Cohen Lior, Mizrahi Adi
Department of Neurobiology, Institute of Life Sciences, Edmond and Lily Safra Center for Brain Sciences, Hebrew University of Jerusalem, Edmond J. Safra Campus, Givat Ram Jerusalem, 91904, Israel.
Department of Neurobiology, Institute of Life Sciences, Edmond and Lily Safra Center for Brain Sciences, Hebrew University of Jerusalem, Edmond J. Safra Campus, Givat Ram Jerusalem, 91904, Israel
J Neurosci. 2015 Jan 28;35(4):1806-15. doi: 10.1523/JNEUROSCI.1786-14.2015.
Maternal behavior can be triggered by auditory and olfactory cues originating from the newborn. Here we report how the transition to motherhood affects excitatory and inhibitory neurons in layer 2/3 (L2/3) of the mouse primary auditory cortex. We used in vivo two-photon targeted cell-attached recording to compare the response properties of parvalbumin-expressing neurons (PVNs) and pyramidal glutamatergic neurons (PyrNs). The transition to motherhood shifts the average best frequency of PVNs to higher frequency by a full octave, with no significant effect on average best frequency of PyrNs. The presence of pup odors significantly reduced the spontaneous and evoked activity of PVN. This reduction of feedforward inhibition coincides with a complimentary increase in spontaneous and evoked activity of PyrNs. The selective shift of PVN frequency tuning should render pup odor-induced disinhibition more effective for high-frequency stimuli, such as ultrasonic vocalizations. Indeed, pup odors increased neuronal responses of PyrNs to pup ultrasonic vocalizations. We conclude that plasticity in the mothers is mediated, at least in part, via modulation of the feedforward inhibition circuitry in the auditory cortex.
母性行为可由源自新生儿的听觉和嗅觉线索触发。在此,我们报告了向母亲身份的转变如何影响小鼠初级听觉皮层第2/3层(L2/3)中的兴奋性和抑制性神经元。我们使用体内双光子靶向细胞贴附记录来比较表达小白蛋白的神经元(PVNs)和锥体谷氨酸能神经元(PyrNs)的反应特性。向母亲身份的转变使PVNs的平均最佳频率向更高频率移动了整整一个八度,对PyrNs的平均最佳频率没有显著影响。幼崽气味的存在显著降低了PVN的自发活动和诱发活动。这种前馈抑制的减少与PyrNs的自发活动和诱发活动的互补性增加相吻合。PVN频率调谐的选择性转变应该使幼崽气味诱导的去抑制对高频刺激(如超声波发声)更有效。事实上,幼崽气味增加了PyrNs对幼崽超声波发声的神经元反应。我们得出结论,母亲体内的可塑性至少部分是通过调节听觉皮层中的前馈抑制回路来介导的。