摘要
Experimental DermatologyVolume 20, Issue 5 p. 413-419 Original Article Stress-induced epinephrine levels compromise murine dermal fibroblast activity through β-adrenoceptors Bruna Romana-Souza, Bruna Romana-Souza Department of Histology and Embryology, Rio de Janeiro State University, Rio de Janeiro, Brazil Department of Animal Biology, Rural Federal University of Rio de Janeiro, Rio de Janeiro, BrazilSearch for more papers by this authorMarcela Otranto, Marcela Otranto Department of Histology and Embryology, Rio de Janeiro State University, Rio de Janeiro, BrazilSearch for more papers by this authorTaís Fontoura Almeida, Taís Fontoura Almeida Department of Histology and Embryology, Rio de Janeiro State University, Rio de Janeiro, BrazilSearch for more papers by this authorLuis Cristóvão Porto, Luis Cristóvão Porto Department of Histology and Embryology, Rio de Janeiro State University, Rio de Janeiro, BrazilSearch for more papers by this authorAndréa Monte-Alto-Costa, Andréa Monte-Alto-Costa Department of Histology and Embryology, Rio de Janeiro State University, Rio de Janeiro, BrazilSearch for more papers by this author Bruna Romana-Souza, Bruna Romana-Souza Department of Histology and Embryology, Rio de Janeiro State University, Rio de Janeiro, Brazil Department of Animal Biology, Rural Federal University of Rio de Janeiro, Rio de Janeiro, BrazilSearch for more papers by this authorMarcela Otranto, Marcela Otranto Department of Histology and Embryology, Rio de Janeiro State University, Rio de Janeiro, BrazilSearch for more papers by this authorTaís Fontoura Almeida, Taís Fontoura Almeida Department of Histology and Embryology, Rio de Janeiro State University, Rio de Janeiro, BrazilSearch for more papers by this authorLuis Cristóvão Porto, Luis Cristóvão Porto Department of Histology and Embryology, Rio de Janeiro State University, Rio de Janeiro, BrazilSearch for more papers by this authorAndréa Monte-Alto-Costa, Andréa Monte-Alto-Costa Department of Histology and Embryology, Rio de Janeiro State University, Rio de Janeiro, BrazilSearch for more papers by this author First published: 01 March 2011 https://doi.org/10.1111/j.1600-0625.2010.01239.xCitations: 25 Dr Andréa Monte-Alto-Costa, Department of Histology and Embryology, Rio de Janeiro State University (UERJ), Rua Professor Manoel de Abreu, 444, 3° andar, 20550-170 Rio de Janeiro, RJ, Brazil, Tel.: +55-21-2587-6509, Fax: +55-21-2587-6511, e-mails: [email protected]; [email protected] Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat Abstract Abstract: Stress-induced catecholamine impairs the formation of granulation tissue acting directly in fibroblast activity; however, the mechanism by which high levels of catecholamines alter the granulation tissue formation is still unclear. Thus, the aim of this study was to investigate how high levels of epinephrine compromise the activity of murine dermal fibroblasts. Dermal fibroblasts isolated from the skin of neonatal Swiss mice were preincubated with α- or β-adrenoceptor antagonists. Thereafter, cells were exposed to physiologically elevated levels of epinephrine or epinephrine plus α- or β-adrenoceptor antagonists, and fibroblast activity was evaluated. The blockade of β1- and β2-adrenoceptors reversed the increase in fibroblast proliferation, ERK 1/2 phosphorylation, myofibroblastic differentiation and the reduction of collagen deposition induced by epinephrine. In addition, the blockade of β3-adrenoceptors reversed the increase in fibroblast