scholarly journals Pauses in Cholinergic Interneuron Activity Are Driven by Excitatory Input and Delayed Rectification, with Dopamine Modulation

Neuron ◽  
2018 ◽  
Vol 98 (5) ◽  
pp. 918-925.e3 ◽  
Author(s):  
Yan-Feng Zhang ◽  
John N.J. Reynolds ◽  
Stephanie J. Cragg
2021 ◽  
pp. JN-RM-0967-20
Author(s):  
Noorya Yasmin Ahmed ◽  
Yadollah Ranjbar-Slamloo ◽  
Alice Shaam Al Abed ◽  
Lingxiao Gao ◽  
Yovina Sontani ◽  
...  

2007 ◽  
Vol 27 (3) ◽  
pp. 496-506 ◽  
Author(s):  
M. Narushima ◽  
M. Uchigashima ◽  
M. Fukaya ◽  
M. Matsui ◽  
T. Manabe ◽  
...  

IBRO Reports ◽  
2019 ◽  
Vol 6 ◽  
pp. S402
Author(s):  
Yadollah Ranjbar-Slamloo ◽  
Noorya Ahmed ◽  
Lingxiao Gao ◽  
Shaam Al Abed ◽  
Alexander Rcom-H’cheo-Gauthier ◽  
...  

eNeuro ◽  
2021 ◽  
pp. ENEURO.0196-21.2021
Author(s):  
Samira Ztaou ◽  
Soo Jung Oh ◽  
Sophia Tepler ◽  
Sixtine Fleury ◽  
Miriam Matamales ◽  
...  

2018 ◽  
Vol 137 ◽  
pp. 309-321 ◽  
Author(s):  
Rodrigo Manuel Paz ◽  
Cecilia Tubert ◽  
Agostina Stahl ◽  
Analía López Díaz ◽  
Roberto Etchenique ◽  
...  

2020 ◽  
Author(s):  
Karen A Bell ◽  
Rayne Delong ◽  
Priyodarshan Goswamee ◽  
A Rory McQuiston

Abstract The entorhinal cortex alvear pathway is a major excitatory input to hippocampal CA1, yet nothing is known about its physiological impact. We investigated the alvear pathway projection and innervation of neurons in CA1 using optogenetics and whole cell patch clamp methods in transgenic mouse brain slices. Using this approach, we show that the medial entorhinal cortical alvear inputs onto CA1 pyramidal cells (PCs) and interneurons with cell bodies located in stratum oriens were monosynaptic, had low release probability, and were mediated by glutamate receptors. Optogenetic theta burst stimulation was unable to elicit suprathreshold activation of CA1 PCs but was capable of activating CA1 interneurons. However, different subtypes of interneurons were not equally affected. Higher burst action potential frequencies were observed in parvalbumin-expressing interneurons relative to vasoactive-intestinal peptide-expressing or a subset of oriens lacunosum-moleculare (O-LM) interneurons. Furthermore, alvear excitatory synaptic responses were observed in greater than 70% of PV and VIP interneurons and less than 20% of O-LM cells. Finally, greater than 50% of theta burst-driven inhibitory postsynaptic current amplitudes in CA1 PCs were inhibited by optogenetic suppression of PV interneurons. Therefore, our data suggest that the alvear pathway primarily affects hippocampal CA1 function through feedforward inhibition of select interneuron subtypes.


1983 ◽  
Vol 49 (3) ◽  
pp. 674-685 ◽  
Author(s):  
L. Z. Wise ◽  
D. R. Irvine

1. The auditory responses of 207 single neurons in the intermediate and deep layers of the superior colliculus (SC) of barbiturate -or chloralose-anesthetized cats were recorded extracellularly. Sealed stimulating systems incorporating calibrated probe microphone assemblies were employed to present tone- and noise-burst stimuli. 2. All acoustically activated neurons responded with onset responses to noise bursts. Of those neurons also tested with tonal stimuli, approximately 30% were unresponsive over the frequency range tested (0.1-40 kHz), while the others had higher thresholds to tones than to noise. 3. Details of frequency responsiveness were obtained for 55 neurons; 21 were broadly tuned, while 34 were sharply tuned with clearly defined characteristic frequencies (CFs). All sharply tuned neurons had CFs greater than or equal to 10 kHz. 4. The majority of neurons (81%) responded with latencies in the range 8-20 ms; only 11% of neurons had latencies greater than 30 ms. 5. Binaural response properties were examined for 165 neurons. The great majority (79%) received monaural excitatory input only from the contralateral ear (EO). However, most EO cells were binaurally influenced, the contralateral response being either inhibited (EO/I; 96 of 131 units) or facilitated (EO/F; 33 of 131 units) by simultaneous ipsilateral stimulation. Small subgroups were monaurally excited by either ear (EE cells; 8%) or were unresponsive monaurally but responded strongly to binaural stimulation (OO/F cells; 7%). 6. EO/I, EO/F, and OO/F neurons showed characteristic forms of sensitivity to interaural intensity differences (IIDs). The IID functions of EO/I neurons would be expected to produce large contralateral spatial receptive fields with clearly defined medial borders, such as have been described in studies of deep SC neurons employing free-field stimuli. 7. Preliminary evidence suggests a possible topographic organization of IID sensitivity in deep SC, such that the steeply sloping portion of the function (corresponding to the medial edge of the receptive field) is shifted laterally for EO/I neurons located more caudally in the nucleus. 8. The auditory properties of deep SC neurons are compared with previous reports and implications for the organization of auditory input are considered. The binaural properties and auditory spatial fields of deep SC neurons suggest that any representation of auditory space in this structure is unlikely to be based on restricted spatial fields.


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