Please enter verification code
Confirm
Stem Cells Take Part in Regulation of Prooxidant Activity and Immunity at Liver Fibrosis
American Journal of Biomedical and Life Sciences
Volume 2, Issue 6-1, December 2014, Pages: 5-12
Received: Oct. 13, 2014; Accepted: Nov. 20, 2014; Published: Nov. 26, 2014
Views 3584      Downloads 172
Authors
Anatoliy Ivanovich Bozhkov, Biology Research Institute of V. N. Karazin Kharkov National University, Kharkov, Ukraine
Elena Mikhajlovna Klimova, State Institution “Institute of General and Urgent Surgery NAMS of Ukraine”, Kharkov, Ukraine
Yuriy Viktorovich Nikitchenko, Biology Research Institute of V. N. Karazin Kharkov National University, Kharkov, Ukraine
Vadim Vyacheslavovich Davydov, State Institution “Institute of Children and Adolescent Health NAMS of Ukraine”, Kharkov, Ukraine
Oxana Vladimirovna Zvyagintseva, State Institution “Institute of General and Urgent Surgery NAMS of Ukraine”, Kharkov, Ukraine
Natalia Igorevna Kurguzova, Biology Research Institute of V. N. Karazin Kharkov National University, Kharkov, Ukraine
Vadim Ivanovich Sidorov, Biology Research Institute of V. N. Karazin Kharkov National University, Kharkov, Ukraine
Alexandr Vladimirovich Naglov, Biology Research Institute of V. N. Karazin Kharkov National University, Kharkov, Ukraine
Article Tools
Follow on us
Abstract
It has been explored the possibility of correction of prooxidant-antioxidant parameters at rats with experimental liver fibrosis and immunological status of these animals using xenogeneic embryonic stem cells. It is shown that the threefold sequential administration of copper sulfate in dose 1 mg / 100 g of body weight, which amounted to 30% of the lethal dose in 48 hour intervals between administrations induced liver fibrosis in 24 hours after the last administration to 3 month animals. It was found that the development of fibrosis, was accompanied 50 per cent increase in TBA-active products in the mitochondria and 25% of the increase in the microsomes of liver cells. Content of Ig A, IgM, circulating immune complexes (CIC) and the average molecular weight peptides was increased to 2-3 times in the same time. Introduction of xenogenic embryonic stem cells in animals with experimental fibrosis accompanied by decrease in the amount of TBA-active products to almost intact control. It coincided with the 60% increase in the activity of glutathione peroxidase in the mitochondria. Introduction of stem cells to experimental animals provide a normalization of the content of Ig A, Ig M, the CiC and the average molecular weight of the peptides.
Keywords
Embryonic Stem Cells, Fibrosis, Prooxidant-Antioxidant System, Immune Parameters
To cite this article
Anatoliy Ivanovich Bozhkov, Elena Mikhajlovna Klimova, Yuriy Viktorovich Nikitchenko, Vadim Vyacheslavovich Davydov, Oxana Vladimirovna Zvyagintseva, Natalia Igorevna Kurguzova, Vadim Ivanovich Sidorov, Alexandr Vladimirovich Naglov, Stem Cells Take Part in Regulation of Prooxidant Activity and Immunity at Liver Fibrosis, American Journal of Biomedical and Life Sciences. Special Issue: Mechanisms of Protection Against Oxidative Stress. Vol. 2, No. 6-1, 2014, pp. 5-12. doi: 10.11648/j.ajbls.s.2014020601.12
References
[1]
Choi J., Corder N.L., Koduru B. and Wang Y. (2014) Oxidative stress and hepatic Nox proteins in chronic hepatitis C and hepatocellular carcinoma. Free Radic. Bio.l Med, 72, 267–84.
[2]
Ma B., Meng X., Wang J., Sun J., Ren X., Qin M., Sun J., Sun G. and Sun X. (2014) Notoginsenoside R1 attenuates amyloid-β-induced damage in neurons by inhibiting reactive oxygen species and modulating MAPK activation. Int. Immunopharmacol, 22, 151–159.
