Skip to main content
Log in

Tinospora cordifolia attenuates oxidative stress and distorted carbohydrate metabolism in experimentally induced type 2 diabetes in rats

  • Original Paper
  • Published:
Journal of Natural Medicines Aims and scope Submit manuscript

Abstract

Diabetes is a chronic metabolic disorder affecting a vast number of people worldwide. Oxidative stress is the causative agent amplifying diabetic complications in various organs by generating noxious amount of free radicals. A huge interest always exists in exploring nutraceuticals from plant materials to replace synthetic drugs in order to overcome their adverse effects and also for economic reasons. The anti-diabetic efficiency of a medicinal plant, Tinospora cordifolia (TC) was studied in experimentally induced type 2 diabetes in Sprague–Dawley rats. Diabetes was induced by a combination of high fat diet (HFD) for a period of 10 weeks followed by intraperitoneal injection of streptozotocin (STZ, 35 mg/kg of body weight). Oral treatment of TC (100 and 200 mg/kg body weight) for 14 days regulated blood glucose, provoked insulin secretion and also suppressed oxidative stress marker, thiobarbituric acid reactive substances (TBARS), formation and restored cellular defence anti-oxidant markers including superoxide dismutase (SOD), glutathione peroxidase (GPx) and glutathione (GSH), in liver. Treatment with TC (100 and 200 mg/kg) also inhibited glucose 6-phosphatase and fructose 1,6-diphosphatase (p < 0.001); and restored glycogen content in liver (p < 0.005), which was also studied by histopathological staining with periodic acid–Schiff stain. In conclusion, the traditional plant Tinospora cordifolia mediates its anti-diabetic potential through mitigating oxidative stress, promoting insulin secretion and also by inhibiting gluconeogenesis and glycogenolysis, thereby regulating blood glucose.

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. Singh SS, Pandey SC, Srivastava S, Gupta VS, Patro B, Ghosh AC (2003) Chemistry and medicinal properties of Tinospora cordifolia (Guduchi). Indian J Pharmacol 35:83–91

    CAS  Google Scholar 

  2. Raghunathan K, Sharma PV (1969) The aqueous extract of T. cordifolia caused reduction of blood sugar in alloxan induced hyperglycemic rats and rabbits. J Res Ind Med 3:203–211

    Google Scholar 

  3. Gupta SS, Varma SCL, Garg VP, Rai M (1967) Effect on fasting blood sugar level, glucose tolerance and adrenaline induced hyperglycemia. Indian J Exp Biol 55:733–745

    CAS  Google Scholar 

  4. Reddy SS, Ramatholisammab P, Karunaa R, Saralakumaria D (2009) Preventive effect of Tinospora cordifolia against high-fructose diet-induced insulin resistance and oxidative stress in male Wistar rats. Food Chem Toxicol 47:2224–2229

    Article  PubMed  CAS  Google Scholar 

  5. Zhang M, Lv X, Li J, Xu Z, Chen L (2008) The characterization of high-fat diet and multiple low-dose streptozotocin induced type II diabetes rat model. Exp Diabetes Res 2008:704045. doi:10.1155/2008/704045

    PubMed  Google Scholar 

  6. Buettner R, Parhofer KG, Woenckhaus WCE, Kunz-Schughart LA, Scholmerich J, Bollheimer LC (2006) Defining high-fat-diet rat models: metabolic and molecular effects of different fat types. J Mol Endocrinol 36:485–501

    Article  PubMed  CAS  Google Scholar 

  7. Srinivasan K, Viswanad B, Lydia A, Kaul CL, Ramarao P (2005) Combination of high fat diet and low dose streptozotocin treated rat: a model for type 2 diabetes and pharmacological screening. Pharmacol Res 52:313–320

    Article  PubMed  CAS  Google Scholar 

  8. Kokate CK (1996) Practical pharmacognosy, 4th edn. Vallabh prakashan, Pune

    Google Scholar 

  9. Wagner H, Bladt S (1996) Plant drug analysis: a thin layer chromatography atlas, 2nd edn. Springer-Verlag, Berlin Heidelberg

    Google Scholar 

  10. Ohkawa H, Ohishi N, Yagi K (1979) Assay of lipid peroxides in animal tissues by thiobabituric acid reaction. Anal Biochem 95:351–358

