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中空纤维型肝辅助装置的体内评估

In vivo evaluation of a hollow fiber liver assist device.

作者信息

Jauregui H O, Mullon C J, Trenkler D, Naik S, Santangini H, Press P, Muller T E, Solomon B A

机构信息

Department of Pathology, Rhode Island Hospital, Providence 02903.

出版信息

Hepatology. 1995 Feb;21(2):460-9.

PMID:7843721
Abstract

Orthotopic liver transplantation is the only effective form of therapy currently available for patients with fulminant hepatic failure (FHF). The use of an extracorporeal (EC) liver assist device (LAD) may result in improved presurgical clinical management. Alternatively, patients treated with LADs could avoid the transplantation procedure if they are able to regenerate a critical mass of hepatocytes that will sustain functional viability. In this study, the efficacy of a prototype hollow fiber LAD seeded with rabbit hepatocytes was assessed in vivo by the use of two different animal models: (1) normal rabbits injected with diazepam or lidocaine, and (2) a galactosamine (Gal)-intoxicated rabbit model of FHF. The EC LAD clearly decreased the blood levels of the two drugs and significantly generated diazepam and lidocaine metabolites indicating the maintenance of active P450 forms in the cellular component of the devices. A 6-hour EC treatment significantly increased the survival time and delayed the onset of hepatic encephalopathy (HE) in the Gal-intoxicated rabbits. Histological evaluations of postmortem livers showed greater hepatocyte regenerative activity in the animals treated with hepatocyte-seeded LADs than in the two control groups, e.g., rabbits not treated or treated with unseeded devices. These findings support the concept that a microporous hollow fiber LAD seeded with rabbit hepatocytes is able to sustain drug detoxification in vivo as well as to modify the course of FHF in a well-characterized animal model.

摘要

原位肝移植是目前治疗暴发性肝衰竭(FHF)患者唯一有效的治疗方式。使用体外(EC)肝辅助装置(LAD)可能会改善术前临床管理。另外,如果接受LAD治疗的患者能够再生出足够数量的肝细胞以维持功能存活,他们就可以避免移植手术。在本研究中,通过使用两种不同的动物模型在体内评估了接种兔肝细胞的原型中空纤维LAD的疗效:(1)注射地西泮或利多卡因的正常兔,以及(2)半乳糖胺(Gal)诱导的FHF兔模型。EC LAD明显降低了两种药物的血药浓度,并显著产生了地西泮和利多卡因代谢物,表明装置细胞成分中的活性P450形式得以维持。6小时的EC治疗显著延长了Gal中毒兔的存活时间,并延迟了肝性脑病(HE)的发作。死后肝脏的组织学评估显示,接种肝细胞的LAD治疗的动物比两个对照组(即未治疗或接受未接种装置治疗的兔)具有更强的肝细胞再生活性。这些发现支持了这样一种概念,即接种兔肝细胞的微孔中空纤维LAD能够在体内维持药物解毒,并在一个特征明确的动物模型中改变FHF的病程。

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