Nephroprotective Effect of Methanol Extract of Crassocephalum Crepidioides (Benth.) S. Moore (Ebolo) during Paracetamol- Induced toxicity in Wistar Rats

Fausat Kikelomo Ola- Mudathir, Ighorhiowhoaro M. Ajekevwoda, S. Jeje, Ogheneoruese F. Onoharigho, Kelechi Adikaesieme
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Abstract

The effect of Crassocephalum crepidioides (Benth.) S. Moore against Paracetamol (PCM)-induced oxidative stress was investigated. Wistar rats were divided into five groups of six rats. The control was group 1, Groups 2 and 3 were administered 250 mg/kg/bwt PCM and 300 mg/kg/bwt methanol extract of C. crepidioides leaves (MECL) respectively, group 4 and 5 were co-administered with 250 mg/kg/bwt PCM + 300 mg/kg/bwt MECL and 250 mg/kg/bwt PCM + 50 mg acetylcysteine (NAC) respectively for 2 weeks, following 1week pre-administration with 300 mg/kg/bwt MECL and 50mg NAC respectively. Kidney damage was measured by evaluating serum urea and creatinine, while antioxidant status was assessed by evaluating glutathione (GSH) level, glutathione-S-transferase (GST), superoxide dismutase (SOD) and catalase activities. Lipid peroxidation (LPO) was determined from malondialdehyde (MDA) levels. PCM had no significant effect on serum urea and creatinine levels, but significantly decreased glutathione levels, SOD and catalase activities, while the activity of glutathione-S-transferase and level of malondialdehyde (MDA) was increased significantly. Co-administration with MECL or NAC reversed these effects. In conclusion, C. crepidioides. protects against PCM-induced oxidative stress in the Kidneys of Wistar rats.
粗头草甲醇提取物的肾保护作用S. Moore (Ebolo)对Wistar大鼠扑热息痛毒性的影响
粗头草(Crassocephalum crepidioides)的作用研究了S. Moore抗扑热息痛(Paracetamol, PCM)诱导的氧化应激。Wistar大鼠分为5组,每组6只。对照组为1组,2组和3组分别给药250 mg/kg/bwt PCM和300 mg/kg/bwt crepidiides叶片甲醇提取物(MECL), 4组和5组分别给药250 mg/kg/bwt PCM + 300 mg/kg/bwt MECL和250 mg/kg/bwt PCM + 50mg乙酰半胱氨酸(NAC),连续2周,1周前分别给药300 mg/kg/bwt MECL和50mg NAC。通过测定血清尿素和肌酐来评估肾脏损害,通过测定谷胱甘肽(GSH)水平、谷胱甘肽s转移酶(GST)、超氧化物歧化酶(SOD)和过氧化氢酶活性来评估抗氧化状态。脂质过氧化(LPO)测定丙二醛(MDA)水平。PCM对血清尿素和肌酐水平无显著影响,但显著降低谷胱甘肽水平、SOD和过氧化氢酶活性,显著升高谷胱甘肽- s转移酶活性和丙二醛(MDA)水平。与MECL或NAC合用可逆转这些效应。综上所述。对pcm诱导的Wistar大鼠肾脏氧化应激有保护作用。
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