Nephroprotective Effects of Manjeonmoktong-san on Cisplatin-induced Rat Acute Renal Failure

만전목통산(萬全木通散)이 Cisplatin으로 유발(誘發)된 흰쥐의 급성신부전(急性腎不全)에 미치는 영향(影響)

  • Kim, Do-Nyeon (Dept. of Oriental Internal Medicine Graduate School, Deagu Haany University) ;
  • Yoon, Gyeong-Min (Dept. of Oriental Internal Medicine Graduate School, Deagu Haany University) ;
  • Shin, Hyeon-Chul (Dept. of Oriental Internal Medicine Graduate School, Deagu Haany University) ;
  • Kang, Seok-Bong (Dept. of Oriental Internal Medicine Graduate School, Deagu Haany University)
  • 김도년 (대구한의대학교 부속한방병원 신계내과학교실) ;
  • 윤경민 (대구한의대학교 부속한방병원 신계내과학교실) ;
  • 신현철 (대구한의대학교 부속한방병원 신계내과학교실) ;
  • 강석봉 (대구한의대학교 부속한방병원 신계내과학교실)
  • Published : 2010.09.30

Abstract

Purpose : The object of this study was to observe the nephroprotective effects of Manjeonmoktong-san(MJMTS), which has traditionally been used as Korean medicine for treating various renal diseases, on cisplatin-induced rat acute renal failure. Methods : At first, three different dosages of MJMTS extract were orally administered once a day for 28 days. On the 23rd day after MJMTS extract treatment, cisplatin was treated. Then, 5 days after cisplatin treatment, all the rats (6 groups of 8 rats each) were checked in the present study. The changes to the body weight, kidney weight, serum BUN and creatinine levels were observed with changes on the kidney MDA and GSH contents. The results were compared with captopril 100mg/kg in which the effects on cisplatin-induced acute renal failures were already confirmed. Results : It showed dramatical decrease on the body weight, increase of serum BUN and creatinine levels were detected in cisplatin control as compared with intact control. In addition marked increase of kidney MDA contests and decrease of kidney GSH contents were also detected in cisplatin control as compared with intact control. it means that cisplatin induced ARF are induced by oxiidative stress and related lipid peroxidation in the present study. However, these ARFs and inhibition of antioxidant effects induced by cisplatin were dose-dependently reduced by treatment of all three different dosages of MJMTS extracts. Conclusion : This study suggests that MJMTS extracts have favorable effects on the cisplatin-induced rat ARF.

