Nephroprotective Effect of Pentoxyphylline Through Improvement in the Expression of TGF-beta1, Collagen Type-1, and Renal Interstitial Fibrosis in Swiss Strain Mice After Being Induced by Doxorubicin
Abstract
BACKGROUND: Use of doxorubicin (DXR) in the treatment of cancer has been increasing along with the increase in cancer morbidity. Nephrotoxic effects of DXR are still a problem. Pentoxyphylline (PTX) as an electron-donor material can be nephroprotective, so the combination of DXR and PTX might reduce the nephrotoxic effects of DXR. The aim of this study was to prove the nephroprotective effect of PTX and DXR nephrotoxicity through the improvement of TGF-β1, collage type-1, and renal interstitial fibrosis.
METHODS: Twenty-four males Swiss strain mice, divided into three groups namely Control (C) injected with NaCl 0.9%; DXR induced nephrotoxicity (D); and effect of PTX on D (P/D) by intraperitoneally, respectively, each group consisted of 8 mice. Injections were given once a week for three consecutive weeks. At 8th week post-treatment, all eight mice of each group were sacrificed. Examination of TGF-β1 and collagen type-I expression was done by immunohistochemistry with monoclonal antibody. Renal interstitial fibrosis examination was done by a histopathologist, using Verheoff van Giesen staining. The statistic analysis was carried out using one-way ANOVA.
RESULTS: TGF-β1 expression increased from C to D and subsequently decreased in P/D (4.50±3.89 vs. 177.88±68.78 vs. 36.88±9.51). Collagen type-I expression increased from C to D and subsequently decreased in P/D (12.00±14.32 vs. 186.25±125.62 vs. 36.00±29.14). Renal interstitial fibrosis expression increased from C to D and subsequently decreased in P/D (16.75±6.14 vs. 85.00±7.33 vs. 60.50±11.40). The expression of TGF-β1, collagen type-1, and renal interstitial fibrosis were higher significantly in D group as compared to C group (p<0,001). The expression of TGF-β1, collagen type-1, and renal interstitial fibrosis were lower significantly in P/D group as compared to D group (p<0.005).
CONCLUSIONS: PTX was proved to be nephroprotector inducing by DXR.
KEYWORDS: PTX, nephroprotector, TGF-β1, collagen type-I, renal interstitial fibrosis
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Lin SL, Chen YM, Chien CT, Chiang WC, Tsai CC, Tsai TJ. Pentoxyphylline attenuated the renal disease progression in rats with remnant kidney. J Am Soc Nephrol. 2002; 13: 2916-29, CrossRef.
World Health Organization. Geneva: Cancer; [n.y] [cited 2010 Februari 12]. Available from: http://www.who.int/cancer.
Wang Y, Wang YP. Role of CD 8th cells in the progression of murine adiramycin neprhropaty. Kidney International. 2001; 59: 941-9, CrossRef.
Erlan JF, Desmant. Transfers of ferritin-bound iron to andriamicyn. FEBS letters. 2001; 176: 97-100, CrossRef.
Epstein FH, Blobe GC, Schiemann WP, Lodish HF. Role of transforming growth factor ß in human Disease. N Engl J Med. 2000; 343: 1350-8, CrossRef.
Tamaki K, Seiya O, Takashi A. TGF-β in glomerulosklerosis and interstitial fibrosis, of andriamicyn neprhopaty. Kidney International. 1994; 45: 525 -36, CrossRef.
Suryohudoyo P. Oxidant, Anti-oxidant and Free Radical (Oksidan, Anti-okisdan dan Radikal Bebas). Jakarta: CV Agung Seto; 2000.
Kupsakova, Docolomansky P, Ryber M, Brier A. Carbonyl group of aliphatic side chain on pentoxyphylline does not play role for P.glycoprotein antagonizing effect of pentoxyphylline. Gen Physol Biophys. 2002; 21: 471-8, PMID.
Mayes PA. Structure and function of lipofilic vitamin. In: Robert K, Granner DK, Mayes PA, Rodw M. Harper's Biochemistry. 26th ed. New York: McGraw-Hill; 2003. p.613-22, NLMID.
Davila ME, Esqueda, Martinez F, Morales. Pentoxyphylline diminshes the oxidative damage to renal tissue induced shreptotozocin in rat. Experimental Diab Res. 2004; 5: 245-51, CrossRef.
David D, Abbe S. Protective effect of recombinant human interlukin-1α in doxorubicin treated normal and tumor bearing mice. Cancer Research.1993; S3:1565-70, PMID.
Belloc F, Dumani P. Effect of pentoxyphylline on apoptosis of cultural cells. J.Cardiovase Pharmacal.1995; 25: S71-4, CrossRef.
Guntur AH. SIRS and SEPSIS: Immunology, Diagnosis, and Management (SIRS dan SEPSIS: Imunologi, Diagnosis, Penatalaksanaan). Surakarta: Sebelas Maret University Press; 2006.
Onat A, Can G, Hergenç G, Yazıcı M, Karabulut A, Albayrak S. Serum apolipoprotein B predicts dyslipidemia, metabolic syndrome and, in women, hypertension and diabetes, independent of markers of central obesity and inflammation. International Journal of Obesity. 2007; 31: 1119-25, CrossRef.
Sakai N, Uchida Y, Ohashi K, Hibuse T, Saika Y, Tomari Y, et al. Measurement of fasting serum apoB-48 levels in normolipidemic and hyperlipidemic subjects by ELISA. Journal of Lipid Research. 2003; 44: 1256-62, CrossRef.
Baratawidjaja KG, Iris R. Basic Immunology (Imunologi Dasar). 8th Ed. Jakarta: University of Indonesia; 2009.
Koli K, Saharinen J, Hyytiainen M, Penttinen C, Keski-Oja J. Latency, activation, and binding proteins of TGF-beta. Microsc Res Tech. 2001; 52: 354-62, CrossRef.
Wang W, Koka V, Lan HY. Transforming growth factor-beta and Smad signalling in kidney diseases. Nephrology. 2005; 10: 48-56, CrossRef.
Gameson R, Reeves WB. TNF-α mediates chemokine and sitokine expression and renal injury in cesplation nephrotoxcity. J Clin Invest. 2007; 110: 835-42, CrossRef.
Xiong LJ, Zhu JF, Luo DD, Zen LL, Cai SQ. Effects of pentoxyphylline on the hepatic content of TGF-b1 and collagen in Schistosomiasis japonica mice with liver fibrosis. World J Gastroenterol. 2003; 9: 152-4, PMID.
Fang CC, Lai MN, Chien CT, Hung KY, Tsai CC, Tsai TJ, et al. Effects of pentoxyphylline on peritoneal fibroblasts and silica-induced peritoneal fibrosis. Peritoneal Dialysis International. 2003; 23: 228-36, PMID.
Strutz F, Heeg M, Kochsiek T, Siemers G, Zeisberg M, Muller GA. Effects of pentoxyphylline, pentiphylline and gamma-interferon on proliferation, differentiation, and matrix synthesis of human renal fibroblasts. Nephrol Dial Transplant. 2000; 15: 1535-46, CrossRef.
Li J, Campanale NV, Liang RJ, Deane JA, Bertram JF, Ricardo SD. Inhibition of p38 mitogen-activated protein kinase and transforming growth factor-β1/smad signaling pathways modulates the development of fibrosis in adriamycin-induced nephropathy. Am J Pathol. 2006; 169: 1527-40, CrossRef.
DOI: https://doi.org/10.18585/inabj.v2i2.119
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