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Open Access
Copyright: The authors. This article is an open access
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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. Shivakumar
Veterinary 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. |
|
|