Skip to main content
Log in

Ipomoea staphylina Attenuates Potassium Dichromate-Induced Nephrotoxicity in Wistar Rats via Antioxidant and Antiapoptotic Effects

  • BIOCHEMISTRY, BIOPHYSICS, AND MOLECULAR BIOLOGY
  • Published:
Doklady Biochemistry and Biophysics Aims and scope Submit manuscript

Abstract

Occupational and environmental exposure to chromium compounds leads to nephrotoxicity to humans and animals due to the overproduction of ROS. Our study was aimed to demonstrate the shielding effect of hydroethanolic extract of Ipomoea staphylina (HEIS) bark on male Wistar rats challenged with potassium dichromate (K2Cr2O7). Division of animals was done in 4 groups’ viz., normal control, K2Cr2O7 control, K2Cr2O7+HEIS (100 mg/kg), and K2Cr2O7+HEIS (200 mg/kg). Except for the normal control group, other groups were challenged with a single dose (subcutaneous) of K2Cr2O7 (15 mg/kg) and then treated with HEIS (100 and 200 mg/kg) for 1 week. It was observed that animals treated with K2Cr2O7 showed a notable increase in serum creatinine, blood urea, and BUN and dwindles in protein level. These changes were significantly reversed after a 1-week treatment with HEIS (100 and 200 mg/kg). Moreover, HEIS (100 and 200 mg/kg) showed a remarkable improvement in the activity of antioxidant enzymes (GPx, CAT, and SOD) and decreased the levels of TNF-α and IL-1β in the kidney. Furthermore, treatment with HEIS (100 and 200 mg/kg) notably decreased the activity of caspase-3 and improved the level of HO-1 especially in the K2Cr2O7+ HEIS (200 mg/kg) group. Also, the histopathological study of the kidney supported the protective effects of HEIS. Hence, HEIS bark holds a notable protective effect against K2Cr2O7-induced nephrotoxicity in rats.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1.
Fig. 2.

Similar content being viewed by others

REFERENCES

  1. Yatera, K., Morimoto, Y., Ueno, S., Noguchi, S., Kawaguchi, T., Tanaka, F., Suzuki, H., and Higashi, T., Cancer risks of hexavalent chromium in the respiratory tract, J. Uoeh., 2018, vol. 40, pp. 157–172.

    Article  CAS  Google Scholar 

  2. Pechova, A. and Pavlata, L., Chromium as an essential nutrient: a review, Vet. Med., 2007, vol. 52, no. 1, pp. 1–18.

    Article  CAS  Google Scholar 

  3. Suh, M., Wikoff, D., Lipworth, L., Goodman, M., Fitch, S., Mittal, L., Ring, C., and Proctor, D., Hexavalent chromium and stomach cancer: a systematic review and meta-analysis, Crit. Rev. Toxicol., 2019, vol. 49, no. 2, pp. 140–159.

    Article  CAS  Google Scholar 

  4. Guo, Y., Wang, Y., and Huang, B., The acute toxicity effects of hexavalent chromium in antioxidant system and gonad development to male clam Geloina coaxans, Eur. Zool. J., 2020, vol. 87, no. 1, pp. 325–335.

    Article  Google Scholar 

  5. EL-Guendouz, S., Zizi, S., Elamine, Y., and Lyoussi, B., Preliminary screening of the possible protective effect of moroccan propolis against chromium induced nephrotoxicity in animal model, Vet. World, 2020, vol. 13, no. 7, pp. 1327–1333.

    Article  CAS  Google Scholar 

  6. Wu, F., Li, S., Zhang, N., Huang, W., Li, X., Wang, M., Bai, D., and Han, B., Hispidulin alleviates high-glucose-induced podocyte injury by regulating protective autophagy, Biomed. Pharmacother., 2018, vol. 104, pp. 307–314.

    Article  CAS  Google Scholar 

  7. Athira, K., Madhana, R.M., and Lahkar, M., Flavonoids, the emerging dietary supplement against cisplatin-induced nephrotoxicity, Chem. Biol. Interact., 2016, vol. 248, pp. 18–20.

    Article  CAS  Google Scholar 

  8. Bag, A.K. and Mumtaz, S.M.F., Hepatoprotective and nephroprotective activity of hydroalcoholic extract of Ipomoea staphylina leaves, Bangladesh J. Pharmacol., 2013, vol. 8, pp. 263–268.

    Article  Google Scholar 

  9. OECD, 2002. Acute Oral Toxicity. Acute Oral Toxic Class Method Guideline 423 Adopted 3.03.1996, in Eleventh Addendum to the OECD Guidelines for the Testing of Chemicals Organisation for Economic Co-Operation Development, Paris, June, 2000.

