The potential protective effect of two actinomycete extracts against carbon tetrachloride-induced hepatotoxicity in rats

被引:7
作者
Hozzein, Wael N. [1 ,2 ]
Al-Khalaf, Areej Abdulkareem [3 ]
Mohany, Mohamed [4 ]
Al-Rejaie, Salim S. [4 ]
Ali, Dalia M. I. [5 ]
Amin, Asmaa A. [2 ]
机构
[1] King Saud Univ, Coll Sci, Bioprod Res Chair, Zool Dept, POB 2455, Riyadh 11451, Saudi Arabia
[2] Beni Suef Univ, Fac Sci, Bot & Microbiol Dept, Bani Suwayf, Egypt
[3] Princess Nourah bint Abdulrahman Univ, Coll Sci, Biol Dept, Riyadh, Saudi Arabia
[4] King Saud Univ, Coll Pharm, Dept Pharmacol & Toxicol, Riyadh 11451, Saudi Arabia
[5] Cairo Univ, Fac Sci, Bot Dept, Giza, Egypt
关键词
Actinomycete extracts; CCl4; Hepatotoxicity; Liver enzymes; Oxidative stress; OXIDATIVE STRESS; INJURY; BLOOD; LIVER; IDENTIFICATION; CATALASE; DAMAGE; CCL4;
D O I
10.1007/s11356-018-3904-z
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The aim of this study was to investigate the potential protective effect of two extracts derived from two soil actinomycete strains, designated S19 and G30, against CCl4-induced hepatotoxicity in male rats. Sixty-four male rats were divided into four groups of 16 rats per group. The first group was a control group given corn oil and the nutritive medium which is composed of a mixture of the two used media. The second group received CCl4 only, the third group was administered CCl4 and the extract S19, and the fourth group was administered CCl4 and the extract G30. The results were taken after a treatment period of 8weeks. Our data demonstrated that the two actinomycete extracts significantly (P<0.01) lowered the CCl4-induced elevation of serum levels of alanine aminotransferase (ALT), aspartate aminotransferase (AST), and alkaline phosphatase (ALP) after 8weeks of treatment. The extract S19 had no effect on serum lactate dehydrogenase (LDH) and total bilirubin, whereas the extract G30 significantly decreased (P<0.01) the elevated levels of these parameters in the serum, especially after 4weeks of treatment. The levels of hepatic glutathione (GSH), glutathione peroxidase (GSH-Px), peroxidase (Px), catalase (CAT), and superoxide dismutase (SOD) significantly increased (P<0.01), while those of malondialdehyde (MDA) markedly decreased in rats treated with the two extracts. Furthermore, histopathological lesions in the liver, including necrosis, inflammatory cell infiltration, hydropic degeneration, and congestion of the central vein, were partially reversed by treatment with the two microbial extracts. Our results provided evidence for the protective effect of the two used actinomycete extracts against CCl4-induced liver damage occurred through the reduction of oxidative stress and improvement of antioxidant defense markers.
引用
收藏
页码:3834 / 3847
页数:14
相关论文
共 49 条
[21]  
Kuriakose GC, 2008, INDIAN J EXP BIOL, V46, P52
[22]  
Lechevalier H.A., 1989, Bergey's Manual of Systematic Bacteriology, V4, P2344
[23]   A Phenotypic and Genotypic Analysis of the Antimicrobial Potential of Cultivable Streptomyces Isolated from Cave Moonmilk Deposits [J].
Maciejewska, Marta ;
Adam, Delphine ;
Martinet, Loic ;
Naome, Aymeric ;
Calusinska, Magdalena ;
Delfosse, Philippe ;
Carnol, Monique ;
Barton, Hazel A. ;
Hayette, Marie-Pierre ;
Smargiasso, Nicolas ;
De Pauw, Edwin ;
Hanikenne, Marc ;
Baurain, Denis ;
Rigali, Sebastien .
FRONTIERS IN MICROBIOLOGY, 2016, 7
[24]  
MARKLUND S, 1974, EUR J BIOCHEM, V47, P469
[25]  
MARSH WH, 1959, CLIN CHEM, V5, P119
[26]  
Matkovics Bela, 1997, Acta Physiologica Hungarica, V85, P29
[27]   Potential of rare actinomycetes in the production of metabolites against multiple oxidant agents [J].
Mohammadipanah, Fatemeh ;
Momenilandi, Mana .
PHARMACEUTICAL BIOLOGY, 2017, 56 (01) :51-59
[28]   Hepato- and Nephroprotective Activities of a Nigerian Local King Tuber Oyster Mushroom, Pleurotus tuberregium (Higher Basidiomycetes), in Chemically-Induced Organ Toxicities in Rats [J].
Nworu, Chukwuemeka S. ;
Ihim, Stella A. ;
Ugwu, Loveth E. ;
Laiyemo, Kolawole A. ;
Akah, Peter A. .
INTERNATIONAL JOURNAL OF MEDICINAL MUSHROOMS, 2014, 16 (04) :305-318
[29]  
Oskay M., 2004, African Journal of Biotechnology, V3, P441
[30]   Redox therapeutics in hepatic ischemia reperfusion injury [J].
Patel, Rakesh P. ;
Lang, John D. ;
Smith, Alvin B. ;
Crawford, Jack H. .
WORLD JOURNAL OF HEPATOLOGY, 2014, 6 (01) :1-8