S-nitrosoglutathione-containing hydrogel accelerates rat cutaneous wound repair

被引:82
作者
Amadeu, T. P.
Seabra, A. B.
de Oliveira, M. G.
Costa, A. M. A.
机构
[1] State Univ Rio de Janeiro UERJ, Dept Histol & Embryol, BR-20550170 Rio De Janeiro, Brazil
[2] Univ Estadual Campinas, UNICAMP, Inst Chem, Sao Paulo, Brazil
关键词
collagen; mast cells; nitric oxide; skin; vessels; wound healing;
D O I
10.1111/j.1468-3083.2006.02032.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background Nitric oxide (NO) plays a key role in wound repair and S-nitrosothiols like S-nitrosoglutathione (GSNO) are well known NO donors. Methods Animals were separated in two groups and submitted to excisional wounds on the dorsal surface at the first day. GSNO (100 mu m)-containing hydrogels were topically applied on the wound bed in the GSNO group, daily, during the first 4 days. Control group was topically treated with hydrogel without GSNO for the same period. Wound contraction and re-epithelialization were measured. Animals were sacrificed 21 days after wounding. Samples of lesion and normal tissue were formalin-fixed, paraffin embedded for histological analysis. Results Wound contraction, measured 14 and 21 days after wounding, was greater in the GSNO group than in the control group (P < 0.05 for both). The re-epithelialized wound area, measured 14 days after wounding, was higher in the GSNO group than in the control group (P < 0.05). A higher amount of inflammatory cells was observed in superficial and deep areas of the granulation tissue of the control group compared to the GSNO group. Twenty-one days after wounding, thin red-yellow collagen fibers arranged perpendicularly to the surface were found in the granulation tissue of the control group, whereas in the GSNO-treated group collagen fibers were thicker and arranged parallel to the surface. Increased number of mast cells was observed in the GSNO group compared with that in the control group. Vascularization and myofibroblast distribution were similar in both groups. Conclusion Topical application of GSNO-containing hydrogel during the early phases of rat cutaneous wound repair accelerates wound closure and re-epithelialization and affects granulation tissue organization.
引用
收藏
页码:629 / 637
页数:9
相关论文
共 53 条
[1]   Nitrosoglutathione triggers collagen deposition in cutaneous wound repair [J].
Achuth, HN ;
Moochhala, SM ;
Mahendran, R ;
Tan, WTL .
WOUND REPAIR AND REGENERATION, 2005, 13 (04) :383-389
[2]   Nitric oxide synthesis inhibition alters rat cutaneous wound healing [J].
Amadeu, Thais P. ;
Costa, Andrea M. A. .
JOURNAL OF CUTANEOUS PATHOLOGY, 2006, 33 (07) :465-473
[3]  
BARBUL A, 1990, SURGERY, V108, P331
[4]   Controlled release of estradiol solubilized in carbopol/surfactant aggregates [J].
Barreiro-Iglesias, R ;
Alvarez-Lorenzo, C ;
Concheiro, A .
JOURNAL OF CONTROLLED RELEASE, 2003, 93 (03) :319-330
[5]   Constitutive nitric oxide synthase is present in normal human keratinocytes [J].
Baudouin, JE ;
Tachon, P .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1996, 106 (03) :428-431
[6]   Hydroxocobalamins as biologically compatible donors of nitric oxide implicated in the acceleration of wound healing [J].
Bauer, JA .
MEDICAL HYPOTHESES, 1998, 51 (01) :65-67
[7]  
Bauer Joseph A., 1998, Wound Repair and Regeneration, V6, P569, DOI 10.1046/j.1524-475X.1998.60609.x
[8]   EXPRESSION OF VASCULAR-PERMEABILITY FACTOR (VASCULAR ENDOTHELIAL GROWTH-FACTOR) BY EPIDERMAL-KERATINOCYTES DURING WOUND-HEALING [J].
BROWN, LF ;
YEO, KT ;
BERSE, B ;
YEO, TK ;
SENGER, DR ;
DVORAK, HF ;
VANDEWATER, L .
JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 176 (05) :1375-1379
[9]   Nitric oxide in human skin: Current status and future prospects [J].
Bruch-Gerharz, D ;
Ruzicka, T ;
Kolb-Bachofen, V .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1998, 110 (01) :1-7
[10]   Nitric-oxide releasing molecules: A new class of drugs with several major indications [J].
Burgaud, JL ;
Riffaud, JP ;
Del Soldato, P .
CURRENT PHARMACEUTICAL DESIGN, 2002, 8 (03) :201-213