Evaluation of Protective Effect of Tageteserecta Against Mercuric Chloride Induced Nephrotoxicity

P. N. Saxena, B. Bhushan
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引用次数: 3

Abstract

The toxicity of various forms of mercury to the living organisms is well documented. Mammalian kidney is the main site of decomposition of inorganic mercury as well as the target organ for its toxicity in majority of the animals including human beings. Present study has been aimed to investigate the role of Tageteserecta(family-Astereacea) as a possible modifier of mercury induced renal damages. Experimentation was conducted on one hundred female albino rats, divided into five equal groups, each group again sub-divided into four sub-groups having five rats each: Control group- Orally administrated distilled water only. T. erecta flower extract treated group-10mg/kg b. wt./day for 1, 7, 14, 21 days was administrated orally. Mercuric chloride treatment groups-A dose of 0.926 mg/kg b.wt. for 01 day, 0.132 mg/kg b.wt. for 7 days, 0.066 mg/kg b.wt. for 14 days and 0.044 for 21 days was administrated through oral route. Oral administration of T. erecta flower extract followed by mercuric chloride treatment for 1, 7, 14 and 21 days. Oral administration of Mercuric chloride followed by T. erectaflower extractadministration for 1, 7, 14 and 21 days. These animals were then sacrificed after 1, 7, 14 and 21 days treatment respectively. Controls were also run respectively. Mercuric chloride intoxication resulted in pathological alterations in the kidney of albino rats, such as degradation of glomerulus, proximal and distal tubules. Combined pre and post treatment of T. erectawith mercuric chloride has been found to reduce the pathological alterations in the kidney. Thus, the results from the present study suggest that T. erectacan modify the renal damages against mercuric chloride induced toxicity.
泰吉替利对氯化汞所致肾毒性的保护作用评价
各种形式的汞对生物体的毒性是有据可查的。哺乳动物肾脏是无机汞分解的主要部位,也是包括人类在内的大多数动物体内无机汞中毒的靶器官。本研究的目的是探讨石斛属植物作为汞致肾损害的可能调节剂的作用。实验选用雌性白化大鼠100只,随机分为5组,每组再分为4个亚组,每组5只:对照组:只口服蒸馏水。直立花提取物处理组(10mg/kg b. wt./d),连续1、7、14、21 d口服。氯化汞处理组-剂量为0.926 mg/kg b.wt。第01天,0.132 mg/kg b.wt。连续7天,0.066 mg/kg b.wt。口服给药14 d, 0.044给药21 d。口服直立木花提取物后加氯化汞处理1、7、14和21天。口服氯化汞,然后分别给药1、7、14和21天。分别于1、7、14、21 d后处死。对照组也分别运行。氯化汞中毒导致白化大鼠肾脏病理改变,如肾小球、近端小管和远端小管退化。研究发现,用氯化汞治疗前后联合治疗可减少肾的病理改变。因此,本研究结果表明,直立木可改善氯化汞引起的肾脏损伤。
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