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替非罗和蜂胶对减轻铍诱导的肝肾毒性的药理干预。

Pharmacological intervention of tiferron and propolis to alleviate beryllium-induced hepatorenal toxicity.

作者信息

Nirala Satendra Kumar, Bhadauria Monika, Shukla Sangeeta, Agrawal Om Prakash, Mathur Asha, Li Pei Qiang, Mathur Ramesh

机构信息

School of Studies in Zoology, Jiwaji University, Gwalior 474011, India.

出版信息

Fundam Clin Pharmacol. 2008 Aug;22(4):403-15. doi: 10.1111/j.1472-8206.2008.00603.x.

Abstract

Intervention of chelating agent tiferron (sodium-4,5-dihydroxy-1,3-benzene disulfonate; 300 mg/kg, intraperitoneal) with propolis (honey beehive product; 200 mg/kg, p.o.) was evaluated to encounter the characteristic biochemical and ultra-morphological alterations following subchronic exposure to beryllium. Female albino rats were challenged with beryllium nitrate (1 mg/kg, i.p.) daily for 28 days followed by treatment of the above-mentioned therapeutic agents either individually or in combination for five consecutive days. Exposure to beryllium increased its concentration in the serum, liver and kidney, and caused significant alterations in cytochrome P450 activity, microsomal lipid peroxidation and proteins. Activities of alkaline phosphatase, lactate dehydrogenase, gamma-glutamyl transpeptidase, bilirubin, creatinine and urea in the serum and activity of acid phosphatase, alkaline phosphatase, adenosine triphosphatase, glucose-6-phophatase and succinic dehydrogenase in the liver and kidney were significantly altered after beryllium administration. Beryllium exposure also induced severe hepatorenal alterations at histopathological and ultra-morphological level. Tiferron along with propolis dramatically reversed the alterations in all the variables more towards control rather than their individual treatment. The study concludes that pharmacological intervention of tiferron and propolis is beneficial in attenuating beryllium-induced systemic toxicity.

摘要

评估了螯合剂替弗隆(4,5-二羟基-1,3-苯二磺酸钠;300毫克/千克,腹腔注射)与蜂胶(蜂巢产品;200毫克/千克,口服)的干预措施,以应对亚慢性接触铍后出现的特征性生化和超微形态学改变。雌性白化大鼠每天腹腔注射硝酸铍(1毫克/千克),持续28天,随后连续5天单独或联合使用上述治疗剂进行治疗。接触铍会增加其在血清、肝脏和肾脏中的浓度,并导致细胞色素P450活性、微粒体脂质过氧化和蛋白质发生显著改变。铍给药后,血清中的碱性磷酸酶、乳酸脱氢酶、γ-谷氨酰转肽酶、胆红素、肌酐和尿素的活性以及肝脏和肾脏中的酸性磷酸酶、碱性磷酸酶、三磷酸腺苷酶、葡萄糖-6-磷酸酶和琥珀酸脱氢酶的活性均发生了显著改变。铍暴露还在组织病理学和超微形态学水平上诱发了严重的肝肾改变。替弗隆与蜂胶一起显著地使所有变量的改变更多地向对照方向逆转,而不是它们各自治疗时的情况。该研究得出结论,替弗隆和蜂胶的药物干预有助于减轻铍诱导的全身毒性。

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