Research Article Volume 14 Issue 1 - 2026

Modulation of Mitochondrial Stress by Nano-Curcumin in the Liver of Arsenic Treated Rats

Lalit Mohan Vashistha, Yeshvandra Verma and Suresh Vir Singh Rana*

Department of Toxicology, Ch. Charan Singh University, Meerut, India

*Corresponding Author: Suresh Vir Singh Rana, Professor Emeritus, Department of Toxicology, Ch. Charan Singh University, Meeru, India.
Received: November 12, 2025; Published: December 31, 2025



Background: Several therapeutic strategies have been employed in the past to combat arsenic toxicity in animal models. Recent advent in nano-phyto-medicine now offers new pharmaco-therapeutic platforms to restore organ/system function affected by arsenicals. One amongst these is nano-curcumin, a product of rhizome, Curcuma longa. Since arsenic is considered as one of the potent mitochondrial toxicants, a comparative study on the protective effects of nano-curcumin and curcumin on mitochondrial function in arsenic treated rats was proposed.

Objectives: The objective of present study was to investigate the effects of N-CUR on mitochondrial function in the liver of arsenic treated rats. The hallmark indicators selected for present study include-mitochondrial lipid peroxidation, oxidative phosphorylation, adenosine triphosphatase, cytochrome c, and caspase-3.

Result: Present report describes the protective effects of nano-curcumin on mitochondrial toxicity of arsenic in the liver of laboratory rat. Results demonstrated that nano-curcumin treatment to arsenic fed rats significantly improved the mitochondrial function in the liver and shows protective effects against apoptosis and genotoxicity induced by arsenic.

Conclusion: Present results confer that CUR and N-CUR ameliorated mitochondrial stress and attenuated AsIII induced hepatotoxicity. N-CUR expressed stronger protective efficacy compared to CUR. These beneficial effects may precisely be associated with suppression of pro-inflammatory factors, TLR4/NFkB and MAPKs signalling. Further studies are in progress.

