A mathematical model for histamine synthesis, release, and control in varicosities.

Q1 Mathematics
Janet Best, H F Nijhout, Srimal Samaranayake, Parastoo Hashemi, Michael Reed
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引用次数: 17

Abstract

Background: Histamine (HA), a small molecule that is synthesized from the amino acid histidine, plays an important role in the immune system where it is associated with allergies, inflammation, and T-cell regulation. In the brain, histamine is stored in mast cells and other non-neuronal cells and also acts as a neurotransmitter. The histamine neuron cell bodies are in the tuberomammillary (TM) nucleus of the hypothalamus and these neurons send projections throughout the central nervous system (CNS), in particular to the cerebral cortex, amygdala, basal ganglia, hippocampus, thalamus, retina, and spinal cord. HA neurons make few synapses, but release HA from the cell bodies and from varicosities when the neurons fire. Thus the HA neural system seems to modulate and control the HA concentration in projection regions. It is known that high HA levels in the extracellular space inhibit serotonin release, so HA may play a role in the etiology of depression.

Results: We compare model predictions to classical physiological experiments on HA half-life, the concentration of brain HA after histidine loading, and brain HA after histidine is dramatically increased or decreased in the diet. The model predictions are also consistent with in vivo experiments in which extracellular HA is measured, using Fast Scan Cyclic Voltammetry, in the premammillary nucleus (PM) after a 2 s antidromic stimulation of the TM, both without and in the presence of the H 3 autoreceptor antagonist thioperamide. We show that the model predicts well the temporal behavior of HA in the extracellular space over 30 s in both experiments.

Conclusions: Our ability to measure in vivo histamine dynamics in the extracellular space after stimulation presents a real opportunity to understand brain function and control. The observed extracellular dynamics depends on synthesis, storage, neuronal firing, release, reuptake, glial cells, and control by autoreceptors, as well as the behavioral state of the animal (for example, depression) or the presence of neuroinflammation. In this complicated situation, the mathematical model will be useful for interpreting data and conducting in silico experiments to understand causal mechanisms. And, better understanding can suggest new therapeutic drug targets.

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组胺合成、释放和控制的数学模型。
背景:组胺(HA)是一种由氨基酸组氨酸合成的小分子,在免疫系统中起着重要作用,与过敏、炎症和t细胞调节有关。在大脑中,组胺储存在肥大细胞和其他非神经元细胞中,也作为一种神经递质。组胺神经元细胞体位于下丘脑的结节乳头核(TM),这些神经元通过中枢神经系统(CNS)发送投射,特别是大脑皮层、杏仁核、基底神经节、海马、丘脑、视网膜和脊髓。血凝素神经元产生的突触很少,但当神经元放电时,会从细胞体和静脉曲张中释放血凝素。因此,HA神经系统似乎调节和控制投影区的HA浓度。众所周知,细胞外空间的高HA水平会抑制血清素的释放,因此HA可能在抑郁症的病因中发挥作用。结果:我们将模型预测的HA半衰期、组氨酸负荷后的脑HA浓度以及组氨酸在饮食中显著增加或减少后的脑HA与经典生理实验进行了比较。模型预测也与体内实验一致,在对TM进行2 s的反激刺激后,使用快速扫描循环伏安法在乳前核(PM)中测量细胞外HA,无论是否存在h3自身受体拮抗剂硫哌丁胺。我们在两个实验中表明,该模型很好地预测了HA在细胞外空间超过30 s的时间行为。结论:我们在刺激后细胞外空间测量体内组胺动力学的能力为了解大脑功能和控制提供了真正的机会。观察到的细胞外动力学取决于合成、储存、神经元放电、释放、再摄取、胶质细胞和自受体的控制,以及动物的行为状态(例如,抑郁)或神经炎症的存在。在这种复杂的情况下,数学模型将有助于解释数据和进行计算机实验,以了解因果机制。而且,更好的理解可以提出新的治疗药物靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Theoretical Biology and Medical Modelling
Theoretical Biology and Medical Modelling MATHEMATICAL & COMPUTATIONAL BIOLOGY-
自引率
0.00%
发文量
0
审稿时长
6-12 weeks
期刊介绍: Theoretical Biology and Medical Modelling is an open access peer-reviewed journal adopting a broad definition of "biology" and focusing on theoretical ideas and models associated with developments in biology and medicine. Mathematicians, biologists and clinicians of various specialisms, philosophers and historians of science are all contributing to the emergence of novel concepts in an age of systems biology, bioinformatics and computer modelling. This is the field in which Theoretical Biology and Medical Modelling operates. We welcome submissions that are technically sound and offering either improved understanding in biology and medicine or progress in theory or method.
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