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双重酪氨酸激酶抑制剂AEE788对大鼠肝切除模型再生的影响及风险

Effect and risk of AEE788, a dual tyrosine kinase inhibitor, on regeneration in a rat liver resection model.

作者信息

Deng M, Huang H, Dirsch O, Dahmen U

机构信息

Department of General, Visceral and Transplantation Surgery, University Hospital Essen, Hufelandstrasse 55, Essen, Germany.

出版信息

Eur Surg Res. 2010;44(2):82-95. doi: 10.1159/000275818. Epub 2010 Jan 19.

Abstract

BACKGROUND

AEE788, a dual tyrosine kinase inhibitor, has antiproliferative effects on diverse tumor models in mice. We aimed to investigate whether AEE788 blocks liver regeneration and causes drug-related side effects.

METHODS

Rats treated orally with 50 mg/kg AEE788 or solvent every 2 days were subjected to 70% partial hepatectomy (PH) and sacrificed on postoperative days 1, 2, 7, and 28. Liver regeneration was evaluated using liver weight to body weight ratio, BrdU-staining, mitotic index, and PCR for PCNA (proliferating cell nuclear antigen). Side effects on the gastrointestinal system and liver were assessed using clinical chemistry, histology, silver staining, and immunohistochemistry. Plasma and liver tissue levels of AEE788 were measured using spectrometry.

RESULTS

AEE788 treatment did not inhibit liver regeneration. No obvious drug-related systemic or hepatic side effects were observed. Restoration of liver architecture during liver regeneration was not obviously impaired, even after 4 weeks' AEE788 treatment. After a 1-week treatment, AEE788 concentrations in plasma and liver tissue in the PH group were 3-fold and 8-fold higher than the non-PH group, respectively.

CONCLUSION

Its antiproliferative properties, good tolerance, and lack of inhibition on liver regeneration make AEE788 a potential candidate for clinical study with oncological PH, but one that carries the risk of overexposure in the early postoperative phase.

摘要

背景

AEE788是一种双酪氨酸激酶抑制剂,对小鼠的多种肿瘤模型具有抗增殖作用。我们旨在研究AEE788是否会阻断肝再生并引起药物相关的副作用。

方法

每2天口服给予50mg/kg AEE788或溶剂的大鼠接受70%部分肝切除术(PH),并在术后第1、2、7和28天处死。使用肝重与体重比、BrdU染色、有丝分裂指数和PCNA(增殖细胞核抗原)的PCR来评估肝再生。使用临床化学、组织学、银染色和免疫组织化学评估对胃肠道系统和肝脏的副作用。使用光谱法测量AEE788的血浆和肝组织水平。

结果

AEE788治疗并未抑制肝再生。未观察到明显的药物相关全身或肝脏副作用。即使经过4周的AEE788治疗,肝再生过程中肝脏结构的恢复也未受到明显损害。治疗1周后,PH组血浆和肝组织中AEE788的浓度分别比非PH组高3倍和8倍。

结论

AEE788的抗增殖特性、良好的耐受性以及对肝再生无抑制作用,使其成为肿瘤性PH临床研究的潜在候选药物,但在术后早期存在过度暴露的风险。

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