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Toxicity of carbon tetrachloride, free radicals and role of antioxidants

dc.authorid 0000-0003-1415-0563
dc.authorid 0000-0001-8925-0230
dc.authorid 0000-0002-0773-2752
dc.contributor.author Unsal, Velid
dc.contributor.author Çiçek, Mustafa
dc.contributor.author Sabancılar, İlhan
dc.contributor.other Department of Nutrition and Dietetics/ Beslenme ve Diyetetik Bölümü
dc.date.accessioned 2021-06-25T11:27:47Z
dc.date.available 2021-06-25T11:27:47Z
dc.date.issued 2020
dc.department MAÜ, Fakülteler, Sağlık Bilimleri Fakültesi, Beslenme ve Diyetetik Bölümü en_US
dc.description.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. CCl4 is strong toxic in the kidney, testicle, brain, heart, lung, other tissues, and particularly in the liver. CCl4 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 CCl4 in tissues can be explained as oxidative damage caused by lipid peroxidation which starts after the conversion of CCl4 to free radicals of highly toxic trichloromethyl radicals (•CCl₃) and trichloromethyl peroxyl radical (•CCl₃O2) 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. CCl4-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 CCl4-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 CCI4 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 CCl4 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 CCl4 and increase the antioxidant capacity of cells. en_US
dc.description.citation Unsal V, Cicek M, Sabancilar İ. Toxicity of carbon tetrachloride, free radicals and role of antioxidants. Rev Environ Health. 2020 Sep 24:/j/reveh.ahead-of-print/reveh-2020-0048/reveh-2020-0048.xml. doi: 10.1515/reveh-2020-0048. Epub ahead of print. PMID: 32970608. en_US
dc.identifier.doi 10.1515/reveh-2020-0048
dc.identifier.issn 2191-0308
dc.identifier.issue 2 en_US
dc.identifier.pmid 32970608
dc.identifier.scopus 2-s2.0-85094100740
dc.identifier.scopusquality Q1
dc.identifier.uri https://doi.org/10.1515/reveh-2020-0048
dc.identifier.uri https://pubmed.ncbi.nlm.nih.gov/32970608/
dc.identifier.uri https://hdl.handle.net/20.500.12514/2622
dc.identifier.volume 36 en_US
dc.identifier.wos WOS:000656354100012
dc.identifier.wosquality Q2
dc.indekslendigikaynak Web of Science en_US
dc.indekslendigikaynak Scopus en_US
dc.indekslendigikaynak PubMed en_US
dc.language.iso en en_US
dc.publisher De Gruyter en_US
dc.relation.ispartof Reviews on Environmental Health en_US
dc.relation.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.scopus.citedbyCount 210
dc.subject antioxidants; carbon tetrachloride; hepatotoxicity; nephrotoxicity; neurotoxicity; oxidative stress. en_US
dc.title Toxicity of carbon tetrachloride, free radicals and role of antioxidants en_US
dc.type Article en_US
dc.wos.citedbyCount 174
dspace.entity.type Publication
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relation.isAuthorOfPublication.latestForDiscovery 7c3a66b7-a957-40d9-a628-a536a623b015
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