scholarly journals Efferent projections of Vglut2 , Foxp2 , and Pdyn parabrachial neurons in mice

2020 ◽  
Vol 529 (4) ◽  
pp. 657-693 ◽  
Author(s):  
Dake Huang ◽  
Fillan S. Grady ◽  
Lila Peltekian ◽  
Joel C. Geerling
Keyword(s):  
Efferent Projections

scholarly journals Understanding Emotions: Origins and Roles of the Amygdala

Biomolecules ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 823
Author(s):  
Goran Šimić ◽  
Mladenka Tkalčić ◽  
Vana Vukić ◽  
Damir Mulc ◽  
Ena Španić ◽  
...  
Keyword(s):  
Sensory Information ◽  
Anterior Cingulate ◽  
Central Nucleus ◽  
Subcortical Structures ◽  
Neuronal Populations ◽  
Efferent Projections ◽  
Short And Long Term ◽  
Understanding Emotions ◽  
Fight Or Flight Response ◽  
And Behavior

Emotions arise from activations of specialized neuronal populations in several parts of the cerebral cortex, notably the anterior cingulate, insula, ventromedial prefrontal, and subcortical structures, such as the amygdala, ventral striatum, putamen, caudate nucleus, and ventral tegmental area. Feelings are conscious, emotional experiences of these activations that contribute to neuronal networks mediating thoughts, language, and behavior, thus enhancing the ability to predict, learn, and reappraise stimuli and situations in the environment based on previous experiences. Contemporary theories of emotion converge around the key role of the amygdala as the central subcortical emotional brain structure that constantly evaluates and integrates a variety of sensory information from the surroundings and assigns them appropriate values of emotional dimensions, such as valence, intensity, and approachability. The amygdala participates in the regulation of autonomic and endocrine functions, decision-making and adaptations of instinctive and motivational behaviors to changes in the environment through implicit associative learning, changes in short- and long-term synaptic plasticity, and activation of the fight-or-flight response via efferent projections from its central nucleus to cortical and subcortical structures.

scholarly journals The Possible Role of the Uropygial Gland on Mate Choice in Domestic Chicken

2011 ◽  
Vol 2011 ◽  
pp. 1-5 ◽  
Author(s):  
Atsushi Hirao
Keyword(s):  
Mate Choice ◽  
Visual Cues ◽  
Individual Recognition ◽  
Copulatory Behavior ◽  
Uropygial Gland ◽  
Odor Cues ◽  
Histocompatibility Complex ◽  
Efferent Projections ◽  
Opposite Sex

In avian mating systems, male domestic fowls are polygamous and mate with a number of selected members of the opposite sex. The factors that influence mating preference are considered to be visual cues. However, several studies have indicated that chemosensory cues also affect socio-sexual behavior, including mate choice and individual recognition. The female uropygial gland appears to provide odor for mate choice, as uropygial gland secretions are specific to individual body odor. Chicken olfactory bulbs possess efferent projections to the nucleus taeniae that are involved in copulatory behavior. From various reports, it appears that the uropygial gland has the potential to act as the source of social odor cues that dictate mate choice. In this review, evidence for the possible role of the uropygial gland on mate choice in domestic chickens is presented. However, it remains unclear whether a relationship exists between the uropygial gland and major histocompatibility complex-dependent mate choice.

The organization of the gastric efferent projections in the brainstem of monkey: An HRP study

1984 ◽  
Vol 293 (2) ◽  
pp. 231-240 ◽  
Author(s):  
M.A. Karim ◽  
Engku Shaikh ◽  
Jeanette Tan ◽  
Zurina Ismail
Keyword(s):  
Efferent Projections

Efferent projections of the anterior perirhinal cortex in the rat

1996 ◽  
Vol 369 (2) ◽  
pp. 302-318 ◽  
Author(s):  
Dan C. McIntyre ◽  
Mary Ellen Kelly ◽  
William A. Staines
Keyword(s):  
Perirhinal Cortex ◽  
Efferent Projections

scholarly journals Tracheal occlusion-evoked respiratory load compensation and inhibitory neurotransmitter expression in rats

2014 ◽  
Vol 116 (8) ◽  
pp. 1006-1016 ◽  
Author(s):  
Hsiu-Wen Tsai ◽  
Paul W. Davenport
Keyword(s):  
Neural Network ◽  
Brain Stem ◽  
Breathing Pattern ◽  
Respiratory Rhythm ◽  
Inhibitory Neurotransmitter ◽  
Load Compensation ◽  
Efferent Projections ◽  
Motor Reflex ◽  
Sensory Pathway ◽  
The Brain

Respiratory load compensation is a sensory-motor reflex generated in the brain stem respiratory neural network. The nucleus of the solitary tract (NTS) is thought to be the primary structure to process the respiratory load-related afferent activity and contribute to the modification of the breathing pattern by sending efferent projections to other structures in the brain stem respiratory neural network. The sensory pathway and motor responses of respiratory load compensation have been studied extensively; however, the mechanism of neurogenesis of load compensation is still unknown. A variety of studies has shown that inhibitory interconnections among the brain stem respiratory groups play critical roles for the genesis of respiratory rhythm and pattern. The purpose of this study was to examine whether inhibitory glycinergic neurons in the NTS were activated by external and transient tracheal occlusions (ETTO) in anesthetized animals. The results showed that ETTO produced load compensation responses with increased inspiratory, expiratory, and total breath time, as well as elevated activation of inhibitory glycinergic neurons in the caudal NTS (cNTS) and intermediate NTS (iNTS). Vagotomized animals receiving transient respiratory loads did not exhibit these load compensation responses. In addition, vagotomy significantly reduced the activation of inhibitory glycinergic neurons in the cNTS and iNTS. The results suggest that these activated inhibitory glycinergic neurons in the NTS might be essential for the neurogenesis of load compensation responses in anesthetized animals.

Efferent projections of the periaqueductal gray in the rabbit

Neuroscience ◽  
1991 ◽  
Vol 40 (1) ◽  
pp. 191-216 ◽  
Author(s):  
S.T. Meller ◽  
B.J. Dennis
Keyword(s):  
Periaqueductal Gray ◽  
Efferent Projections
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