scholarly journals Opposing expression gradients of calcitonin-related polypeptide alpha (Calca/Cgrpα) and tyrosine hydroxylase (Th) in type II afferent neurons of the mouse cochlea

2018 ◽  
Vol 526 (6) ◽  
pp. 1073-1073 ◽  
Author(s):  
Jingjing Sherry Wu ◽  
Pankhuri Vyas ◽  
Elisabeth Glowatzki ◽  
Paul Albert Fuchs
1993 ◽  
Vol 271 (1) ◽  
pp. 135-144 ◽  
Author(s):  
Wolfgang Kummer ◽  
Sebastian Bachmann ◽  
Winfried L. Neuhuber ◽  
J�rg H�nze ◽  
Rudolf E. Lang

2015 ◽  
Vol 6 (1) ◽  
Author(s):  
Kristina E. Froud ◽  
Ann Chi Yan Wong ◽  
Jennie M. E. Cederholm ◽  
Matthias Klugmann ◽  
Shaun L. Sandow ◽  
...  

Author(s):  
Megan B Wood ◽  
Nathaniel Nowak ◽  
Keira Mull ◽  
Adam Goldring ◽  
Mohamed Lehar ◽  
...  

AbstractOuter hair cells (OHCs) in the mouse cochlea are contacted by up to three type II afferent boutons. On average, only half of these are postsynaptic to presynaptic ribbons. Mice of both sexes were subjected to acoustic trauma that produced a threshold shift of 44.2 ± 9.1 dB 7 days after exposure. Ribbon synapses of OHCs were quantified in post-trauma and littermate controls using immunolabeling of CtBP2. Visualization with virtual reality was used to determine 3-D cytoplasmic localization of CtBP2 puncta to the synaptic pole of OHCs. Acoustic trauma was associated with a statistically significant increase in the number of synaptic ribbons per OHC. Serial section TEM was carried out on similarly treated mice. This also showed a significant increase in the number of ribbons in post-trauma OHCs, as well as a significant increase in ribbon volume compared to ribbons in control OHCs. An increase in OHC ribbon synapses after acoustic trauma is a novel observation that has implications for OHC:type II afferent signaling. A mathematical model showed that the observed increase in OHC ribbons considered alone could produce a significant increase in action potentials among type II afferent neurons during strong acoustic stimulation.


2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Pankhuri Vyas ◽  
Jingjing Sherry Wu ◽  
Adrian Jimenez ◽  
Elisabeth Glowatzki ◽  
Paul Albert Fuchs

2021 ◽  
Vol 17 ◽  
pp. 174480692110212
Author(s):  
Yuya Okutsu ◽  
Akihiro Yamada ◽  
Sotatsu Tonomura ◽  
Ryan J Vaden ◽  
Jianguo G Gu

Aβ-afferents in maxillary or V2 trigeminal ganglion (TG) neurons are somatosensory neurons that may be involved in both non-nociceptive and nociceptive functions in orofacial regions. However, electrophysiological properties of these V2 trigeminal Aβ-afferent neurons have not been well characterized so far. Here, we used rat ex vivo trigeminal nerve preparations and applied patch-clamp recordings to large-sized V2 TG neurons to characterize their electrophysiological properties. All the cells recorded had afferent conduction velocities in the range of Aβ-afferent conduction speeds. However, these V2 trigeminal Aβ-afferent neurons displayed different action potential (AP) properties. APs showed fast kinetics in some cells but slow kinetics with shoulders in repolarization phases in other cells. Based on the derivatives of voltages in AP repolarization with time (dV/dt), we classified V2 trigeminal Aβ-afferent neurons into four types: type I, type II, type IIIa and type IIIb. Type I V2 trigeminal Aβ-afferent neurons had the largest dV/dt of repolarization, the fastest AP conduction velocities, the shortest AP and afterhyperpolarization (AHP) durations, and the highest AP success rates. In contrast, type IIIb V2 trigeminal Aβ-afferent neurons had the smallest dV/dt of AP repolarization, the slowest AP conduction velocities, the longest AP and AHP durations, and the lowest AP success rates. The type IIIb cells also had significantly lower voltage-activated K+ currents. For type II and type IIIa V2 trigeminal Aβ-afferent neurons, AP parameters were in the range between those of type I and type IIIb V2 trigeminal Aβ-afferent neurons. Our electrophysiological classification of V2 trigeminal Aβ-afferent neurons may be useful in future to study their non-nociceptive and nociceptive functions in orofacial regions.


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