[3]
Hseu Y.C. et al. (2014) Humic acid in drinking well water induces inflammation through reactive oxygen species generation and activation of nuclear factor-κB/activator protein-1 signaling pathways: a possible role in atherosclerosis. Toxico.l Appl. Pharmacol, 274, 249–262.
[4]
Rottenberg H. (2014) Exceptional longevity and exceptionally high metabolic rates in anthropoid primates are linked to a major modification of the ubiquinone reduction site of cytochrome b. J. Bioenerg. Biomembr, 46, 435–445.
[5]
Rottenberg H. (2007) Exceptional longevity in songbirds is associated with high rates of evolution of cytochrome b, suggesting selection for reduced generation of free radicals. J Exp Biol, 210, 2170–2180.
[6]
Andziak B. et al. (2006) High oxidative damage levels in the longest-living rodent, the naked mole-rat. Aging Cell, 5, 463–471.
[7]
Cardoso A,R., Kakimoto P.A. and Kowaltowski A.J. (2013) Diet-sensitive sources of reactive oxygen species in liver mitochondria: role of very long chain acyl-CoA dehydrogenases. PLoS One, 7, e77088.
[8]
Hagopian K. et al. (2011) Caloric restriction influences hydrogen peroxide generation in mitochondrial sub-populations from mouse liver. J. Bioenerg. Biomembr, 43, 227–236.
[9]
Ramírez-Vélez R. et al. (2013) Effect of exercise training on eNOS expression, NO production and oxygen metabolism in human placenta. PLoS One, 14, e80225.
[10]
Guedouari H. et al. (2014) Changes in glutathione-dependent redox status and mitochondrial energetic strategies are part of the adaptive response during the filamentation process in Candida albicans. Biochim Biophys Acta, 1842, 1855–1869.
[11]
Ayala A., Muñoz M.F. and Argüelles S. (2014) Lipid peroxidation: production, metabolism, and signaling mechanisms of malondialdehyde and 4-hydroxy-2-nonenal. Oxid. Med. Cell Longev, 2014:360438.
[12]
Liu Y., Long J. and Liu J. (2014) Mitochondrial free radical theory of aging: Who moved my premise? Geriatr. Gerontol. Int,18. doi: 10.1111/ggi.12296. [Epub ahead of print].
[13]
Lapointe J. and Hekimi S. (2010) When a theory of aging ages badly. Cell Mol. Life Sci, 67, 1–8.
[14]
Hekimi S., Lapointe J. and Wen Y. (2011) Taking a "good" look at free radicals in the aging process. Trends Cell Bio., 21, 569–576.
[15]
Sanz A. and Stefanatos R.K. (2008) The mitochondrial free radical theory of aging: a critical view. , Curr. Aging Sci, 1, 10–21.
[16]
Barja G. (2014) The mitochondrial free radical theory of aging. Prog. Mol. Biol. Transl. Sci, 127, 1–27.
[17]
Bozhkov A.I. et al. (2010) Appearance of the imprinting effect on the specific pattern of intracellular distribution of copper ions in the liver after exposure to high concentrations of copper sulfate. Biomeditsinskaya khimiya, 56, 195–208. (in Russian).
[18]
Bozhkov A. I., Sidorov V. I., Kurguzova N. I.and Dlubovskaya V. L. (2014) Metabolic memory enhances hormesis effect to the copper ions in age-depended manner. Uspekhy gerontologii, 27, 72–80. (in Russian).
[19]
Lopes R.A. et al. (2014) Testosterone induces apoptosis in vascular smooth muscle cells via extrinsic apoptotic pathway with mitochondria-generated reactive oxygen species involvement. Am. J. Physiol. Heart Circ. Physiol., 306, 1485–1494.
[20]
Zhang H.M. and Zhang Y. (2014) Melatonin: a well-documented antioxidant with conditional pro-oxidant actions. J. Pineal Res, 57, 131–146.