proliferation and nitric oxide synthesis as well as the reduction of fibroblast migration, AKT phosphorylation and active matrix metalloproteinase-2 expression induced by epinephrine. However, the blockade of α1- and α2-adrenoceptors did not alter the effects of epinephrine on the activity of murine dermal fibroblasts. In conclusion, high levels of epinephrine directly compromise the activity of neonatal mouse skin fibroblasts through the activation of β1-, β2- and β3-adrenoceptors, but not through α1- and α2-adrenoceptors. Supporting Information Figure S1. Cell migration observed at the edge of a scratch wound in confluent fibroblast cultures treated with epinephrine (E) or epinephrine plus propranolol (PP), SR-59230A (SR), or phentolamine (PT) for 24 hours. Filename Description EXD_1239_sm_figureS1.jpg44 KB Supporting info item Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article. References 1 Li J, Chen J, Kirsner R. Clin Dermatol 2007: 25: 9–18. 2 Gurtner G C, Werner S, Barrandon Y et al. Nature 2008: 453: 314–321. 3 Avitsur R, Kavelaars A, Heijnen C et al. Brain Behav Immun 2005: 19: 311–317. 4 Vileikyte L. Clin Dermatol 2007: 25: 49–55. 5 Gosain A, Muthu K, Gamelli R L et al. Surgery 2007: 142: 170–179. 6 Sivamani R K, Pullar C E, Manabat-Hidalgo C G et al. PLoS Med 2009: 6: 105–115. 7 Romana-Souza B, Otranto M, Vieira A M et al. Brain Behav Immun 2010: 24: 427–437. 8 Humar R, Kiefer F N, Berns H et al. FASEB J 2002: 16: 771–780. 9 Romana-Souza B, Porto L C, Monte-Alto-Costa A. Exp Dermatol 2010: 19: 821–829. 10 Saito T, Tazawa K, Yokoyama Y et al. Surg Today 1997: 27: 627–631. 11 Morellini N M, Giles N L, Rea S et al. Wound Repair Regen 2008: 16: 682–690. 12 Green L C, Wagner D A, Glogowski J et al. Anal Biochem 1982: 126: 131–138. 13 Romana-Souza B, Nascimento A P, Monte-Alto-Costa A. Eur J Pharmacol 2009: 611: 77–84. 14 Schaffer M R, Tantry U, Efron P A et al. Surgery 1997: 121: 513–519. 15 Villarreal F J, Kim N N, Ungab G D et al. Circulation 1993: 88: 2849–2861. 16 Woessner J F. Arch Biochem Biophys 1961: 93: 440–447. 17 Nankova B B, Sabban E L. Acta Physiol Scand 1999: 167: 1–9. 18 Boucek R J, Noble N L. Proc Soc Exp Biol Med 1973: 144: 929–933. 19 Makman M H. Science 1970: 170: 1421–1423. 20 Pullar C E, Isseroff R R. J Cell Sci 2006: 119: 592–602. 21 Colombo F, Noel J, Mayers P et al. J Mol Cell Cardiol 2001: 33: 1091–1106. 22 Anesini C, Borda E. Auton Autacoid Pharmacol 2002: 22: 177–186. 23 Furlan C, Sterin-Borda L, Borda E. Cell Physiol Biochem 2005: 16: 175–182. 24 Gurjar M V, Sharma R V, Bhalla R C. Arterioscler Thromb Vasc Biol 1999: 19: 2871–2877. 25 Kahn A M, Allen J C, Seidel C L et al. Hypertension 2000: 35: 303–306. 26 Yano N, Ianus V, Zhao T C et al. Am J Physiol Heart Circ Physiol 2007: 293: H385–H393. 27 Ciccarelli M, Cipolletta E, Santulli G et al. Cell Signal 2007: 19: 1949–1955. 28 Berg R A, Moss J, Baum B J et al. J Clin Invest 1981: 67: 1457–1462. 29 Swaney J S, Roth D M, Olson E R et al. Proc Natl Acad Sci U S A 2005: 102: 437–442. 30 Baouz S, Giron-Michel J, Azzarone B et al. Int Immunol 2005: 17: 1473–1481. 31 Bhambi B, Eghbali M. Am J Pathol 1991: 139: 1131–1142. 32 Akiyama-Uchida Y, Ashizawa N, Ohtsuru A et al. Hypertension 2002: 40: 148–154. 33 Eijkelkamp N, Engeland C G, Gajendrareddy P K et al. Brain Behav Immun 2007: 21: 409–412. 34 Zhang H, Facemire C S, Banes A J et al. Am J Physiol Heart Circ Physiol 2002: 282: H2364–H2370. Citing Literature Volume20, Issue5May 2011Pages 413-419 ReferencesRelatedInformation