Effect of turmeric on amelioration of arsenic induced toxicity in grass carp (Ctenopharyngodon idella) fingerlings


105 / 1

Authors

  • Manoj Kumar Tripathi ICAR-RCER, Patna
  • Rajni Kumari ICAR-RCER, Patna
  • Vivekanand Bharti ICAR-RCER, Patna https://orcid.org/0000-0003-0415-2776
  • P. K. Ray ICAR-RCER, Patna
  • Jyoti Kumar ICAR-RCER, Patna
  • P. C. Chandran ICAR-RCER, Patna
  • S. Dayal ICAR-RCER, Patna
  • Tarkeshwar Kumar ICAR-RCER, Patna
  • Saurabh Kumar ICAR-RCER, Patna
  • A. Dey ICAR-RCER, Patna
  • Kamal Sarma ICAR-RCER, Patna
  • Anup Das ICAR-RCER, Patna

https://doi.org/10.21077/ijf.2026.73.1.172305-13

Keywords:

Turmeric, arsenic toxicity, gene expression and amelioration

Abstract

The present study evaluated the protective effects of turmeric against arsenic (AS) toxicity in grass carp (Ctenopharyngodon idella) fingerlings. Four experimental groups were maintained for the study: Control (commercial feed only), T1 (turmeric powder @ 1.2% of daily feed), T2 (sodium meta-arsenite @ 3200 µg l-1 + commercial feed), and T3 (sodium meta-arsenite @ 3200 µg l-1 + turmeric powder @ 1.2% of daily feed). The fish fingerlings were randomly assigned to the four groups, each comprising two replicate tanks containing ten fish per tank; and the experiment was conducted over a period of three months. At the end of the experiment, growth performance was assessed, and blood samples were collected for haemoglobin and haematocrit estimation. Liver samples from the Control, T2, and T3 groups were analysed for the expression of metallothionein, tumour necrosis factor-α (TNF-α), and NF-κB p65 genes, which are key markers of detoxification, immunity, and inflammation. Total RNA was extracted andreverse-transcribed into cDNA for gene expression studies. Results showed that arsenic exposure significantly reduced weight gain, haemoglobin, and haematocrit levels, tTrmeric supplementation partly restored these parameters. Arsenic exposure also led to significant upregulation of metallothionein, TNF-α, and NF-κB p65, indicating oxidative and inflammatory stress. Interestingly, turmeric supplementation downregulated the expression of these genes, highlighting its protective role. Overall, the findings of the study indicated that turmeric has a potential ameliorative role in mitigating arsenic-induced toxicity in grass carp. 
Keywords: cDNA, Gene expression, Haematocrit metallothionein, NF-κB p65, TNF-α

Downloads

Download data is not yet available.

Author Biography

  • Vivekanand Bharti, ICAR-RCER, Patna

    Division of Livestock and Fisheries Management

References

1. Albores, A., Koropatnick, J., Cherian, M. G. and Zelazowski, A. J. 1992. Arsenic induces and enhances rat hepatic metallothionein production in vivo. Chem. Biol. Interact., 85(2-3): 127-140. https://doi.org/10.1016/0009-2797(92)90057-R

2. Al-Faragi, J. K. and Hassan, M. A. H. 2017. Efficiency of dietary turmeric on growth performance, hematology and survival rate in common carp Cyprinus carpio challenged with Flexibacter columnaris. Kufa J. Vet. Med. Sci., 8(1): 130-140. https://doi.org/10.36326/kjvs/2017/v8i14307

3. Anene, A., Okorie, E. O., Ajima, M. N. and Onyemaonwu, J. 2021. Dietary supplement of tumeric (Curcuma longa) powder: Impact on haematological and biochemical responses in Clarias gariepinus (burchell, 1822) fingerlings. Aquac. Stud., 22 (2): AQUAST714. http://doi.org/10.4194/AQUAST714

4. Arkoudi, K., Yuan, Y., Cumine, A. P., Dyer, C., Busch-Nentwich, E., Bravo, I., Feng, Y. and Knight, R. D. 2025. An NF-kB/TNF-alpha signalling feedback loop acts to coordinate tissue regeneration and macrophage behaviour in zebrafish. NPJ Regen. Med, 10 (1): 27. http://doi.org/10.1038/s41536-025-00414-1

