Effects of shark hepatic stimulator substance on the function and antioxidant capacity of liver mitochondria in an animal model of acute liver injury

Acta Biochimica et Biophysica Sinica

Volumn 37, Issue 8, 2005, Pages 507-514

  Fan, Qiu Ling ^a,b   Huang, Cai Guo ^b   Jin, Yan ^b   Feng, Bo ^b   Miao, Hui Nan ^b   Li, Wen Jie ^b   Jiao, Bing Hua ^b   Yuan, Qin Sheng ^a  

^a EAST CHINA UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

^b SECOND MILITARY MEDICAL UNIVERSITY   (China)

Author keywords

Acute liver injury; Antioxidant capacity; Mitochondrion; Respiratory function; Shark hepatic stimulator substance

Indexed keywords

ANTIOXIDANT; HEPATIC STIMULATOR SUBSTANCE; PEPTIDE; REACTIVE OXYGEN METABOLITE; THIOACETAMIDE;

ANIMAL; ARTICLE; CELL RESPIRATION; CHEMICALLY INDUCED DISORDER; DISEASE MODEL; DRUG EFFECT; LIVER FAILURE; LIVER MITOCHONDRION; LIVER REGENERATION; MALE; METABOLISM; RAT; SHARK; SPRAGUE DAWLEY RAT; TREATMENT OUTCOME;

ANIMALS; ANTIOXIDANTS; CELL RESPIRATION; DISEASE MODELS, ANIMAL; LIVER FAILURE, ACUTE; LIVER REGENERATION; MALE; MITOCHONDRIA, LIVER; PEPTIDES; RATS; RATS, SPRAGUE-DAWLEY; REACTIVE OXYGEN SPECIES; SHARKS; THIOACETAMIDE; TREATMENT OUTCOME;

ANIMALIA; CHONDRICHTHYES;

EID: 27744566432     PISSN: 16729145     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1745-7270.2005.00081.x     Document Type: Article

References (45)

