Kikuchi Hirosato
Department of Anesthesiology, Saitama Medical University Hospital, Saitama 350-0495.
Masui. 2009 Sep;58(9):1084-5.
The regulation of biotransformation started with the mechanism of mass action between the concentrations of the substrates (product) and enzyme. Thereafter by understanding the protein tertiary structure, allosteric control mechanism appeared. The enzyme induction was brought into a new aspect by the development of genetic analysis. As a cellular economy, energy charge was found to be a new regulatory mechanism for glycolytic pathway. These regulatory systems showed a single concentration-effect curve of pharmacodynamics. By introduction of silent or non sense gene as in atypical cholinesterase, a given function was not operated. As most doctors are aware of the diverse sensitivity to opioids among patients, numbers and species of opioid receptors might be the cause. By extensive gene analysis, polymorphism may explain this phenotype. The polymorphism may also play an important role in the pain mechanism such as incidence of neuropathic pain and in the modulation of pain. You will find several curves of pharmocodynamics.
生物转化的调节始于底物(产物)浓度与酶之间的质量作用机制。此后,通过对蛋白质三级结构的理解,变构控制机制出现了。随着遗传分析的发展,酶诱导被带入了一个新的层面。作为一种细胞经济性,能量电荷被发现是糖酵解途径的一种新的调节机制。这些调节系统呈现出药效学的单一浓度-效应曲线。通过引入沉默或无义基因,如非典型胆碱酯酶,特定的功能无法发挥作用。正如大多数医生所意识到的,患者对阿片类药物的敏感性各不相同,阿片受体的数量和种类可能是原因所在。通过广泛的基因分析,多态性可能解释这种表型。多态性也可能在疼痛机制中发挥重要作用,如神经性疼痛的发生率以及疼痛的调节。你会发现几条药效学曲线。