Effects of Sotosaja-hwan on the Generation of ROS, RNS, and on the Expression of NF-${\kappa}B$-dependent Proteins in ob/ob Mouse

소도사자환이 ob/ob mouse에서 ROS/ RNS 생성 억제 및 NF-${\kappa}B$ 의존성 단백질에 미치는 영향

  • Bang, Yong-Suk (Dept. of Internal Medicine, College of Korean Medicine, Dongguk University) ;
  • Jeong, Ji-Cheon (Dept. of Internal Medicine, College of Korean Medicine, Dongguk University)
  • 방용석 (동국대학교 한의과대학 내과학교실) ;
  • 정지천 (동국대학교 한의과대학 내과학교실)
  • Published : 2009.01.30

Abstract

Objectives: Peroxynitrite ($ONOO^-$), superoxide anion radical (${\cdot}{O_2}^-$ and nitric oxide (NO) are cytotoxic because they can oxidize several cellular components such as proteins, lipids and DNA. They have been implicated in the aging processes, and age-related diseases such as Alzheimer's disease, rheumatoid arthritis, cancer, diabetes, obesity and atherosclerosis. The aim of this study was to investigate the $ONOO^-$, NO, ${\cdot}{O_2}^-$ scavenging and NF-${\kappa}B$ related anti-inflammatory activities of Sotosaja-hwan in ob/ob mice. Methods: Mice were grouped and treated for 5 weeks as follows. Both the normal lean (C57/BL6J black mice) and control obese (ob/ob mice) groups have received standard chow. The experimental groups were fed with a diet of chow supplemented with 30 and 90 mg Sotosaja-hwan per 1 kg of body weight for 14 days. For this study, the fluorescent probes, namely 2',7'-dichlorodihydrofluorescein diacetate (DCFDA), 4,5-diaminofluorescein (DAF-2) and dihydrorhodamine 123 (DHR 123) were used. Western blotting was performed using anti-phospho-$I{\kappa}B$-${\alpha}$, anti-IKK-${\alpha}$, anti-NF-${\kappa}B$ (p50, p65), anti-COX-2, anti-iNOS, anti-YCAM-1 and anti-MMP-9 antibodies, respectively. Results: Sotosaja-hwan inhibited the generation of $ONOO^-$, NO and ${\cdot}{O_2}^-$ in the lipopolysaccharide (LPS)-treated mouse kidney postmitochondrial fraction in vitro. The generation of $ONOO^-$, NO, ${\cdot}{O_2}^-$ and PGE2 were inhibited in the Sotosaja-hwan-administered ob/ob mice groups. The GSH/GSSG ratio was decreased in the ob/ob mice, whereas the ratio was improved in the Sotosaja-hwan-administered groups. Sotosaja-hwan inhibited the protein expression levels of phospho-$I{\kappa}B$-${\alpha}$, IKK-${\alpha}$, NF-${\kappa}B$ (p50, p65), COX-2, iNOS, YCAM-1 and MMP-9 genes. Conclusions: These results suggest that Sotosaja-hwan is an effective $ONOO^-$, ${\cdot}{O_2}^-$ and NO scavenger and has NF-kB related anti-inflammatory activity in ob/ob mice. Therefore, Sotosaja-hwan might be a potential therapeutic drug against the inflammation process and inflammation-related diseases.

