Maria Francis Yuvaraj, Karunakaran Balaji, Ashfaq Fauzia, Yahia Qattan Malak, Ahmad Irfan, Alkhathami Ali G, Idreesh Khan Mohammad, Varadhan Mohan, Govindan Lakshmanan, Ponnusamy Kasirajan Sankaran
Department of Anatomy, Saveetha Medical College and Hospital, Saveetha Institute of Medical and Technical Sciences, Chennai 602105, Tamil Nadu, India.
Department of Clinical Nutrition, College of Applied Medical Sciences, Jazan University, Jazan 45142, Saudi Arabia.
ACS Omega. 2023 Jun 5;8(24):21696-21708. doi: 10.1021/acsomega.3c01045. eCollection 2023 Jun 20.
The present study analyzes the efficacy of the ethanolic extract of leaves (ECP) against HgCl-induced nephrotoxicity. The effects on the biochemical and percentage of body and organ weight against HgCl-induced nephrotoxicity in female Wistar rats were studied. Wistar rats were divided into five groups with six animals in each group: control, HgCl (2.5 mg/kg b.w.), -acetylcysteine (NAC 180 mg/kg) + HgCl, ECP (300 mg/kg b.w.) + HgCl, and ECP (600 mg/kg) + HgCl groups. After 28 days of study, animals were sacrificed on the 29th day to harvest the blood and kidneys for further analysis. The effect ECP was analyzed by immunohistochemistry (NGAL) and real-time PCR (KIM-1 and NGAL mRNA) in HgCl-induced nephrotoxicity. The results revealed that the HgCl group showed prominent damage in the proximal tubules and glomerulus of nephrons and enormous expression of NGAL in immunohistochemistry and KIM-1 and NGAL in real-time PCR compared to the control group. The simultaneous pretreatment with NAC (180 mg/kg) and ECP (600 and 300 mg/kg) reduced renal damage and expression of NGAL in immunohistochemistry and KIM-1 and NGAL gene in real-time PCR. This study attests to the nephroprotective effect of ECP against HgCl-induced toxicity.
本研究分析了叶乙醇提取物(ECP)对氯化汞诱导的肾毒性的疗效。研究了其对雌性Wistar大鼠氯化汞诱导的肾毒性的生化指标以及体重和器官重量百分比的影响。Wistar大鼠分为五组,每组六只动物:对照组、氯化汞(2.5毫克/千克体重)组、N-乙酰半胱氨酸(NAC 180毫克/千克)+氯化汞组、ECP(300毫克/千克体重)+氯化汞组和ECP(600毫克/千克)+氯化汞组。经过28天的研究,在第29天处死动物以采集血液和肾脏进行进一步分析。通过免疫组织化学(NGAL)和实时PCR(KIM-1和NGAL mRNA)分析ECP在氯化汞诱导的肾毒性中的作用。结果显示,与对照组相比,氯化汞组在肾单位的近端小管和肾小球中表现出明显损伤,免疫组织化学中NGAL以及实时PCR中KIM-1和NGAL表达大量增加。NAC(180毫克/千克)与ECP(600和300毫克/千克)同时预处理可减轻肾脏损伤,降低免疫组织化学中NGAL以及实时PCR中KIM-1和NGAL基因的表达。本研究证明了ECP对氯化汞诱导的毒性具有肾保护作用。