Koppensteiner Peter, Galvin Christopher, Ninan Ipe
Department of Psychiatry, NYU Langone Medical Center, NY, United States.
Department of Psychiatry, NYU Langone Medical Center, NY, United States.
Mol Cell Neurosci. 2016 Dec;77:105-112. doi: 10.1016/j.mcn.2016.10.006. Epub 2016 Oct 26.
Of the two major subdivisions of the habenula, the medial and lateral nuclei, the medial habenula is the least understood in terms of synaptic transmission, intrinsic properties and plasticity. The medial habenula (MHb) is composed of glutamatergic neurons which receive the majority of their inputs from the septal region and project predominantly to the interpeduncular nucleus (IPN). To understand the synaptic transmission, we studied both glutamatergic and GABAergic synaptic transmission in the dorsal region of the medial habenula (dMHb). While glutamatergic transmission dominates during early development, an attenuation of glutamatergic transmission and an enhancement of GABAergic transmission occur during development leading into adulthood. Furthermore, as reported previously, GABA receptor-mediated transmission is excitatory in the adult dMHb, which is consistent with the reduced expression of the K-Cl co-transporter KCC2. Given the potential role of the dMHb in aversive behaviors, we examined whether fear conditioning or exposure to foot shock affects excitability in dMHb neurons. We observed a suppression of the excitability of dMHb neurons in mice that either underwent fear conditioning or were exposed to foot shock. Furthermore, we observed a suppression of GABAergic but not glutamatergic transmission in the dMHb neurons following fear conditioning. These results suggest that aversive experience produces a suppression of the dMHb neuronal activity. Given that the medial habenula is upstream of the median raphe nucleus which is believed to be involved in the negative regulation of aversive memory, the suppression of dMHb neurons following an aversive experience might play a role in strengthening of aversive memories.
在缰核的两个主要亚区,即内侧核和外侧核中,内侧缰核在突触传递、内在特性和可塑性方面是了解最少的。内侧缰核(MHb)由谷氨酸能神经元组成,这些神经元的大部分输入来自隔区,主要投射到脚间核(IPN)。为了了解突触传递,我们研究了内侧缰核背侧区域(dMHb)的谷氨酸能和GABA能突触传递。虽然谷氨酸能传递在早期发育过程中占主导地位,但在发育至成年的过程中,谷氨酸能传递会减弱,GABA能传递会增强。此外,如先前报道的那样,GABA受体介导的传递在成年dMHb中是兴奋性的,这与K-Cl共转运体KCC2表达降低一致。鉴于dMHb在厌恶行为中的潜在作用,我们研究了恐惧条件反射或足部电击暴露是否会影响dMHb神经元的兴奋性。我们观察到,经历恐惧条件反射或暴露于足部电击的小鼠中,dMHb神经元的兴奋性受到抑制。此外,我们观察到恐惧条件反射后,dMHb神经元中的GABA能传递而非谷氨酸能传递受到抑制。这些结果表明,厌恶经历会抑制dMHb神经元的活动。鉴于内侧缰核位于中缝核的上游,而中缝核被认为参与厌恶记忆的负调控,厌恶经历后dMHb神经元的抑制可能在强化厌恶记忆中起作用。