The effect of sulforaphane on oxidative stress and inflammation in rats with toxic hepatitis induced by acetaminophene

被引:11
作者
Dokumacioglu, E. [1 ]
Iskender, H. [1 ]
Aktas, M. S. [1 ,2 ]
Hanedan, B. [1 ,2 ]
Dokumacioglu, A. [1 ,3 ]
Sen, T. M. [1 ,4 ]
Musmul, A. [1 ,5 ]
机构
[1] Artvin Coruh Univ, Fac Hlth Sci, Dept Nutr & Dietet, Artvin, Turkey
[2] Ataturk Univ, Fac Vet Med, Dept Internal Med, Erzurum, Turkey
[3] Hopa Govt Hosp, Dept Med Biochem, Artvin, Turkey
[4] Karadeniz Tech Univ, Dept Med Biochem, Fac Med, Trabzon, Turkey
[5] Eskisehir Osmangazi Univ, Fac Med, Dept Biostat, Eskisehir, Turkey
来源
BRATISLAVA MEDICAL JOURNAL-BRATISLAVSKE LEKARSKE LISTY | 2017年 / 118卷 / 08期
关键词
acetaminophen; lipid peroxidation; neopterin; oxidative stress; sulforaphane; CHRONIC LIVER-DISEASE; INDUCED HEPATOTOXICITY; ISCHEMIA-REPERFUSION; LIPID-PEROXIDATION; NEOPTERIN LEVELS; DAMAGE; MODEL; ACID; ASSOCIATION; PROTECTS;
D O I
10.4149/BLL_2017_088
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
OBJECTIVE: The aim of the present study was to reveal the possible effect of sulforaphane on oxidative stress and inflammation in rats liver with toxic hepatitis induced by acetaminophene. BACKGROUND: Sulforaphane is a compound with high antioxidant properties. Acetaminophen, which is a para-aminophenol derivative, can lead to fatal hepatic necrosis with direct hepatotoxic effects at high doses. METHODS: Thirty six male Sprague-Dawley rats were randomly divided into four groups. Control group (n = 9) was fed with standard rat chow and water for 3 days. Group APAP (n = 9) received a single dose acetaminophen 1 g/kg by oral gavage in addition to standard chow and water. Group SFN (n = 9) received sulforaphane 500 mu g/kg by oral gavage in addition to standard chow and water for 3 days. Group APAP+SFN (n = 9) received sulforaphane 500 mu g/kg and a single dose acetaminophen 1 g/kg by oral gavage in addition to standard chow and water. Acetaminophen was administered three hours after SFN administration. RESULTS: Neopterin, MDA, AST, ALT and CRP levels of group APAP were significantly increased compared to control group. GSH level of group APAP was significantly lower than in the control group. CONCLUSION: Sulforaphane is a protective agent against acetaminophen-induced liver damage and it can be added in the treatment protocol (Tab. 1, Fig. 5, Ref. 51). Text in PDF www.elis.sk.
引用
收藏
页码:453 / 459
页数:7
相关论文
共 50 条
[1]
Adeneye Adejuwon Adewale, 2015, J Tradit Complement Med, V5, P106, DOI 10.1016/j.jtcme.2014.11.001
[2]
The effects of L-carnitine on acetaminophen induced hepatotoxicity in rats [J].
Aktas, Ozgur ;
Eskiocak, Sevgi ;
Ozgun, Gulben Sayilan ;
Yalcin, Omer ;
Sut, Necdet .
TURKISH JOURNAL OF BIOCHEMISTRY-TURK BIYOKIMYA DERGISI, 2013, 38 (04) :475-482
[3]
[Anonymous], GLOBAL J HLTH SCI
[4]
Arici S, 2008, PAMUKKALE M J, V1, P113
[5]
Protective effects of an extract of young radish (Raphanus sativus L) cultivated with sulfur (sulfur-radish extract) and of sulforaphane on carbon tetrachloride-induced hepatotoxicity [J].
Baek, Seung-Hae ;
Park, Min ;
Suh, Jae-Hee ;
Choi, Hye-Seon .
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 2008, 72 (05) :1176-1182
[6]
Glutathione dysregulation and the etiology and progression of human diseases [J].
Ballatori, Nazzareno ;
Krance, Suzanne M. ;
Notenboom, Sylvia ;
Shi, Shujie ;
Tieu, Kim ;
Hammond, Christine L. .
BIOLOGICAL CHEMISTRY, 2009, 390 (03) :191-214
[7]
Baydar T, 2009, TURK KLIN TIP BILIM, V29, P1280
[8]
BEUTLER E, 1963, J LAB CLIN MED, V61, P882
[9]
The association between neopterin and acetaminophen-induced nephrotoxicity [J].
Cakir, Erdinc ;
Akgul, Ozgur E. ;
Aydin, Ibrahim ;
Cayci, Tuncer ;
Kurt, Yasemin Gulcan ;
Onguru, Onder ;
Aydin, Fevzi N. ;
Agilli, Mehmet ;
Yaman, Halil ;
Ersoz, Nail ;
Bilgic, Serkan ;
Guven, Ahmet ;
Turker, Turker ;
Bilgi, Cumhur ;
Erbil, Kemal M. .
RENAL FAILURE, 2010, 32 (06) :740-746
[10]
Çayci T, 2009, TURK J BIOCHEM, V34, P134