Keywords

References

  1. 대한비뇨기과학회.비뇨기과학 3판. 서울: 고려의학출판사; 2001, p. 91-2.
  2. Fischereder M. Trick W, Nath KA. Therapeutic strategies in the prevention of acute renal failure. Semin Nephrol. 1994;14:41-52.
  3. 李梴. 編註醫學入門3권. 서울: 고려의학출판사; 1989, p. 341.
  4. 우성순. 萬全木通散水性엑기스가 개의 신장기능에 미치는 영향. 圓光大大學院. 碩士學位論文. 1982;1-20.
  5. Safirstein R, Winston J, Goldstein M, Moel D, Dikman S, Guttenplan J. Cisplatin nephrotoxicity. Am J Kidney Dis. 1986;8:356-67. https://doi.org/10.1016/S0272-6386(86)80111-1
  6. Lippman AJ, Helson C, Helson L, Krakoff IH. Clinical trials of cis-diamminedichloroplatinum (NSC-119875). Cancer Chemother Rep. 1973;57 :191-200.
  7. Gordon JA, Peterson LN, Anderson RJ. Water metabolism after cisplatin in the rat. Am J Physiol. 1982;243:F36-43.
  8. Seguro AC, Shimizu MH, Kudo LH, dos Santos Rocha A. Renal concentration defect induced by cisplatin. The role of thick ascending limb and papillary collecting duct. Am J Nephrol. 1989;9 :59-65. https://doi.org/10.1159/000167938
  9. Wong NL, Walker VR, Wong EF, Sutton RA. Mechanism of polyuria after cisplatin therapy. Nephron. 1993;65:623-7. https://doi.org/10.1159/000187575
  10. Kavutcu M, Canbolat O, Ozturk S, Olcay E, Ulutepe S, Ekinci C, Gokhun IH, Durak I. Reduced enzymatic antioxidant defense mechanism in kidney tissues from gentamicin-treated guinea pigs: effects of vitamins E, C. Nephron. 1996;72 :269-74. https://doi.org/10.1159/000188853
  11. Lowry OH, Rosenbrough NJ, Farr AL, Randall RJ. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951;193:265-75.
  12. Dahle LK, Hill EG, Holman RT. The thiobarbituric acid reaction and the autoxidations of polyunsaturated fatty acid methyl esters. Arch Biochem Biophys. 1962;98:221-53.
  13. Eyer P, Podhradsky D. Evaluation of the micromethod for determination of glutathione using enzymatic cycling and Ellman's reagent. Anal Biochem. 1986;153:57-66. https://doi.org/10.1016/0003-2697(86)90061-8
  14. Salahudeen A, Badr K, Morrow J, Roberts J. Hydrogen peroxide induces 21-aminosteroidinhibitable F2-isoprostane production and cytolysis in renal tubular epithelial cells. J Am Soc Nephrol. 1995;6:1300-3.
  15. Lieberthal W, Triaca V, Levine J. Mechanisms of death induced by cisplatin in proximal tubular epithelial cells: apoptosis vs. necrosis. Am J Physiol. 1996;270:F700-8.
  16. Masuda H, Tanaka T, Takahama U. Cisplatin generates superoxide anion by interaction with DNA in a cell-free system. Biochem Biophys Res Commun. 1994;203:1175-80. https://doi.org/10.1006/bbrc.1994.2306
  17. Kuhlmann MK, Burkhardt G, Köhler H. Insights into potential cellular mechanisms of cisplatin nephrotoxicity and their clinical application. Nephrol Dial Transplant. 1997;12:2478-80. https://doi.org/10.1093/ndt/12.12.2478
  18. Davis CA, Nick HS, Agarwal A. Manganese superoxide dismutase attenuates Cisplatin-induced renal injury: importance of superoxide. J Am Soc Nephrol. 2001;12:2683-90.
  19. Cetin R, Devrim E, Kilicoglu B, Avci A, Candir O, Durak I. Cisplatin impairs antioxidant system and causes oxidation in rat kidney tissues: possible protective roles of natural antioxidant foods. J Appl Toxicol. 2006;26:42-6. https://doi.org/10.1002/jat.1103
  20. Ahn H, Lee E, Kim K, Lee C. Effect of glutathione and its related enzymes on chemosensitivity of renal cell carcinoma and bladder carcinoma cell lines. J Urol. 1994;151 :263-7. https://doi.org/10.1016/S0022-5347(17)34929-7
  21. Baldew GS, McVie JG, van der Valk MA, Los G, de Goeij JJ, Vermeulen NP. Selective reduction of cis-diamminedichloroplatinum(II) nephrotoxicity by ebselen. Cancer Res. 1990;50:7031-6.
  22. Suzuki CA, Cherian MG. The interactions of cis-diamminedichloroplatinum with metallothionein and glutathione in rat liver and kidney. Toxicology. 1990;64:113-27. https://doi.org/10.1016/0300-483X(90)90129-5
  23. Kang DG, Lee AS, Mun YJ, Woo WH, Kim YC, Sohn EJ, Moon MK, Lee HS. Butein ameliorates renal concentrating ability in cisplatin-induced acute renal failure in rats. Biol Pharm Bull. 2004;27:366-70. https://doi.org/10.1248/bpb.27.366
  24. Karimi G, Ramezani M, Tahoonian Z. Cisplatin nephrotoxicity and protection by milk thistle extract in rats. Evid Based Complement Alternat Med. 2005;2:383-6. https://doi.org/10.1093/ecam/neh103
  25. Shimeda Y, Hirotani Y, Akimoto Y, Shindou K, Ijiri Y, Nishihori T, Tanaka K. Protective effects of capsaicin against cisplatin-induced nephrotoxicity in rats. Biol Pharm Bull. 2005; 28:1635-8. https://doi.org/10.1248/bpb.28.1635