5. Banerjee, S., Mitra, T., Purohit, G. K., Mohanty, S. and Mohanty, B. P. 2015. Immunomodulatory effect of arsenic on cytokine and HSP gene expression in Labeo rohita fingerlings. Fish Shellfish Immunol., 44(1): 43-49. http://doi.org/10.1016/j.fsi.2015.01.029

6. Bhattacharya, S., Bhattacharya, A. and Roy, S. 2007. Arsenic-induced responses in freshwater teleosts. Fish Physiol. Biochem., 33(4): 463-473. http://doi.org/10.1007/s10695-007-9173-2

7. Byeon, E., Kang, H. M., Yoon, C. and Lee, J. S. 2021. Toxicity mechanisms of arsenic compounds in aquatic organisms. Aquat. Toxicol., 237: 105901. http://doi.org/10.1016/j.aquatox.2021.105901

8. Cao, L., Ding, W., Du, J., Jia, R., Liu, Y., Zhao, C., Shen, Y. and Yin, G. 2015. Effects of curcumin on antioxidative activities and cytokine production in Jian carp (Cyprinus carpio var. Jian) with CCl4-induced liver damage. Fish Shellfish Immunol., 43(1): 150-157. https://doi.org/10.1016/j.fsi.2014.12.025

9. Castaldo, G., Pillet, M., Slootmaekers, B., Bervoets, L., Town, R. M., Blust, R. and De Boeck, G. J. A. T. 2020. Investigating the effects of a sub-lethal metal mixture of Cu, Zn and Cd on bioaccumulation and ionoregulation in common carp, Cyprinus carpio. Aquat. Toxicol., 218: 105363. http://doi.org/10.1016/j.aquatox.2021.105875

10. Chandel, M., Sharma, A. K., Thakur, K., Sharma, D., Brar, B., Mahajan, D., Kumari, H., Pankaj, P. P. and Kumar, R. 2024. Poison in the water: Arsenic's silent assault on fish health. J. Appl. Toxicol., 44(9): 1282-1301. https://doi.org/10.1002/jat.4581

11. Duan, X., Xu, G., Li, J., Yan, N., Li, X., Liu, X. and Li, B. 2022. Arsenic induces continuous inflammation and regulates Th1/Th2/Th17/Treg balance in liver and kidney in vivo. Mediators Inflamm., 2022(1): 8414047. https://doi.org/10.1155/2022/8414047

12. El-Demerdash, F. M., Yousef, M. I. and Radwan, F. M. 2009. Ameliorating effect of curcumin on sodium arsenite-induced oxidative damage and lipid peroxidation in different rat organs. Food Chem. Toxicol., 47(1): 249-254. https://doi.org/10.1016/j.fct.2008.11.013

13. Fatima, A., Makhdoom Hussain, S., Ali, S., Rizwan, M., Al-Ghanim, K. A. and Yong, J. W. H. 2024. Ameliorating effects of natural herbal supplements against water-borne induced toxicity of heavy metals on Nile tilapia,(Oreochromis niloticus). Sci. Rep., 14(1): 22571. https://doi.org/10.1038/s41598-024-72268-4

14. García-Niño, W. R. and Pedraza-Chaverrí, J. 2014. Protective effect of curcumin against heavy metals-induced liver damage. Food Chem. Toxicol., 69:182-201. https://doi.org/10.1016/j.fct.2014.04.016

15. Giri, S. S., Sukumaran, V. and Park, S. C. 2019. Effects of bioactive substance from turmeric on growth, skin mucosal immunity and antioxidant factors in common carp, Cyprinus carpio. Fish Shellfish Immunol., 92: 612-620. https://doi.org/10.1016/j.fsi.2019.06.053

16. Hino, K., Nakamura, O., Yoshiura, Y., Suetake, H., Suzuki, Y., and Watanabe, T. (2006). TNF induces the growth of thymocytes in rainbow trout. Dev. Comp. Immunol. 30: 639-647. https://doi.org/10.1016/j.dci.2005.09.005

17. Jabeen, G., Ishaq, S., Arshad, M., Fatima, S., Kanwal, Z. and Ali, F. 2022. Investigation on Immune‐Related Protein (Heat Shock Proteins and Metallothionein) Gene Expression Changes and Liver Histopathology in Cadmium‐Stressed Fish. BioMed. Res. Int., 2075791. https://doi.org/10.1155/2022/2075791

