2011, Número 4
Rev Invest Clin 2011; 63 (4)
Nuevo modelo microquirúrgico para el estudio de la respuesta morfológica adaptativa de injertos venosos
Quiroga-Garza A, Delgado-Brito M, Bazaldúa-Cruz JJ, Villarreal-Silva E, Velázquez-Gauna SE, Elizondo-Omaña RE, Guzmán-López S
Idioma: Español
Referencias bibliográficas: 37
Paginas: 399-406
Archivo PDF: 163.75 Kb.
RESUMEN
Introducción. Se han desarrollado modelos animales para el estudio de la hiperplasia de la túnica íntima, una causa de la estenosis que sufren los injertos venosos.
Objetivo. Establecer un modelo animal de injerto venoso para el estudio de la respuesta morfológica adaptativa a la circulación arterial.
Material y métodos. El estudio se realizó en los Laboratorios de Microcirugía e Histología de la Facultad de Medicina de la Universidad Autónoma de Nuevo León. Se realizó un modelo animal de injerto venoso colocado en la circulación arterial. Para desarrollar el modelo se realizó un estudio morfológico de los vasos sanguíneos de la extremidad caudal de la rata Wistar. Se evaluaron tres posibles sitios para la obtención del injerto venoso.
Resultados. Se observó permeabilidad y viabilidad del injerto sólo en un segmento comprendido entre los ramos musculares y el origen de la vena safena. El segmento venoso obtenido fue colocado en la circulación arterial de la extremidad caudal opuesta al lugar donde se obtuvo el injerto.
Conclusiones. Se estableció un modelo animal de injerto venoso utilizando el segmento de la vena femoral, comprendido entre los ramos musculares y el origen de la vena safena, se colocó en la arteria homónima del lado opuesto.
REFERENCIAS (EN ESTE ARTÍCULO)
Clause BT. The Wistar Institute Archives: rats (not mice) and history. Mendel Newsletter 1998; 7: 2-7.
Sata M, Nagai R. Origin of neointimal cells in autologous vein graft. Arterioscler Thromb Vasc Biol 2004; 24: 1147-9.
Schachner T, Yping Z, Oberhuber A, et al. Local application of rapamycin inhibits neointimal hyperplasia in experimental vein grafts. Ann Thorac Surg 2004; 77: 1580-5.
Asaoka D, Nagahara A, Oguro M, et al. Characteristic pathological findings and effects of ecabet sodium in rat reflux esophagitis. World J Gastroenterol 2009; 15: 3480-5.
Brouwers JEM, Lamberst FM, Gasser JA, et al. Bone degeneration and recovery alter early and late bosphosphonate treatment of ovariectomized Wistar rats assessed by in vivo micro-computed tomography. Calcif Tissue Int 2008; 82: 202-11.
Hidaka S, Okamoto Y, Uchiyama S, et al. Royal jelly prevents osteoporosis in rats: beneficial effects in ovariectomy model and in bone tissue culture model. Evid Based Complement Alternat Med 2006; 3: 339-48.
Mansuroglu T, Dudas J, Elmaouhoub A, et al. Hepatoblast and mesechymal cell-specific gene-expression in fetal rat liver and in cultured fetal rat liver cells. Histochem Cell Biol 2009; 132: 11-9.
Primeaux SE, Barnes MJ, Bray GA. Olfactory bulbectomy increases food intake and hypothalamic neuropeptide Y in obesity- prone but not obesity-resistant rats. Behav Brain Res 2008; 180: 190-6.
Cottone P, Sabino V, Nagy TR, et al. Feed microstructure in diet-induced obesity susceptible versus resistant rats: central effects of urocortin2. J Physiol 2007; 583: 487-504.
Pacharinsak C, Beitz A. Animal models of cancer Pain. Comp Med 2008; 58: 220-33.
Morrone FB, Oliveira DL, Gamermann P, et al. In vivo glioblastoma growth is reduced by apyrase activity in a rat glioma model. BMC Cancer 2006; 6: 226.
Andersen ML, Martins RCS, Elvarenga TAF, et al. Progesterone reduces erectile dysfunction in sleep-deprived spontaneously hypertensive rats. Reprod Biol Endocrinol 2007; 1(5): 7.
Vieyra-Reyes P, Mineur YS, Tunez I, et al. Antidepressant like effects of nicotine and transcranial magnetic stimulation in the olfactory bulbectomy rat model of depresión. Brain Res Bull 2008; 77: 13-8.
