|  | 
              
  
              
              Open Access  
Copyright: The authors. This article is an open access 
article licensed under the terms of the Creative Commons Attribution License 
(http://creativecommons.org/licenses/by/2.0) which permits unrestricted use, 
distribution and reproduction in any medium, provided the work is properly 
cited. 
 
              
              
              Research (Published 
online :  05-10-2013) 
7. Protective role of turmeric on histological, 
ultrastructural and sero-biochemical changes in cisplatin-induced nephrotoxicity 
in female rats - B. Ramya, Y. Anjaneyulu, A. Gopala Reddy, D. Madhuri, 
M. Lakshman and P. ShivakumarVeterinary World, 6(11): 865-869
 
                
              doi: 
              10.14202/vetworld.2013.865-869 
                
              
              
          
 
              Abstract 
 
              Aim: Protective role of 
              turmeric was assessed against cisplatin-induced histological and 
              ultra-structural changes in kidney. Materials and Methods: A total of 48 rats were divided into 
              4 groups of 12 rats in each. Group 1 was kept as sham control, 
              group 2 was treated with cisplatin (@ 2 mg/kg b.wt, 
              intraperitoneally on day 1, 7, 14 and 21), group 3 with turmeric 
              (@ 0.05 mg/kg b.wt. p.o. once daily for 28 days) and group 4 with 
              cisplatin + turmeric (as per above schedule). Blood was collected 
              at fortnight intervals and serum was separated for estimation of 
              kidney biomarkers. Six rats in each group were then euthanized on 
              day 14 and 28 for histopathology, and tissue parameters were 
              assayed on day 28.
 Results: Thibarbituric acid reacting substances (TBARS), 
              protein carbonyls, serum creatinine, blood urea nitrogen (BUN) 
              were significantly (P < 0.05) increased, while GSH was 
              significantly (P < 0.05) decreased in group 2 as compared to other 
              groups. Histological sections of kidney from group 2 rats showed 
              marked inter-tubular haemorrhages, congestion, marked dilation of 
              tubules, and other lesions of pathological significance. 
              Ultrastructural changes of pathological significance were also 
              recorded in group 2. Kidney sections of group 4 showed nucleus 
              with uniform size with well differentiated nuclear membrane and 
              nucleolus, and prominent inter tubular and inter cellular 
              junctions.
 Conclusion: The study revealed that cisplatin induces 
              nephrotoxicity due to oxidative stress and turmeric was found 
              beneficial in countering the adverse effects.
 Key words: cisplatin, nephrototoxicity, oxidative stress, 
              turmeric.
 
