Department of Mathematics, The Ohio State University, Columbus, OH 43210, USA.
Pharmacopsychiatry. 2011 May;44 Suppl 1:S76-83. doi: 10.1055/s-0031-1273697. Epub 2011 May 5.
We present a new hypothesis for the efficacy of selective serotonin reuptake inhibitors (SSRIs). We propose that SSRIs bring the response to the phasic firing of raphe nucleus cells back to normal, even though the average extracellular 5HT concentration remains low. We discuss burst firing in the raphe nuclei and use mathematical models to argue that tonic firing and phasic firing may be decoupled and may come from different mechanisms. We use a mathematical model for serotonin synthesis, release, and reuptake in terminals to illustrate the responses in terminal regions to bursts in a normal individual and in an individual with low vesicular serotonin. We then show that acute doses of SSRIs do not bring the response to bursts back to normal, but that chronic doses do return the response to normal. These model results need to be confirmed by new electrophysiological and pharmacological experiments.
我们提出了一个选择性 5-羟色胺再摄取抑制剂(SSRIs)疗效的新假说。我们提出,SSRIs 使反应恢复到中缝核细胞的相位发射正常,尽管平均细胞外 5HT 浓度仍然较低。我们讨论了中缝核的爆发发射,并使用数学模型来论证紧张发射和相位发射可能是分离的,可能来自不同的机制。我们使用一个用于终端中的 5-羟色胺合成、释放和再摄取的数学模型来举例说明正常个体和低囊泡 5-羟色胺个体中终端区域对爆发的反应。然后我们表明,SSRIs 的急性剂量不会使反应恢复到正常,而慢性剂量确实会使反应恢复正常。这些模型结果需要通过新的电生理和药理学实验来验证。