Fikru A., Makonnen E., Eguale T., Debella A., Abie Mekonnen G.
Faculty of Veterinary Medicine, University of Gondar, P.O. Box 196, Gondar, Ethiopia; Department of Pharmacology, School of Medicine, Addis Ababa University, P.O. Box 9086, Addis Ababa, Ethiopia; Akililu Lemma Institute of Pathobiology, Addis Ababa University, P.O. Box 1176, Addis Ababa, Ethiopia; Department of Drug Research, Ethiopian Health and Nutrition Research Institute, P.O. Box 1242, Addis Ababa, Ethiopia; Department of Pathology, National Animal Health Diagnostic and Investigation Center, P.O. Box, 04, Sebeta, Ethiopia
Fikru, A., Faculty of Veterinary Medicine, University of Gondar, P.O. Box 196, Gondar, Ethiopia; Makonnen, E., Department of Pharmacology, School of Medicine, Addis Ababa University, P.O. Box 9086, Addis Ababa, Ethiopia; Eguale, T., Akililu Lemma Institute of Pathobiology, Addis Ababa University, P.O. Box 1176, Addis Ababa, Ethiopia; Debella, A., Department of Drug Research, Ethiopian Health and Nutrition Research Institute, P.O. Box 1242, Addis Ababa, Ethiopia; Abie Mekonnen, G., Department of Pathology, National Animal Health Diagnostic and Investigation Center, P.O. Box, 04, Sebeta, Ethiopia
Ethnopharmacological relevance: The leaves of Achyranthes aspera L. (Amarenthacea) has been used traditionally for the treatment of wound in various parts of Ethiopia. However, the plant has not been explored scientifically for its wound healing activity. Therefore, this study was designed to investigate the wound healing activity of methanol extract of Achyranthes aspera L. leaves in rats. Materials and methods: Incision and excision wounds were inflicted on albino rats of either sex, under diethyl ether anesthesia. Group I served as positive control and was treated with 1% silver sulphadiazine, group II, III, IV treated with simple ointment containing 2.5%, 5% and 10% (w/w) methanol extract of the leaves of Achyranthes aspera L.; respectively, whereas group V served as negative control and was treated with simple ointment. All the animals were treated topically once a day. Wound healing potential was assessed with excision and incision wound model. Excision wound model was used to assess the change in percentage contraction of wound, epithelization time, DNA content and histological features whereas rats inflicted with the incision wounds were used to determine breaking strength. Results: Based on the results of percentage wound contraction, the DNA content and epithelization time, all groups of rats treated with methanol extract of the leaves of Achyranthes aspera L. showed significant (p<0.05) wound healing activity compared to group of rats treated with simple ointment (negative control) group. The difference in breaking strength was, however, significant (p<0.05) only for the 5% and 10% methanol extract of Achyranthes aspera (w/w) ointment treated groups. Histological evaluation showed well organized epidermal layer, increased number of fibrocytes, remarkable degree of neovascularization and epithelization which was comparable to the standard on the 21st day after treatment; especially in the 5% and 10% (w/w) extract treated group. Conclusion: The present study provides a scientific rationale for the traditional use of the leaf extracts of Achyranthes aspera L. in the treatment of wound. © 2012 Elsevier Ireland Ltd.
Achyranthes aspera extract; ether; sulfadiazine silver; wound healing promoting agent; Achyranthes aspera; animal experiment; animal model; article; controlled study; DNA content; epidermis; epithelization; excision; female; in vivo study; incision; male; medicinal plant; nonhuman; plant leaf; rat; wound contraction; wound healing; Achyranthes; Animals; DNA; Ethiopia; Female; Male; Medicine, African Traditional; Methanol; Phytotherapy; Plant Extracts; Plant Leaves; Rats; Skin; Solvents; Wound Healing; Achyranthes aspera; Animalia; Rattus