IDENTIFICATION OF HEAVY METAL TOXICITY INDUCED BIOMARKERS AND THE PROTECTIVE ROLE OF ASCORBIC ACID SUPPLEMENTATION IN CHANNA PUNCTATUS

被引:2
作者
Singh, Sohini [1 ]
Srivastava, Arti [1 ]
Allen, Tanu [1 ]
Bhagat, Neeta [1 ]
Singh, Neetu [1 ]
机构
[1] Amity Univ, Amity Inst Biotechnol, Noida 201303, Uttar Pradesh, India
关键词
Metal toxicity; Lysosomal markers; Mitochondrial damage; Arsenic; Mercury; Ascorbic acid; LIPID-PEROXIDATION; VITAMIN-C; LIVER; RATS; KIDNEY;
D O I
10.13040/IJPSR.0975-8232.11(3).1098-09
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Arsenic and mercury are presently the most common pollutants of freshwater bodies. There is a continuous increase in the toxic level of these pollutants with some seasonal changes, affecting the aquatic biota. The present study aimed to identify cellular biomarkers of arsenic and mercury toxicity in freshwater fish Channa punctatus. Antioxidant defense like catalase (CAT), superoxide dismutase (SOD), ascorbate, reduced glutathione (GSH), oxidative stress marker lipid peroxidation (LPO), lysosomal marker like acid phosphatases and apoptotic marker namely caspases-3 were employed to check the damage caused to the fish as a result of arsenic and mercury contamination of water. Results indicate that increased lipid peroxidation induced apoptosis in arsenic toxicity. On the other hand, mercury toxicity induced necrosis mediated by lysosomal induction. These results further significantly indicate the protective effects of ascorbic acid that reduces the increased level of hepatic oxidative stress during metal toxicity. This study suggests that ascorbic acid supplementation can be a good option to save fish, which are at high risk of heavy metal-induced damage resulting in the availability of healthy edible fish in the market.
引用
收藏
页码:1098 / 1109
页数:12
相关论文
共 33 条
[1]   Effect of arsenic (AsIII) on glutathione-dependent enzymes in liver and kidney of the freshwater fish channa punctatus [J].
Allen, T ;
Rana, SVS .
BIOLOGICAL TRACE ELEMENT RESEARCH, 2004, 100 (01) :39-48
[2]  
Anderson KA, 2012, ESSAYS BIOCHEM, V52, P23, DOI [10.1042/BSE0520023, 10.1042/bse0520023]
[3]  
BERGMAN F, 1981, MED BIOL, V59, P92
[4]  
Boyd C.E., 2005, Global Aquaculture Advocate, P84
[5]   Enzyme activity alteration by cadmium administration to rats: The possibility of iron involvement in lipid peroxidation [J].
Casalino, E ;
Sblano, C ;
Landriscina, C .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1997, 346 (02) :171-179
[6]   Pharmacologic ascorbic acid concentrations selectively kill cancer cells: Action as a pro-drug to deliver hydrogen peroxide to tissues [J].
Chen, Q ;
Espey, MG ;
Krishna, MC ;
Mitchell, JB ;
Corpe, CP ;
Buettner, GR ;
Shacter, E ;
Levine, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (38) :13604-13609
[7]   Ascorbic acid: Chemistry, biology and the treatment of cancer [J].
Du, Juan ;
Cullen, Joseph J. ;
Buettner, Garry R. .
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER, 2012, 1826 (02) :443-457
[8]   TISSUE SULFHYDRYL GROUPS [J].
ELLMAN, GL .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1959, 82 (01) :70-77
[9]   Meso 2,3-dimercaptosuccinic acid (DMSA) and monoisoamyl DMSA effect on gallium arsenide induced pathological liver injury in rats [J].
Flora, SJS ;
Dubey, R ;
Kannan, GM ;
Chauhan, RS ;
Pant, BP ;
Jaiswal, DK .
TOXICOLOGY LETTERS, 2002, 132 (01) :9-17
[10]   Lipid peroxidation in cell death [J].
Gaschler, Michael M. ;
Stockwell, Brent R. .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2017, 482 (03) :419-425