Department of Pharmacology and Toxicology and Center for Addiction Research, University of Texas Medical Branch, Galveston, Texas, United States of America.
PLoS One. 2011;6(6):e20508. doi: 10.1371/journal.pone.0020508. Epub 2011 Jun 7.
The serotonin 5-HT(2C) receptor (5-HT(2C)R) is localized to the limbic-corticostriatal circuit, which plays an integral role in mediating attention, motivation, cognition, and reward processes. The 5-HT(2C)R is linked to modulation of mesoaccumbens dopamine neurotransmission via an activation of γ-aminobutyric acid (GABA) neurons in the ventral tegmental area (VTA). However, we recently demonstrated the expression of the 5-HT(2C)R within dopamine VTA neurons suggesting the possibility of a direct influence of the 5-HT(2C)R upon mesoaccumbens dopamine output. Here, we employed double-label fluorescence immunochemistry with the synthetic enzymes for dopamine (tyrosine hydroxylase; TH) and GABA (glutamic acid decarboxylase isoform 67; GAD-67) and retrograde tract tracing with FluoroGold (FG) to uncover whether dopamine and GABA VTA neurons that possess 5-HT(2C)R innervate the nucleus accumbens (NAc). The highest numbers of FG-labeled cells were detected in the middle versus rostral and caudal levels of the VTA, and included a subset of TH- and GAD-67 immunoreactive cells, of which >50% also contained 5-HT(2C)R immunoreactivity. Thus, we demonstrate for the first time that the 5-HT(2C)R colocalizes in DA and GABA VTA neurons which project to the NAc, describe in detail the distribution of NAc-projecting GABA VTA neurons, and identify the colocalization of TH and GAD-67 in the same NAc-projecting VTA neurons. These data suggest that the 5-HT(2C)R may exert direct influence upon both dopamine and GABA VTA output to the NAc. Further, the indication that a proportion of NAc-projecting VTA neurons synthesize and potentially release both dopamine and GABA adds intriguing complexity to the framework of the VTA and its postulated neuroanatomical roles.
5-羟色胺 5-HT(2C)受体(5-HT(2C)R)位于边缘皮质纹状体回路中,该回路在介导注意力、动机、认知和奖励过程中起着重要作用。5-HT(2C)R 通过激活腹侧被盖区(VTA)中的γ-氨基丁酸(GABA)神经元来调节中脑伏隔核多巴胺神经传递。然而,我们最近证明了 5-HT(2C)R 在多巴胺 VTA 神经元中的表达,这表明 5-HT(2C)R 可能直接影响中脑伏隔核多巴胺的输出。在这里,我们采用合成多巴胺(酪氨酸羟化酶;TH)和 GABA(谷氨酸脱羧酶同工型 67;GAD-67)的酶的双重荧光免疫化学和 FluoroGold(FG)逆行追踪来揭示是否具有 5-HT(2C)R 受体的多巴胺和 GABA VTA 神经元支配伏隔核(NAc)。在 VTA 的中间水平相对于前颅和后颅水平检测到最多的 FG 标记细胞,并且包括一部分 TH 和 GAD-67 免疫反应性细胞,其中>50%也包含 5-HT(2C)R 免疫反应性。因此,我们首次证明 5-HT(2C)R 与投射到 NAc 的多巴胺和 GABA VTA 神经元共定位,详细描述了投射到 NAc 的 GABA VTA 神经元的分布,并确定了投射到 NAc 的相同 VTA 神经元中 TH 和 GAD-67 的共定位。这些数据表明 5-HT(2C)R 可能直接影响到投射到 NAc 的多巴胺和 GABA VTA 神经元的输出。此外,有证据表明,一部分投射到 NAc 的 VTA 神经元合成并可能释放多巴胺和 GABA,这为 VTA 及其假设的神经解剖学作用增加了有趣的复杂性。