  26. Sakemi T, Baba N. Effects of antihypertensive drugs on the progress of renal failure in hyperlipidemic Imai rats. Nephron. 1993;63:323-9. https://doi.org/10.1159/000187217
  27. Krishan P, Sharma A, Singh M. Effect of angiotensin converting enzyme inhibitors on ischaemia-reperfusion-induced renal injury in rats. Pharmacol Res. 1998;37:23-9. https://doi.org/10.1006/phrs.1997.0259
  28. Durmus A, Dogan E, Erkoc R, Sayarlioglu H, Topal C, Dilek I. Effect of valsartan on erythropoietin and hemoglobin levels in stage III-IV chronic kidney disease patients. Int J Clin Pract. 2005;59:1001-4. https://doi.org/10.1111/j.1742-1241.2005.00606.x
  29. El-Sayed el-SM, Abd-Ellah MF, Attia SM. Protective effect of captopril against Cisplatin -induced nephrotoxicity in rats. Pak J Pharm Sci. 2008;21:255-61.
  30. Latha PG, Panikkar KR. Chemoprotective effect of Ixora coccinea L. flowers on cisplatin induced toxicity in mice. Phytother Res. 2001 ;15:364-6. https://doi.org/10.1002/ptr.727
  31. Yatsu T, Aoki M, Inagaki O. Preventive effect of zelandopam, a dopamine D1 receptor agonist, on cisplatin-induced acute renal failure in rats. Eur J Pharmacol. 2003;461:191-5. https://doi.org/10.1016/S0014-2999(03)01305-0
  32. Saleh S, El-Demerdash E. Protective effects of L-arginine against cisplatin-induced renal oxidative stress and toxicity: role of nitric oxide. Basic Clin Pharmacol Toxicol. 2005;97:91-7. https://doi.org/10.1111/j.1742-7843.2005.pto_114.x
  33. Mansour MA, Mostafa AM, Nagi MN, Khattab MM, Al-Shabanah OA. Protective effect of aminoguanidine against nephrotoxicity induced by cisplatin in normal rats. Comp Biochem Physiol C Toxicol Pharmacol. 2002;132:123-8. https://doi.org/10.1016/S1532-0456(02)00062-5
  34. Shirwaikar A, Malini S, Kumari SC. Protective effect of Pongamia pinnata flowers against cisplatin and gentamicininduced nephrotoxicity in rats. Indian J Exp Biol. 2003;41:58-62.
  35. Sodikoff CH. Laboratory profiles of small animal diseases. A guide to laboratory diagnosis. 2nd ed., Mosby: St. Louise, 1995:1-36.
  36. Kim YK, Choi TR, Kwon CH, Kim JH, Woo JS, Jung JS. Beneficial effect of pentoxifylline on cisplatin-induced acute renal failure in rabbits. Ren Fail. 2003;25:909-22. https://doi.org/10.1081/JDI-120026026
  37. Nishida M, Fujimoto S, Toiyama K, Sato H, Hamaoka K. Effect of hematopoietic cytokines on renal function in cisplatin-induced ARF in mice. Biochem Biophys Res Commun. 2004;324 :341-7. https://doi.org/10.1016/j.bbrc.2004.09.051
  38. Ramesh G, Reeves WB. p38 MAP kinase inhibition ameliorates cisplatin nephrotoxicity in mice. Am J Physiol Renal Physiol. 2005;289:F166-74. https://doi.org/10.1152/ajprenal.00401.2004
  39. Satoh M, Kashihara N, Fujimoto S, Horike H, Tokura T, Namikoshi T, Sasaki T, Makino H. A novel free radical scavenger, edarabone, protects against cisplatin-induced acute renal damage in vitro and in vivo. J Pharmacol Exp Ther. 2003;305:1183-90. https://doi.org/10.1124/jpet.102.047522
  40. Jung HJ, Lee CO, Lee KT, Choi J, Park HJ. Structure-activity relationship of oleanane disaccharides isolated from Akebia quinata versus cytotoxicity against cancer cells and NO inhibition. Biol Pharm Bull. 2004;27:744-7. https://doi.org/10.1248/bpb.27.744
  41. Schinella GR, Tournier HA, Prieto JM, Mordujovich de Buschiazzo P, Rios JL. Antioxidant activity of anti-inflammatory plant extracts. Life Sci. 2002;70:1023-33. https://doi.org/10.1016/S0024-3205(01)01482-5
  42. Park BG, Lee HS, Jung SH, Hong CO, Won HJ, Park HY, Ryu YS, Lee SJ, Kim KH, Park KW, Lee KW. A 90 day repeated oral toxicity study on plantamajoside concentrate from Plantago asiatica. Phytother Res. 2007;21 :1118-23. https://doi.org/10.1002/ptr.2217
  43. Joannidis M. Medical therapy of acute kidney injury. Acta Clin Belg Suppl. 2007;9(1):353-6.
  44. Choi J, Jung HJ, Lee KT, Park HJ. Antinociceptive and anti-inflammatory effects of the saponin and sapogenins obtained from the stem of Akebia quinata. J Med Food. 2005;8:78-85. https://doi.org/10.1089/jmf.2005.8.78
  45. Yasukawa K, Kaminaga T, Kitanaka S, Tai T, Nunoura Y, Natori S, Takido M. 3 beta-phydroxybenzoyldehydrotumulosic acid from Poria cocos, and its anti-inflammatory effect. Phytochemistry. 1998;48:1357-60. https://doi.org/10.1016/S0031-9422(97)01063-7
  46. Murai M, Tamayama Y, Nishibe S. Phenylethanoids in the herb of Plantago lanceolata and inhibitory effect on arachidonic acid-induced mouse ear edema. Planta Med. 1995;61:479-80. https://doi.org/10.1055/s-2006-958143