铅诱导的Cepa根尖细胞有丝分裂抑制作用的逆转研究

H. Rathore, Ranjana Punyasi, P. Joshi, Deepika Rathore, D. Bhatnagar
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引用次数: 3

摘要

本研究探讨了myrobalan对铅诱导的洋葱根尖细胞有丝分裂的保护作用。洋葱首先在去离子水中培养3天,然后在100、1000、3000和10,000 ppm的硝酸铅溶液中暴露1小时。暴露于铅后,洋葱被允许自然恢复或在myrobalan悬浮液(0.01 mg/ml)中恢复72小时。记录根颜色、平均根长(MRL)和线粒体分裂指数(MI),并对中期和后期染色体畸变进行评分。在自然恢复(NR)过程中,1000ppm、3000ppm和10000ppm Pb处理下的根不生长,而myrobalan处理的药物恢复(DR)在1000ppm和3000ppm Pb处理下的根生长。在100ppm Pb处理下,NR和DR均能观察到根的生长,DR的根生长更明显。在对照组中,这些时期的根系生长和MI在整个试验过程中没有变化。在所有浓度的铅暴露下,降低了MI。NR对铅处理的根尖细胞无效,因为这些细胞在核仁肥大的间期表现出有丝分裂作用。DR不能恢复暴露于10,000 ppm Pb的根尖细胞的有丝分裂抑制作用,而药物可以恢复暴露于100、1000和3000 ppm Pb的根尖细胞的有丝分裂抑制作用。NR和DR均能恢复100ppm Pb后的有丝分裂抑制作用,且作用在DR中较早观察到,1小时未见染色体畸变,细胞未表现出典型的中期排列。效果表现为剂量依赖性。在1000ppm和3000ppm的铅暴露中,DR从1小时起恢复核分裂抑制作用,并在72小时时完成。在100ppm Pb暴露下,NR组的核分裂抑制作用在48小时后消失,DR组的核分裂抑制作用在24小时后恢复。对照根尖细胞无丝分裂抑制作用。
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Studies on the reversal of lead induced mitostatic effect in Allium Cepa root tip cells with myrobalan (fruit of Terminalia Chebula, Retz, Combretaceae)
The present study was undertaken to find the protective role of myrobalan against lead (Pb) induced cytogenetic effects on mitosis in Allium-cepa root tip cells. Onions were initially cultivated in deionized water for 3 days and were then exposed at 100, 1000, 3000 and 10,000 ppm of lead nitrate solution for 1 hr. After exposure to lead, the onions were allowed to recover naturally or in myrobalan suspension (0.01 mg/ml) for 72 hrs. The root color, mean root length (MRL) and mitolic index (MI) were recorded and the metaphases and anaphases were scored for chromosomal aberrations. During the natural recovery (NR), roots did not grow following 1000, 3000 and 10,000 ppm Pb exposure but myrobalan treated drug recovery (DR) showed root growth following 1000 and 3000 ppm Pb exposure. The root growth was observed in both NR and DR, more in DR in 100 ppm Pb exposure. Among the control, root growth during these periods and MI did not change throughout the experimentation. Pb exposure at all concentrations, lowered MI. NR was ineffective in Pb treated root tip cells as these were seen in interphase with hypertrophied nucleoli showing mitostatic effect. DR could not revert the mitostatic effect in root tip cells exposed at 10,000 ppm Pb, however, drug could do so in 100, 1000 ppm and 3000 ppm Pb exposure. Both, NR and DR reverted mitostatic effect after 100 ppm Pb exposure and the effect was observed earlier in DR. No chromosomal aberrations could be seen at 1 hr, the cells failed to show typical metaphase arrangement. The effect appeared dose dependent. DR reverted mitostatic effect from 1 hr onwards and completed at 72 hrs in 1000 and 3000 ppm Pb exposure. At 100 ppm Pb exposure, mitostatic effect disappeared at 48 hr in NR while in DR, it reverted after 24 hr. Control root tip cells showed no mitostatic effect.
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