Stoichiometry Based Steady-State Hepatic Flux Analysis: Computational and Experimental Aspects

被引:7
作者
Orman, Mehmet A. [1 ]
Mattick, John [1 ]
Androulakis, Ioannis P. [1 ,2 ]
Berthiaume, Francois [2 ]
Ierapetritou, Marianthi G. [1 ]
机构
[1] Rutgers State Univ, Dept Chem & Biochem Engn, Piscataway, NJ 08854 USA
[2] Rutgers State Univ, Dept Biomed Engn, Piscataway, NJ 08854 USA
关键词
hepatocytes; perfused livers; metabolic flux analysis; flux balance analysis; metabolic pathway analysis;
D O I
10.3390/metabo2010268
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The liver has many complex physiological functions, including lipid, protein and carbohydrate metabolism, as well as bile and urea production. It detoxifies toxic substances and medicinal products. It also plays a key role in the onset and maintenance of abnormal metabolic patterns associated with various disease states, such as burns, infections and major traumas. Liver cells have been commonly used in in vitro experiments to elucidate the toxic effects of drugs and metabolic changes caused by aberrant metabolic conditions, and to improve the functions of existing systems, such as bioartificial liver. More recently, isolated liver perfusion systems have been increasingly used to characterize intrinsic metabolic changes in the liver caused by various perturbations, including systemic injury, hepatotoxin exposure and warm ischemia. Metabolic engineering tools have been widely applied to these systems to identify metabolic flux distributions using metabolic flux analysis or flux balance analysis and to characterize the topology of the networks using metabolic pathway analysis. In this context, hepatic metabolic models, together with experimental methodologies where hepatocytes or perfused livers are mainly investigated, are described in detail in this review. The challenges and opportunities are also discussed extensively.
引用
收藏
页码:268 / 291
页数:24
相关论文
共 100 条
[1]   In vitro zonation and toxicity in a hepatocyte bioreactor [J].
Allen, JW ;
Khetani, SR ;
Bhatia, SN .
TOXICOLOGICAL SCIENCES, 2005, 84 (01) :110-119
[2]   Microfluidic-based measurements of cytochrome P450 enzyme activity of primary mammalian hepatocytes [J].
Anderson, Keith ;
Cooper, Jonathan M. ;
Haswell, Stephen J. ;
Marshall, Damian ;
Yin, Huabing ;
Zhang, Xunli .
ANALYST, 2010, 135 (06) :1282-1287
[3]   Intrahepatic amino acid and glucose metabolism in a D-galactosamine-induced rat liver failure model [J].
Arai, K ;
Lee, K ;
Berthiaume, F ;
Tompkins, RG ;
Yarmush, ML .
HEPATOLOGY, 2001, 34 (02) :360-371
[4]   Effects of dehydroepiandrosterone administration on rat hepatic metabolism following thermal injury [J].
Banta, S ;
Yokoyama, T ;
Berthiaume, F ;
Yarmush, ML .
JOURNAL OF SURGICAL RESEARCH, 2005, 127 (02) :93-105
[5]   Contribution of gene expression to metabolic fluxes in hypermetabolic livers induced through burn injury and cecal ligation and puncture in rats [J].
Banta, Scott ;
Vemula, Murali ;
Yokoyama, Tadaaki ;
Jayaraman, Arul ;
Berthiaume, Francois ;
Yarmush, Martin L. .
BIOTECHNOLOGY AND BIOENGINEERING, 2007, 97 (01) :118-137
[6]   Xenobiotic metabolism by cultured primary porcine hepatocytes [J].
Behnia, K ;
Bhatia, S ;
Jastromb, N ;
Balis, U ;
Sullivan, S ;
Yarmush, M ;
Toner, M .
TISSUE ENGINEERING, 2000, 6 (05) :467-479
[7]   INDUCTION OF TRYPTOPHAN OXYGENASE BY DEXAMETHASONE IN ISOLATED HEPATOCYTES - DEPENDENCE ON COMPOSITION OF MEDIUM AND PH [J].
BERG, T ;
MORLAND, J .
BIOCHIMICA ET BIOPHYSICA ACTA, 1975, 392 (02) :233-241
[8]  
BISSELL DM, 1981, FED PROC, V40, P2469
[9]   LIVER-CELL HETEROGENEITY - FUNCTIONS OF NONPARENCHYMAL CELLS [J].
BOUWENS, L ;
DEBLESER, P ;
VANDERKERKEN, K ;
GEERTS, B ;
WISSE, E .
ENZYME, 1992, 46 (1-3) :155-168
[10]   Mass flux balance-based model and metabolic flux analysis for collagen synthesis in the fibrogenesis process of human liver [J].
Çalik, P ;
Akbay, A .
MEDICAL HYPOTHESES, 2000, 55 (01) :5-14