Siddiqi Afsheen, Nazneen Zainab, Alam Saadia Shahzad, Tariq Sumbal
Department of Pharmacology, Ayub Medical College, Abbottabad, Pakistan.
Department of Community Medicine, Ayub Medical College, Abbottabad, Pakistan.
J Ayub Med Coll Abbottabad. 2018 Apr-Jun;30(2):184-186.
Humans are exposed either deliberately or unintentionally to a variety of diverse chemicals that harm the kidney. To reduce the alarming high incidence of nephrotoxicity, some chemical as well as herbal alternatives are needed. Nimesulide belongs to a group of antiinflammatory drugs that are in common use in our society. Like all non-steroidal antiinflammatory drugs, it carries a potential threat of nephrotoxicity especially when other risk factors are present in user. The objective of this study was to find herbal alternative with antiinflammatory and nephroprotective qualities and to bring into light its mechanism of nephroprotection.
This experimental study was conducted on mice at National Institute of Health, Islamabad from Feb 2013 to March 2014. Nimesulide was given in a dosage of 750 mg/kg body weight for 3 days to induce nephrotoxicity and protective effect of Picrorhiza kurroa was noted in two doses of 250 mg/kg and 500 mg/kg for 14 days. Renal function tests were done and urinary PGE2 was measured to assess the effect of nimesulide and Pk on kidneys.
In our study, significant improvement was seen in serum urea and creatinine levels in mice receiving low and high dose Picrorhiza kurroa. However, no significant improvement was noted in urinary PGE2 showing that the mechanism of nephroprotection is not by vasodilatory effect of Pk.
This study showed nimesulide nephrotoxic potential and Pk is a good herbal antiinflammatory and nephroprotective alternative for nimesulide but its mechanism of nephroprotection is not by PGE2.
人类有意或无意地接触到各种损害肾脏的不同化学物质。为降低令人担忧的高肾毒性发病率,需要一些化学及草药替代品。尼美舒利属于我们社会中常用的一类抗炎药物。与所有非甾体抗炎药一样,它存在肾毒性的潜在威胁,尤其是当使用者存在其他风险因素时。本研究的目的是寻找具有抗炎和肾保护特性的草药替代品,并揭示其肾保护机制。
本实验研究于2013年2月至2014年3月在伊斯兰堡国立卫生研究所的小鼠身上进行。给予尼美舒利750毫克/千克体重的剂量,持续3天以诱导肾毒性,并观察了胡黄连在250毫克/千克和500毫克/千克两种剂量下,持续14天的保护作用。进行了肾功能测试并测量了尿PGE2,以评估尼美舒利和胡黄连对肾脏的影响。
在我们的研究中,接受低剂量和高剂量胡黄连的小鼠血清尿素和肌酐水平有显著改善。然而,尿PGE2没有显著改善,表明肾保护机制不是通过胡黄连的血管舒张作用。
本研究显示了尼美舒利的肾毒性潜力,胡黄连是一种很好的替代尼美舒利的具有抗炎和肾保护作用的草药,但其肾保护机制不是通过PGE2。