Browse > Article

Electrical Stimulation Induces the Collagen Deposition and TGF-${\beta}$1 mRNA Expression in Skin Wound of Rat  

Lee, Jae-Hyoung (Department of Physical Therapy, Wonkwang Health Science University)
Park, Chan-Eui (Department of Physical Therapy, College of Physical Therapy, Southwestern University)
Park, Rae-Joon (Department of Physical Therapy, College of Rehabilitation Sciences, Daegu University)
Publication Information
The Journal of Korean Physical Therapy / v.22, no.3, 2010 , pp. 87-92 More about this Journal
Abstract
Purpose: The purpose of this study was to investigate the effect of electrical stimulation (ES) on the wound closure rate, collagen deposition, and TGF-${\beta}$1 mRNA expression in skin wound of rat. Methods: Twenty male Sprague-Dawley rats (222~271 g) were randomly divided into ES (n=10) and control group (n=10). The ES group received a cathodal stimulation with 50 V at 100 pps for 30 minutes for 7 days, while the control group was not given electrical stimulation. The wound closure rate, collagen density and TGF-${\beta}$1 mRNA ratio were measured. Results: The mean wound closure rates in the ES and control groups were $83.79{\pm}16.35$% and $51.57{\pm}17.76$%, respectively (p<0.001). The collagen density in the ES and control groups were $46.67{\pm}10.68$% and $25.03{\pm}13.09$%, respectively (p<0.001). The TGF-${\beta}$1 mRNA ratio in the ES and control groups were $1.35{\pm}0.60$ and $0.63{\pm}0.30$, respectively at 6 hours post-wound (p<0.01) and $1.69{\pm}0.47$ and $1.32{\pm}0.28$, respectively, at 7 days post-wound (p<0.05). Conclusions: ES accelerated the wound closure rate of skin incision wounds and was accompanied by an increase in collagen deposition in the regenerating dermis. In addition, ES increased TGF-${\beta}$1 mRNA expression during wound healing process. These findings suggest that ES may activate TGF-${\beta}$1 expression, and may increase synthesis activities of fibroblasts in regenerating skin wounds in rats.
Keywords
Electrical stimulation; Wound healing; Collagen density; TGF-${\beta}$1 mRNA; Rat;
Citations & Related Records
Times Cited By KSCI : 2  (Citation Analysis)
연도 인용수 순위
1 Klass BR, Grobbelaar AO, Rolfe KJ. Transforming growth factor beta1 signalling, wound healing and repair: a multifunctional cytokine with clinical implications for wound repair, a delicate balance. Postgrad Med J. 2009;85(999):9-14.   DOI   ScienceOn
2 Rolfe KJ, Richardson J, Vigor C et al. A role for TGFbeta1- induced cellular responses during wound healing of the non-scarring early human fetus? J Invest Dermatol. 2007; 127(11):2656-67.   DOI   ScienceOn
3 Kim YV, Conover DL, Lotz WG et al. Electric field-induced changes in agonist-stimulated calcium fluxes of human HL- 60 leukemia cells. Bioelectromagnetics. 1998;19(6):366-76.   DOI   ScienceOn
4 Aaron RK, Boyan BD, Ciombor DM et al. Stimulation of growth factor synthesis by electric and electromagnetic fields. Clin Orthop Relat Res. 2004;(419):30-7.
5 Zhao M. Electrical fields in wound healing-An overriding signal that directs cell migration. Semin Cell Dev Biol. 2009; 20(6):674-82.   DOI   ScienceOn
6 Bourguignon GJ, Bourguignon LY. Electric stimulation of protein and DNA synthesis in human fibroblasts. FASEB J. 1987;1(5):398-402.   DOI
7 Lee JH, Jekal SJ, Park RJ. Enhance of migration and proliferation of cells from tendon biopsies by high voltage pulsed current stimulation. J Kor Soci Phys Ther. 2002;14(2):53-8.   과학기술학회마을
8 Mani H, Sidhu GS, Kumari R et al. Curcumin differentially regulates TGF-beta1, its receptors and nitric oxide synthase during impaired wound healing. Biofactors. 2002;16(1-2): 29-43.   DOI   ScienceOn
9 Lee JH, Song IY, Kim JG. Acceleration of wound healing and collagen deposition in rat skin by high voltage pulsed current stimulation. J Kor Soci Phys Ther. 2003;15(4):1-12.   과학기술학회마을   DOI
10 Jennings J, Chen D, Feldman D. Transcriptional response of dermal fibroblasts in direct current electric fields. Bioelectromagnetics. 2008;29(5):394-405.   DOI   ScienceOn
11 Barrientos S, Stojadinovic O, Golinko MS et al. Growth factors and cytokines in wound healing. Wound Repair Regen. 2008;16(5):585-601.   DOI   ScienceOn
12 Martinez-Ferrer M, Afshar-Sherif AR, Uwamariya C et al. Dermal transforming growth factor-beta responsiveness mediates wound contraction and epithelial closure. Am J Pathol. 2010;176(1):98-107.   DOI   ScienceOn
13 Heldin CH, Eriksson U, Ostman A. New members of the platelet-derived growth factor family of mitogens. Arch Biochem Biophys. 2002;398(2):284-90.   DOI
14 Riedel K, Riedel F, Goessler UR et al. Tgf-beta antisense therapy increases angiogenic potential in human keratinocytes in vitro. Arch Med Res. 2007;38(1):45-51.   DOI   ScienceOn
15 Harding KG, Morris HL, Patel GK. Science, medicine and the future: healing chronic wounds. BMJ. 2002;324(7330): 160-3.   DOI   ScienceOn
16 Schultz GS, Wysocki A. Interactions between extracellular matrix and growth factors in wound healing. Wound Repair Regen. 2009;17(2):153-62.   DOI   ScienceOn
17 Werner S, Grose R. Regulation of wound healing by growth factors and cytokines. Physiol Rev 2003;83(3):835-70.   DOI
18 Kloth LC, Feedar JA. Acceleration of wound healing with high voltage, monophasic, pulsed current. Phys Ther. 1988;68(4):503-8.   DOI
19 Fitzgerald GK, Newsome D. Treatment of a large infected thoracic spine wound using high voltage pulsed monophasic current. Phys Ther. 1993;73(6):355-60..   DOI
20 Burdge JJ, Hartman JF, Wright ML. A retrospective study of high-voltage, pulsed current as an adjunctive therapy in limb salvage for chronic diabetic wounds of the lower extremity. Ostomy Wound Manage. 2009;55(8):30-8.
21 Bourguignon GJ, Jy W, Bourguignon LY. Electric stimulation of human fibroblasts causes an increase in $Ca^{2+}$ influx and the exposure of additional insulin receptors. J Cell Physiol. 1989;140(2):379-85.   DOI
22 Brown M, McDonnell MK, Menton DN. Electrical stimulation effects on cutaneous wound healing in rabbits. A follow-up study. Phys Ther. 1988;68(6):955-60.   DOI