1. Krahenbuhl L, Ledermann M, Lang C, Krahenbuhl S. Relationship between hepatic mitochondrial functions in vivo and in vitro in rats with carbon tetrachloride-induced liver cirrhosis. J Hepatol 2000, 33: 216-223
2. Nagamura Y, Uesugi K, Naito J, Ishiguro I. Cinnabarinic acid was formed in damaged mitochondria and its effect on mitochondrial respiration. Adv Exp Med Biol 1999, 467: 419-423
3. Yang S, Tana TMC, Weeb A, Leowc CK. Mitochondrial respiratory function and antioxidant capacity in normal and cirrhotic livers following partial hepatectomy. Cell Mol Life Sci 2004, 61: 220-229
4. Ferreira FML, Palmeira CM, Mates MJ, Seiqa R, Santos MS. Decreased susceptibility to lipid peroxidation of goto-kakizaki rats: Relationship to mitochondrial antioxidant capacity. Life Sci 1999, 65: 1013-1025
5. Rikans LE, Hornbrook KR. Lipid peroxidation, antioxidant protection and aging. Biochim Biophys Acta 1997, 1362: 116-127
6. Fernandez-Checa JC, Kaplowitz N, Garcia-Ruiz C, Colell A, Miranda M, Mari M, Ardite E et al. GSH transport in mitochondria: Defense against TNF-induced oxidative stress and alcohol-induced defect. Am J Physiol Gastrointest Liver Physiol 1997, 273: 7-17
7. Ratan RR, Murphy TH, Baraban JM. Oxidative stress induces apoptosis in embryonic cortical neurons. J Neurochem 1994, 62: 376-379
8. Kaneto H, Fujii J, Myint T, Miyanawz N, Islam KN, Kawasaki Y, Islam KN et al. Reducing sugars trigger oxidative modification and apoptosis in pancreatic β-cells by provoking oxidative stress through the glycation reaction. Biochem J 1996, 320: 855-863
9. Guerrieri F, Vendemiale G, Grattagliano I, Cocco T, Pellecchia G, Altomare E. Mitochondrial oxidative alterations following partial hepatectomy. Free Radic Biol Med 1999, 26: 34-41
10. Turrens JB, Boveris A. Generation of superoxide anion by the NADH dehydrogenase of bovine heart mitochondria. Biochem J 1980, 191: 421-427
11. 4 administration. Hepatology 1996, 24: 657-662
12. Francavilla A, di Leo A, Polimeno L, Gavaler J, Pellici R, Todo S, Kam I et al. The effect of hepatic stimulatory substance, isolated from regenerating hepatic cytosol, and 50,000 and 300,000 subfractions in enhancing survival in experimental acute hepatic failure in rats treated with D-galactosamine. Hepatology 1986, 6: 1346-1351
13. Fleig WE, Lehmann H, Wagner H, Hoss G, Ditschuneit H. Hepatic regenerative stimulator substance in the rabbit. Relation to liver regeneration after partial hepatectomy. J Hepatol 1986, 3: 19-26
14. Gupta S, Labrecque DR, Shafritz DA. Mitogenic effects of hepatic stimulator substance on cultured nonparenchymal liver epithelial cells. Hepatology 1992, 15: 485-491
15. Terbalache J, Porter KA, Starzl TE, Moore J, Patzelt L, Hayashida N. Stimulation of hepatic regeneration after partial hepatectomy by infusion of a cytosol extract from regenerating dog liver. Surg Gynecol Obstet 1980, 151: 538-544
16. Kahn D, Hickman R, Terblanche J, Kirch RE. Hepatic stimulator substance in extracts from regenerating porcine liver. Eur Surg Res 1988, 20: 168-174
17. LaBrecque DR, Pesh LA. Preparation and partial characterization of hepatic regenerative stimulator substance (SS) from rat liver. J Physiol 1975, 248: 273-284
18. Francavilla A, Ove P, Polimeno L, Coetzee M, Makowka L, Rose J, van Thiel DH et al. Extraction and partial purification of hepatic stimulatory substance in rats, mice and dogs. Cancer Res 1987, 47: 5600-5605
19. Mei MH, An W, Zhang BH, Shao Q, Gong DZ. Hepatic stimulator substance protects against acute liver failure induced by carbon tetrachloride poisoning in mice. Hepatology 1993, 17: 638-644
20. Theocharis SE, Margeli AP, Spiliopoulou C, Skaltsas S, Kittas C, Koutselinis A. Hepatic stimulator substance administration enhances regenerative capacity of hepatocytes in cadmium-pretreated partially hepatectomized rats. Dig Dis Sci 1996, 41: 1475-1480
21. Lü ZB, Li Q, Ye BP, Bian S, Wang Y, Ruan QP, Wu WT. Protective effects of shark hepatic stimulator substance against acute hepatic injury induced by acetaminophen in mice. Acta Pharmaceutica Sinica 2004, 39: 17-21
22. Okajima A, Miyazawa K, Kitamura N. Primary structure of rat hepatocyte growth factor and induction of its mRNA during liver regeneration following hepatic injury. Eur J Biochem 1990, 193: 375-381
