WOUND-HEALING ACTIVITY OF ASTRAGALI RADIX IN RATS

被引:14
作者
Han, D. -O. [1 ]
Lee, H. -J. [1 ]
Hahm, D. -H. [1 ]
机构
[1] Kyung Hee Univ, Acupuncture & Meridian Sci Res Ctr, Seoul, South Korea
来源
METHODS AND FINDINGS IN EXPERIMENTAL AND CLINICAL PHARMACOLOGY | 2009年 / 31卷 / 02期
关键词
Astragali Radix; Wound healing; Inflammation; Rat; EPIDERMAL-GROWTH-FACTOR; SKIN; ACTIVATION; EXPRESSION; SAPONINS;
D O I
10.1358/mf.2009.31.2.1353846
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Inhibition of inflammatory responses, acceleration of basal cell growth and balanced synthesis of the extracellular matrix (ECM) ate important in the healing of open cutaneous Wounds. To evaluate the wound-healing effects of Astragali Radix (AR) (the root of Astragalus membranaceus [Fisch.]), experimental open wounds were made on the dorsal side of rats under anesthesia. Boiling water extracts of AR, soaked into a hydrophilic foam dressing, were topically applied to the wounds once a day for 71 consecutive days. The healing process was assessed by scoring macroscopic appearance and measuring the area of the open wounds. Molecular aspects of the healing skin area were also investigated via histological observation indicating cell density and linear alignment Of the granulation tissue. The AR extracts significantly accelerated cutaneous Wound healing by suppressing inflammation and stimulating basal cell growth in the wound area compared to epidermal growth factor as a positive control. Promotion of basal cell proliferation and angiogenesis by the AR extracts was remarkable in the early stages of wound healing, resulting in a significant reduction in the duration of the wound-healing process. We Conclude 0301 extracts of AR could be useful in enhancing cutaneous wound healing.
引用
收藏
页码:95 / 100
页数:6
相关论文
共 33 条
[1]
Wound healing acceleration of a novel transforming growth factor-β inducer, SEK-1005 [J].
Abe, Y ;
Inagaki, K ;
Fujiwara, A ;
Kuriyama, K .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2000, 408 (02) :213-218
[2]
Methylglyoxal administration induces diabetes-like microvascular changes and perturbs the healing process of cutaneous wounds [J].
Berlanga, J ;
Cibrian, D ;
Guillén, I ;
Freyre, F ;
Alba, JS ;
Lopez-Saura, P ;
Merino, N ;
Aldama, A ;
Quintela, AM ;
Triana, ME ;
Montequin, JF ;
Ajamieh, H ;
Urquiza, D ;
Ahmed, N ;
Thornalley, PJ .
CLINICAL SCIENCE, 2005, 109 (01) :83-95
[3]
Fibroblast growth factor 22 and its potential role during skin development and repair [J].
Beyer, TA ;
Werner, S ;
Dickson, C ;
Grose, R .
EXPERIMENTAL CELL RESEARCH, 2003, 287 (02) :228-236
[4]
SUSTAINED-RELEASE OF EPIDERMAL GROWTH-FACTOR ACCELERATES WOUND REPAIR [J].
BUCKLEY, A ;
DAVIDSON, JM ;
KAMERATH, CD ;
WOLT, TB ;
WOODWARD, SC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (21) :7340-7344
[5]
CARE KRG, 2002, ADV WOUND CARE, P43
[6]
Chao JCJ, 2003, WORLD J GASTROENTERO, V9, P2261
[7]
CHU J, 2001, BONKYUNGSOJENG, V1, P107
[8]
Towards a molecular definition of keratinocyte activation after acute injury to stratified epithelia [J].
Coulombe, PA .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 236 (02) :231-238
[9]
CZAP K, 2003, ALTERN MED REV, V8, P72
[10]
Role for gap junctional intercellular communications in wound repair [J].
Ehrlich, HP ;
Diez, T .
WOUND REPAIR AND REGENERATION, 2003, 11 (06) :481-489