Skip to main content
Top
Published in: Clinical and Experimental Nephrology 2/2015

01-04-2015 | Original Article

Nephroprotective effect of catechin on gentamicin-induced experimental nephrotoxicity

Authors: Ankush Sardana, Sanjeev Kalra, Deepa Khanna, Pitchai Balakumar

Published in: Clinical and Experimental Nephrology | Issue 2/2015

Login to get access

Abstract

Background

Gentamicin is an effective aminoglycoside antibiotic employed against severe Gram-negative bacterial infections, but induction of nephrotoxicity limits its frequent clinical use. This study was undertaken to investigate the effect of catechin hydrate on gentamicin-induced nephrotoxicity in rats.

Methods

Rats were administered nephrotoxic dose of gentamicin (100 mg/kg/day, i.p.) once daily for 14 days. Gentamicin-administered rats were treated with catechin hydrate (50 mg/kg/day, per os), the treatment was started 3 days before the administration of gentamicin while it was continued for 14 days from the day of gentamicin administration.

Results

Two weeks administration of gentamicin significantly increased the serum creatinine and blood urea nitrogen levels. Renal histopathological examination of gentamicin-administered rats revealed degenerative changes in glomeruli and tubules after 2 weeks. These renal structural and functional abnormalities in gentamicin-administered rats were accompanied with renal oxidative stress as assessed in terms of marked decrease in renal-reduced glutathione (GSH). However, catechin hydrate treatment showed considerably nephroprotective action against gentamicin-induced nephrotoxicity in rats by preventing aforementioned renal structural and functional abnormalities and oxidative stress.

