药物反应的系统视角。

IF 7.7 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Vlad Elgart, Joseph Loscalzo
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引用次数: 0

摘要

通过测量特定表型来量化药物扰动的影响。虽然药物作用发生在分子(微观)水平上,但测量的表型通常表征系统水平(宏观)变量,如血压或细胞活力。现有的药物扰动模型旨在通过分析药物引起的微观变量(如基因表达或代谢物浓度)的变化来推断(剂量依赖性)药物对表型的影响。这些变化被用来建立观察到的宏观变量的模式。在这里,我们回顾了药物反应的传统分析,并在宏观层面上直接介绍了药物反应的简单现象学描述。我们演示了如何使用这种方法来建立一个框架,用于量化由低浓度的单一药物或药物组合引起的表型剂量依赖性变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A system perspective on drug response.

The effect of drug perturbation(s) is quantified by measuring a specific phenotype. While drug action occurs on a molecular (microscopic) level, the measured phenotypes typically characterise system-level (macroscopic) variables, such as blood pressure or cell viability. Existing drug perturbation models are designed to infer (dosage-dependent) drug effects on the phenotype by analysis of the drug-induced changes in microscopic variables, such as gene expression or metabolite concentration. These changes are used to establish patterns in observed macroscopic variables. Here, we review conventional analysis of drug response and introduce a simple phenomenological description of drug response directly on a macroscopic level. We demonstrate how this approach can be used to establish a framework for quantifying dose-dependent changes in phenotype induced by low concentrations of a single drug or drug combinations.

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来源期刊
CiteScore
15.40
自引率
12.30%
发文量
270
审稿时长
2.0 months
期刊介绍: The British Journal of Pharmacology (BJP) is a biomedical science journal offering comprehensive international coverage of experimental and translational pharmacology. It publishes original research, authoritative reviews, mini reviews, systematic reviews, meta-analyses, databases, letters to the Editor, and commentaries. Review articles, databases, systematic reviews, and meta-analyses are typically commissioned, but unsolicited contributions are also considered, either as standalone papers or part of themed issues. In addition to basic science research, BJP features translational pharmacology research, including proof-of-concept and early mechanistic studies in humans. While it generally does not publish first-in-man phase I studies or phase IIb, III, or IV studies, exceptions may be made under certain circumstances, particularly if results are combined with preclinical studies.
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