Therapeutic efficacy of Glycyrrhiza glabra and Curcuma longa on adenine induced chronic kidney disease in rats

Vicky M Patel, K. Sadariya, Darshan R Patel, Ravi D Patel, V. Sarvaiya, S. Bhavsar
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Abstract

The current investigation was designed to assess the therapeutic efficacy of aqueous and alcoholic bi-herbal extracts of Glycyrrhiza glabra (GG) and Curcuma longa (CL) on adenine-induced chronic kidney disease (CKD) using 36 male Sprague-Dawley rats. The rats were randomly allocated into six different groups, each group comprising six rats. CKD was induced in groups II to VI by administering adenine at a dose of 200 mg/kg orally once daily for 28 days. Group I served as the control. Group II was adenine control, received adenine (200 mg/kg orally) for 28 days. Groups III, IV, V and VI were therapeutic groups, received adenine @ 200 mg/kg orally once daily for 28 days to induce CKD, after that rats were given bi-herbal aqueous and alcoholic extracts of GG and CL (1.5:1) orally for another 42 days. Groups III and IV, received bi-herbal aqueous extract of GG and CL @ 250 and 500 mg/kg, respectively. Groups V and VI, received bi-herbal alcoholic extracts of GG and CL @ 250 and 500 mg/kg, respectively. Blood samples were collected twice during the experiment, on day 28 and day 70. Various assessments including haematology, serum biochemistry, urine analysis, renal ultrasonography and histopathology were conducted. Adenine administration for 28 days resulted in significant decrease in haemoglobin, total erythrocyte count and lymphocyte, while significant increase in TLC and granulocyte, however treatment with bi-herbal aqueous and alcoholic extracts significantly ameliorated haematological alterations. Adenine induced CKD resulted in elevated serum creatinine, uric acid, BUN, ALT and Phosphorus while significantly reduced levels of serum uromodulin, albumin, total protein, and calcium. Conversely, treatment with aqueous and alcoholic bi-herbal extract significantly improved biochemical changes as compared to adenine control rats. Notably, the therapeutic efficacy was most pronounced in rats treated with bi-herbal alcoholic extracts at the dose rate of 500 mg/kg. In addition, significant increased levels of urine calcium and total protein, with decreased levels of urine creatinine, phosphorus and urine pH were observed in adenine control group as compared to normal control group. These changes were significantly reverted with treatment of aqueous and alcoholic bi-herbal extracts for 42 days. Following CKD induction, treatment with aqueous and alcoholic extracts of GG and CL attenuated ultrasonographic changes and improved histopathological damage in the kidney. Results of the present study showed that the bi-herbal alcoholic extracts of Glycyrrhiza glabra and Curcuma longa in the ratio of 1.5:1 given at the dose rate of 500 mg/kg once orally daily for 42 days after induction of CKD is more efficacious in the treatment of CKD in rats.
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甘草和莪术对腺嘌呤诱导的大鼠慢性肾病的疗效
本研究旨在使用 36 只雄性 Sprague-Dawley 大鼠,评估甘草(GG)和莪术(CL)双草本水提取物和酒精提取物对腺嘌呤诱导的慢性肾病(CKD)的疗效。大鼠被随机分为六个不同的组,每组六只。第 II 组至第 VI 组大鼠每天口服一次腺嘌呤,剂量为 200 毫克/千克,连续 28 天,诱发慢性肾脏病。第一组为对照组。第二组为腺嘌呤对照组,连续 28 天口服腺嘌呤(200 毫克/千克)。第三组、第四组、第五组和第六组为治疗组,每天一次口服腺嘌呤 200 毫克/千克,连续 28 天,以诱导慢性肾功能衰竭,之后再口服 GG 和 CL(1.5:1)的双草本水提取物和酒精提取物,连续 42 天。第三组和第四组分别接受 250 毫克/千克和 500 毫克/千克的 GG 和 CL 双草本水提取物。第五组和第六组分别服用 250 毫克/千克和 500 毫克/千克的 GG 和 CL 双草本酒精提取物。实验期间,分别在第 28 天和第 70 天采集两次血样。进行了各种评估,包括血液学、血清生化学、尿液分析、肾脏超声波检查和组织病理学。连续 28 天服用腺嘌呤会导致血红蛋白、红细胞总数和淋巴细胞显著下降,而 TLC 和粒细胞则显著增加,但使用双草本水提取物和酒精提取物治疗会显著改善血液学变化。腺嘌呤诱导的慢性肾功能衰竭导致血清肌酐、尿酸、尿素氮、谷丙转氨酶和磷升高,而血清尿蛋白、白蛋白、总蛋白和钙的水平则明显降低。相反,与腺嘌呤对照组大鼠相比,水性和酒精性双草本提取物能明显改善生化变化。值得注意的是,使用双草本酒精提取物(剂量为 500 毫克/千克)治疗大鼠的疗效最为明显。此外,与正常对照组相比,腺嘌呤对照组的尿钙和总蛋白水平明显升高,尿肌酐、磷和尿 pH 值下降。使用双草本植物水提取物和酒精提取物治疗 42 天后,这些变化得到明显恢复。在诱发慢性肾功能衰竭后,使用 GG 和 CL 的水提取物和酒精提取物治疗可减轻超声波变化并改善肾脏的组织病理学损伤。本研究结果表明,甘草和莪术以 1.5:1 的比例制成双草本酒精提取物,在诱导 CKD 后以 500 毫克/千克的剂量每日口服一次,持续 42 天,对治疗大鼠的 CKD 更为有效。
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