Conclusion

Catechin hydrate has a potential to prevent gentamicin-induced experimental nephrotoxicity. The renoprotective effect of catechin hydrate against gentamicin-induced nephrotoxicity might be mediated through its antioxidant and possible direct nephroprotective actions.
Literature
1.
go back to reference Pokrovskaya V, Nudelman I, Kandasamy J, Baasov T. Aminoglycosides redesign strategies for improved antibiotics and compounds for treatment of human genetic diseases. Methods Enzymol. 2010;478:437–62.CrossRefPubMed Pokrovskaya V, Nudelman I, Kandasamy J, Baasov T. Aminoglycosides redesign strategies for improved antibiotics and compounds for treatment of human genetic diseases. Methods Enzymol. 2010;478:437–62.CrossRefPubMed
2.
go back to reference Begg EJ, Barclay ML. Aminoglycosides—50 years on. Br J ClinPharmacol. 1995;39:597–603. Begg EJ, Barclay ML. Aminoglycosides—50 years on. Br J ClinPharmacol. 1995;39:597–603.
4.
go back to reference Khoory BJ, Fanos V, Dall’Agnola A, Cataldi L. Aminoglycosides, risk factors and neonatal kidney. Pediatr Med Chir. 1996;18:495–9.PubMed Khoory BJ, Fanos V, Dall’Agnola A, Cataldi L. Aminoglycosides, risk factors and neonatal kidney. Pediatr Med Chir. 1996;18:495–9.PubMed
5.
go back to reference Martínez-Salgado C, López-Hernández FJ, LópezNovoa JM. Glomerular nephrotoxicity aminoglycosides. Toxicol Appl Pharmacol. 2007;223(1):86–98.CrossRefPubMed Martínez-Salgado C, López-Hernández FJ, LópezNovoa JM. Glomerular nephrotoxicity aminoglycosides. Toxicol Appl Pharmacol. 2007;223(1):86–98.CrossRefPubMed
6.
go back to reference Balakumar P, Rohilla A, Thangathirupathi A. Gentamicin-induced nephrotoxicity: do we have a promising therapeutic approach to blunt it? Pharmacol Res. 2010;62:179–86.CrossRefPubMed Balakumar P, Rohilla A, Thangathirupathi A. Gentamicin-induced nephrotoxicity: do we have a promising therapeutic approach to blunt it? Pharmacol Res. 2010;62:179–86.CrossRefPubMed
7.
go back to reference Ali BH. Gentamicin nephrotoxicity in humans and animals: some recent research. Gen Pharmacol. 1995;26:1477–87.CrossRefPubMed Ali BH. Gentamicin nephrotoxicity in humans and animals: some recent research. Gen Pharmacol. 1995;26:1477–87.CrossRefPubMed
8.
9.
go back to reference Yang CL, Du XH, Han YX. Renal cortical mitochondria are the source of oxygen free radicals enhanced by gentamicin. Ren Fail. 1995;17:21–6.CrossRefPubMed Yang CL, Du XH, Han YX. Renal cortical mitochondria are the source of oxygen free radicals enhanced by gentamicin. Ren Fail. 1995;17:21–6.CrossRefPubMed
10.
go back to reference Cuzzocrea S, Mazzon E, Dugo L, Serraino I, Di Paola R, Britti D, De Sarro A, Pierpaoli S, Caputi A, Masini E, Salvemini D. A role for superoxide in gentamicin-mediated nephropathy in rats. Eur J Pharmacol. 2002;450:67–76.CrossRefPubMed Cuzzocrea S, Mazzon E, Dugo L, Serraino I, Di Paola R, Britti D, De Sarro A, Pierpaoli S, Caputi A, Masini E, Salvemini D. A role for superoxide in gentamicin-mediated nephropathy in rats. Eur J Pharmacol. 2002;450:67–76.CrossRefPubMed
11.
go back to reference Bledsoe G, Shen B, Yao YY, Hagiwara M, Mizell B, Teuton M, Grass D, Chao L, Chao J. Role of tissue kallikrein in prevention and recovery of gentamicin-induced renal injury. Toxicol Sci. 2008;102:433–43.CrossRefPubMed Bledsoe G, Shen B, Yao YY, Hagiwara M, Mizell B, Teuton M, Grass D, Chao L, Chao J. Role of tissue kallikrein in prevention and recovery of gentamicin-induced renal injury. Toxicol Sci. 2008;102:433–43.CrossRefPubMed
12.
go back to reference Graham HN. Green tea composition, consumption, and polyphenol chemistry. Prev Med. 1992;21:334–50.CrossRefPubMed Graham HN. Green tea composition, consumption, and polyphenol chemistry. Prev Med. 1992;21:334–50.CrossRefPubMed
13.
go back to reference Kobayashi H, Tanaka Y, Asagiri K, Asakawa T, Tanikawa K, Kage M, Yagi M. The antioxidant effect of green tea catechin ameliorates experimental liver injury. Phytomedicine. 2010;17:197–202.CrossRefPubMed Kobayashi H, Tanaka Y, Asagiri K, Asakawa T, Tanikawa K, Kage M, Yagi M. The antioxidant effect of green tea catechin ameliorates experimental liver injury. Phytomedicine. 2010;17:197–202.CrossRefPubMed
14.
go back to reference Abd El-Aziz TA, Mohamed RH, Pasha HF, Abdel-Aziz HR. Catechin protects against oxidative stress and inflammatory-mediated cardiotoxicity in adriamycin-treated rats. Clin Exp Med. 2012;12(4):223–40.CrossRef Abd El-Aziz TA, Mohamed RH, Pasha HF, Abdel-Aziz HR. Catechin protects against oxidative stress and inflammatory-mediated cardiotoxicity in adriamycin-treated rats. Clin Exp Med. 2012;12(4):223–40.CrossRef
15.
go back to reference Farooqui AA. Beneficial effects of green tea catechins on neurological disorders. In: Phytochemicals, signal transduction, and neurological disorders. Springer: New York; 2012. p. 117–49. Farooqui AA. Beneficial effects of green tea catechins on neurological disorders. In: Phytochemicals, signal transduction, and neurological disorders. Springer: New York; 2012. p. 117–49.
16.