23. Webber EM, Fitzgerald MJ, Brown PI, Bartlett MH, Fausto N. Transforming growth factor-alpha expression during liver regeneration after partial hepatectomy and toxic injury, and potential interactions between transforming growth factor-alpha and hepatocyte growth factor. Hepatology 1993, 18: 1422-1431
24. Liatsos GD, Mykoniatis MG, Margeli A, Liakos AA, Theocharis SE. Effect of acute ethanol exposure on hepatic stimulator substance (HSS) levels during liver regeneration (protective function of HSS). Dig Dis Sci 2003, 48: 1929-1938
25. Theocharis SE, Margeli AP, Agapitos EV, Mykoniatis MG, Kittas CN, Davaris PS. Effect of hepatic stimulator substance administration on tissue regeneration due to thioacetamide-induced liver injury in rats. Scand J Gastroenterol 1998, 33: 656-663
26. Tzirogiannis KN, Panoutsopoulos GI, Demonakou MD, Hereti RI, Alexandropoulou KN, Mykoniatis MG. Effect of hepatic stimulator substance (HSS) on cadmium-induced acute hepatotoxicity in the rat liver. Dig Dis Sci 2004, 49: 1019-1028
27. Yao ZQ, Yang WS, Zhang WB, Chen YN, Yang FY. Human hepatic regenerative stimulator substance: Partial purification and biological characterization of hepatic stimulator substance from human fetal liver cells. Hepatology 1990, 12: 1144-1151
28. Mangipudy RS, Chanda S, Mehendale HM. Tissue repair response as a function of dose in thioacetamide hepatotoxicity. Environ Health Perspect 1995, 103: 260-267
29. Reddy J, Chiga M, Svoboda D. Initiation of the division cycle of rat hepatocytes following a single injection of thioacetamide. Lab Invest 1969, 20: 405-411
30. Trennery PN, Waring RH. Early changes in thioacetamide-induced liver damage. Toxicol Lett 1983, 19: 299-307
31. LaBrecque DR, Ssteele G, Fogerty S, Wilson M, Barton J. Purification and physical-chemical characterization of hepatic stimulator substance. Hepatology 1988, 7: 100-106
32. LaBrecque DR, Bachur NR. Hepatic stimulator substance: Physicochemical characteristics and specificity. Am J Physiol 1982, 242: G281-G288
33. Estabrook R. Mitochondrial respiratory control and the polarographic measurement of ADP/O ratios. Methods Enzymol 1967, 10: 41-47
34. Salazar I, Pavani M, Aranda W, Maya JD, Morello A, Ferreira J. Alterations of rat liver mitochondrial oxidative phosphorylation and calcium uptake by benzo [a]pyrene. Toxicol Appl Pharmacol 2004, 198: 1-10
35. Zhang BH, Gong DZ, Mei MH. Protection of regenerating liver after partial hepatectomy from carbon tetrachloride hepatotoxicity in rats: Role of hepatic stimulator substance. J Gastroenterol Hepatol 1999; 14: 1010-1017
36. Ludwig B, Bender E, Arnold S, Huttemann M, Lee I, Kadenbach B. Cytochrome c oxidase and the regulation of oxidative phosphorylation. Chembiochem 2001, 2: 392-403
37. Wallace DC. Mitochondrial diseases in man and mouse. Science 1999, 283: 1482-1488
38. Beckman KB, Ames BN. The free radical theory of aging mitomatures. Physiol Rev 1998, 78: 547-581
39. Murphy MP, Robin A, Smith J. Drug delivery to mitochondria: The key to mitochondrial medicine. Adv Drug Deliv Rev 2000, 41: 235-250
40. Navarro A, del Pino MJS, Gómez C, Peralta JL, Boveris A. Behavioral dysfunction, brain oxidative stress, and impaired mitochondrial electron transfer in aging mice. Am J Physiol Regul Integr Comp Physiol 2002, 282: R985-R992
41. Ip SP, Ma CY, Che CT, Ko KM. Methylenedioxy group as determinant of schisandrin in enhancing hepatic mitochondrial glutathione in carbon tetrachloride-intoxicated mice. Biochem Pharmacol 1997, 54: 317-319
42. Tsai J, King K, Chang C, Wei Y. Changes of mitochondrial respiratory functions and superoxide dismutase activity during liver regeneration. Biochem Int 1992, 28: 205-217
43. Ahmad A, Pillai KK, Najmi AK, Ahmad SJ, Pal SN, Balani DK. Evaluation of hepatoprotective potential of jigrine post-treatment against thioacetamide induced hepatic damage. J Ethnopharmacol 2002, 79: 35-41
44. Bruck R, Aeed H, Avni Y, Shirin H, Matas Z, Shahmurov M, Avinoach I et al. Melatonin inhibits nuclear factor kappa B activation and oxidative stress and protects against thioacetamide-induced liver damage in rats. J Hepatol 2004, 40: 86-93
45. Bruck R, Aeed H, Shirin H, Matas Z, Zaidel L, Avni Y, Halpern Z. The hydroxyl radical scavengers dimethylsulfoxide and dimethylthiourea protect rats against thioacetamide-induced fulminant hepatic failure. J Hepatol 1999, 31: 27-38