 
              References 
 
                
                  | 1. Nanda Kumar, A. (1990-1996) National Cancer Registry 
                  Program, Indian Council of Medical Research, Consolidated 
                  Report of Population Based Cancer Registries, New Delhi, 
                  India. |  
                  |  |  
                  | 2. Stephen, T. (2005) Cisplatin. Chemical and Engineering News 
                  83: 52. |  
                  |  |  
                  | 3. Noori, S. and Mahboob, T. (2010). Protective role of 
                  carnosine pretreatment on cisplatin- induced kidney damage in 
                  rats. Indian Journal of Clinical Biochemistry 25: 86-91. http://dx.doi.org/10.1007/s12291-010-0018-x
 PMid:23105891 PMCid:PMC3453019
 |  
                  |  |  
                  | 4. Pratibha, R., Sameer, R., Padmanabh, V., Rataboli., 
                  Dayanand, A., Bhiwgade. and Chitra, Y. D. (2006) Enzyme 
                  studies of cisplatin induced hepatic tissue damage in rats. 
                  European Journal of Pharmacology 532:290-293. http://dx.doi.org/10.1016/j.ejphar.2006.01.007
 PMid:16458885
 |  
                  |  |  
                  | 5. Naqshbandi, A., Khan, M. W., Rizwan, S., Yusufi, A. N. K. 
                  and Khan, F. (2011) Protective role of fish oil in cisplatin 
                  induced liver toxicity.Biology and Medicine 3:86-97. |  
                  |  |  
                  | 6. Zafar, A. B. R., David, B. and Pradip, D. (2010) Prevention 
                  of Cisplatin Induced Nephrotoxicity by Ethanolic Extract of 
                  Embelia ribes Fruits and a Tocopherol in Experimental Animals. 
                  Journal of Complementary and Integrative Medicine 7:53. |  
                  |  |  
                  | 7. Sudhavani, V., Chinnikrishnaiah, V., Raghu, Moorthy, V., 
                  Raghavendra, H.G. and Ranganayakulu, D. (2010) 
                  Merremiaemarginata burmprotects against cisplatin induced 
                  nephrotoxicity rats. Journal of Advances in Drug Research 1: 
                  2230-7761. |  
                  |  |  
                  | 8. Ulkan, K., Ertugrul, K., Zeynep, T., Mehmet, T., Ibrahim H. 
                  O., Okkes, Y., Fikrettin, S., and Kazim, S.(2013) Melatonin 
                  suppresses cisplatin-induced nephrotoxicity via activation of 
                  Nrf-2/HO-1 pathway.Nutrition & Metabolism 10:7. http://dx.doi.org/10.1186/1743-7075-10-7
 PMid:23311701 PMCid:PMC3561216
 |  
                  |  |  
                  | 9. Zsuzsanna, K.,Zsengeller,L. E., Dan, B., Bela, H., Partha, 
                  M. B. K., Samir M. P., Ananth. K., Isaac E. S., Pal, P. (2012) 
                  Cisplatin Nephrotoxicity Involves Mitochondrial Injury with 
                  Impaired Tubular Mitochondrial Enzyme Activity. Journal of 
                  Histochemistryand Cytochemistry 60: 521-529. |  
                  |  |  
                  | 10. Deeb, D., Xu, Y. X., Jiang, H., Gao, X., Janakiram, N., 
                  Chapman, R. A. and Gautam, S. C. (2003) Curcumin enhances TNF-related 
                  apoptosis enhancing ligand-induced apoptosis in LNCaPprostate 
                  cancer cells. Molecular Cancer Therapeutics 2: 95–103. PMid:12533677
 |  
                  |  |  
                  | 11. Ramya, B., Anjaneyulu,Y.,Gopalareddy, A.(2013)A study on 
                  cisplatin-induced hepatotoxicity and protectiverole of 
                  turmeric in rats. International Journal of Pharma and Bio 
                  Sciences 4(1): (b) 133 – 143. |  
                  |  |  
                  | 12. Snedecor, G. W. and Cochran, W. G. (1994) Statistical 
                  methods, 8th edition, IOWA State University Press, Amer, IOWA, 
                  USA. Pp. 237-252. |  
                  |  |  
                  | 13. Satia, N. C., Dawani, R. R. and Goyal, R. K. 
                  (1997)Benefical effects of clonidine in streptozocine induced 
                  Diabetes and Doca-hypersensitive rats. Journal of Pharmacy and 
                  Pharmacology 49:1030-1035. http://dx.doi.org/10.1111/j.2042-7158.1997.tb06036.x
 PMid:9364415
 |  
                  |  |  
                  | 14. Culling C F A,Handbook of Histopathological Technique, 
                  (Butterworth & Company (Publishers) Limited Landon) 1957. Pp. 
                  1-50. |  
                  |  |  
                  | 15. Bozzola, J. J. and Russell, L. D. 1999. Electron 
                  Microscopy: Principles and Techniques for Biologists. 2ndEdn., 
                  Jones and Bartlett, Boston. |  
                  |  |  
                  | 16. Moron, M. S., Depierre, J. W. and Mannervik, B. (1979) 
                  Levels of GSH, glutathione reductase and GST in rat lung and 
                  liver. Biochimica et Biophysica Acta. 582: 67-68. http://dx.doi.org/10.1016/0304-4165(79)90289-7
 |  
                  |  |  
                  | 17. Balasubramanian, K. A., Manohar, M. and Mathan, V. I. 
                  (1988)An unidentified inhibitor of lipid peroxidation in 
                  intestinal mucosa. Biochimicaet Biophysica Acta. 962:51- 58. http://dx.doi.org/10.1016/0005-2760(88)90094-X
 |  
                  |  |  
                  | 18. Levine, R. L., Garland, D., Oliver, C. N., Amici, A., 
                  Climent, I., Lenz, A, G., Ahn, B, W., Shaltiel, S. and 
                  Stadtman, E. R. (1990) Determination of carbonyl concentration 
                  in oxidative proteins. Methods in Enzymology. 186: 464-478. http://dx.doi.org/10.1016/0076-6879(90)86141-H
 |  
                  |  |  
                  | 19. Yousef, M. I., Saad, A. A. and El-Shennawy, L. K. (2009) 
                  Role of grape seedextract in by cisplatininduced oxidative 
                  damagein rats. Food and Chemical Toxicology 47: 1176 – 1183. http://dx.doi.org/10.1016/j.fct.2009.02.007
 PMid:19425235
 |  
                  |  |  
                  | 20. Marie, H. H. and Prasad, D. (2003) Molecular mechanisms 
                  inCisplatin renal-toxicity.Cancer Therapeutics.1: 47–61. |  
                  |  |  
                  | 21. Santos, N. A., Catao, C. S., Martins, N. M., Curti, C., 
                  Bianchi, M.L. and Santos, A.C. (2007)Cisplatin induced 
                  nephrotoxicity is associated with redox state imbalance, 
                  impairedenergy metabolism and apoptosis in rat kidney 
                  mitochondria. Archieves of Toxicology. 81:495-504. http://dx.doi.org/10.1007/s00204-006-0173-2
 PMid:17216432
 |  
                  |  |  
                  | 22. Pratibha, R., Dayanand, A., Bhiwgade., Sameer, K., 
                  Padmanabh, V., Rataboli. And Chitra, Y. D. (2010) Cisplatin 
                  induced histological changes in renal tissue of rat. Journal 
                  of Cell and Animal Biology.4: 108-111. |  
                  |  |  
                  | 23. Chattopadhyay, I., Kaushik, B., Bandyopadhyay, U. and 
                  Banerjee, R.K. (2004) Biological effects and medicinal 
                  properties of turmeric and curcumin, Current Science,87 :44- 
                  53. |  |  |