Department of Chemistry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, USA.
J Neurochem. 2011 Sep;118(5):749-59. doi: 10.1111/j.1471-4159.2011.07352.x. Epub 2011 Jul 18.
Exploring the mechanisms of serotonin [5-hydroxytryptamine (5-HT)] in the brain requires an in vivo method that combines fast temporal resolution with chemical selectivity. Fast-scan cyclic voltammetry is a technique with sufficient temporal and chemical resolution for probing dynamic 5-HT neurotransmission events; however, traditionally it has not been possible to probe in vivo 5-HT mechanisms. Recently, we optimized fast-scan cyclic voltammetry for measuring 5-HT release and uptake in vivo in the substantia nigra pars reticulata (SNR) with electrical stimulation of the dorsal raphe nucleus (DRN) in the rat brain. Here, we address technical challenges associated with rat DRN surgery by electrically stimulating 5-HT projections in the medial forebrain bundle (MFB), a more accessible anatomical location. MFB stimulation elicits 5-HT in the SNR; furthermore, we find simultaneous release of an additional species. We use electrochemical and pharmacological methods and describe physiological, anatomical and independent chemical analyses to identify this species as histamine. We also show pharmacologically that increasing the lifetime of extracellular histamine significantly decreases 5-HT release, most likely because of increased activation of histamine H-3 receptors that inhibit 5-HT release. Despite this, under physiological conditions, we find by kinetic comparisons of DRN and MFB stimulations that the simultaneous release of histamine does not interfere with the quantitative 5-HT concentration profile. We therefore present a novel and robust electrical stimulation of the MFB that is technically less challenging than DRN stimulation to study 5-HT and histamine release in the SNR.
探索大脑中 5-羟色胺(5-HT)的机制需要一种结合快速时间分辨率和化学选择性的体内方法。快速扫描循环伏安法是一种具有足够时间和化学分辨率的技术,可用于探测动态 5-HT 神经传递事件;然而,传统上不可能在体内探测 5-HT 机制。最近,我们优化了快速扫描循环伏安法,用于在大鼠脑的背侧中缝核(DRN)电刺激下测量黑质网状部(SNR)中的 5-HT 释放和摄取。在这里,我们通过电刺激内侧前脑束(MFB)中的 5-HT 投射来解决与大鼠 DRN 手术相关的技术挑战,MFB 是一个更容易接近的解剖位置。MFB 刺激会在 SNR 中引发 5-HT;此外,我们发现同时释放了另一种物质。我们使用电化学和药理学方法,并描述了生理学、解剖学和独立的化学分析,以确定这种物质为组胺。我们还表明,通过增加细胞外组胺的寿命,可以显著降低 5-HT 的释放,这很可能是因为组胺 H3 受体的激活增加,从而抑制 5-HT 的释放。尽管如此,在生理条件下,我们通过对 DRN 和 MFB 刺激的动力学比较发现,组胺的同时释放不会干扰定量 5-HT 浓度曲线。因此,我们提出了一种新的、稳健的 MFB 电刺激方法,与 DRN 刺激相比,技术上的挑战较小,可用于研究 SNR 中的 5-HT 和组胺释放。