Díaz-Mataix Llorenç, Artigas Francesc, Celada Pau
Department of Neurochemistry, Institut d' Investigacions Biomèdiques de Barcelona, CSIC, IDIBAPS, Rosselló, 161, 6th floor, 08036 Barcelona, Spain.
Eur Neuropsychopharmacol. 2006 May;16(4):288-96. doi: 10.1016/j.euroneuro.2005.10.003. Epub 2005 Nov 14.
5-HT(1A) receptor agonists increase the activity of dopamine (DA) neurons in the ventral tegmental area (VTA) and DA release in medial prefrontal cortex (mPFC). The mPFC is enriched in 5-HT(1A) receptors and projects to the VTA, where mesocortical dopaminergic neurons originate. We examined whether 5-HT(1A) receptor activation can modulate the activity of mPFC pyramidal neurons projecting to VTA. These were identified by antidromic stimulation from the VTA and were recorded extracellularly in anesthetized rats. The selective 5-HT(1A) agonist BAY x 3,702 (10-80 microg/kg i.v.) increased the firing rate in 14/19 neurons (283 +/- 79%) and reduced the activity of 5/19 neurons (22 +/- 11%), resulting in an overall 2.2-fold increase of the firing rate. Both effects were blocked by the selective 5-HT(1A) antagonist WAY-100635. These results suggest that the increase in dopaminergic activity produced by 5-HT(1A) receptor activation can be driven by an increase in the activity of projection neurons in mPFC.
5-羟色胺(5-HT)(1A)受体激动剂可增加腹侧被盖区(VTA)中多巴胺(DA)神经元的活性以及内侧前额叶皮质(mPFC)中的DA释放。mPFC富含5-HT(1A)受体,并投射至VTA,中皮质多巴胺能神经元即起源于此。我们研究了5-HT(1A)受体激活是否能调节投射至VTA的mPFC锥体神经元的活性。通过从VTA进行逆向刺激来识别这些神经元,并在麻醉大鼠中进行细胞外记录。选择性5-HT(1A)激动剂BAY x 3,702(10 - 80微克/千克静脉注射)使19个神经元中的14个神经元的放电频率增加(283±79%),并使19个神经元中的5个神经元的活性降低(22±11%),导致放电频率总体增加2.2倍。这两种效应均被选择性5-HT(1A)拮抗剂WAY - 100635阻断。这些结果表明,5-HT(1A)受体激活所产生的多巴胺能活性增加可能是由mPFC中投射神经元活性的增加所驱动的。