Different role of Schisandrin B on mercury-induced renal damage in vivo and in vitro

Toxicology

Volumn 286, Issue 1-3, 2011, Pages 48-57

  Stacchiotti, Alessandra ^a   Li Volti, Giovanni ^b   Lavazza, Antonio ^c   Schena, Ilaria ^a   Aleo, Maria Francesca ^a   Rodella, Luigi Fabrizio ^a   Rezzani, Rita ^a  

^a UNIVERSITY OF BRESCIA   (Italy)

^b UNIVERSITY OF CATANIA   (Italy)

^c ISTITUTO ZOOPROFILATTICO SPERIMENTALE DELLA LOMBARDIA E DELL EMILIA ROMAGNA   (Italy)

Author keywords

Heat shock proteins; Kidney; Mercuric chloride; Nitric oxide synthase; NRK52E; Schisandrin B

Indexed keywords

BIOLOGICAL MARKER; CYTOCHROME C OXIDASE; ENDOTHELIAL NITRIC OXIDE SYNTHASE; GLUCOSE REGULATED PROTEIN 75; HEAT SHOCK PROTEIN; HEAT SHOCK PROTEIN 25; HEAT SHOCK PROTEIN 72; INDUCIBLE NITRIC OXIDE SYNTHASE; ISOPROTEIN; MERCURY; REACTIVE OXYGEN METABOLITE; SCHIZANDRIN B; UNCLASSIFIED DRUG;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; DRUG EFFICACY; GLOMERULUS; HISTOPATHOLOGY; IMMUNOHISTOCHEMISTRY; IN VITRO STUDY; IN VIVO STUDY; KIDNEY CORTEX; KIDNEY INJURY; KIDNEY TUBULE DAMAGE; MALE; MERCURIALISM; MITOCHONDRION; NEPHROTOXICITY; NONHUMAN; OXIDATIVE STRESS; PRIORITY JOURNAL; PROTEIN LOCALIZATION; RAT; RENAL PROTECTION;

ANIMALS; CELL LINE; CYCLOOCTANES; CYTOCHROMES C; DOSE-RESPONSE RELATIONSHIP, DRUG; HSP27 HEAT-SHOCK PROTEINS; HSP70 HEAT-SHOCK PROTEINS; HSP72 HEAT-SHOCK PROTEINS; KIDNEY CORTEX; KIDNEY DISEASES; KIDNEY TUBULES, PROXIMAL; LIGNANS; MALE; MEMBRANE PROTEINS; MERCURIC CHLORIDE; MITOCHONDRIA; NITRIC OXIDE SYNTHASE TYPE I; NITRIC OXIDE SYNTHASE TYPE III; OXIDATIVE STRESS; POLYCYCLIC COMPOUNDS; RATS; RATS, WISTAR;

RATTUS NORVEGICUS; SCHISANDRA CHINENSIS;

EID: 80955177119     PISSN: 0300483X     EISSN: 18793185     Source Type: Journal    
DOI: 10.1016/j.tox.2011.05.005     Document Type: Article

References (61)

