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Safoof-e-Pathar Phori(一种用于治疗尿石症的多草药尤纳尼配方)的药理学评价

Pharmacological Evaluation of Safoof-e-Pathar Phori- A Polyherbal Unani Formulation for Urolithiasis.

作者信息

Ahmad Wasim, Khan Mohammad Ahmed, Ashraf Kamran, Ahmad Ayaz, Daud Ali Mohammad, Ansari Mohd Nazam, Kamal Y T, Wahab Shadma, Zaidi Sm Arif, Mujeeb Mohd, Ahmad Sayeed

机构信息

Department of Pharmacy, Mohammed Al-Mana College for Medical Sciences, Dammam-34222, Saudi Arabia.

Bioactive Natural Product Laboratory, Department of Pharmacognosy and Phytochemistry, School of Pharmaceutical Education and Research, Jamia Hamdard, India.

出版信息

Front Pharmacol. 2021 Apr 14;12:597990. doi: 10.3389/fphar.2021.597990. eCollection 2021.

Abstract

Safoof-e-Pathar phori (SPP) is an Unani poly-herbomineral formulation, which has for a long time been used as a medicine due to its antiurolithiatic activity, as per the Unani Pharmacopoeia. This powder formulation is prepared using six different plant/mineral constituents. In this study, we explored the antiurolithiatic and antioxidant potentials of SPP (at 700 and 1,000 mg/kg) in albino Wistar rats with urolithiasis induced by 0.75% ethylene glycol (EG) and 1% ammonium chloride (AC). Long-term oral toxicity studies were performed according to the Organization for Economic Co-operation and Development (OECD) guidelines for 90 days at an oral dose of 700 mg/kg of SPP. The EG urolithiatic toxicant group had significantly higher levels of urinary calcium, serum creatinine, blood urea, and tissue lipid peroxidation and significantly ( < 0.001 vs control) lower levels of urinary sodium and potassium than the normal control group. Histopathological examination revealed the presence of refractile crystals in the tubular epithelial cell and damage to proximal tubular epithelium in the toxicant group but not in the SPP treatment groups. Treatment of SPP at 700 and 1,000 mg/kg significantly ( < 0.001 vs toxicant) lowered urinary calcium, serum creatinine, blood urea, and lipid peroxidation in urolithiatic rats, 21 days after induction of urolithiasis compared to the toxicant group. A long-term oral toxicity study revealed the normal growth of animals without any significant change in hematological, hepatic, and renal parameters; there was no evidence of abnormal histology of the heart, kidney, liver, spleen, or stomach tissues. These results suggest the usefulness of SPP as an antiurolithiatic and an antioxidant agent, and long-term daily oral consumption of SPP was found to be safe in albino Wistar rats for up to 3 months. Thus, SPP may be safe for clinical use as an antiurolithiatic formulation.

摘要

Safoof-e-Pathar phori(SPP)是一种尤纳尼多草药矿物制剂,根据尤纳尼药典,由于其抗尿路结石活性,长期以来一直被用作药物。这种粉末制剂是用六种不同的植物/矿物成分制备的。在本研究中,我们探讨了SPP(700和1000毫克/千克)对由0.75%乙二醇(EG)和1%氯化铵(AC)诱导的尿路结石白化Wistar大鼠的抗尿路结石和抗氧化潜力。根据经济合作与发展组织(OECD)指南,以700毫克/千克的口服剂量对SPP进行了90天的长期口服毒性研究。与正常对照组相比,EG尿路结石毒物组的尿钙、血清肌酐、血尿素和组织脂质过氧化水平显著更高,尿钠和钾水平显著更低(与对照组相比<0.001)。组织病理学检查显示,毒物组肾小管上皮细胞中存在折光晶体,近端肾小管上皮受损,但SPP治疗组未出现这种情况。与毒物组相比,在尿路结石诱导21天后,700和1000毫克/千克的SPP治疗显著降低了尿路结石大鼠的尿钙、血清肌酐、血尿素和脂质过氧化水平(与毒物组相比<0.001)。长期口服毒性研究显示,动物生长正常,血液学、肝脏和肾脏参数无任何显著变化;没有证据表明心脏、肾脏、肝脏、脾脏或胃组织的组织学异常。这些结果表明SPP作为一种抗尿路结石和抗氧化剂是有用的,并且发现在白化Wistar大鼠中长达3个月每天口服SPP是安全的。因此,SPP作为一种抗尿路结石制剂临床使用可能是安全的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76f3/8081291/9245fd6e5ba1/fphar-12-597990-g001.jpg

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