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在大鼠中通过甲磺酸伊马替尼和血管紧张素转换酶抑制剂联合双重抑制血小板衍生生长因子(PDGF)和转化生长因子-β(TGF-β)改善肝纤维化形成

Amelioration of liver fibrogenesis by dual inhibition of PDGF and TGF-beta with a combination of imatinib mesylate and ACE inhibitor in rats.

作者信息

Yoshiji Hitoshi, Kuriyama Shigeki, Noguchi Ryuichi, Ikenaka Yasuhide, Yoshii Junichi, Yanase Koji, Namisaki Tadashi, Kitade Mitsuteru, Yamazaki Masaharu, Asada Kiyoshi, Akahane Takemi, Tsujimoto Tatsuhiro, Uemura Masahito, Fukui Hiroshi

机构信息

Third Department of Internal Medicine, Nara Medical University, Kashihara, Nara 634-8522, Japan.

出版信息

Int J Mol Med. 2006 May;17(5):899-904.

Abstract

Both platelet-derived growth factor (PDGF) and transforming growth factor-beta (TGF-beta) are known to be pivotal cytokines in liver fibrosis development. The aim of our current study was to elucidate the effects of dual inhibition of PDGF and TGF-beta by combination of the clinically used imatinib mesylate (STI-571) and perindopril (an ACE-inhibitor; ACE-I), respectively, on ongoing liver fibrosis development in rats. The effects of STI-571 and ACE-I at clinically comparable low doses were examined in a rat model of CCl4-induced liver fibrogenesis. Treatment with both STI-571 and ACE-I inhibited liver fibrogenesis and suppressed activation of hepatic stellate cells (HSCs). Administration of both agents exerted a more potent inhibitory effect than administration of either single agent. Our in vitro study demonstrated that STI-571 and ACE-I suppressed PDGF receptor (PDGFR) phosphorylation and TGF-beta expression in activated HSCs, respectively. Dual suppression of PDGF and TGF-beta with a combination of clinically comparable low doses of STI-571 and ACE-I exerted a significant inhibitory effect on ongoing liver fibrosis development. Since both agents are widely used in clinical practice, this combination therapy may provide a new strategy against liver fibrosis in the future.

摘要

血小板衍生生长因子(PDGF)和转化生长因子-β(TGF-β)均为肝纤维化发展过程中的关键细胞因子。我们当前研究的目的是分别通过临床使用的甲磺酸伊马替尼(STI-571)和培哚普利(一种血管紧张素转换酶抑制剂;ACE-I)联合使用,阐明对PDGF和TGF-β的双重抑制作用对大鼠肝纤维化进展的影响。在四氯化碳诱导的肝纤维化大鼠模型中,研究了临床可比低剂量的STI-571和ACE-I的作用。STI-571和ACE-I联合治疗均抑制了肝纤维化,并抑制了肝星状细胞(HSCs)的激活。两种药物联合给药比单一药物给药具有更强的抑制作用。我们的体外研究表明,STI-571和ACE-I分别抑制了活化HSCs中PDGF受体(PDGFR)的磷酸化和TGF-β的表达。临床可比低剂量的STI-571和ACE-I联合使用对PDGF和TGF-β的双重抑制对正在进行的肝纤维化发展具有显著的抑制作用。由于这两种药物在临床实践中广泛使用,这种联合治疗可能为未来抗肝纤维化提供一种新策略。

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