International Journal of Medical Sciences
.: Home > International Journal of Medical Sciences > 2008 > Volume 5 Number 4 > Walter Fries1, Carmelo Muja2, Carmela Crisafulli2, Giuseppe Costantino1, Giuseppe Longo1, Salvatore Cuzzocrea2,3, Emanuela Mazzon2,3
Infliximab and Etanercept Are Equally Effective in Reducing Enterocyte APOPTOSIS in Experimental Colitis
Walter Fries1, Carmelo Muja2, Carmela Crisafulli2, Giuseppe Costantino1, Giuseppe Longo1, Salvatore Cuzzocrea2,3, Emanuela Mazzon2,3
1. Dipartimento di Medicina Interna e Terapia Medica, Sezione di Farmacologia, Università di Messina, Messina, Italy. 2. Dipartimento Clinico-Sperimentale di Medicina e Farmacologia, Sezione di Farmacologia, Università di Messina, Messina, Italy. 3. IRCCS Centro Neurolesi “Bonino-Pulejo”, Messina, Italy.
Loss of epithelial barrier integrity is considered an early step in the pathogenesis of Crohn’s disease (CD), and the rate of enterocyte apoptosis is one of the determinants of the intestinal barrier function. Tumor necrosis factor-ل (TNF-ل), one of the major proinflammatory mediators in CD, is one of the extrinsic signals which initiate apoptosis of enterocytes. The aim of this study was to investigate the early effects of experimental colitis on enterocyte apoptosis, and the effects of two anti-TNF treatments, infliximab (IFX) and etanercept (ETC). In addition, the importance of receptor I for TNF was tested in TNFR-1-/- mice. Circulating TNF-ل levels were effectively reduced by IFX and ETC (p<0.01, both) at 3 and 6 h. Apoptosis of the ileal enterocytes, assessed by TUNEL staining, staining for Fas-ligand, and bax, increased at 3 and 6h. These alterations were prevented by both anti-TNF strategies, and in TNFR-1-/- animals. The anti-apoptotic protein Bcl-2 was expressed in the ileal epithelium under control conditions, but was suppressed in DNB-colitis. Expression of Bcl-2 was maintained in both anti-TNF treatments and TNFR-1-/- mice.
TNF-ل, Enterocyte, Apoptosis, Experimental Colitis
Date Deposited : 28 Jul 2011 11:10
Official URL: http://www.medsci.org/archive
Last Modified : 28 Jul 2011 11:10
Volume 5, Number 4, - 2008 , ISSN 1449-1907
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