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二甲双胍抑制小鼠海绵模型中的炎症性血管生成。

Metformin inhibits inflammatory angiogenesis in a murine sponge model.

机构信息

FUMEC University, Physiology, Rua da Paisagem 240, Bairro Vila da Serra, Nova Lima, Minas Gerais, Brazil.

出版信息

Biomed Pharmacother. 2010 Mar;64(3):220-5. doi: 10.1016/j.biopha.2009.08.004. Epub 2009 Oct 24.

Abstract

To investigate the effects of metformin on angiogenesis, on inflammatory cell accumulation and on production of endogenous cytokines in sponge implant in mice. Polyester-polyurethane sponges were implanted in Swiss mice and metformin (40 or 400mg/kg/day) was given orally for six days. The implants collected at day 7 postimplantation were processed for the assessment of hemoglobin (Hb), myeloperoxidase (MPO), N-acetylglucosaminidase (NAG) e collagen used as indexes for angiogenesis, neutrophil and macrophage accumulation and extracellular matrix deposition, respectively. Relevant inflammatory, angiogenic and fibrogenic cytokines were also determined. Metformin treatment attenuated the main components of the fibrovascular tissue, wet weight, vascularization (Hb content), macrophage recruitment (NAG activity), collagen deposition and the levels of transforming growth factor (TGF-beta1) intraimplant. A regulatory function of metformin on multiple parameters of main components of inflammatory angiogenesis has been revealed giving insight into the potential therapeutic underlying the actions of metformin.

摘要

研究二甲双胍对小鼠海绵植入物中血管生成、炎性细胞积聚和内源性细胞因子产生的影响。将聚酯-聚氨基甲酸乙酯海绵植入瑞士小鼠体内,并口服给予二甲双胍(40 或 400mg/kg/天)六天。在植入后第 7 天收集植入物,用于评估血红蛋白(Hb)、髓过氧化物酶(MPO)、N-乙酰氨基葡萄糖苷酶(NAG)和胶原蛋白,分别作为血管生成、中性粒细胞和巨噬细胞积聚以及细胞外基质沉积的指标。还测定了相关的炎症、血管生成和纤维生成细胞因子。二甲双胍治疗减轻了纤维血管组织的主要成分、湿重、血管化(Hb 含量)、巨噬细胞募集(NAG 活性)、胶原沉积和植入物内转化生长因子(TGF-β1)的水平。二甲双胍对炎症性血管生成的主要成分的多个参数的调节作用表明了其对二甲双胍作用的潜在治疗机制。

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