1. Ahn J., Baik S., Ko M., Shin H., Chung H., Jeong H. Effects of mercuric chloride on gene expression in NRK52E cells. Genomics Inform. 2010, 8:50-57.
2. Ait-Aissa S., Porcher J., Arrigo A., Lambre C. Activation of the hsp70 promoter by environmental inorganic and organic chemicals: relationships with cytotoxicity and lipophilicity. Toxicology 2000, 145:147-157.
3. Arrigo A., Virot S., Chaufour S., Firdaus W., Kretz-Remy C., Diaz-Latoud C. HSP27 consolidates intracellular redox homeostasis by upholding glutathione in its reduced form and by decreasing iron intracellular levels. Antioxid. Redox Signal. 2005, 7:414-422.
4. Augusti P., Conterato G., Somacal S., Einsfeld l., Ramos A., Hosom Y., Graca D., Emanuelli T. Effect of lycopene on nephrotoxicity induced by mercuric chloride in rats. Basic Clin. Pharmacol. Toxicol. 2007, 100:398-402.
5. Bachmann M., Mundel P. Nitric oxide in the kidney: synthesis, localization, and function. Am. J. Kidney Dis. 1994, 24:112-129.
6. Bartosiewicz M., Jenkins D., Penn S., Emery J., Buckpitt A. Unique gene expression patterns in liver and kidney associated with exposure to chemical toxicants. J. Pharmacol. Exp. Ther. 2001, 297:895-905.
7. Capaldi R.A. Structure and assembly of cytochrome c oxidase. Arch. Biochem. Biophys. 1990, 280:252-262.
8. Chen N., Ko K.M. Schisandrin B-induced glutathione antioxidant response and cardioprotection are mediated by reactive oxidant species production in rat hearts. Biol. Pharm. Bull. 2010, 33:825-829.
9. Chiu P., Ko K. Schisandrin B-induced increase in cellular glutathione level and protection against oxidant injury are mediated by the enhancement of glutathione synthesis and regeneration in AML12 and H9C2 cells. Biofactors 2006, 26:221-230.
10. Chiu P., Mak D., Poon M., Ko K. Role of cytochrome P-450 in schisandrin B-induced antioxidant and heat shock responses in mouse liver. Life Sci. 2005, 77:2887-2895.
11. Chiu P., Leung H., Poon M., Ko K. Chronic schisandrin B treatments improves mitochondrial antioxidant status and tissue heat shock protein production in various tissues of young adult and middle-aged rats. Biogerontology 2006, 7:199-210.
12. 2+-induced mitochondrial permeability transition and mitochondrial membrane potential in H9c2 cardiomyocytes. Life Sci. 2008, 82:1092-1101.
13. Chiu P., Leung H., Ko K.M. Schisandrin B enhances renal mitochondrial antioxidant status, functional and structural integrity, and protects against gentamicin-induced nephrotoxicity in rats. Biol. Pharm. Bull. 2008, 31:602-605.
14. Clarkson T., Magos L., Myers G. The toxicology of mercury-current exposures and clinical manifestations. N. Engl. J. Med. 2003, 349:1731-1737.
15. Davidson P., Myers G., Weiss B. Mercury exposure and child development outcomes. Pediatrics 2004, 113:1023-1029.
16. El-Shenawy S., Hassan N. Comparative evaluation of the protective effect of selenium and garlic against liver and kidney damage induced by mercury chloride in the rats. Pharmacol. Rep. 2008, 60:199-208.
17. Girardi G., Saball D., Salvarrey M., Elias M. Glomerular compromise in mercuric chloride-induced nephrotoxicity. J. Biochem. Toxicol. 1996, 11:189-196.
18. Girolami J., Orfila C., Cabos-Boutot G., Pecher C., Bascands J., Colle A. Early acute effects of mercuric chloride on synthesis and release of kallikrein and on distal tubular morphology of rat renal cortical slices. Ren. Physiol. Biochem. 1990, 13:223-232.
19. Goering P.L., Fisher B.R., Noren B.T., Papaconstantinou A., Rojko J., Marler R. Mercury induces regional and cell-specific stress protein expression in rat kidney. Toxicol. Sci. 2000, 53:447-457.
20. Golpon H., Puchner A., Barth P., Wetle T., Wichert P., Feddersen C. Nitric oxide-dependent vasorelaxion and endothelial cell damage caused by mercuric chloride. Toxicology 2003, 192:179-188.
