Topical pretreatment of diabetic rats with all-trans retinoic acid improves healing of subsequently induced abrasion wounds

被引:31
作者
Lateef, H
Abatan, OI
Aslam, MN
Stevens, MJ
Varani, J
机构
[1] Univ Michigan, Dept Pathol, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Internal Med, Ann Arbor, MI 48109 USA
[3] Ann Arbor Vet Adm Hosp, Ann Arbor, MI USA
关键词
D O I
10.2337/diabetes.54.3.855
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In the current study, rats were made diabetic with streptozotocin (STZ) and maintained for 8 weeks, during which time they were treated topically on alternative days with a solution of 0.1% all-trans retinoic acid in a vehicle of 70:30% ethanol/propylene glycol. STZ-induced diabetic rats treated with vehicle served as controls. Additional nondiabetic rats were treated with all-trans retinoic acid or vehicle in parallel. At the end of the 8-week period, rats from all four treatment groups were subjected to abrasion wound formation, Wounds healed more rapidly in vehicle-treated nondiabetic skin than in vehicle-treated diabetic skin (96% of the wound surface area closed in nondiabetic rats within 6 days vs. 41% closed in diabetic rats). Wounds in all-trans retinoic acid-treated diabetic skin healed more rapidly than wounds in vehicle-treated diabetic skin (85% of the wound surface area closed in all-trans retinoic acid-treated diabetic rats vs. 41% closed in vehicle-treated diabetic rats). At the histological level, recently healed skin from vehicle-treated diabetic rats was shown to contain a thin, wispy provisional matrix in which many of the embedded cells were rounded and some were pycnotic. In contrast, a much denser provisional matrix with large numbers of embedded spindle-shaped cells was observed in healed wounds from diabetic skin that had been pretreated with all-trans retinoic acid. The all-trans retinoic acid-treated diabetic skin was histologically similar to vehicle-treated (or all-trans retinoic acid-treated) skin from nondiabetic animals. In light of these findings, we suggest that prophylactic use of retinoid-containing preparations might be useful in preventing the development of non-healing skin ulcers resultant from minor traumas in at-risk skin.
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收藏
页码:855 / 861
页数:7
相关论文
共 53 条
[1]   HISTOLOGIC-CHANGES IN THE SKIN OF THE RHINO MOUSE (HRRHHRRH) INDUCED BY RETINOIDS [J].
ASHTON, RE ;
CONNOR, MJ ;
LOWE, NJ .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1984, 82 (06) :632-635
[2]  
ASLAM MN, IN PRESS J INVEST DE
[3]   UNCOORDINATE EXPRESSIONS OF TYPE-I AND TYPE-III COLLAGENS, COLLAGENASE AND TISSUE INHIBITOR OF MATRIX METALLOPROTEINASE-1 ALONG IN-VITRO PROLIFERATIVE LIFE-SPAN OF HUMAN SKIN FIBROBLASTS - REGULATION BY ALL-TRANS-RETINOIC ACID [J].
BIZOTFOULON, V ;
BOUCHARD, B ;
HORNEBECK, W ;
DUBERTRET, L ;
BERTAUX, B .
CELL BIOLOGY INTERNATIONAL, 1995, 19 (02) :129-135
[4]   ALTERED TRANSCRIPTIONAL REGULATION OF HUMAN INTERSTITIAL COLLAGENASE IN CULTURED SKIN FIBROBLASTS FROM OLDER DONORS [J].
BURKE, EM ;
HORTON, WE ;
PEARSON, JD ;
CROW, MT ;
MARTIN, GR .
EXPERIMENTAL GERONTOLOGY, 1994, 29 (01) :37-53
[5]   RETINOIC ACID RECEPTOR-GAMMA MEDIATES TOPICAL RETINOID EFFICACY AND IRRITATION IN ANIMAL-MODELS [J].
CHEN, S ;
OSTROWSKI, J ;
WHITING, G ;
ROALSVIG, T ;
HAMMER, L ;
CURRIER, SJ ;
HONEYMAN, J ;
KWASNIEWSKI, B ;
YU, KL ;
STERZYCKI, R ;
KIM, CU ;
STARRETT, J ;
MANSURI, M ;
RECZEK, PR .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1995, 104 (05) :779-783
[6]  
ELIAS PM, 1981, LAB INVEST, V44, P531
[7]   Molecular basis of sun-induced premature skin ageing and retinoid antagonism [J].
Fisher, GJ ;
Datta, SC ;
Talwar, HS ;
Wang, ZQ ;
Varani, J ;
Kang, S ;
Voorhees, JJ .
NATURE, 1996, 379 (6563) :335-339
[8]   Pathophysiology of premature skin aging induced by ultraviolet light [J].
Fisher, GJ ;
Wang, ZQ ;
Datta, SC ;
Varani, J ;
Kang, S ;
Voorhees, JJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 337 (20) :1419-1428
[9]   THE STEADY-STATE LEVELS OF TYPE-I COLLAGEN MESSENGER-RNA ARE REDUCED IN SENESCENT FIBROBLASTS [J].
FURTH, JJ .
JOURNALS OF GERONTOLOGY, 1991, 46 (03) :B122-B124
[10]   Characterization of matrix metalloproteinases produced by rat alveolar macrophages [J].
Gibbs, DF ;
Warner, RL ;
Weiss, SJ ;
Johnson, KJ ;
Varani, J .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1999, 20 (06) :1136-1144