Vasopressin differentially modulates the excitability of rat olfactory bulb neuron subtypes.

Front Neural Circuits

Institute of Zoology, Neurophysiology, University of Regensburg, Regensburg, Germany.

Published: September 2024

AI Article Synopsis

  • Vasopressin (VP) is important for social memory and affects the olfactory bulb (OB) during social interactions, specifically by modulating olfactory processing to help distinguish similar odors.
  • In experiments, VP was found to reduce the firing rates of mitral cells (MCs) and diminish excitatory responses in another type of neuron, the middle tufted cells (mTCs), but had no effect on MCs.
  • The study demonstrated that VP enhances calcium influx in juxtaglomerular and granule cell layers when stronger odor signals are presented, suggesting that VP increases inhibition through interneuron activity, ultimately improving the ability to differentiate similar smells like rat body odors.

Article Abstract

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 and decreases the amplitudes of olfactory nerve-evoked excitatory postsynaptic potentials (ON-evoked EPSPs) in external tufted cells . We performed whole-cell patch-clamp recordings and population Ca 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 Ca 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 Ca 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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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11390533PMC
http://dx.doi.org/10.3389/fncir.2024.1448592DOI Listing

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  • In experiments, VP was found to reduce the firing rates of mitral cells (MCs) and diminish excitatory responses in another type of neuron, the middle tufted cells (mTCs), but had no effect on MCs.
  • The study demonstrated that VP enhances calcium influx in juxtaglomerular and granule cell layers when stronger odor signals are presented, suggesting that VP increases inhibition through interneuron activity, ultimately improving the ability to differentiate similar smells like rat body odors.
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