go back to reference Ihm SH, Lee JO, Kim SJ, Seung KB, Schini-Kerth VB, Chang K, Oak MH. Catechin prevents endothelial dysfunction in the prediabetic stage of OLETF rats by reducing vascular NADPH oxidase activity and expression. Atherosclerosis. 2009;206:47–53.CrossRefPubMed Ihm SH, Lee JO, Kim SJ, Seung KB, Schini-Kerth VB, Chang K, Oak MH. Catechin prevents endothelial dysfunction in the prediabetic stage of OLETF rats by reducing vascular NADPH oxidase activity and expression. Atherosclerosis. 2009;206:47–53.CrossRefPubMed
17.
go back to reference Chander V, Singh D, Chopra K. Catechin, a natural antioxidant protects against rhabdomyolysis-induced myoglobinuric acute renal failure. Pharmacol Res. 2003;48:503–9.CrossRefPubMed Chander V, Singh D, Chopra K. Catechin, a natural antioxidant protects against rhabdomyolysis-induced myoglobinuric acute renal failure. Pharmacol Res. 2003;48:503–9.CrossRefPubMed
18.
go back to reference Cao Y, He XJ, Xiang W, Yi ZW. Protective effect of catechin on renal microvessels in 5/6 nephrectomized rats and its mechanism. Zhong Xi Yi Jie He XueBao. 2009;7:557–62.CrossRef Cao Y, He XJ, Xiang W, Yi ZW. Protective effect of catechin on renal microvessels in 5/6 nephrectomized rats and its mechanism. Zhong Xi Yi Jie He XueBao. 2009;7:557–62.CrossRef
19.
go back to reference Hase M, Babazono T, Karibe S, Kinae N, Iwamoto Y. Renoprotective effects of tea catechin in streptozotocin- induced diabetic rats. Int Urol Nephrol. 2006;38:693–9.CrossRefPubMed Hase M, Babazono T, Karibe S, Kinae N, Iwamoto Y. Renoprotective effects of tea catechin in streptozotocin- induced diabetic rats. Int Urol Nephrol. 2006;38:693–9.CrossRefPubMed
20.
go back to reference Chennasamudram SP, Kudugunti S, Boreddy PR, Moridani MY, Vasylyeva TL. Renoprotective effects of (+)-catechin in streptozotocin-induced diabetic rat model. Nutr Res. 2012;32:347–56.CrossRefPubMed Chennasamudram SP, Kudugunti S, Boreddy PR, Moridani MY, Vasylyeva TL. Renoprotective effects of (+)-catechin in streptozotocin-induced diabetic rat model. Nutr Res. 2012;32:347–56.CrossRefPubMed
21.
go back to reference Cekmen M, Otunctemur A, Ozbek E, Cakir SS, Dursun M, Polat EC, Somay A, Ozbay N. Pomegranate extract attenuates gentamicin-induced nephrotoxicity in rats by reducing oxidative stress. Ren Fail. 2013;35:268–74.CrossRefPubMed Cekmen M, Otunctemur A, Ozbek E, Cakir SS, Dursun M, Polat EC, Somay A, Ozbay N. Pomegranate extract attenuates gentamicin-induced nephrotoxicity in rats by reducing oxidative stress. Ren Fail. 2013;35:268–74.CrossRefPubMed
22.
go back to reference Otunctemur A, Ozbek E, Cekmen M, Cakir SS, Dursun M, Polat EC, Somay A, Ozbay N. Protective effect of montelukastwhich is cysteinyl-leukotriene receptor antagonist on gentamicin-induced nephrotoxicity and oxidative damage in rat kidney. Ren Fail. 2013;35:403–10.CrossRefPubMed Otunctemur A, Ozbek E, Cekmen M, Cakir SS, Dursun M, Polat EC, Somay A, Ozbay N. Protective effect of montelukastwhich is cysteinyl-leukotriene receptor antagonist on gentamicin-induced nephrotoxicity and oxidative damage in rat kidney. Ren Fail. 2013;35:403–10.CrossRefPubMed
23.
go back to reference Kadian S, Mahadevan N, Balakumar P. Differential effects of low-dose fenofibrate treatment in diabetic rats with early onset nephropathy and established nephropathy. Eur J Pharmacol. 2013;698:388–96.CrossRefPubMed Kadian S, Mahadevan N, Balakumar P. Differential effects of low-dose fenofibrate treatment in diabetic rats with early onset nephropathy and established nephropathy. Eur J Pharmacol. 2013;698:388–96.CrossRefPubMed
24.
go back to reference Ellman GL. Tissue sulfhydryl groups. Arch Biochem Bio phys. 1959;82:70–7.CrossRef Ellman GL. Tissue sulfhydryl groups. Arch Biochem Bio phys. 1959;82:70–7.CrossRef
25.
go back to reference Boyne AF, Ellman GL. A methodology for analysis of tissue sulfhydryl components. Anal Biochem. 1972;46:639–53.CrossRefPubMed Boyne AF, Ellman GL. A methodology for analysis of tissue sulfhydryl components. Anal Biochem. 1972;46:639–53.CrossRefPubMed
26.
go back to reference Patel Manali B, Deshpande S, Shah G. Evaluation of efficacy of vitamin E and N-acetyl cysteine in gentamicin-induced nephrotoxicity in rats. Ren Fail. 2011;33(3):341–7.CrossRefPubMed Patel Manali B, Deshpande S, Shah G. Evaluation of efficacy of vitamin E and N-acetyl cysteine in gentamicin-induced nephrotoxicity in rats. Ren Fail. 2011;33(3):341–7.CrossRefPubMed
27.
go back to reference Pai PG, ChamariNawarathna S, Kulkarni A, Habeeba U, Reddy CS, Teerthanath S, Shenoy JP. Nephroprotective effect of ursolic acid in a murine model of gentamicin-induced renal damage. ISRN Pharmacol. 2012;2012:410902. doi:10.5402/2012/410902. Pai PG, ChamariNawarathna S, Kulkarni A, Habeeba U, Reddy CS, Teerthanath S, Shenoy JP. Nephroprotective effect of ursolic acid in a murine model of gentamicin-induced renal damage. ISRN Pharmacol. 2012;2012:410902. doi:10.​5402/​2012/​410902.
28.
go back to reference Arora MK, Reddy K, Balakumar P. The low dose combination of fenofibrate and rosiglitazone halts the progression of diabetes-induced experimental nephropathy. Eur J Pharmacol. 2010;636:137–44.CrossRefPubMed Arora MK, Reddy K, Balakumar P. The low dose combination of fenofibrate and rosiglitazone halts the progression of diabetes-induced experimental nephropathy. Eur J Pharmacol. 2010;636:137–44.CrossRefPubMed
