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在严重慢性肝损伤大鼠模型中,骨髓多能间充质基质细胞不会减轻纤维化或改善功能。

Bone marrow multipotent mesenchymal stromal cells do not reduce fibrosis or improve function in a rat model of severe chronic liver injury.

作者信息

Carvalho Adriana B, Quintanilha Luiz Fernando, Dias Juliana V, Paredes Bruno D, Mannheimer Elida G, Carvalho Felipe G, Asensi Karina D, Gutfilen Bianca, Fonseca Lea Mirian B, Resende Celia Maria C, Rezende Guilherme F M, Takiya Christina M, de Carvalho Antonio Carlos Campos, Goldenberg Regina C S

机构信息

Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.

出版信息

Stem Cells. 2008 May;26(5):1307-14. doi: 10.1634/stemcells.2007-0941. Epub 2008 Feb 28.

Abstract

The objective of our study was to evaluate the therapeutic potential of bone marrow mesenchymal stromal cells (MSC) in a rat model of severe chronic liver injury. Fourteen female Wistar rats were fed exclusively an alcoholic liquid diet and received intraperitoneal injections of carbon tetrachloride every other day during 15 weeks. After this period, eight animals (MSC group) had 1 x 10(7) cells injected into the portal vein while six animals (placebo group) received vehicle. Blood analysis was performed to evaluate alanine aminotransferase (ALT), aspartate aminotransferase (AST), and albumin before cell therapy and 1 and 2 months after cell or placebo infusion. Fibrosis was evaluated before and 1 month after cell or placebo injection by liver biopsies. Two months after cell delivery, animals were sacrificed and histological analysis of the livers was performed. Fibrosis was quantified by histomorphometry. Biopsies obtained before cell infusion showed intense collagen deposition and septa interconnecting regenerative nodules. One month after cell injection, this result was unaltered and differences in fibrosis quantification were not found between MSC and placebo groups. ALT and AST returned to normal values 2 weeks after cell or placebo infusion, without significant differences between experimental groups. Two months after cell or placebo injection, albumin had also returned to normal values and histological results were maintained, again without differences between MSC and placebo groups. Therefore, under our experimental conditions, MSC were unable to reduce fibrosis or improve liver function in a rat model of severe chronic liver injury.

摘要

我们研究的目的是评估骨髓间充质基质细胞(MSC)在严重慢性肝损伤大鼠模型中的治疗潜力。14只雌性Wistar大鼠仅给予酒精性液体饮食,并在15周内每隔一天接受腹腔注射四氯化碳。在此期间过后,8只动物(MSC组)经门静脉注射1×10⁷个细胞,而6只动物(安慰剂组)接受赋形剂。在细胞治疗前以及细胞或安慰剂输注后1个月和2个月进行血液分析,以评估丙氨酸转氨酶(ALT)、天冬氨酸转氨酶(AST)和白蛋白。在细胞或安慰剂注射前及注射后1个月通过肝活检评估纤维化情况。细胞递送2个月后,处死动物并对肝脏进行组织学分析。通过组织形态计量学对纤维化进行定量。细胞输注前获取的活检显示有强烈的胶原沉积以及连接再生结节的间隔。细胞注射1个月后,该结果未改变,且MSC组和安慰剂组之间在纤维化定量方面未发现差异。细胞或安慰剂输注2周后,ALT和AST恢复到正常水平,实验组之间无显著差异。细胞或安慰剂注射2个月后,白蛋白也恢复到正常水平,组织学结果得以维持,MSC组和安慰剂组之间同样没有差异。因此,在我们的实验条件下,在严重慢性肝损伤大鼠模型中,MSC无法减轻纤维化或改善肝功能。

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