Keywords

References

  1. Chung HY, Kim HJ, Jung KJ, Yoon JS, Yoo MA, Kim KW, Yu BP. The inflammatory process in aging. Reviews in Clinical Gerontology. 2000;10:207-22. https://doi.org/10.1017/S0959259800010327
  2. Chung HY, Kim HJ, and Kim JW. The inflammation hypothesis of aging : Molecular modulation by calorie restriction. Ann. N. Y. Acad. Sci. 2001;928:327-35. https://doi.org/10.1111/j.1749-6632.2001.tb05662.x
  3. Kim HJ, Kim KW, Yu BP, Chung HY. The effect of age on cyclooxygenase-2 gene expression : $NF-_{\kappa}B$ activation and IκBα degradation. Free Radical Biol Med. 2000;28:683-92. https://doi.org/10.1016/S0891-5849(99)00274-9
  4. Collins T. Endotherial nuclear factor-kappa B and the initiation of the atherosclerotic lesion. Lab Invest 1993:68:499-508.
  5. Chung HY, Kim HJ, Shim KH, Kim KW. Dietary modulation of prostanoid synthesis in the aging process : role of cyclooxygenase-2. Mech Ageing Dev. 1999;111:97-106. https://doi.org/10.1016/S0047-6374(99)00061-5
  6. Luo SF, Wang CC, Chien CS, Hsiao LD, Yang CM, Induction of cyclooxygenase-2 by lipopolysaccharide in canine tracheal smooth muscle cells : involvement of p42/p44 and p38 mitogen-activated protein kinases and nuclear factor-kappa B pathways. Cell Signal. 2003;15:497-509. https://doi.org/10.1016/S0898-6568(02)00135-3
  7. Korhonen P, Helenius M, Salminen A. Age-related changes in the regulation of transcription factor NF-kappa B in rat brain. Neurosci Lett. 1997;225:61-4. https://doi.org/10.1016/S0304-3940(97)00190-0
  8. Ghosh S, May MJ, Kopp EB. $NF-_{\kappa}B$ and Rel proteins : Evolutionarity conserved mediators of immune responses. Annu Rev Immunol. 1998;16:225-60. https://doi.org/10.1146/annurev.immunol.16.1.225
  9. Halushka PV, Mais DE, Mayeux PR and Morinelli TA. Thromboxane, prostaglandin and leukotriene receptors. Annu Rev Pharmacol Toxicol. 1989;29;213-39. https://doi.org/10.1146/annurev.pa.29.040189.001241
  10. Martel-Pelletier J, Pelletier JP, Fahmi H. Cyclooxygenase-2 and prostaglandins in articular tissues. Semin Arthritis Rheum. 2003;33(3);155-67. https://doi.org/10.1016/S0049-0172(03)00134-3
  11. 陳師文 등 編. 太平惠民和劑局方. 臺北:旋風出版社. 1985:(卷五)10.
  12. 失震亨. 丹溪心法. 北京:北京市中國書店. 1986:221.
  13. 王毅, 靳長金 失君波 編著. 益壽效方 120. 北京:中國醫藥科技出版社. 1989:52-3.
  14. Kooy NW, Royall JA, Ischiropoulos H, Beckman JS. Peroxynitrite-mediated oxidation of dihydrorhodamine 123. Free Radic Res Commun. 1994;16:149-56.
  15. Nagata N, Momose K, Ishida Y. Inhibitory effects of catecholamines and anti-oxidants on the fluorescence reaction of 4,5-diaminofluorescein, DAF-2, a novel indicator of nitric oxide. J Biochem Tokyo. 1999;125:658-61. https://doi.org/10.1093/oxfordjournals.jbchem.a022333
  16. Cathcart R, Schwiers E, Ames BN. Detection of picomole levels of hydroperoxides using a fluorescent dichlorofluorescein fluorescent assay. Anal Biochem. 1983;134:111-6. https://doi.org/10.1016/0003-2697(83)90270-1
  17. Gaitonide MK. A spectrophotometric method for the direct determination of cystein in the presense of other naturally occuring amino acid. Biochem. J. 1967;104:627.
  18. Lowry OH, Rosebrough NJ, Farr AL, Randall RJ. Protein measurement with folin phenol reagent. J Biol Chem. 1951;193:265-75.
