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小鼠中骨形态发生蛋白2(BMP2)的生理药代动力学模型(PBPK)的建立。

Development of Physiologically Based Pharmacokinetic Model (PBPK) of BMP2 in Mice.

作者信息

Utturkar Aditya, Paul Bikram, Akkiraju Hemanth, Bonor Jeremy, Dhurjati Prasad, Nohe Anja

机构信息

Department of Chemical and Biomolecular Engineering, University of Delaware, USA.

Department of Biological Sciences, University of Delaware, USA.

出版信息

Biol Syst Open Access. 2013;2. doi: 10.4172/2329-6577.1000123.

Abstract

Bone Morphogenetic protein 2 holds great promise for potential applications in the clinic. It is a potent growth factor for the use in the cervical spine surgery (FDA approved 2002) and has been marketed as "Infuse" for treating open tibial shaft fractures (FDA approved 2004). However, its use is limited by several significant side effects that maybe due to its potency and effect on different stem cell populations in the spine. BMP2 is expressed throughout the human body in several tissues and at a very high concentration in the blood. BMP receptors, especially BMP receptor type Ia, is ubiquitously expressed in most tissues. Currently, it is difficult to determine how BMP2 is physiologically distributed in mice or humans and no quantitative models are available. A Physiologically-Based Pharmaco-Kinetic (PBPK) model has been developed to determine steady-state distribution of BMP2 in mice. The multi-compartmental PBPK model represents relevant organ/tissues with physiological accuracy. The organs/tissue compartments chosen were brain, lung, heart, liver, pancreas, kidney, uterus, bone and fat. A blood compartment maintained connectivity among the various organs. Four processes characterized the change in the concentration of the protein in every compartment: blood flow in, blood flow out, protein turnover and receptor binding in the organ. The unique aspects of the model are the determination of elimination using receptor kinetics and generation using protein turnover. The model also predicts steady state concentrations of BMP2 in tissues in mice and may be used for possible scale-up of dosage regimens in humans.

摘要

骨形态发生蛋白2在临床潜在应用方面具有巨大前景。它是一种用于颈椎手术的强效生长因子(2002年获美国食品药品监督管理局批准),并已作为“Infuse”上市用于治疗开放性胫骨干骨折(2004年获美国食品药品监督管理局批准)。然而,其应用受到一些显著副作用的限制,这些副作用可能归因于其效力以及对脊柱中不同干细胞群体的影响。骨形态发生蛋白2在人体的多种组织中均有表达,且在血液中的浓度非常高。骨形态发生蛋白受体,尤其是I型骨形态发生蛋白受体,在大多数组织中广泛表达。目前,很难确定骨形态发生蛋白2在小鼠或人类体内的生理分布情况,也没有定量模型可用。已开发出一种基于生理的药代动力学(PBPK)模型来确定骨形态发生蛋白2在小鼠体内的稳态分布。多室PBPK模型以生理准确性代表相关器官/组织。所选择的器官/组织隔室包括脑、肺、心脏、肝脏、胰腺、肾脏、子宫、骨骼和脂肪。一个血液隔室维持着各个器官之间的连通性。四个过程表征了每个隔室中蛋白质浓度的变化:血流进入、血流流出、蛋白质周转以及器官中的受体结合。该模型的独特之处在于使用受体动力学确定消除以及使用蛋白质周转确定生成。该模型还预测了小鼠组织中骨形态发生蛋白2的稳态浓度,并且可用于可能的人类给药方案放大。

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本文引用的文献

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MOPED: Model Organism Protein Expression Database.MOPED:模式生物蛋白质表达数据库。
Nucleic Acids Res. 2012 Jan;40(Database issue):D1093-9. doi: 10.1093/nar/gkr1177. Epub 2011 Dec 1.
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Bone morphogenetic proteins: a critical review.骨形态发生蛋白:一项关键性综述。
Cell Signal. 2011 Apr;23(4):609-20. doi: 10.1016/j.cellsig.2010.10.003. Epub 2010 Oct 16.
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