Castilla-Cortázar Inma, Pascual María, Urdaneta Elena, Pardo Javier, Puche Juan Enrique, Vivas Bárbara, Díaz-Casares Amelia, García María, Díaz-Sánchez Matías, Varela-Nieto Isabel, Castilla Alberto, González-Barón Salvador
Department of Physiology, Clínica Universitaria, University of Navarra, Pamplona, Spain.
BMC Gastroenterol. 2004 Jun 14;4:12. doi: 10.1186/1471-230X-4-12.
Previous results have shown that in rats with non-ascitic cirrhosis there is an altered transport of sugars and amino acids associated with elongated microvilli. These alterations returned to normal with the administration of Insulin-Like Growth Factor-I (IGF-I). The aims of this study were to explore the evolution of these alterations and analyse the effect of IGF-I in rats with advanced cirrhosis and ascites. Thus, jejunal structure and nutrient transport (D-galactose, L-leucine, L-proline, L-glutamic acid and L-cystine) were studied in rats with ascitic cirrhosis.
Advanced cirrhosis was induced by CCl4 inhalation and Phenobarbital administration for 30 weeks. Cirrhotic animals were divided into two groups which received IGF-I or saline during two weeks. Control group was studied in parallel. Jejunal microvilli were studied by electron microscopy. Nutrient transport was assessed in brush border membrane vesicles using 14C or 35S-labelled subtracts in the three experimental groups.
Intestinal active Na+-dependent transport was significantly reduced in untreated cirrhotic rats. Kinetic studies showed a decreased Vmax and a reduced affinity for sugar and four amino acids transporters (expressed as an increased Kt) in the brush border membrane vesicles from untreated cirrhotic rats as compared with controls. Both parameters were normalised in the IGF-I-treated cirrhotic group. Electron microscopy showed elongation and fusion of microvilli with degenerative membrane lesions and/or notable atrophy.
The initial microvilli elongation reported in non ascitic cirrhosis develops into atrophy in rats with advanced cirrhosis and nutrient transports (monosaccharides and amino acids) are progressively reduced. Both morphological and functional alterations improved significantly with low doses of IGF-I.
先前的研究结果表明,在非腹水型肝硬化大鼠中,存在与微绒毛延长相关的糖类和氨基酸转运改变。给予胰岛素样生长因子-I(IGF-I)后,这些改变恢复正常。本研究的目的是探讨这些改变的演变过程,并分析IGF-I对晚期肝硬化伴腹水大鼠的影响。因此,对腹水型肝硬化大鼠的空肠结构和营养物质转运(D-半乳糖、L-亮氨酸、L-脯氨酸、L-谷氨酸和L-胱氨酸)进行了研究。
通过吸入四氯化碳和给予苯巴比妥30周诱导晚期肝硬化。将肝硬化动物分为两组,在两周内分别给予IGF-I或生理盐水。同时对对照组进行研究。通过电子显微镜研究空肠微绒毛。在三个实验组中,使用14C或35S标记的底物评估刷状缘膜囊泡中的营养物质转运。
未经治疗的肝硬化大鼠肠道依赖钠的主动转运显著降低。动力学研究表明,与对照组相比,未经治疗的肝硬化大鼠刷状缘膜囊泡中糖类和四种氨基酸转运体的Vmax降低,亲和力降低(表现为Kt增加)。在IGF-I治疗的肝硬化组中,这两个参数均恢复正常。电子显微镜显示微绒毛延长和融合,伴有退行性膜病变和/或明显萎缩。
非腹水型肝硬化中最初报道的微绒毛延长在晚期肝硬化大鼠中发展为萎缩,营养物质转运(单糖和氨基酸)逐渐减少。低剂量的IGF-I可使形态和功能改变均得到显著改善。