[21]
Liu Q. et al. (2013) Polymorphism of rs1836882 in NOX4 gene modifies associations between dietary caloric intake and ROS levels in peripheral blood mononuclear cells. PLoS One, 12, e85660.
[22]
de Paula A Sousa A. et al. (2014) Autologous haematopoietic stem cell transplantation reduces abnormalities in the expression of immune genes in multiple sclerosis. Clin. Sci. (Lond), 128, 111–120.
[23]
Capitelli C.S. et al. (2014) Opposite effects of bone marrow-derived cells transplantation in MPTP-rat model of Parkinson's disease: a comparison study of mononuclear and mesenchymal stem cells. Int J Med Sci, 11, 1049–1064.
[24]
Liu X. et al. (2014) Transplantation of SIRT1-engineered aged mesenchymal stem cells improves cardiac function in a rat myocardial infarction model. J. Heart Lung Transplant 33, 1083–1092.
[25]
Peng S.Y. (2014) Therapeutic potential of amniotic-fluid-derived stem cells on liver fibrosis model in mice. Taiwan J. Obstet. Gyneco, 53, 151–157.
[26]
Persky E.E., Nikitina N.A., Naglov A.V.and J.G. Kot (2006) Age features of induction and synthesis of intensity of certain processing steps of collagen in the connective tissue under the influence of mechanical loading. Biologicheskii vestnik, 10, 126–129. (in Russian).
[27]
Kamath S.A. and Narayan K.A. (1972) Interaction of Ca 2+ with endoplasmic reticulum of rat liver: a standardized procedure for the isolation of rat liver microsomes. Anal. Biochem, 48, 53–61.
[28]
Ohkawa H., Ohishi N. and Yagi K. (1979) Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal. Biochem, 95, 351–358.
[29]
Paglia D.E. and Valentine W.N. (1967) Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase. J. Lab. Clin. Med., 70, 158–169.
[30]
Younes M., Schlichting R. and Siegers C.P. (1980) Glutathione S-transferase activities in rat liver: effect of some factors influencing the metabolism of xenobiotics. Pharmacol. Res. Commun, 12, 115–129.
[31]
Khaitov R.М., Pinegin B.V. and Yarilin А.А. (2009) Manual of Clinical Immunology. Diagnosis of diseases of the immune system: a guide for physicians. Moskow: GEOTAR Media, 352 s. (in Russian).
[32]
Khan H.Y. et al. (2014) Plant polyphenol induced cell death in human cancer cells involves mobilization of intracellular copper ions and reactive oxygen species generation: a mechanism for cancer chemopreventive action. Mol. Nutr. Food Res., 58, 437-446.
[33]
Sornchuer P. et al. (2014) Copper chloride induces antioxidant gene expression but reduces ability to mediate H2O2 toxicity in Xanthomonas campestris. Microbiology. 160 (Pt 2), 458–466.
[34]
Arain S.A. et al. (2014) Estimation of copper and iron burden in biological samples of various stages of hepatitis C and liver cirrhosis patients. Biol. Trace Elem. Res., 160, 197–205.
[35]
Casey C.A. Tuma DJ., McVicker B.L. (2014) Sy39-2 chronic ethanol consumption: its effects on liver inflammation. Alcohol Alcohol. 49, Suppl 1, i 33.
[36]
Roychowdhury S., Chiang D.J., McMullen M.R. and Nagy L.E. (2014) Moderate, chronic ethanol feeding exacerbates carbon-tetrachloride-induced hepatic fibrosis via hepatocyte-specific hypoxia inducible factor 1α. Pharmacol. Res. Perspect, 2, e00061.
[37]
Chrostek L, Panasiuk A. (2014) Liver fibrosis markers in alcoholic liver disease. World J. Gastroenterol, 20, 8018–1823.
ADDRESS
Science Publishing Group
1 Rockefeller Plaza,
10th and 11th Floors,
New York, NY 10020
U.S.A.
Tel: (001)347-983-5186