Salvaging the Zone of Stasis By Simvastatin: An Experimental Study in Rats

被引:21
作者
Uygur, Fatih [1 ,2 ]
Evinc, Rahmi [1 ,2 ]
Urhan, Muammer [3 ]
Celikoz, Bahattin [1 ,2 ]
Haholu, Aptullah [4 ,5 ]
机构
[1] Haydarpasa Training Hosp, Dept Plast & Reconstruct Surg, Istanbul, Turkey
[2] Haydarpasa Training Hosp, Burn Unit, Istanbul, Turkey
[3] Haydarpasa Training Hosp, Dept Nucl Med, Istanbul, Turkey
[4] Haydarpasa Training Hosp, Dept Pathol, Gulhane Mil Med Acad, Istanbul, Turkey
[5] Haydarpasa Training Hosp, Fac Med, Istanbul, Turkey
关键词
COA REDUCTASE INHIBITOR; NITRIC-OXIDE SYNTHASE; ENDOTHELIAL-CELLS; PROTEIN-C; THROMBOMODULIN EXPRESSION; BURN INJURY; STATINS; ISCHEMIA; PATHOPHYSIOLOGY; FLUVASTATIN;
D O I
10.1097/BCR.0b013e3181b47eb8
中图分类号
R4 [临床医学];
学科分类号
100218 [急诊医学];
摘要
Salvaging the zone of stasis is important for burn researchers because this can prevent an increase in the depth and width of the injured area. Statin analogues have many pleiotropic effects on the vessel walls and the coagulation and fibrinolytic systems. In this study, we investigated the effects of simvastatin, a statin analogue, administered to rats burned with a metal comb. No treatment was given to the control group (n = 10). Simvastatin was given at a dose of 5 mg/kg/d by intraperitoneal injection in treatment group (n = 10) for 7 days. Phosphate-buffered saline was given I mg/kg/d by intraperitoneal injection in sham group (n = 10). The groups were randomly divided into two subgroups (n = 5) for evaluation at 24 hours and 7 days. It was observed that there were necrotic areas and viable interspaces in both the experimental and control groups at 24 hours. The interspaces progressed to necrotic areas in the control and sham groups at 7 days. However, viable interspaces were separated from necrotic areas clearly in the treatment group at 7 days. In the samples taken from interspaces at 24 hours, positive staining for thrombomodulin (TM) for all groups was noted. In the samples taken from the control and phosphate-buffered saline groups at 7 days, there was negative staining for TM. However, in the samples taken from interspaces of the treatment group, positive staining for TM was observed. The conclusion of this study was that simvastatin potently increased endothelial TM expression in the zone of stasis and preserved the zone. (J Burn Care Res 2009;30:872-879)
引用
收藏
页码:872 / 879
页数:8
相关论文
共 50 条
[1]
THE EFFECTS OF BURN INJURY ON VASOACTIVITY IN HAMSTER PERIPHERAL MICROCIRCULATION [J].
AGGARWAL, SJ ;
DACOSTA, R ;
DILLER, KR ;
HINICH, MJ .
MICROVASCULAR RESEARCH, 1990, 40 (01) :73-87
[2]
Pathophysiology of the burn wound and pharmacological treatment. The Rudi Hermans lecture, 1995 [J].
Arturson, G .
BURNS, 1996, 22 (04) :255-274
[3]
Basse P, 1993, Acta Chir Plast, V35, P86
[4]
Endothelial function and hemostasisEndothelfunktion und Hämostase [J].
B. F. Becker ;
B. Heindl ;
C. Kupatt ;
S. Zahler .
Zeitschrift für Kardiologie, 2000, 89 (3) :160-167
[5]
MICROVASCULAR PATHOPHYSIOLOGY OF BURNED TISSUE [J].
BRANEMAR.PI ;
BREINE, U ;
JOSHI, M ;
URBASCHE.B .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1968, 150 (A3) :474-&
[6]
REDUCTION OF BURN INJURY BY INHIBITING CD18-MEDIATED LEUKOCYTE ADHERENCE IN RABBITS [J].
BUCKY, LP ;
VEDDER, NB ;
HONG, HZ ;
EHRLICH, HP ;
WINN, RK ;
HARLAN, JM ;
MAY, JW .
PLASTIC AND RECONSTRUCTIVE SURGERY, 1994, 93 (07) :1473-1480
[7]
Simvastatin improves endothelial function in spontaneously hypertensive rats through a superoxide dismutase mediated antioxidant effect [J].
Carneado, J ;
de Sotomayor, MA ;
Perez-Guerrero, C ;
Jimenez, L ;
Herrera, MD ;
Pamies, E ;
Martin-Sanz, MDV ;
Stiefel, P ;
Miranda, M ;
Bravo, L ;
Marhuenda, E .
JOURNAL OF HYPERTENSION, 2002, 20 (03) :429-437
[8]
Effects of allopurinol, ibuprofen and cyclosporin A on local microcirculatory disturbances due to burn injuries [J].
Cetinkale, O ;
Demir, M ;
Sayman, HB ;
Ayan, F ;
Onsel, C .
BURNS, 1997, 23 (01) :43-49
[9]
PREVENTING THE INFILTRATION OF LEUKOCYTES BY MONOCLONAL-ANTIBODY BLOCKS THE DEVELOPMENT OF PROGRESSIVE ISCHEMIA IN RAT BURNS [J].
CHOI, M ;
RABB, H ;
ARNAOUT, MA ;
EHRLICH, HP .
PLASTIC AND RECONSTRUCTIVE SURGERY, 1995, 96 (05) :1177-1185
[10]
CHOI MY, 1993, AM J PATHOL, V142, P519