{"title":"药物反应的系统视角。","authors":"Vlad Elgart, Joseph Loscalzo","doi":"10.1111/bph.70128","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":9262,"journal":{"name":"British Journal of Pharmacology","volume":" ","pages":""},"PeriodicalIF":7.7000,"publicationDate":"2025-07-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A system perspective on drug response.\",\"authors\":\"Vlad Elgart, Joseph Loscalzo\",\"doi\":\"10.1111/bph.70128\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>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.</p>\",\"PeriodicalId\":9262,\"journal\":{\"name\":\"British Journal of Pharmacology\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":7.7000,\"publicationDate\":\"2025-07-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"British Journal of Pharmacology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1111/bph.70128\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PHARMACOLOGY & PHARMACY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"British Journal of Pharmacology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1111/bph.70128","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
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.
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.