21. Guo S., Wharton W., Moseley P., Shi H. Heat shock protein 70 regulates cellular redox status by modulating glutathione-related enzyme activities. Cell Stress Chaperones 2007, 12:245-254.
22. Guo L., Hung T., Bae K., Shin E., Zhou H., Hong Y., Kang S., Kim H., Kim Y. Anti-inflammatory effects of schisandrin isolated from the fruit of Schisandra chinensis Baill. Eur. J. Pharmacol. 2008, 591:293-299.
23. Guzzi G., La Porta C. Molecular mechanisms triggered by mercury. Toxicology 2008, 244:1-12.
24. 2+ induced changes in cell volume. Cell Biochem. Biophys. 2008, 51:21-32.
25. Ko K.M., Chiu P.Y. Structural determinants of schisandrin B which enhance mitochondrial functional ability and glutathione status as well as heat shock protein expression in rat hearts and H9c2 cells. Mol. Cell. Biochem. 2005, 276:227-234.
26. Kovacs G., Komlosi P., Fuson A., Peti-Peterdi J., Rosivall L., Darwin Bell P. Neuronal nitric oxide synthase: its role and regulation in macula densa cells. J. Am. Soc. Nephrol. 2003, 14:2475-2483.
27. Kozma L., Lenkey A., Varga E., Gomba S. Induction of renin release from isolated glomeruli by inorganic mercury (II). Toxicol. Lett. 1996, 85:49-54.
28. Lash L.H. Cytoprotective systems within the kidney. Compr. Toxicol. 2010, 7:117-150.
29. Lash L., Putt D., Hueni S., Cao W., Xu F., Kulidjian S., Horwitz J. Cellular energetics and glutathione status in NRK52E cells: toxicological implications. Biochem. Pharmacol. 2002, 64:1533-1546.
30. Lash L., Putt D., Zalups R. Influence of compensatory renal growth on susceptibility of primary cultures of renal cells to chemically induced injury. Toxicol. Sci. 2006, 94:417-427.
31. Li Y., Gong M., Konishi T. Antioxidant synergism among component herbs of traditional chinese medicine formula, ShengMai San studied in vitro and in vivo. J. Health Sci. 2007, 53:692-699.
32. Lim K., Kim S., Noh J., Kim K., Jang W., Bae O., Chung S., Chung J. Low-level mercury can enhance procoagulant activity of erythrocytes: a new contributing factor for mercury-related thrombotic disease. Environ. Health Perspect. 2010, 118:928-935.
33. Liu R., Carretero O., Ren Y., Garvin J. Increased intracellular pH at the macula densa activates nNOS during tubuloglomerular feedback. Kidney Int. 2005, 67:1837-1843.
34. Liu W., Xu Z., Yang H., Deng Y., Xu B., Wei Y. The protective effects of tea polyphenols and Schisandrin B on nephrotoxicity of mercury. Biol. Trace Elem. Res. 2011, 10.1007/s12011-011-8996-y.
35. 2 formation and oxidative stress in vivo and in vitro in rat kidney mitochondria. Biochem. Pharmacol. 1993, 45:2017-2024.
36. Merzoug S., Toumi M., Oumeddour A., Boukhris N., Baudin B., Tahraoui A., Bairi A. Effect of inorganic mercury on biochemical parameters in Wistar rat. J. Cell Anim. Biol. 2009, 3:222-230.
37. Opletal L., Sovova H., Bartlova M. Dibenzo [a, c] cyclooctadiene lignans of the genus Schisandra: importance, isolation and determination. J. Chromatogr. B 2004, 812:357-371.
38. Park J.Y., Shin H., Lee Y., Choi Y., Bae S., Kim C. The mechanism of vasorelaxation induced by Schisandra chinensis. J. Ethnopharmacol. 2009, 121:69-73.
39. Piacenza F., Malavolta M., Cipriano C., Costarelli L., Giacconi R., Muti E., Tesei S., Pierpaoli S., Basso A., Bracci M., Bonacucina V., Santarelli L., Moccheggiani E. L-Arginine normalizes NOS activity and zinc-MT homeostasis in the kidney of mice chronically exposed to inorganic mercury. Toxicol. Lett. 2009, 189:200-205.
40. Ren Y., Garvin J., Liu R., Carretero O. Cross-talk between arterioles and tubules in the kidney. Pediatr. Nephrol. 2009, 24:31-35.
41. Rezzani R., Rodella L., Corsetti G., Bianchi R. Does methylene blue protect the kidney tissues from damage induced by cyclosporine A treatment?. Nephron 2001, 89:329-336.