29.
go back to reference Whiting PH, Brown PA. The relationship between enzymuria and kidney enzyme activities in experimental gentamicin nephrotoxicity. Ren Fail. 1996;18:899–909.CrossRefPubMed Whiting PH, Brown PA. The relationship between enzymuria and kidney enzyme activities in experimental gentamicin nephrotoxicity. Ren Fail. 1996;18:899–909.CrossRefPubMed
30.
go back to reference Elfarra AA, Duescher RJ, Sausen PJ, O’hara TM, Cooley AJ. Methimazole protection of rats against gentamicin-induced nephrotoxicity. Can J Physiol Pharmacol. 1994;72:1238–44.CrossRefPubMed Elfarra AA, Duescher RJ, Sausen PJ, O’hara TM, Cooley AJ. Methimazole protection of rats against gentamicin-induced nephrotoxicity. Can J Physiol Pharmacol. 1994;72:1238–44.CrossRefPubMed
31.
go back to reference Geleilete TJ, Melo GC, Costa RS, Volpini RA, Soares TJ, Coimbra TM. Role of myofibroblasts, macrophages, transforming growth factor-beta endothelin, angiotensin-II, and fibronectin in the progression of tubulointerstitial nephritis induced by gentamicin. J Nephrol. 2002;15:633–42.PubMed Geleilete TJ, Melo GC, Costa RS, Volpini RA, Soares TJ, Coimbra TM. Role of myofibroblasts, macrophages, transforming growth factor-beta endothelin, angiotensin-II, and fibronectin in the progression of tubulointerstitial nephritis induced by gentamicin. J Nephrol. 2002;15:633–42.PubMed
32.
go back to reference Abdel-Raheem IT, Abdel-Ghany AA, Mohamed GA. Protective effect of quercetin against gentamicin-induced nephrotoxicity in rats. Biol Pharm Bull. 2009;32:61–7.CrossRefPubMed Abdel-Raheem IT, Abdel-Ghany AA, Mohamed GA. Protective effect of quercetin against gentamicin-induced nephrotoxicity in rats. Biol Pharm Bull. 2009;32:61–7.CrossRefPubMed
33.
go back to reference Pedraza-Chaverri J, Maldonado PD, Medina-Campos ON, Olivares-Corichi IM, Granados-Silvestre MA, Hernandez-Pando R, et al. Garlic ameliorates gentamicin nephrotoxicity: relation to antioxidant enzymes. Free RadicBiol Med. 2000;29:602–11.CrossRef Pedraza-Chaverri J, Maldonado PD, Medina-Campos ON, Olivares-Corichi IM, Granados-Silvestre MA, Hernandez-Pando R, et al. Garlic ameliorates gentamicin nephrotoxicity: relation to antioxidant enzymes. Free RadicBiol Med. 2000;29:602–11.CrossRef
34.
go back to reference Maldonado PD, Barrera D, Medina-Campos ON, Hernandez-Pando R, Ibarra-Rubio ME, Pedraza-Chaverri J. Aged garlic extract attenuates gentamicin induced renal damage and oxidative stress in rats. Life Sci. 2003;73:2543–56.CrossRefPubMed Maldonado PD, Barrera D, Medina-Campos ON, Hernandez-Pando R, Ibarra-Rubio ME, Pedraza-Chaverri J. Aged garlic extract attenuates gentamicin induced renal damage and oxidative stress in rats. Life Sci. 2003;73:2543–56.CrossRefPubMed
35.
go back to reference Harada M, Kan Y, Naoki H, Fukui Y, Kageyama N, Nakai M, Miki W, Kiso Y. Identification of the major antioxidative metabolites in biological fluids of the rat with ingested (+)-catechin and (-)-epicatechin. Biosci Biotechnol Biochem. 1999;63(6):973–7.CrossRefPubMed Harada M, Kan Y, Naoki H, Fukui Y, Kageyama N, Nakai M, Miki W, Kiso Y. Identification of the major antioxidative metabolites in biological fluids of the rat with ingested (+)-catechin and (-)-epicatechin. Biosci Biotechnol Biochem. 1999;63(6):973–7.CrossRefPubMed
36.
go back to reference Bharrhan S, Koul A, Chopra K, Rishi P. Catechin suppresses an array of signalling molecules and modulates alcohol-induced endotoxin mediated liver injury in a rat model. PLoS One. 2011;6:e20635.CrossRefPubMedCentralPubMed Bharrhan S, Koul A, Chopra K, Rishi P. Catechin suppresses an array of signalling molecules and modulates alcohol-induced endotoxin mediated liver injury in a rat model. PLoS One. 2011;6:e20635.CrossRefPubMedCentralPubMed
37.
go back to reference Raj Vasanth, et al. Protective Role of catechin on d-galactosamineinduced hepatotoxicity through a p53 dependent pathway. Indian J ClinBiochem. 2010;25:349–56. Raj Vasanth, et al. Protective Role of catechin on d-galactosamineinduced hepatotoxicity through a p53 dependent pathway. Indian J ClinBiochem. 2010;25:349–56.
38.
go back to reference Bhardwaj P, Khanna D, Balakumar P. Catechin averts experimental diabetes mellitus-induced vascular endothelial structural and functional abnormalities. Cardio Vasc Toxicol. 2014;14:41–51.CrossRef Bhardwaj P, Khanna D, Balakumar P. Catechin averts experimental diabetes mellitus-induced vascular endothelial structural and functional abnormalities. Cardio Vasc Toxicol. 2014;14:41–51.CrossRef
39.
go back to reference Hamaishi K, Kojima R, Ito M. Anti-ulcer effect of tea catechin in rats. Biol Pharm Bull. 2006;29:2206–13.CrossRefPubMed Hamaishi K, Kojima R, Ito M. Anti-ulcer effect of tea catechin in rats. Biol Pharm Bull. 2006;29:2206–13.CrossRefPubMed
Metadata
Title
Nephroprotective effect of catechin on gentamicin-induced experimental nephrotoxicity
Authors
Ankush Sardana
Sanjeev Kalra
Deepa Khanna
Pitchai Balakumar
Publication date
01-04-2015
Publisher
Springer Japan
Published in
Clinical and Experimental Nephrology / Issue 2/2015
Print ISSN: 1342-1751
Electronic ISSN: 1437-7799
DOI
https://doi.org/10.1007/s10157-014-0980-3

