Axonal patterns in olfactory cortex after olfactory bulb removal in newborn rats

1975 ◽  
Vol 47 (3) ◽  
pp. 442-447 ◽  
Author(s):  
Lesnick E. Westrum
Neuroenology ◽  
2016 ◽  
pp. 128-134
Author(s):  
Gordon M. Shepherd

We compare the initial experience of the aroma of the wine in the glass with the experience of the retronasal aroma as it contributes to the full flavor of the wine in the mouth and throat. We discuss the controversy over whether retronasal smell is less sensitive than orthonasal smell, and what could be the reasons. The processing of retronasal smell images is described from the olfactory receptors to the olfactory bulb, olfactory cortex, and highest cortical levels.


2014 ◽  
pp. 133-160 ◽  
Author(s):  
Shin Nagayama ◽  
Kei M. Igarashi ◽  
Hiroyuki Manabe ◽  
Kensaku Mori

2021 ◽  
pp. 851-861
Author(s):  
Kelly D. Flemming

This chapter briefly repeats key anatomic characteristics and then reviews clinical disorders affecting each cranial nerve in addition to the brainstem. More specifically, this chapter covers cranial nerves I, V, VII, and IX through XII plus the brainstem. The olfactory nerve is a special visceral afferent nerve that functions in the sense of smell. The axons of the olfactory receptor cells within the nasal cavity extend through the cribriform plate to the olfactory bulb. These olfactory receptor cell axons synapse with mitral cells in the olfactory bulb. Mitral cell axons project to the primary olfactory cortex and amygdala. The olfactory cortex interconnects with various autonomic and visceral centers.


2020 ◽  
Vol 83 (1) ◽  
Author(s):  
Kensaku Mori ◽  
Hitoshi Sakano

In mammals, odor information detected by olfactory sensory neurons is converted to a topographic map of activated glomeruli in the olfactory bulb. Mitral cells and tufted cells transmit signals sequentially to the olfactory cortex for behavioral outputs. To elicit innate behavioral responses, odor signals are directly transmitted by distinct subsets of mitral cells from particular functional domains in the olfactory bulb to specific amygdala nuclei. As for the learned decisions, input signals are conveyed by tufted cells as well as by mitral cells to the olfactory cortex. Behavioral scene cells link the odor information to the valence cells in the amygdala to elicit memory-based behavioral responses. Olfactory decision and perception take place in relation to the respiratory cycle. How is the sensory quality imposed on the olfactory inputs for behavioral outputs? How are the two types of odor signals, innate and learned, processed during respiration? Here, we review recent progress on the study of neural circuits involved in decision making in the mouse olfactory system. Expected final online publication date for the Annual Review of Physiology, Volume 83 is February 10, 2021. Please see http://www.annualreviews.org/page/journal/pubdates for revised estimates.


2017 ◽  
Vol 12 (5) ◽  
pp. 1355-1362 ◽  
Author(s):  
Linyin Yao ◽  
Xiaoli Yi ◽  
Jayant Marian Pinto ◽  
Xiandao Yuan ◽  
Yichen Guo ◽  
...  

2018 ◽  
Author(s):  
Koshi Murata ◽  
Tomoki Kinoshita ◽  
Yugo Fukazawa ◽  
Kenta Kobayashi ◽  
Kazuto Kobayashi ◽  
...  

AbstractOlfaction guides goal-directed behaviours including feeding. To investigate how central olfactory neural circuits control feeding behaviour in mice, we performed retrograde tracing from the lateral hypothalamus (LH), an important feeding centre. We observed a cluster of retrogradely labelled cells distributed in the posteroventral region of the olfactory peduncle. Histochemical analyses revealed that a majority of these retrogradely labelled projection neurons expressed glutamic acid decarboxylase 65/67 (GAD65/67), but not vesicular glutamate transporter 1 (VGluT1). We named this region with GABAergic projection neurons the ventral olfactory nucleus (VON) to discriminate it from the conventional olfactory peduncle. VON neurons were less immunoreactive for DARPP-32, a striatal neuron marker, in comparison to those in the olfactory tubercle and nucleus accumbens, which distinguished the VON from the ventral striatum. Fluorescent labelling confirmed synaptic contacts between VON neurons and olfactory bulb projection neurons. Rabies-virus-mediated trans-synaptic labelling revealed that VON neurons received synaptic inputs from the olfactory bulb, other olfactory cortices, horizontal limb of the diagonal band, and prefrontal cortex. Collectively, these results identified novel GABAergic projection neurons in the olfactory cortex that can integrate olfactory sensory and top-down inputs and send inhibitory output to the LH, which may contribute to forming odour-guided LH-related behaviours.


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