Acute paracetamol toxicity-induced inflammatory and oxidative effects are relieved by Aleppo galls: a novel experimental study.

Ahmed Alamir Mahmoud Abdallah, Rawan Bafail, Amal Yaseen Zaman, Ahmed J Aldhafiri, Ali Alalawi, Faten M Omran, Hussam H Baghdadi, Wafaa A Abdellah, Abdullah Mahfouz Alsharif, Sultan S Al Thagfan, Ibrahim M Abdel-Rahman, Samer A El-Sawy, Mehrevan M Abd Elmoniem, Salah Mohamed El Sayed, Hytham Mahmoud Abdel-Latif
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Abstract

Background: Paracetamol (acetaminophen) is an over-the-counter non-steroidal anti-inflammatory drug that may cause acute toxic overdosage particularly in neuropsychiatric patients. Paracetamol is also very commonly prescribed as an analgesic and antipyretic agent. Paracetamol toxicity causes decreased reduced glutathione and oxidative tissue damage. Aleppo galls is a promising natural remedy exerting antioxidant and tissue-protective effects that may combat acetaminophen-induced oxidative tissue damage.

Methodology: Biochemical and toxicological effects of a toxic dose of paracetamol (250 mg/kg) were investigated for three consecutive days versus the tissue-protective effects of Aleppo galls. Eighteen white albino mice were randomly allocated in this study and divided into three experimental groups (six mice per group): negative control (received intraperitoneal sterile water injection), paracetamol toxicity group (received intraperitoneal paracetamol injection) and the third group (received paracetamol injection at 250 mg/kg/day together with oral Aleppo galls treatment at 250 mg/kg/day for 3 consecutive days). All mice were sacrificed by the end of the study.

Results: Our data revealed that paracetamol toxicity exerted significant oxidative stress damaging effects (high serum malondialdehyde, decreased serum catalase and decreased total antioxidant capacity), and significant inflammatory effects (high serum IL-6) and significant tissue-damaging effects (high serum LDH). Aleppo galls treatment significantly protected against acetaminophen toxicity-induced oxidative stress effects (P<0.001), inflammatory effects (P<0.001) and tissue-damaging effects (P<0.001).

Conclusion: Aleppo galls are promising for future drug therapeutics and for the synthesis of natural remedies for treating paracetamol toxicity. We recommend formulating Aleppo galls extract as a pharmaceutical nutrition and to be given to those who need to take large doses of paracetamol.

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急性扑热息痛毒性诱导的炎症和氧化作用由阿勒颇胆囊缓解:一项新的实验研究。
背景:扑热息痛(扑热息痛)是一种非处方非甾体抗炎药,可引起急性毒性过量,特别是对神经精神病人。扑热息痛也是常用的止痛药和解热药。扑热息痛毒性导致还原性谷胱甘肽减少和氧化性组织损伤。阿勒颇胆是一种很有前途的自然疗法,具有抗氧化和保护组织的作用,可以对抗对乙酰氨基酚引起的氧化性组织损伤。方法:连续3天研究有毒剂量扑热息痛(250 mg/kg)与阿勒颇胆的组织保护作用的生化和毒理学效应。本研究随机选取白化小鼠18只,分为3个实验组(每组6只):阴性对照组(腹腔注射无菌水)、扑热息痛毒性组(腹腔注射扑热息痛)和第三组(注射扑热息痛250 mg/kg/d,同时口服阿勒波胆250 mg/kg/d,连续3天)。研究结束时,所有小鼠都被处死。结果:我们的数据显示,扑热息痛毒性具有显著的氧化应激损伤作用(高血清丙二醛,降低血清过氧化氢酶和降低总抗氧化能力),显著的炎症作用(高血清IL-6)和显著的组织损伤作用(高血清LDH)。结论:阿勒颇胆在未来的药物治疗和对乙酰氨基酚毒性的自然疗法合成中具有广阔的应用前景。我们建议将阿勒颇胆囊提取物作为一种药物营养制剂,给那些需要服用大剂量扑热息痛的人服用。
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