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促红细胞生成素在半乳糖胺诱导的大鼠肝损伤期间抑制肝脏明胶酶。

Erythropoietin inhibits liver gelatinases during galactosamine-induced hepatic damage in rats.

机构信息

Department of Gastroenterology with Endoscopic Unit, Medical University of Lublin, Jaczewskiego 8, PL 20-954 Lublin, Poland.

出版信息

Pharmacol Rep. 2009 Sep-Oct;61(5):917-23. doi: 10.1016/s1734-1140(09)70149-5.

DOI:10.1016/s1734-1140(09)70149-5
PMID:19904016
Abstract

Matrix metalloproteinase (MMP)-2 and -9 (gelatinases) participate in extracellular protein remodeling. Moreover, they are involved in the development of hepatic fibrosis. The goal of this study was to evaluate liver gelatinase activities after erythropoietin (Epo) treatment (1U/dose, sc) in experimentally damaged livers of rats treated with D-galactosamine (Gal, 800 mg/kg/dose, ip). Sixty rats were divided into six equal groups: I - received 5 doses of Epo and a single dose of Gal [the experiment duration (ED): 10 days]; II - received 5 doses of Epo and 3 doses of Gal (ED: 14 days); III - received only 5 doses of Epo (ED: 9 days); IV - received 3 doses of Gal (ED: 5 days);V - received a single dose of Gal (ED: 1 day); VI - control group (ED: 9 days). The animals were sacrificed and the livers were collected 48 h after the last drug administration. The activity of gelatinases was measured using gelatin zymography. No fluctuations in gelatinase activities were observed after the administration of a single dose of Gal in comparison to the control group. However, a significant increase in gelatinase activities was observed after treatment with three doses of Gal. Five doses of Epo administrated before Gal treatment prevented elevated gelatinase activities: MMP-9 activity was comparable to control, and MMP-2 activity was decreased (group II). The gelatinase activities was lower in group I and II in comparison to the control group. These results revealed that Epo decreases MMP-2 and MMP-9 activity, suggesting that it is a hepatoprotective agent against hepatic damage induced by galactosamine injection.

摘要

基质金属蛋白酶(MMP)-2 和 -9(明胶酶)参与细胞外蛋白质重塑。此外,它们还参与肝纤维化的发展。本研究的目的是评估红细胞生成素(Epo)(1U/剂量,sc)治疗后实验性损伤大鼠肝脏中明胶酶活性,这些大鼠用半乳糖胺(Gal,800mg/kg/剂量,ip)处理。60 只大鼠分为 6 组,每组相等:I - 接受 5 剂 Epo 和 1 剂 Gal [实验持续时间(ED):10 天];II - 接受 5 剂 Epo 和 3 剂 Gal(ED:14 天);III - 仅接受 5 剂 Epo(ED:9 天);IV - 接受 3 剂 Gal(ED:5 天);V - 接受 1 剂 Gal(ED:1 天);VI - 对照组(ED:9 天)。最后一次给药后 48 小时处死动物并收集肝脏。使用明胶酶谱法测量明胶酶的活性。与对照组相比,单次给予 Gal 后明胶酶活性没有波动。然而,给予三剂 Gal 后,明胶酶活性显著增加。Gal 治疗前给予 5 剂 Epo 可预防明胶酶活性升高:MMP-9 活性与对照组相当,MMP-2 活性降低(组 II)。与对照组相比,组 I 和 II 的明胶酶活性较低。这些结果表明,Epo 降低 MMP-2 和 MMP-9 的活性,提示其是一种对抗半乳糖胺注射诱导肝损伤的肝保护剂。

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