42. Riordan M., Garg V., Thulin G., Kashgarian M., Siegel N. Differential inhibition of HSP72 and HSP25 produces profound impairment of cellular integrity. J. Am. Soc. Nephrol. 2004, 15:1557-1566.
43. Risher J., Amler S. Mercury exposure: evaluation and intervention: the inappropriate use of chelating agents in the diagnosis and treatment of putative mercury. NeuroToxicology 2005, 26:691-699.
44. Salonen J., Seppanen K., Lakka T., Salonen R., Kaplan G. Mercury accumulation and accelerated progression of carotid atherosclerosis: a population-based prospective 4-year follow-up study in men in eastern Finland. Atherosclerosis 2000, 148:265-273.
45. Sands J.M., Verlander W. Functional anatomy of the kidney. Compr. Toxicol. 2010, 7:1-22.
46. Sarwar Alam M., Kaur G., Jabbar Z., Javed K., Athar M. Eruca sativa seeds possess antioxidant activity and exert a protective effect on mercuric chloride induced renal toxicity. Food Chem. Toxicol. 2007, 45:910-920.
47. Sener G., Sehirli O., Tozan A., Velioglu-Ovunc A., Gedik N., Omurtag G. Ginkgo biloba extracts protects against mercury (II)-induced oxidative tissue damage in rats. Food Chem. Toxicol. 2007, 45:543-550.
48. Soti C., Csermely P. Protein stress and stress proteins: implications in aging and disease. J. Biosci. 2007, 32:511-515.
49. Stacchiotti A., Borsani E., Rodella L., Rezzani R., Bianchi R. Dose-dependent mercuric chloride tubular injury in rat kidney. Ultrastr. Pathol. 2003, 27:253-259.
50. Stacchiotti A., Lavazza A., Rezzani R., Borsani E., Rodella L., Bianchi R. Mercuric chloride-induced alterations in stress protein distribution in rat kidney. Histol. Histopathol. 2004, 19:1209-1218.
51. Stacchiotti A., Ricci F., Rezzani R., Li Volti G., Borsani E., Lavazza A., Bianchi R., Rodella L. Tubular stress proteins and nitric oxide synthase expression in rat kidney exposed to mercuric chloride and melatonin. J. Histochem. Cytochem. 2006, 54:1149-1157.
52. Stacchiotti A., Morandini F., Bettoni F., Schena I., Lavazza A., Grigolato P.G., Apostoli P., Rezzani R., Aleo M.F. Stress proteins and oxidative damage in a renal derived cell line exposed to inorganic mercury and lead. Toxicology 2009, 264:215-224.
53. Stacchiotti A., Li Volti G., Lavazza A., Rezzani R., Rodella L.F. Schisandrin B stimulates a cytoprotective response in rat liver exposed to mercuric chloride. Food Chem. Toxicol. 2009, 47:2834-2840.
54. 2+ channels. J. Cell Biol. 2006, 175:901-911.
55. Virtanen J.K., Rissanen T.H., Voutilainen S., Tuomainen T.P. Mercury as a risk factor for cardiovascular diseases. J. Nutr. Biochem. 2007, 18:75-85.
56. Wadhwa R., Taira K., Kaul S. An HSP70 family chaperone, mortalin/mthsp70/PBP74/Grp75: what, when, and where?. Cell Stress Chaperones 2002, 7:309-316.
57. Wiggers G., Stefanon I., Padilha A., Pecanha F., Vassallo D., Oliveira E. Low nanomolar concentration of mercury chloride increases vascular reactivity to phenylephrine and local angiotensin production in rats. Comp. Biochem. Physiol. Part C 2008, 147:252-260.
58. Wiggers G., Peçanha F., Briones A., Perez-Giron J., Miguel M., Vassallo D., Cachofeiro V., Alonso M., Salaices M. Low mercury concentrations cause oxidative stress and endothelial dysfunction in conductance and resistance arteries. Am. J. Physiol. Circ. Physiol. 2008, 295:H1033-H1043.
59. Yanagisawa H., Nodera M., Sato M., Moridaira K., Sato G., Wada O. Decreased expression of brain nitric oxide synthase in macula densa cells and glomerular epithelial cells of rats with mercury chloride-induced acute renal failure. Toxicol. Appl. Pharmacol. 2002, 184:165-171.
60. 2-induced acute renal failure. Toxicol. Lett. 1998, 98:181-188.
61. Zalups R.K. Renal handling and toxicity of mercury. Compr. Toxicol. 2010, 7:475-493.