Principles:: Mechanisms and modeling of synergism in cellular responses

被引:36
作者
Barrera, NP
Morales, B
Torres, S
Villalón, M
机构
[1] Univ Cambridge, Dept Pharmacol, Cambridge CB2 1PD, England
[2] Univ Santiago Chile, Dept Biol, Alameda 3363, Chile
[3] Univ Valparaiso, Dept Stat, Valparaiso 1111, Chile
[4] Pontificia Univ Catolica Chile, Dept Physiol Sci, Santiago 340, Chile
关键词
D O I
10.1016/j.tips.2005.08.003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cells can be considered as integrators of simultaneous stimuli, in which cross-talk between transduction pathways can eventually produce responses that are significantly different from simply additive responses. Synergism represents an efficient means of increasing the amplitude of cellular responses induced by low levels of stimulation. Recently, several kinetic and physicochemical models have been developed to describe and predict synergistic responses. In this article, the mechanisms that control the magnitude and timing of cellular synergism are discussed. We suggest that the analysis of theoretical models could enable a general prediction of synergism despite the presence of signal-specific synergistic responses. In addition, application of the proposed concepts should aid understanding of the wide occurrence of synergism induced by interacting transduction pathways in multidrug clinical treatment.
引用
收藏
页码:526 / 532
页数:7
相关论文
共 32 条
[1]   Effect of agmatine on the development of morphine dependence in rats: potential role of cAMP system [J].
Aricioglu, F ;
Means, A ;
Regunathan, S .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2004, 504 (03) :191-197
[2]   Agmatine reduces only peripheral-related behavioral signs, not the central signs, of morphine withdrawal in nNOS deficient transgenic mice [J].
Aricioglu, F ;
Paul, IA ;
Regunathan, S .
NEUROSCIENCE LETTERS, 2004, 354 (02) :153-157
[3]   CHEMICAL AND PHYSICAL SPUTTERING OF FLUORINATED SILICON [J].
BARONE, ME ;
GRAVES, DB .
JOURNAL OF APPLIED PHYSICS, 1995, 77 (03) :1263-1274
[4]   Prediction of synergism on frequency of responses in the attojoule range [J].
Barrera, NP ;
Torres, S ;
Morales, B ;
Villalon, M .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2004, 6 (08) :1806-1814
[5]   The community of the self [J].
Buchman, TG .
NATURE, 2002, 420 (6912) :246-251
[6]   TIME-RESOLVED OPTICAL DIAGNOSTICS OF RADIO-FREQUENCY PLASMAS [J].
GOTTSCHO, RA ;
MANDICH, ML .
JOURNAL OF VACUUM SCIENCE & TECHNOLOGY A-VACUUM SURFACES AND FILMS, 1985, 3 (03) :617-624
[7]   Isobolographic analysis for combinations of a full and partial agonist: Curved isoboles [J].
Grabovsky, Y ;
Tallarida, RJ .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2004, 310 (03) :981-986
[8]   Synergistic activation of transcription by CBP and p53 [J].
Gu, W ;
Shi, XL ;
Roeder, RG .
NATURE, 1997, 387 (6635) :819-823
[9]   Synergistic interactions of lipids and myelin basic protein [J].
Hu, YF ;
Doudevski, I ;
Wood, D ;
Moscarello, M ;
Husted, C ;
Genain, C ;
Zasadzinski, JA ;
Israelachvili, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (37) :13466-13471
[10]   Quantitative prediction of in vivo drug clearance and drug interactions from in vitro data on metabolism, together with binding and transport [J].
Ito, K ;
Iwatsubo, T ;
Kanamitsu, S ;
Nakajima, Y ;
Sugiyama, Y .
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 1998, 38 :461-499