18. Kong, Y., Li, M., Guo, G., Yu, L., Sun, L., Yin, Z., Li, R., Chen, X. and Wang, G. 2021. Effects of dietary curcumin inhibit deltamethrin-induced oxidative stress, inflammation and cell apoptosis in Channa argus via Nrf2 and NF-κB signaling pathways. Aquac. Rep., 540: 736744. https://doi.org/10.1016/j.aqrep.2021.100981

19. Kovendan, K., Vincent, S., Janarthanan, S. and Saravanan, M. 2013. Expression of metallothionein in liver and kidney of freshwater fish Cyprinus carpio var. communis (Linn) exposed to arsenic trioxide. Am J Sci Ind Res., 4(1): 1-10. https://doi.org/10.5251/ajsir.2013.4.1.1.10

20. Kreppel, H., Bauman, J. W., Liu, J. I. E., McKim Jr, J. M. and Klaassen, C. D. 1993. Induction of metallothionein by arsenicals in mice. Fundam. Appl. Toxicol., 20(2): 184-189. https://doi.org/10.1006/faat.1993.1025

21. Kumar, R. and Banerjee, T. K. 2016. Arsenic induced hematological and biochemical responses in nutritionally important catfish Clarias batrachus (L.). Toxicol. Rep., 3:148-152. https://doi.org/10.1016/j.toxrep.2016.01.001

22. Kumari, P. and Paul, D. K. 2020. Bioremedial effect of turmeric (Curcuma longa) on haematological and biochemical parameters against fenvalerate induced toxicity in air-breathing fish Clarias batrachus. Int. J. Aquac. Fish. Sci., 6(2): 056-060. https://doi.org/10.17352/2455-8400.000057

23. Kumari, R. R., Kumar, R., Shekhar, P., Tripathi, M. K. and Kumar, P. 2021. Tropical theileriosis in cattle reared in an endemic area of Bihar known for arsenic toxicity: preliminary observations. Indian Vet. J., 98(12): 30-32.

24. Li, M., Kong, Y., Wu, X., Guo, G., Sun, L., Lai, Y., Zhang, J., Niu, X. and Wang, G. 2022. Effects of dietary curcumin on growth performance, lipopolysaccharide-induced immune responses, oxidative stress and cell apoptosis in snakehead fish (Channa argus). Aquac. Rep., 22: 100981. https://doi.org/10.1016/j.aqrep.2021.100981

25. Li, Y., Xiao, T. and Zou, J. 2021. Fish TNF and TNF receptors. Sci. China Life Sci., 64(2): 196-220. https://doi.org/10.1007/s11427-020-1712-4

26. Liu, M., Wang, J., Song, Z. and Pei Y 2025. Regulation mechanism of curcumin mediated inflammatory pathway and its clinical application: A Review. Front. pharmacol., 16: 1642248. https://doi.org/10.3389/fphar.2025.1642248

27. Liu, S., Yu, H., Li, P., Wang, C., Liu, G., Zhang, X., Zhang, C., Qi, M. and Ji, H. 2022. Dietary nano-selenium alleviated intestinal damage of juvenile grass carp (Ctenopharyngodon idella) induced by high-fat diet: Insight from intestinal morphology, tight junction, inflammation, anti-oxidization and intestinal microbiota. Anim. Nutr., 8: 235-248. https://doi.org/10.1016/j.aninu.2021.07.001

28. Liu, T., Zhang, L., Joo, D. and Sun, S.C. 2017. NF-κB signaling in inflammation. Signal transduct. target. ther. 2: 17023. https://doi.org/10.1038/sigtrans.2017.23

29. Livak., K. J. and Schmittgen, T. D. 2001. Analysis of relative gene expression data using real-time quantitative PCR and the 2− ΔΔCT method. Methods., 25: 402-408. https://doi.org/10.1006/meth.2001.1262

30. Lu, H., Zhao, H., Wang, Y., Guo, M., Mu, M., Liu, Y., Nie, X., Huang, P. and Xing, M. 2021. Arsenic (III) induces oxidative stress and inflammation in the gills of common carp, which is ameliorated by zinc (II). J. Inorg. Biochem. 225: 111617. https://doi.org/10.1016/j.jinorgbio.2021.111617

31. Lu, M., Wang, H., Li, X.F., Lu, X., Cullen, W. R., Arnold, L. L., Cohen, S. M. and Le, X. C. 2004. Evidence of hemoglobin binding to arsenic as a basis for the accumulation of arsenic in rat blood. Chem. Res. Toxicol., 17(12): 1733-1742. doi: https://doi.org/10.1021/tx049756s

