乳香油对小剂量扑热息痛大鼠的改善作用

Aml Talaat, Yomna A. Elgendy, Heba F. Mohamed, Nouran M Saed, Noran A. Abd Elrouf, Hend A. Elgendy, Hagar H. Elbalakousy, Nourhan N. El hantoshy, Mohammed S. Elmezaien, Youssef M. Sayed, Yosry El. Hekal, M. Gabr, Nada S. Badr
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引用次数: 0

摘要

扑热息痛是一种广泛使用的镇痛解热药物,但长期使用具有潜在的毒性。本研究的目的是研究乳香油如何预防扑热息痛的毒性。选取雄性白化大鼠20只,分为4组:(G1)对照组,(G2)扑热息痛组,(G3)乳香油组,(G4)扑热息痛+乳香油组。连续3天口服扑热息痛1000 mg/kg,乳香油1000 mg/kg与扑热息痛同时口服。评估血液学参数、血脂、心脏指标、胰腺功能、血液抗氧化能力、髓过氧化物酶活性、血液、脾脏、胰腺、心脏和肺组织病理学。扑热息痛引起氧化应激、血液毒性、血脂异常、心肌损伤、胰腺功能障碍、脾脏改变和肺组织损伤。然而,扑热息痛和乳香油的联合使用可以通过增强抗氧化能力、改善血液学参数、保护胰腺功能、提高脂质谱、保持脾脏形态和防止肺损伤来防止这些影响,这可能是由于乳香油的抗氧化特性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ameliorative effects of frankincense oil on rats treated with a minimum toxic dose of paracetamol
Paracetamol is a widely used analgesic and antipyretic drug, but its long-term usage has been associated with potential toxicity. The goal of this study was to investigate how frankincense oil prevents paracetamol toxicity. The study included twenty male albino rats divided into four groups: (G1) control, (G2) paracetamol, (G3) frankincense oil, and (G4) paracetamol + frankincense oil. For three days, 1000 mg/kg paracetamol was given orally, while frankincense oil was given orally at a dosage of 1000 mg/kg concurrently with paracetamol. Hematological parameters, lipid profile, cardiac markers, pancreatic function, blood antioxidant capacity, myeloperoxidase activity, blood, spleen, pancreas, heart, and lung histopathology were evaluated. Paracetamol caused oxidative stress, hematotoxicity, dyslipidemia, myocardial damage, pancreatic dysfunction, spleen alterations, and lung tissue damage. However, coadministration of paracetamol and frankincense oil protected against these effects by boosting antioxidant capacity, improving hematological parameters, preserving pancreatic function, enhancing lipid profiles, preserving spleen morphology, and preventing lung damage, likely due to the antioxidant properties of frankincense oil.
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