    Article  PubMed  CAS  Google Scholar 

  11. Moren MS, Deplerre JN, Mannevik V (1979) Levels of glutathione-S-transferase activity in rat lung and liver. Arch Biochem Biophys 582:67–74

    Google Scholar 

  12. Kakkar P, Das B, Viswanathan PN (1984) A modified spectrophotometric assay of superoxide dismutase. Indian J Biochem Biophys 21:130–162

    PubMed  CAS  Google Scholar 

  13. Rotruck JT, Pope AL, Ganther HE, Swaason AB, Hafeman DG, Hoekstra WG (1973) Selenium: biochemical role as a component of glutathione peroxidase. Science 179:588–590

    Article  PubMed  CAS  Google Scholar 

  14. Laura B (2005) Prime time for real-time PCR. Nat Methods 2:305–312

    Article  Google Scholar 

  15. Swanson MA (1995) Phosphatases in liver I. Glucose -6-phosphatase. J Appl Biol Chem 184(2):647–706

    Google Scholar 

  16. Gancedo JM, Gancedo C (1971) Fructose-1,6-bisphosphatase, phosphofructokinase and glucose-6-phosphate dehydrogenase from fermenting and nonfermenting yeasts. Arch Mikrobiol 76:132–139

    Article  PubMed  CAS  Google Scholar 

  17. Sadasivam S, Manickam A (1996) Methods in biochemistry. In: Sadasivam S, Manickam A (eds) Carbohydrates. New Age International Pvt. Ltd, New Delhi, pp 11–12

    Google Scholar 

  18. http://www.ihcworld.com/_protocols.htm

  19. Brownlee M (2001) Biochemistry and molecular cell biology of diabetic complications. Nature 414:813–820

    Article  PubMed  CAS  Google Scholar 

  20. Robert JK, Irina M, Joseph FT, Kan L, Jeffrey EK (2001) The potential mechanism of the diabetogenic action of streptozotocin: inhibition of pancreatic beta-cell O-GlcNAc-selective N-acetyl-beta-d-glucosaminidase. J Biochem 356:31–41

    Article  Google Scholar 

  21. Zhao S, Chu Y, Zhang C (2008) Diet induced central obesity and insulin resistance in rabbits. J Anim Physiol Anim Nutr 92:105–111

    CAS  Google Scholar 

  22. Bayens JW (1991) Role of oxidative stress in the development of complications in diabetes. Diabetes 40:405–412

    Article  Google Scholar 

  23. Kakkar R, Kalra J, Mantha SV, Prasad K (1995) Lipid peroxidation and activity of antioxidant enzymes in diabetic rats. Mol Cell Biochem 151:113–119

    Article  PubMed  CAS  Google Scholar 

  24. Andrew A, Richard EG, Thai Kerri, Renae MG, Robyn GL, Alison JC, Kim AC, Yuan Z, Andrew MH, Per KC, Carol AP, Weier Q, Sih MT, Hans-Henrik P, Darren J (2009) Expression, localization, and function of the thioredoxin system in diabetic nephropathy. J Am Soc Nephrol 20:730–741

    Article  Google Scholar 

  25. Consoli A, Nurjhan N, Capani F, Gerich J (1989) Predominant role of gluconeogenesis in increased hepatic glucose production in NIDDM. Diabetes 38:550–557

    Article  PubMed  CAS  Google Scholar 

  26. Nagaraja PK, Kammar KF, Devi Sheela (2007) Modulation of morphology and some gluconeogenic enzymes activity by Tinospora cordifolia (Willd.) in diabetic rat kidney. Biomed Res 18:179–183

    CAS  Google Scholar 

Download references

Acknowledgements

The authors thank the Department of Science and Technology (Govt. of India) for providing fellowship, staff of the Centre for Toxicology and Developmental Research (CEFT) for help in conducting animal studies and the Central Research Facility (CRF) of Sri Ramachandra University for running the RT-PCR.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Hannah R. Vasanthi.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Sangeetha, M.K., Balaji Raghavendran, H.R., Gayathri, V. et al. Tinospora cordifolia attenuates oxidative stress and distorted carbohydrate metabolism in experimentally induced type 2 diabetes in rats. J Nat Med 65, 544–550 (2011). https://doi.org/10.1007/s11418-011-0538-6

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11418-011-0538-6

Keywords

Navigation