32. Maji, C., Sarkar, S., Biswas, S., Patra, P.H., Datta, B.K., Bandyopadhyay, S., Biswas, T.K., Jana, C. and Mandal, T.K. 2016. Experimental assessment of arsenic toxicity in garole sheep in India. Emerg. Contam., 2(3): 128-134. https://doi.org/10.1016/j.emcon.2016.04.002

33. Malik, A., Khalid, F., Hidait, N., Anjum, K. M., Mahad, S., Razaq, A., Azmat, H. and Majeed, M. B. B. 2023. Arsenic toxicity in fish: sources and impacts. In Arsenic in the Environment-Sources, Impacts and Remedies. In: Huq, S. M. I. (Eds.), Arsenic in the Environment - Sources, Impacts and Remedies. IntechOpen. https://doi.org/10.5772/intechopen.1001534

34. Ming, J., Ye, J., Zhang, Y., Xu, Q., Yang, X., Shao, X., Qiang, J. and Xu, P. 2020. Optimal dietary curcumin improved growth performance, and modulated innate immunity, antioxidant capacity and related genes expression of NF-κB and Nrf2 signaling pathways in grass carp (Ctenopharyngodon idella) after infection with Aeromonas hydrophila. Fish Shellfish Immunol., 97: 540-553. https://doi.org/10.1016/j.fsi.2019.12.074

35. Mulla, A. N., Thorat, S. T., Chandramore, K., Kumar, P., Reddy, K. S. and Kumar, N. 2025. Curcumin as a protective agent against chromium and ammonia toxicity using molecular and biochemical approaches in fish. Sci. Rep., 15(1): 12023. https://doi.org/10.1038/s41598-025-95369-0

36. Nambiar, S. P., Banuru, S. C., Vahab, R. A., Ittoop, G., Nair, S. N. and Pillai, D. 2024. Augmentation of the anesthetic potency of clove oil for immersion anesthesia in fishes. Aquacult. Int. 32, 2599-2607. https://doi.org/10.1007/s10499-023-01287-1

37. Oladimeji, A. A., Qadri, S. U. and deFreitas, A. S. 1984. Measuring the elimination of arsenic by the gills of rainbow trout (Salmo gairdneri) by using a two compartment respirometer. Bull. Environ. Contam. Toxicol., 32(6): 661-668. https://doi.org/10.1007/BF01607553

38. Pandey, N. and Bhatt, R. 2015. Exiguobacterium mediated arsenic removal and its protective effect against arsenic induced toxicity and oxidative damage in freshwater fish, Channa striata. Toxicol. Rep., 2: 1367-1375. https://doi.org/10.1016/j.toxrep.2015.10.002

39. Perveen, H., Chattopadhyay, S., Maity, M., Dash, M. and Islam, S. S. 2019. Involvement of proinflammatory cytokines and metallothionein in the repairing of arsenic-mediated uterine tissue damage by curcumin. J. Basic Clin. Physiol. Pharmacol. 30(4): 20170179. https://doi.org/10.1515/jbcpp-2017-0179

40. Rabbane, M. G., Kabir, M. A., Habibullah-Al-Mamun, M. and Mustafa, M. G. 2022. Toxic effects of arsenic in commercially important fish rohu carp, Labeo rohita of Bangladesh. Fishes, 7(5): 217. https://doi.org/10.3390/fishes7050217

41. Rajabiesterabadi, H., Hoseini, S. M., Fazelan, Z., Hoseinifar, S. H. and Doan, H. V. 2020. Effects of dietary turmeric administration on stress, immune, antioxidant and inflammatory responses of common carp (Cyprinus carpio) during copper exposure. Aquac. Nutr., 26(4): 1143-1153. https://doi.org/10.1111/anu.13071

42. Singh, S. and Rana, S. V. S. 2010. Ascorbic acid improves mitochondrial function in liver of arsenic-treated rat. Toxicol. Ind. Health., 26(5): 265-272. https://doi.org/10.1177/0748233710365694

43. Smirnova, E., Moniruzzaman, M., Chin, S., Sureshbabu, A., Karthikeyan, A., Do, K. and Min, T. 2023. A review of the role of curcumin in metal induced toxicity. , 12(2): 243. https://doi.org/10.3390/antiox12020243

