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The Wound Healing Effect of Hydnocarpi Semen Extract on Ulcer in Diabetic Mice

  • Received : 2010.06.08
  • Accepted : 2010.07.16
  • Published : 2010.07.31

Abstract

The extract from Hydnocarpi Semen (HS) has been used to treat leprosy and its anti-inflammatory activity has been reported. However, the effect of HS on the treatment of diabetic or peripheral ulcer is not well known. We therefore examined its wound healing effects on ulcer area in diabetic mice. GC and GC/MS analysis with the total extract of HS show that the main constituents of the extract are chaulmoogric acid, hydnocarpic acid, and gorlic acid. Whereas HS showed wound healing effect in diabetic ulcer, there was no hypoglycemic effect in diabetic mice. The treatment of HS extract significantly decreased the level of total WBC and neutrophils in mice compared to control mice. Cutting ulcer was induced by the round-shaped punch on the backside of diabetic mice and the extract of HS was given orally or topically. The wound area score significantly decreased after treatment of HS at dose of 50 mg/kg. The treatment of HS also induced the activation of macrophages and increased the production of IL-12 and TNF-$\alpha$ in macrophages, indicating that the wound healing by HS extract is associated with the inflammatory effect via the activation of macrophages. Our results suggest that HS extract can be a new therapeutic candidate for treatment of diabetic ulcer.

Keywords

References

  1. Ajabnoor, M. A. (1990). Effect of aloes on blood glucose levels in normal and alloxan diabetic mice. J. Ethnopharmacol. 28, 215-220. https://doi.org/10.1016/0378-8741(90)90031-N
  2. Chithra, P., Sajithlal, G. B., and Chandrakasan. G. (1998). Influnce of aloe vera on the healing of dermal wounds in diabetic rats. J. Ethnopharmacol. 59, 195-201. https://doi.org/10.1016/S0378-8741(97)00124-4
  3. Goodson, W. H. 3rd. and Hunt, T. K. (1979). Wound healing and the diabetic patient. Surg. Gynecol. Obstet. 149, 600-608.
  4. Ivora, M. D., Paya, M. and Villar, A. (1989). A review of natural products and plants as potential antidiabetic drugs. J. Ethnopharmacol. 27, 243-275. https://doi.org/10.1016/0378-8741(89)90001-9
  5. Kang , T. J., Fenton, M. J., Weiner, M. A., Hibbs, S., Baillie, L. and Cross, A. S. (2005). Murine macrophages kill the vegetative form of Bacillus anthracis. Infect. Immun. 73, 7495-7501. https://doi.org/10.1128/IAI.73.11.7495-7501.2005
  6. Levy, L. (1975). The activity of chaulmoogra acids against Mycobacterium leprae. Am. Rev. Respir. Dis. 111, 703-705.
  7. Lukic, M. L., Stosic-Grujicic, S. and Shahin, A. (1998). Effector mechanisms in low dose sterptozotocin induced diabetes. Dev. Immunol. 6, 119-128. https://doi.org/10.1155/1998/92198
  8. Meghana, K., Sanjeev, G. and Ramesh, B. (2007). Curcumin prevents streptozotocin-induced islet damage by scavenging free radicals: a prophylactic and protective role. Eur. J. Pharmacol. 577, 183-191. https://doi.org/10.1016/j.ejphar.2007.09.002
  9. Oommen, S. T. (2000). The effect of oil of hydnocarpus on excision wounds. Int. J. Lepr. Other. Mycobact. Dis. 68, 69-70.
  10. Oommen, S. T., Rao, M. and Raju, C. V. (1999). Effect of oil of hydnocarpus on wound healing. Int. J. Lepr. Other. Mycobact. Dis. 67,154-158.
  11. Park, J. S., Yang, J. S., Hwang, B. Y., Yoo, B. Y. and Han, K. (2009). Hypoglycemic effect of Yacon tuber extract and its constituent chlorogenic acid, in streptozotocin-induced diabetic rats. Biomol. & Ther. 17, 256-262. https://doi.org/10.4062/biomolther.2009.17.3.256
  12. Raghow, R. (1994). The role of extracellular matrix in post inflammatory wound healing and fibrosis. FASEB. J. 8, 823-831. https://doi.org/10.1096/fasebj.8.11.8070631
  13. Sharma, D. K. and Hall, I. H. (1991). Hypolipidemic, anti-inflammatory, and antineoplastic activity and cytotoxicity of flavonolignans isolated from Hydnocarpus wightiana seeds. J. Nat. Prod. 54, 1298-1302. https://doi.org/10.1021/np50077a010
  14. Spinas, G. A. (1999). The Dual Role of Nitric Oxide in Islet beta-Cells. News. Physiol. Sci. 14, 49-54.

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