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四氯化碳的毒性、自由基与抗氧化剂的作用

Toxicity of carbon tetrachloride, free radicals and role of antioxidants.

作者信息

Unsal Velid, Cicek Mustafa, Sabancilar İlhan

机构信息

Department of Nutrition and Dietetics, Faculty of Health Sciences, Mardin Artuklu University, Mardin, Turkey.

Department of Anatomy, Faculty of Medicine, Kahramanmaraş Sütçü imam University, Kahramanmaraş, Turkey.

出版信息

Rev Environ Health. 2020 Sep 25;36(2):279-295. doi: 10.1515/reveh-2020-0048. Print 2021 Jun 25.

Abstract

Several chemicals, including environmental toxicants and clinically useful drugs, cause severe cellular damage to different organs of our body through metabolic activation to highly reactive substances such as free radicals. Carbon tetrachloride is an organic compound of which chemical formula is CCl₄. CCl is strong toxic in the kidney, testicle, brain, heart, lung, other tissues, and particularly in the liver. CCl is a powerful hepatoxic, nephrotoxic and prooxidant agent which is widely used to induce hepatotoxicity in experimental animals and to create hepatocellular carcinoma, hepatic fibrosis/cirrhosis and liver injury, chemical hepatitis model, renal failure model, and nephrotoxicity model in recent years. The damage-causing mechanism of CCl in tissues can be explained as oxidative damage caused by lipid peroxidation which starts after the conversion of CCl to free radicals of highly toxic trichloromethyl radicals (•CCl₃) and trichloromethyl peroxyl radical (•CCl₃O) via cytochrome P450 enzyme. Complete disruption of lipids (i.e., peroxidation) is the hallmark of oxidative damage. Free radicals are structures that contain one or more unpaired electrons in atomic or molecular orbitals. These toxic free radicals induce a chain reaction and lipid peroxidation in membrane-like structures rich in phospholipids, such as mitochondria and endoplasmic reticulum. CCl-induced lipid peroxidation is the cause of oxidative stress, mitochondrial stress, endoplasmic reticulum stress. Free radicals trigger many biological processes, such as apoptosis, necrosis, ferroptosis and autophagy. Recent researches state that the way to reduce or eliminate these CCl-induced negative effects is the antioxidants originated from natural sources. For normal physiological function, there must be a balance between free radicals and antioxidants. If this balance is in favor of free radicals, various pathological conditions occur. Free radicals play a role in various pathological conditions including Pulmonary disease, ischemia / reperfusion rheumatological diseases, autoimmune disorders, cardiovascular diseases, cancer, kidney diseases, hypertension, eye diseases, neurological disorders, diabetes and aging. Free radicals are antagonized by antioxidants and quenched. Antioxidants do not only remove free radicals, but they also have anti-inflammatory, anti-allergic, antithrombotic, antiviral, and anti-carcinogenic activities. Antioxidants contain high phenol compounds and antioxidants have relatively low side effects compared to synthetic drugs. The antioxidants investigated in CCI toxicity are usually antioxidants from plants and are promising because of their rich resources and low side effects. Data were investigated using PubMed, EBSCO, Embase, Web of Science, DOAJ, Scopus and Google Scholar, Carbon tetrachloride, carbon tetrachloride-induced toxicity, oxidative stress, and free radical keywords. This study aims to enlighten the damage-causing mechanism created by free radicals which are produced by CCl on tissues/cells and to discuss the role of antioxidants in the prevention of tissue/cell damage. In the future, Antioxidants can be used as a therapeutic strategy to strengthen effective treatment against substances with high toxicity such as CCl and increase the antioxidant capacity of cells.

摘要

包括环境毒物和临床常用药物在内的几种化学物质,通过代谢活化生成自由基等高活性物质,对人体不同器官造成严重的细胞损伤。四氯化碳是一种化学式为CCl₄的有机化合物。四氯化碳对肾脏、睾丸、大脑、心脏、肺及其他组织具有强烈毒性,尤其对肝脏毒性极大。四氯化碳是一种强大的肝毒性、肾毒性和促氧化剂,近年来被广泛用于在实验动物中诱导肝毒性,建立肝细胞癌、肝纤维化/肝硬化和肝损伤、化学性肝炎模型、肾衰竭模型以及肾毒性模型。四氯化碳在组织中的损伤机制可解释为脂质过氧化引起的氧化损伤,该过程始于四氯化碳通过细胞色素P450酶转化为剧毒的三氯甲基自由基(•CCl₃)和三氯甲基过氧自由基(•CCl₃O)之后。脂质的完全破坏(即过氧化)是氧化损伤的标志。自由基是在原子或分子轨道中含有一个或多个未成对电子的结构。这些有毒自由基在富含磷脂的膜状结构(如线粒体和内质网)中引发连锁反应和脂质过氧化。四氯化碳诱导的脂质过氧化是氧化应激、线粒体应激和内质网应激的原因。自由基触发许多生物学过程,如细胞凋亡、坏死、铁死亡和自噬。最近的研究表明,减少或消除这些四氯化碳诱导的负面影响的方法是天然来源的抗氧化剂。对于正常生理功能而言,自由基和抗氧化剂之间必须保持平衡。如果这种平衡偏向自由基,则会出现各种病理状况。自由基在包括肺病、缺血/再灌注、风湿性疾病、自身免疫性疾病、心血管疾病、癌症、肾脏疾病、高血压、眼部疾病、神经系统疾病、糖尿病和衰老在内的各种病理状况中起作用。自由基被抗氧化剂拮抗并淬灭。抗氧化剂不仅能清除自由基,还具有抗炎、抗过敏、抗血栓形成、抗病毒和抗癌活性。抗氧化剂含有高酚类化合物,与合成药物相比副作用相对较低。在四氯化碳毒性研究中所研究的抗氧化剂通常是植物来源的抗氧化剂,由于其资源丰富且副作用低而颇具前景。使用PubMed、EBSCO、Embase、Web of Science、DOAJ、Scopus和谷歌学术搜索等数据库,以四氯化碳、四氯化碳诱导的毒性、氧化应激和自由基为关键词进行数据检索。本研究旨在阐明四氯化碳产生的自由基对组织/细胞造成损伤的机制,并探讨抗氧化剂在预防组织/细胞损伤中的作用。未来,抗氧化剂可作为一种治疗策略,以加强针对四氯化碳等高毒性物质的有效治疗,并提高细胞的抗氧化能力。

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