Zhou Zhao Sheng, Huang Si Qi, Guo Kai, Mehta Surya Kant, Zhang Peng Chao, Yang Zhi Min
Department of Biochemistry and Molecular Biology, College of Life Science, No. 1 Weigang, Outside the Zhoungshan Men, Building of Life Science, Nanjing Agricultural University, Nanjing 210095, China.
J Inorg Biochem. 2007 Jan;101(1):1-9. doi: 10.1016/j.jinorgbio.2006.05.011. Epub 2006 Jun 7.
Alfalfa (Medicago sativa) roots were treated with mercuric ions in a concentration- and time-dependent manner, and lipid peroxidation was studied biochemically as well as histochemically along with other physiological responses. Histochemical staining with Schiff's reagent and Evans blue revealed that the peroxidation of membrane lipids and loss of plasma membrane integrity in Hg-treated roots occurred in the meristem and the elongation zone. The histochemical observations were supported by the quantitative determinations of thiobarbituric acid reactive substances (TBARS). However, under the mercuric ions stress, the alfalfa plants showed no significant alteration of hydrogen peroxide in roots. Analysis of lipoxygenase activity by non-denaturing polyacrylamide gel electrophoresis (PAGE) showed that there were two isoforms in the root of alfalfa plants, but they showed quite different patterns under the Hg exposure. Also, using non-denaturing PAGE, activities of superoxide dismutase (SOD) and peroxidase (POD) were determined in roots after treatment with Hg ions. The total activities of SOD and POD increased in roots after Hg treatment of roots. Activity of ascorbate peroxides (APX) was stimulated at relatively high concentration of Hg (40microM), and after prolonged Hg exposure (20microM, 24h). In contrast, glutathione reductase activity was depressed at higher concentrations of Hg (10-20microM). Treatments of seedlings with 10-40microM Hg decreased the ascorbate and glutathione amounts but increased total non-protein thiols. The above results indicated that Hg exerted its toxic effect on the root growth of alfalfa by induction of oxidative stress.
用汞离子以浓度和时间依赖的方式处理紫花苜蓿(Medicago sativa)根系,并从生化和组织化学方面研究脂质过氧化以及其他生理反应。用席夫试剂和伊文思蓝进行组织化学染色显示,汞处理根系中膜脂过氧化和质膜完整性丧失发生在分生组织和伸长区。硫代巴比妥酸反应性物质(TBARS)的定量测定支持了组织化学观察结果。然而,在汞离子胁迫下,紫花苜蓿植株根系中的过氧化氢没有明显变化。通过非变性聚丙烯酰胺凝胶电泳(PAGE)分析脂氧合酶活性表明,紫花苜蓿植株根系中有两种同工型,但在汞暴露下它们表现出相当不同的模式。此外,使用非变性PAGE测定了汞离子处理后根系中超氧化物歧化酶(SOD)和过氧化物酶(POD)的活性。汞处理根系后,根系中SOD和POD的总活性增加。在相对较高浓度的汞(40μM)下以及长时间汞暴露(20μM,24小时)后,抗坏血酸过氧化物酶(APX)的活性受到刺激。相反,在较高浓度的汞(10 - 20μM)下,谷胱甘肽还原酶活性受到抑制。用10 - 40μM汞处理幼苗会降低抗坏血酸和谷胱甘肽的含量,但会增加总非蛋白硫醇的含量。上述结果表明,汞通过诱导氧化应激对紫花苜蓿根系生长产生毒性作用。