  10. Bucher, J.R., NTP toxicity studies of sodium dichromate dihydrate (CAS No. 7789-12-0) administered in drinking water to male and female F344/N rats and B6C3F1 mice and male BALB/c and am3-C57BL/6 mice, Toxic Rep. Ser., 2007; 72, pp. 1–G4.

    Google Scholar 

  11. Salminen, A. and Vihko, V., Lipid peroxidation in exercise myopathy, Exp. Mol. Pathol., 1983, vol. 38, pp. 380–388.

    Article  CAS  Google Scholar 

  12. Dennis, J.M. and Witting, P.K., Protective role for antioxidants in acute kidney disease, Nutrients, 2017, vol. 9, no. 7, p. 718.

    Article  Google Scholar 

  13. Araújo, L.S., Torquato, B.G.S., da Silva, C.A., Monteiro, M.L.G.D.R., Martins, A.L.M.D.S., da Silva, M.V., Reis, M.A.D., and Machado, J.R., Renal expression of cytokines and chemokines in diabetic nephropathy, Nephrology, 2020, vol. 21, p. 308.

    PubMed  PubMed Central  Google Scholar 

  14. Yorulmaz, H.O. and Konuskan, D.B., Antioxidant activity, sterol and fatty acid compositions of Turkish olive oils as an indicator of variety and ripening degree, J. Food Sci. Technol., 2017, vol. 54, no. 12, pp. 4067–4077.

    Article  CAS  Google Scholar 

  15. MC, Rimessi, A., Bezzerri, V., Nicolis, E., Guerrini, A., Tacchini, M., Tamanini, A., Munari, S., D’Aversa, E., Santangelo, A., Lippi, G., Sacchetti, G., Pinton, P., Gambari, R., Agostini, M., and Cabrini, G., β-sitosterol reduces the expression of chemotactic cytokine genes in cystic fibrosis bronchial epithelial cells, Front. Pharmacol., 2017, vol. 8, p. 236.

    Article  Google Scholar 

  16. Bashandy, S.A.E., Mohamed, M.A., Morsy, F.A., and El-Marasy SA. Amelioration of the nephrotoxic effect of potassium dichromate by whey protein and/or Nigella sativa oil in male albino rats, J. Appl. Pharm. Sci., 2016, vol. 6, no. 8, pp. 44–50.

    Article  CAS  Google Scholar 

  17. Parveen, K., Khan, M.R., and Siddiqui, W.A., Pycnogenol® prevents potassium dichromate (K2Cr2O7)-induced oxidative damage and nephrotoxicity in rats, Chem. Biol. Interact., 2009, vol. 181, pp. 343–350.

    Article  CAS  Google Scholar 

  18. Shirazi, M., Eslahi, A., Shari, V., Rahimi, F., and Safarpour, A., Evaluation of caspase 3 enzyme and TNF-alpha as biomarkers in ureteropelvic junction obstruction in children—a preliminary report, Pak. J. Med. Sci., 2017, vol. 33, no. 2, pp. 315–319.

    PubMed  PubMed Central  Google Scholar 

  19. Pei, J., Cai, S., Song, S., Xu, Y., Feng, M., Luo, G., Wang, Y., Sun, F., Shi, H., and Xu, S., Normobaric hyperoxia plays a protective role against renal ischemia-reperfusion injury by activating the Nrf2/HO-1 signaling pathway, Biochem. Biophys. Res. Commun., 2020, vol. 532, no. 1, pp. 151–158.

    Article  CAS  Google Scholar 

Download references

ACKNOWLEDGMENTS

The authors gratefully acknowledge Department of Nephrology of Chengdu Fifth People’s Hospital for providing facilities to carry out the work.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Jinping Huang.

Ethics declarations

CONFLICT OF INTEREST

Authors have declared that there is no conflict of interest.

COMPLIANCE WITH ETHICAL STANDARDS

The study on animals was approved by the Animal Ethics Committee of Chengdu Fifth People’s Hospital, Sichuan, China (ethics number: cddwrmyy2019122801).

ABBREVIATIONS

AR—Analytical reagent, BUN—Blood Urea Nitrogen, CAT—Catalase, GSH—Reduced Glutathione, GPx—Glutathione Peroxidase, H&E—Hematoxylin and Eosin, HO-1—Heme Oxygenase 1, IL-1β—Interleukin-1β, LPO—Lipid Peroxidation, O2•−—Superoxide Anion, Nrf2— Nuclear factor erythroid 2-related factor 2, SOD—Superoxide Dismutase, TNF-α—Tumor Necrosis Factor-α.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Feng, H., Feng, Q., Xiao, T. et al. Ipomoea staphylina Attenuates Potassium Dichromate-Induced Nephrotoxicity in Wistar Rats via Antioxidant and Antiapoptotic Effects. Dokl Biochem Biophys 499, 289–295 (2021). https://doi.org/10.1134/S1607672921040074

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1134/S1607672921040074

Keywords:

Navigation