 Keywords: Arsenic Trioxide; Nano-Curcumin; Mitochondrial Stress; Apoptosis

  1. Leonard A and Lauwerys R R. “Carcinogenicity, teratogenicity and mutagenicity of arsenic”. Mutation Research1 (1980): 49-62.
  2. Rana SVS. “Chemoprevention of arseniasis-past, present and future (mini review)”. Austin Environmental Science 4 (2021): 1084-1097.
  3. Chan PC and Huff J. “Arsenic carcinogenesis in animals and in humans: mechanistic, experimental, and epidemiological evidence”. Journal of Environmental Science and Health Part C 2 (1997): 83-122.
  4. International Agency for Research on Cancer (IARC). “Monograph on the Evaluation of Carcinogenic Risks to Humans”. Monograph 84, Lyon, France (2015).
  5. Esatbeyoglu T., et al. “Curcumin-from molecule to biological function”. Angewandte Chemie International Edition22 (2012): 5308-5332.
  6. Karthikeyan A., et al. “Nanocurcumin: A promising candidate for therapeutic applications”. Frontiers in Pharmacology 11 (2020): 487.
  7. Naranmandura H., et al. “Mitochondria are the main target organelle for trivalent monomethylarsonous acid (MMAIII)-induced cytotoxicity”. Chemical Research in Toxicology7 (2011): 1094-1103.
  8. Bhawana R K., et al. “Curcumin nanoparticles: preparation, characterization, and antimicrobial study”. Journal of Agricultural and Food Chemistry 5 (2011): 2056-2061.
  9. Vashistha L M., et al. “Nano-curcumin ameliorates arsenic induced hepatotoxicity in female rats”. Journal of Environmental Biology 44.6 (2023): 775-783.
  10. Jordan RA and Schenkman JB. “Relationship between malondialdehyde production and arachidonate consumption during NADPH-supported microsomal lipid peroxidation”. Biochemical Pharmacology7 (1982): 1393-1400.
  11. Lowry O., et al. “Protein measurement with the Folin phenol reagent”. Journal of Biological Chemistry 193.1 (1951): 265-275.
  12. Hagihara B. “Techniques for the application of polarography to mitochondrial respiration”. Biochimica et Biophysica Acta 46.1 (1961): 134-142.
  13. Jampol LM and Epstein FH. “Sodium-potassium-activated adenosine triphosphatase and osmotic regulation by fishes”. American Journal of Physiology-Legacy Content 218.2 (1970): 607-611.
  14. Fiske CH and Subbarow Y. “The colorimetric determination of phosphorus”. Journal of Biological Chemistry 66.2 (1925): 375-400.
  15. Creutz C and Sutin N. “Reduction of ferricytochrome c by dithionite ion: electron transfer by parallel adjacent and remote pathways”. Proceedings of the National Academy of Sciences 70.6 (1973): 1701-1703.
  16. Gurtu V. “Fluorometric and colorimetric detection of caspase activity associated with apoptosis”. Analytical Biochemistry 251.1 (1997): 98-102.
  17. Kitchin KT. “Recent advances in arsenic carcinogenesis: modes of action, animal model systems, and methylated arsenic metabolites”. Toxicology and Applied Pharmacology172.3 (2001): 249-261.
  18. Rana SVS. “Mitochondrial stress by toxic elements - an overview, Austin Journal of Pharmacology and Therapeutics 6 (2021): 1155-1163.
  19. Valko M. “Free radicals, metals and antioxidants in oxidative stress-induced cancer”. Chemico-biological Interactions 160.1 (2006): 1-40.
  20. Parija SC., et al. “Vasorelaxation to eugenol, curcumin and nanocurcumin is mediated by differential augmentation of Na+, K+-ATPase activity in middle uterine artery of Capra hircus”. Indian Journal of Traditional Knowledge (IJTK), 20.1 (2021): 59-67.
  21. Ashafaq M., et al. “Neuroprotective effects of nano-curcumin against cypermethrin associated oxidative stress and up-regulation of apoptotic and inflammatory gene expression in rat brains”. Antioxidants 12.3 (2023): 644.
  22. Moustapha A., al. “Curcumin induces crosstalk between autophagy and apoptosis mediated by calcium release from the endoplasmic reticulum, lysosomal destabilization and mitochondrial events”. Cell Death Discovery 1.1 (2015): 15017.
  23. Lim HW., et al. “Uncoupling of oxidative phosphorylation by curcumin: implication of its cellular mechanism of action”. Biochemical and Biophysical Research Communications 389.1 (2009): 187-192.
  24. Khan H., et al. “Significance of inflammation and apoptosis in hepatocellular death in rat, co-treated with arsenic and fluoride”. Biological Trace Element Research200.7 (2022): 3227-3235.
  25. Woo JH., et al. “Molecular mechanisms of curcumin-induced cytotoxicity: induction of apoptosis through generation of reactive oxygen species, down-regulation of Bcl-X L and IAP, the release of cytochrome c and inhibition of Akt”. Carcinogenesis 24.7 (2003): 1199-1208.
  26. Saleem TH., et al. “Effect of curcumin-containing chitosan nanoparticle on caspase-3, carcinoembryonic antigen in colorectal cancer induced by dimethylhydrazine”. Journal of Current Medical Research and Practice4.3 (2019): 302-307.
  27. Pistritto G., et al. D. “Apoptosis as anticancer mechanism: function and dysfunction of its modulators and targeted therapeutic strategies”. Aging (Albany NY) 8.4 (2016): 603-619.
  28. Basniwal RK., et al. “Improving the anticancer activity of curcumin using nanocurcumin dispersion in water”. Nutrition and Cancer66.6 (2014): 1015-1022.
  29. Medda N., et al. “Different mechanisms of arsenic related signaling in cellular proliferation, apoptosis and neo-plastic transformation”. Ecotoxicology and Environmental Safety 208 (2021): 111752.
  30. Sikora E., et al. “Curcumin induces caspase-3-dependent apoptotic pathway but inhibits DNA fragmentation factor 40/caspase-activated DNase endonuclease in human Jurkat cells”. Molecular Cancer Therapeutics5.4 (2006): 927-934.

Suresh Vir Singh Rana., et al. “Modulation of Mitochondrial Stress by Nano-Curcumin in the Liver of Arsenic Treated Rats”. EC Pharmacology and Toxicology  14.1 (2026): 01-10.