Chang CC, Hwang JS, Chan CC, et al. Interaction effects of ultrafine carbon Black with iron and nickel on heart rate variability in spontaneously hypertensive rats. Environ Health Perspect 2007; 115: 1012-7.
Nelli S, Craig J, Martin W. Oxidation by trace Cu2+ ions underlies the ability of ascorbate to induce vascular dysfunction in the rat perfused mesentery. Eur J Pharmacol 2009; 614: 84-90.
Chang Y, Hsieh CY, Peng ZA, et al. Neuroprotective mechanisms of puerarin in middle cerebral artery oclusion-induced brain infarction in rats. J Biomed Sci 2009; 19(16): 9.
Cheng J, Alkayed NJ, Hurn PD. Deleterious effects of dihydrotestosterone on cerebral ischemic injury. J Cereb Blood Flow Metab 2007; 27: 1553-62.
Garrett HE, Dennis EW, De Bakey ME. Aortocoronary bypass with saphenous vein graft: seven year follow-up. JAMA 1973; 223: 792-4.
Wei WI, Lam KH, Wong J. Use of the yarsagil aneurismal clamp for end-to-side microvascular anastomosis: an experimental study in rats. British J Plastic Surg 1983; 36: 363-6.
Dobrin PB, Littooy FN, Endean ED. Mechanical factors predisposing to intimal hyperplasia and medial thickening in autogenous vein grafts. Surgery 1989; 105(3): 393-400.
Dilley RJ, McGeachie JK, Tennant M. The role of cell proliferation and migration in the development of a neo-intimal layer in veins grafted into arteries, in rats. Cell Tissue Res 1992; 269(2): 281-7.
McGeachie JK, Tennant M. The role of cell proliferation and migration in the development of a neo-intimal layer in veins grafted into arteries, in rats. Cell Tissue Res 1992; 269: 281-7.
Gupta SK, Girinshkumar H. Lower extremity revascularization. J Cardiovasc Surg 1993; 34: 229-36.
Tennant M, McGeachie JK. Adaptive remodelling of smooth muscle in the neo-intima of vein-to-artery grafts in rats: a detailed morphometric analysis. Anat Embryol 1993; 187(2): 161-6.
Mills JL, Fujitani RM, Taylor SM. The characteristics and anatomic distribution of lesions that cause reversed vein graft failure: a five year prospective study. J Vasc Surg 1993; 17: 195-204.
Davies MG, Hagen PO. Pathobiology of intimal hyperplasia. Br J Surg 1994; 81: 1254-69.
Zou Y, Dietrich H, Hu Y, Metzler B, Wick G, Zu Q. Mouse model of venous bypass graft arteriosclerosis. Am J Pathol 1998; 153: 1301-10.
Motwani JG, Topol EJ. Aortocoronary saphenous vein graft disease: patogenesis, predisposition, and prevention. Circulation 1998; 97: 916-31.
Leville CD, Osipov VO, Jean Claude JM, Seabrook GR, et al. All-trans-retinoic acid decreases cell proliferation and increases apoptosis in an animal model of vein bypass grafting. Surgery 2000; 128: 178-84.
Kwei S, Starvrakis G, Takhas M, et al. Early adaptative responses of the vascular wall Turing venous arterialization in mice. Am J Pathol 2004; 161: 81-9.
Wai-Man NgR. Training model for end-to-side microvascular anastomosis in rat. Surg Pract 2006; 10: 114-6.
Kudo FA, Muto A, Moloney SP, et al. Venous identity is lost but arterial identity is not gained Turing vein graft adaptation. Arterioscler Thromb Vasc Biol 2007; 27: 1562-71.
Elizondo-Omaña RE. Empleo de polidioxanona, polipropileno o seda como materiales de sutura en anastomosis termino-terminal en arterias muscular, elástica o vena. Tesis doctoral. Monterrey: Facultad de Medicina, Universidad Autónoma de Nuevo León; 2008.
Hifny M, El-Shazly M, El-Osaily M, El-Otiefy M. Histo-pathologic spectrum in the different methods of arterial microvascular anastomoses: an experimental study in the rat femoral artery. J Chinese Cli Med 2007; 2(12): 661-6.
Cooley BC. Murine model of neointimal formation and stenosis in vein grafts. Arterioscler Thromb Vasc Biol 2004; 24: 1180-5.
Lidman D, Daniel RK. The normal Ealing process of microvascular anastomoses. Scand J Plast Reconstr Surg 1981; 15: 103-10.
Qingbo X, Sata M, Nagai R. Mouse models of vein grafts. Arterioscler Thromb Vasc Biol 2004; 24: 185-7.