  19. Maziere C, Auclair M, Djavaheri-Mergny M, Packer L, Maziere JC. Oxidized low density lipoprotein induces activation of the transcription factor $NF-{\kappa}B$ in fibroblasts, endothelial and smooth muscle cells. Biochem Mol Biol Int. 1996;39:1201-7.
  20. Kranzhofer R, Schmidt J, Pfeiffer CA, Hagl S, Libby P, Kubler W. Angiotensin induces inflammatory activation of human vascular smooth muscle cells. Arterioscler Thromb Vasc Biol. 1999;19:1623-9. https://doi.org/10.1161/01.ATV.19.7.1623
  21. Mordes JP and Rossini AA. Animal models of diabetes mellitus. Am J Med. 1981;70(2):353-60. https://doi.org/10.1016/0002-9343(81)90772-5
  22. Eleazar S. Animal models of non-insulin-dependent diabetes. Diabetes metabolism reviews. 1992;8(3):179-208. https://doi.org/10.1002/dmr.5610080302
  23. Cai H, Harrison DG. Endothelial dysfunction in cardiovascular diseases ; the role of oxidant stress. Circ Res. 2000;87:840-4. https://doi.org/10.1161/01.RES.87.10.840
  24. Matsubara T, Ziff M. Increased syperoxide anion release from human endothelial cells in response to cytokines. J Immunol. 1986;137:3295-8.
  25. Vendemiale G, Altomare E, Grattagliano I, Albano O. Increased plasma levels of glutathione and malondialdehyde after avute ethanol ingestion in humans. J hepatol. 1989;9:359. https://doi.org/10.1016/0168-8278(89)90146-3
  26. Chung HY, Soung DY, Kim AR, Choi HR, Kim HJ, Choi JS, Yang R, Lee KH and Yu BP. Generation, Toxicity and Scavenging of ONOO : Its Involvement in the Aging Process. Kor J Gerontol. 2000;10:46-59.
  27. Groszmann RJ. Hyperdynamic state in chronic liver disease. J Hepatol. 1993;17(2): S38-40.
  28. Tsujii M, Kawano S, Tsuji S, Sawaoka H, Hori M, DuBois RN. Cyclooxygenase regulates angiogenesis induced by colon cancer cells. Cell. 1998;93(5):705-16. https://doi.org/10.1016/S0092-8674(00)81433-6
  29. Chung HY, Kim HJ, Kim KW, Chio JS, Yu BP. Molecular inflammation hypothesis of aging based on the anti-aging mechanism of calorie restriction. Micro Res Techinq. 2002;59:264-72. https://doi.org/10.1002/jemt.10203
  30. Fries JWU, Williams AJ, Atkins RC, Neman W, Lipscomb MF, Collins T. Expression of VCAM-1 and E-selectin in an in vivo model of endothelial activation. Am J Pathol. 1993;143:725-37.
  31. Baran D, Vendeville B, Ogborn M, Katz N. Cell adhesion molecule expression in murine lupuslike nephritis induced by lipopolysaccharide. Nephron. 2000;84:167-76. https://doi.org/10.1159/000045565
  32. Lakshminarayanan V, Beno DW, Costa RH, Roebuck KA. Differential regulation of interleukine-8 and intercellular adhesion molecule-1 by $H_2O_2$ and tumor necrosis factor-alpha in endothelial and epithelial cells. J Biol Chem. 1997;272(52):32910-8. https://doi.org/10.1074/jbc.272.52.32910
  33. Woessner JF and Nagase H. Matrix metalloproteinases and Timps. Oxford:Oxford university Press. 2000:1-10.
  34. McCawley LJ and Metrisian LM. Matrix metalloproteinases : They're not just for matrix anymore! Curr Opin Cell Biol. 2001:13(5):534-40. https://doi.org/10.1016/S0955-0674(00)00248-9
  35. Liu KJ, Rosenberg GA. Matrix metalloproteinases and free radicals in cerebral ischemia. Free Radic Biol Med. 2005;39:71-80. https://doi.org/10.1016/j.freeradbiomed.2005.03.033