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肝细胞生长因子对大鼠炎症性肠病模型的影响。

Effects of hepatocyte growth factor on rat inflammatory bowel disease models.

作者信息

Ohda Yoshio, Hori Kazutoshi, Tomita Toshihiko, Hida Nobuyuki, Kosaka Tadashi, Fukuda Yoshihiro, Miwa Hiroto, Matsumoto Takayuki

机构信息

Department of Internal Medicine, Hyogo College of Medicine, Nishinomiya, Japan.

出版信息

Dig Dis Sci. 2005 May;50(5):914-21. doi: 10.1007/s10620-005-2664-z.

Abstract

Hepatocyte growth factor (HGF) is a hepatotrophic factor and, also, functions as an epithelial growth factor. We examined the therapeutic effects of HGF on rat inflammatory bowel disease models induced by trinitrobenzensulfonic acid or dextran sulfate sodium. Recombinant human HGF was continuously administered at 50 microg/body/day using an intraperitoneally implanted pump for 7 days. Treatment of HGF reduced the ulcerated area, histological damage score, mucosal myeloperoxidase activity, and epithelial apoptotic rate but did not increase epithelial mitotic rate and immunohistochemical labeling indexes of proliferating cell nuclear antigen, Ki-67, and bromodeoxyuridine as indexes of epithelial cell proliferation in either model. We then examined the epithelial localization of the HGF receptor c-met and identified it on the surface epithelia, where apoptosis was observed, but did not find it in the proliferative zone. These results suggest that HGF exhibits therapeutic effects via anti-inflammation including antiapoptosis rather than epithelial cell proliferation in these inflammatory bowel disease models.

摘要

肝细胞生长因子(HGF)是一种肝营养因子,同时也具有上皮生长因子的功能。我们研究了HGF对三硝基苯磺酸或葡聚糖硫酸钠诱导的大鼠炎症性肠病模型的治疗效果。使用腹腔植入泵以50微克/体/天的剂量连续给予重组人HGF,持续7天。HGF治疗可减少溃疡面积、组织学损伤评分、黏膜髓过氧化物酶活性和上皮细胞凋亡率,但在两种模型中均未增加上皮有丝分裂率以及作为上皮细胞增殖指标的增殖细胞核抗原、Ki-67和溴脱氧尿苷的免疫组化标记指数。然后我们检测了HGF受体c-met在上皮细胞中的定位,发现其位于观察到凋亡的表面上皮细胞上,但在增殖区未发现。这些结果表明,在这些炎症性肠病模型中,HGF通过包括抗凋亡在内的抗炎作用发挥治疗效果,而非通过上皮细胞增殖发挥作用。

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