血清素、组胺和抑郁症的数学模型

Janet Best, A. M. Buchanan, H. F. Nijhout, P. Hashemi, M. Reed
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引用次数: 0

摘要

这两位合著者已经在5 -羟色胺、多巴胺和组胺以及它们与神经精神疾病的关系上合作了10年。Hashemi开创了许多新的实验技术,用于在大脑细胞外空间实时测量血清素和组胺。贝斯特、里德和尼约特一直在建立大脑代谢的数学模型,以帮助他们解释哈希米的数据。Hashemi证明了脑组胺抑制血清素的释放,给出了炎症导致脑血清素减少从而导致抑郁症的直接机制。在他们的共同研究中出现了许多新的生物学现象,包括:1)血清素有两种不同的再摄取机制;2) 5 -羟色胺自身受体的作用不是瞬间的,即使细胞外浓度恢复正常,其作用也是持久的;3)血清素代谢和组胺代谢的数学模型可以解释Hashemi的实验数据;4)血清素自身受体的变化可能是血清素相关情绪障碍的原因之一。在这里,我们回顾了我们近年来为生物学读者、医学读者和从事生物学问题数学建模的研究人员所做的工作。我们讨论了实验技术,数学模型的创建和研究,以及神经精神疾病的后果。
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Mathematical Models of Serotonin, Histamine, and Depression
The coauthors have been working together for ten years on serotonin, dopamine, and histamine and their connection to neuropsychiatric illnesses. Hashemi has pioneered many new experimental techniques for measuring serotonin and histamine in real time in the extracellular space in the brain. Best, Reed, and Nijhout have been making mathematical models of brain metabolism to help them interpret Hashemi’s data. Hashemi demonstrated that brain histamine inhibits serotonin release, giving a direct mechanism by which inflammation can cause a decrease in brain serotonin and therefore depression. Many new biological phenomena have come out of their joint research including 1) there are two different reuptake mechanisms for serotonin; 2) the effect of the serotonin autoreceptors is not instantaneous and is long-lasting even when the extracellular concentrations have returned to normal; 3) that mathematical models of serotonin metabolism and histamine metabolism can explain Hashemi’s experimental data; 4) that variation in serotonin autoreceptors may be one of the causes of serotonin-linked mood disorders. Here we review our work in recent years for biological audiences, medical audiences, and researchers who work on mathematical modeling of biological problems. We discuss the experimental techniques, the creation and investigation of mathematical models, and the consequences for neuropsychiatric diseases.
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