血管加压素以不同方式调节大鼠嗅球神经元亚型的兴奋性

IF 3.4 3区 医学 Q2 NEUROSCIENCES
Hajime Suyama, Gaia Bianchini, Michael Lukas
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引用次数: 0

摘要

即使在嗅球(OB)水平,血管加压素(VP)也在社会记忆中发挥着至关重要的作用,在社会交往过程中,嗅球的VP细胞会被激活。然而,目前仍不清楚 VP 是如何调节嗅觉处理过程以提高对非常相似气味(如大鼠体味)的辨别能力的。迄今为止,已有研究表明,VP 在体内气味呈现过程中会降低有丝分裂细胞(MCs)的发射率,并在体外降低外簇细胞中嗅觉神经诱发的兴奋性突触后电位(ON-evoked EPSPs)的振幅。我们在急性大鼠外耳道切片上进行了全细胞膜片钳记录和群体 Ca2+ 成像。我们记录了两类投射神经元(中间丛细胞(mTCs)和MCs)的导通诱发EPSPs以及自发抑制性突触后电流(IPSCs)。VP 浴降低了 mTCs 的导联诱发 EPSP 的振幅和自发 IPSC 的频率,但并没有改变 MCs 的这些振幅和频率。因此,我们分析了抑制性中间神经元(即肾小球周围细胞(PGC)和颗粒细胞(GC))的ON诱发的EPSPs,以寻找mTCs抑制作用增强的原因。然而,VP 并没有增加这两类中间神经元诱发的 EPSPs 的振幅。接下来,我们在肾小球层和表层 GC 层进行了双光子群体 Ca2+ 成像,以观察对强于贴片钳实验期间的 ON 刺激的反应,因为 ON 刺激应该会在被测细胞中唤起动作电位。我们观察到,施加 VP 增加了并肾小球细胞和 GC 体节中 ON 诱导的 Ca2+ 流入。因此,我们的研究结果表明,VP 可通过强 ON 输入介导的抑制性中间神经元活动抑制投射神经元。这种神经调节可以改善气味的表征,从而提高对类似气味(如同种体味)的辨别能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Vasopressin differentially modulates the excitability of rat olfactory bulb neuron subtypes
Vasopressin (VP) plays a crucial role in social memory even at the level of the olfactory bulb (OB), where OB VP cells are activated during social interactions. However, it remains unclear how VP modulates olfactory processing to enable enhanced discrimination of very similar odors, e.g., rat body odors. Thus far, it has been shown that VP reduces firing rates in mitral cells (MCs) during odor presentation in vivo and decreases the amplitudes of olfactory nerve-evoked excitatory postsynaptic potentials (ON-evoked EPSPs) in external tufted cells in vitro. We performed whole-cell patch-clamp recordings and population Ca2+ imaging on acute rat OB slices. We recorded ON-evoked EPSPs as well as spontaneous inhibitory postsynaptic currents (IPSCs) from two types of projection neurons: middle tufted cells (mTCs) and MCs. VP bath application reduced the amplitudes of ON-evoked EPSPs and the frequencies of spontaneous IPSCs in mTCs but did not change those in MCs. Therefore, we analyzed ON-evoked EPSPs in inhibitory interneurons, i.e., periglomerular cells (PGCs) and granule cells (GCs), to search for the origin of increased inhibition in mTCs. However, VP did not increase the amplitudes of evoked EPSPs in either type of interneurons. We next performed two-photon population Ca2+ imaging in the glomerular layer and the superficial GC layer of responses to stronger ON stimulation than during patch-clamp experiments that should evoke action potentials in the measured cells. We observed that VP application increased ON-evoked Ca2+ influx in juxtaglomerular cells and GC somata. Thus, our findings indicate inhibition by VP on projection neurons via strong ON input-mediated inhibitory interneuron activity. This neural modulation could improve representation of odors, hence, better discriminability of similar odors, e.g., conspecific body odors.
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来源期刊
CiteScore
6.00
自引率
5.70%
发文量
135
审稿时长
4-8 weeks
期刊介绍: Frontiers in Neural Circuits publishes rigorously peer-reviewed research on the emergent properties of neural circuits - the elementary modules of the brain. Specialty Chief Editors Takao K. Hensch and Edward Ruthazer at Harvard University and McGill University respectively, are supported by an outstanding Editorial Board of international experts. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics and the public worldwide. Frontiers in Neural Circuits launched in 2011 with great success and remains a "central watering hole" for research in neural circuits, serving the community worldwide to share data, ideas and inspiration. Articles revealing the anatomy, physiology, development or function of any neural circuitry in any species (from sponges to humans) are welcome. Our common thread seeks the computational strategies used by different circuits to link their structure with function (perceptual, motor, or internal), the general rules by which they operate, and how their particular designs lead to the emergence of complex properties and behaviors. Submissions focused on synaptic, cellular and connectivity principles in neural microcircuits using multidisciplinary approaches, especially newer molecular, developmental and genetic tools, are encouraged. Studies with an evolutionary perspective to better understand how circuit design and capabilities evolved to produce progressively more complex properties and behaviors are especially welcome. The journal is further interested in research revealing how plasticity shapes the structural and functional architecture of neural circuits.
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