用Alamo和Jekomo治疗Wistar大鼠的肝肾功能,Jekomo是尼日利亚的一种酒精草药苦味剂

M. Adeyemi, Olayinka M. Afolabi, Nifemi Balogun
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摘要

对草药的需求增加,对酒精消费的自然追求,使含酒精的草药苦味物成为一种受欢迎的血液解毒和肝脏清洁潜力的理想饮料,但没有经过科学验证。本研究评估了Alomo和Jekomo对雄性Wistar大鼠肝肾的影响。将体重110 ~ 130 g的雄性Wistar大鼠30只分为6组,每组5只,分别用2.68 mL/kg体重的蒸馏水、乙醇、Alomo和Jekomo酒精苦味酒治疗28 d。用血清和肾脏匀浆按标准方法测定总蛋白、白蛋白、肌酐、尿素、胆红素等生化指标。酒精处理组血清和肾脏总蛋白、白蛋白水平显著升高(p < 0.05)。与对照组相比,治疗组乙醇和肾匀浆血清肌酐水平显著升高(p < 0.05)。与对照组相比,各酒精处理组血清和肾脏尿素、胆红素浓度均显著升高(p < 0.05)。尿素、肌酐和胆红素的联合升高提示由含酒精的草药苦味剂引起的中度至重度肾和肝损害。作为肾功能的基本指标,尿素和肌酐的升高记录表明可能存在肾功能障碍。为了防止肝细胞损伤或损害,不鼓励长期和增加饮用这些含酒精的草药苦味酒。
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Hepatorenal function of Wistar rats treated with Alamo and Jekomo, an alcoholic herbal bitters in Nigeria
Increased demand for herbal remedies and natural quest for alcohol consumption has positioned alcoholic herbal bitters an acclaimed blood detoxifying and liver cleansing potential as an ideal drink without scientific validation. This study assessed the hepatorenal effect of Alomo and Jekomo, commonly consumed alcoholic bitters in male Wistar rat. Thirty male Wistar rats weighing 110 to 130 g were divided into six groups of five animals each and treated with distilled water, ethanol, Alomo and Jekomo Alcoholic Bitters at 2.68 mL/kg body weight respectively for 28 days. The serum and kidney homogenate were used to determine biochemical parameters such as total protein, albumin, creatinine, urea and bilirubin following standard methods. There was a significant increase (p < 0.05) in serum and kidney levels of total protein and albumin in alcohol treated groups. A significant increase (p < 0.05) in serum creatinine levels of ethanol and kidney homogenate of Jekomo bitters treated group when compared with control. A significant increase (p < 0.05) in serum and kidney urea and bilirubin concentration was also observed in all alcohol treated groups when compared with control. A combined elevation in urea and creatinine and bilirubin suggest a moderate to severe form of kidney and liver damage induced by the alcoholic herbal bitters. As essential markers of kidney function, the recorded elevation of urea and creatinine shows a potential exposure to renal dysfunction. Prolonged and increased consumption of these alcoholic herbal bitters should be discouraged to prevent hepatocellular injury or damage.
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