44. Smith, T.J. and Ashar, B.H. 2019. Iron Deficiency anemia due to high-dose turmeric. Cureus., 11(1): e3858. https://doi.org/10.7759/cureus.3858

45. Sturve, J., Berglund, A., Balk, L., Broeg, K., Böhmert, B., Massey, S., Savva, D., Parkkonen, J., Stephensen, E., Koehler, A., Förlin, L. 2005. Effects of dredging in Göteborg Harbor, Sweden, assessed by biomarkers in eelpout (Zoarces viviparus) Environ. Toxicol. Chem., 24(8): 1951-1961. https://doi.org/10.1897/04-449r1.1

46. Tang, S., Gao, L., Qin, D., Wang, H., Huang, L., Wu, S., Bai, S., Du, N., Sun, Y., Wang, P. and Chen, Z. 2024. Toxic Effects of Arsenic on Four Freshwater Aquatic Species and Its Transformation Metabolism in Crucian Carp (Carassius auratus). Toxics, 12(3): 221. https://doi.org/10.3390/toxics12030221

47. Wang, W. C., Mao, H., Ma, D. D. and Yang, W. X. 2014. Characteristics, functions, and applications of metallothionein in aquatic vertebrates. Front. Mar. Sci., 1:34. https://doi.org/10.3389/fmars.2014.00034

48. Wei, M., Liu, J., Xu, M., Rui, D., Xu, S., Feng, G., Ding, Y., Li, S. and Guo, S. 2016. Divergent effects of arsenic on NF-κB signaling in different cells or tissues: a systematic review and meta-analysis. Int. J. Environ. Res. Public Health, 13(2): 163. https://doi.org/10.3390/ijerph13020163

49. Yang, R., Roshani, D., Gao, B., Li, P. and Shang, N. 2024. Metallothionein: a comprehensive review of its classification, structure, biological functions, and applications. Antioxidants (Basel), 13(7): 825. https://doi.org/10.3390/antiox13070825

50. Yin, Y., Zhang, P., Liu, J., Wang, N., Shang, X., Zhang, Y. and Li, Y. 2020. Amelioration of Cd-induced oxidative stress, MT gene expression, and immune damage by vitamin C in grass carp kidney cells. Biol. Trace Elem. Res., 194(2): 552-559. https://doi.org/10.1007/s12011-019-01808-1

51. Zhang, W., Miao, A.J., Wang, N.X., Li, C., Sha, J., Jia, J., Alessi, D.S., Yan, B. and Ok, Y.S. 2022. Arsenic bioaccumulation and biotransformation in aquatic organisms. Environ. Int., 163: 107221. https://doi.org/10.1016/j.envint.2022.107221

52. Zhang, X., Liu, Y., Xu S. and Zhang, D., 2025. Arsenic compounds in cancer therapy: mechanistic insights and antitumor activity. Biochem. Pharmacol., 240: 117093. https://doi.org/10.1016/j.bcp.2025.117093

53. Zhang, Z., Pi, R., Luo, J., Liu, J., Zhang, A. and Sun, B. 2022. Association between arsenic exposure and inflammatory cytokines and C-reaction protein: A systematic review and meta-analysis. Medicine (Baltimore), 101(50): e32352. https://doi.org/10.1097/MD.0000000000032352

54. Zhou, X., Medina, S., Bolt, A.M., Zhang, H., Wan, G., Xu, H., Lauer, F.T., Wang, S.C., Burchiel, S.W. and Liu, K.J. 2020. Inhibition of red blood cell development by arsenic-induced disruption of GATA-1. Sci. Rep., 10 (1): 19055. https://doi.org/10.1038/s41598-020-76118-x

Downloads

Submitted

2025-10-03

Published

2026-03-31

Issue

Section

Articles

How to Cite

Tripathi, M. K. ., Rajni Kumari, Vivekanand Bharti, P. K. Ray, Jyoti Kumar, P. C. Chandran, S. Dayal, Tarkeshwar Kumar, Saurabh Kumar, A. Dey, Kamal Sarma, & Anup Das. (2026). Effect of turmeric on amelioration of arsenic induced toxicity in grass carp (Ctenopharyngodon idella) fingerlings. Indian Journal of Fisheries, 73(1). https://doi.org/10.21077/ijf.2026.73.1.172305-13
Citation