van Duuren E, van der Plasse G, van der Blom R, Joosten R N J M A, Mulder A B, Pennartz C M A, Feenstra M G P
Netherlands Institute for Neuroscience, Royal Netherlands Academy of Arts and Sciences, Meibergdreef 47, 1105BA Amsterdam, The Netherlands.
J Pharmacol Exp Ther. 2007 Oct;323(1):61-9. doi: 10.1124/jpet.107.124784. Epub 2007 Jul 12.
To be able to address the question how neurotransmitters or pharmacological agents influence activity of neuronal populations in freely moving animals, the combidrive was developed. The combidrive combines an array of 12 tetrodes to perform ensemble recordings with a moveable and replaceable microdialysis probe to locally administer pharmacological agents. In this study, the effects of cumulative concentrations of tetrodotoxin, lidocaine, and muscimol on neuronal firing activity in the prefrontal cortex were examined and compared. These drugs are widely used in behavioral studies to transiently inactivate brain areas, but little is known about their effects on ensemble activity and the possible differences between them. The results show that the combidrive allows ensemble recordings simultaneously with reverse microdialysis in freely moving rats for periods at least up to 2 wk. All drugs reduced neuronal firing in a concentration dependent manner, but they differed in the extent to which firing activity of the population was decreased and the in speed and extent of recovery. At the highest concentration used, both muscimol and tetrodotoxin (TTX) caused an almost complete reduction of firing activity. Lidocaine showed the fastest recovery, but it resulted in a smaller reduction of firing activity of the population. From these results, it can be concluded that whenever during a behavioral experiment a longer lasting, reversible inactivation is required, muscimol is the drug of choice, because it inactivates neurons to a similar degree as TTX, but it does not, in contrast to TTX, affect fibers of passage. For a short-lasting but partial inactivation, lidocaine would be most suitable.
为了能够回答神经递质或药理剂如何影响自由活动动物中神经元群体活动的问题,研发了组合驱动装置。该组合驱动装置将一个由12个四极管组成的阵列与一个可移动且可更换的微透析探针相结合,以进行整体记录并局部施用药理剂。在本研究中,检测并比较了河豚毒素、利多卡因和蝇蕈醇的累积浓度对前额叶皮质神经元放电活动的影响。这些药物在行为研究中被广泛用于短暂使脑区失活,但它们对整体活动的影响以及它们之间可能存在的差异却鲜为人知。结果表明,组合驱动装置能够在自由活动的大鼠中同时进行整体记录和反向微透析,持续时间至少可达2周。所有药物均以浓度依赖性方式降低神经元放电,但它们在群体放电活动降低的程度以及恢复的速度和程度方面存在差异。在所用的最高浓度下,蝇蕈醇和河豚毒素(TTX)均导致放电活动几乎完全降低。利多卡因显示出最快的恢复速度,但它导致群体放电活动的降低幅度较小。从这些结果可以得出结论,在行为实验中,每当需要更长时间的、可逆的失活时,蝇蕈醇是首选药物,因为它使神经元失活的程度与TTX相似,但与TTX不同的是,它不影响通过的纤维。对于短暂但部分失活,利多卡因将是最合适的。