Other articles of this Issue 2/2015

Clinical and Experimental Nephrology 2/2015 Go to the issue
Live Webinar | 27-06-2024 | 18:00 (CEST)

Keynote webinar | Spotlight on medication adherence

Live: Thursday 27th June 2024, 18:00-19:30 (CEST)

WHO estimates that half of all patients worldwide are non-adherent to their prescribed medication. The consequences of poor adherence can be catastrophic, on both the individual and population level.

Join our expert panel to discover why you need to understand the drivers of non-adherence in your patients, and how you can optimize medication adherence in your clinics to drastically improve patient outcomes.

Prof. Kevin Dolgin
Prof. Florian Limbourg
Prof. Anoop Chauhan
Developed by: Springer Medicine
Obesity Clinical Trial Summary

At a glance: The STEP trials

A round-up of the STEP phase 3 clinical trials evaluating semaglutide for weight loss in people with overweight or obesity.

Developed by: Springer Medicine

Highlights from the ACC 2024 Congress

Year in Review: Pediatric cardiology

Watch Dr. Anne Marie Valente present the last year's highlights in pediatric and congenital heart disease in the official ACC.24 Year in Review session.

Year in Review: Pulmonary vascular disease

The last year's highlights in pulmonary vascular disease are presented by Dr. Jane Leopold in this official video from ACC.24.

Year in Review: Valvular heart disease

Watch Prof. William Zoghbi present the last year's highlights in valvular heart disease from the official ACC.24 Year in Review session.

Year in Review: Heart failure and cardiomyopathies

Watch this official video from ACC.24. Dr. Biykem Bozkurt discusses last year's major advances in heart failure and cardiomyopathies.