Central Mechanisms of Frog Calling

Behaviour ◽  
1966 ◽  
Vol 26 (3-4) ◽  
pp. 251-285 ◽  
Author(s):  
Robert S. Schmidt
Keyword(s):  
Rana Pipiens ◽  
Hormone Receptors ◽  
Acoustic Stimulus ◽  
Control Mechanisms ◽  
Nucleus Isthmi ◽  
Hyla Cinerea ◽  
Midbrain Tegmentum ◽  
Inspiratory Phase ◽  
Ventral Thalamus ◽  
The Brain

AbstractRelease calling and warning crying in Rana pipiens are described and compared with breathing. Vokalizations consist of a vocal phase, which is merely a modification of the expiratory phase of breathing, followed by an inspiratory phase, which is identical to inspiratory phase of breathing. Electrical and mechanical stimulation of the brain and brain lesions are used to locate some of the central mechanisms controlling release calling and warning crying in Rana pipiens, and mating calling in Rana pipiens and a number of hylids (mainly Hyla cinerea). It is concluded that the main control mechanisms are in the trigeminoisthmic tegmentum (below the nucleus isthmi). Mating calling requires, in addition, input transmitted through the ventral thalamus from hormone receptors in the preoptic area. Mating calling can be evoked in hylids by presenting them with recordings of specific calls. The mechanisms for responding to an acoustic stimulus are probably located in the anterior medulla and midbrain tegmentum (below the nucleus isthmi). Mating calling was evoked in two Hyla cinerea females after replacing the ovaries with Rana testes and injecting Rana pituitaries. It is suggested that release calling evolved from breathing, and that warning crying and mating calling may then have evolved from release calling.

scholarly journals Spatial Dependence of Stimulus Competition in the Avian Nucleus Isthmi Pars Magnocellularis

2019 ◽  
Vol 93 (2-3) ◽  
pp. 137-151 ◽  
Author(s):  
Hannah M. Schryver ◽  
Shreesh P. Mysore
Keyword(s):  
Functional Properties ◽  
Sensory Modality ◽  
Barn Owl ◽  
Inhibitory Neurons ◽  
Stimulus Selection ◽  
Nucleus Isthmi ◽  
Midbrain Tegmentum ◽  
The One ◽  
The Brain ◽  
Shed Light

The nucleus isthmi pars magnocellularis (Imc) is a group of specialized inhibitory neurons in the midbrain tegmentum, thought to be conserved across vertebrate classes. Past anatomical work in reptiles has suggested a role for it in stimulus selection, which has been supported by recent studies in avians. Additionally, focal inactivation of Imc neurons is known to abolish all competitive interactions in the optic tectum (OT; SC in mammals), a midbrain sensorimotor hub that is critical for the control of spatial attention, thereby revealing a key role for Imc in stimulus selection. However, the functional properties of Imc neurons are not well understood. Here, with electrophysiological experiments in the barn owl Imc, we show that Imc neurons themselves exhibit signatures of stimulus competition. Distant competing stimuli outside the spatial receptive field (RF) suppressed powerfully, and divisively, the responses of Imc neurons to stimuli inside the RF, and did so from all tested locations along the elevation as well as azimuth. Notably, this held true even for locations encoded by the opposite side of the brain from the one containing the recording site. This global divisive inhibition operated independently of the sensory modality of the competing stimulus. Thus, the Imc not only supplies inhibition to the OT to support competition there, but may itself be an active site of stimulus competition. These results from experiments in the barn owl shed light on the functional properties of a vital node in the vertebrate midbrain selection network.

Modulation of cardiovascular control mechanisms and their interaction

1996 ◽  
Vol 76 (1) ◽  
pp. 193-244 ◽  
Author(s):  
P. B. Persson
Keyword(s):  
Nitric Oxide ◽  
Black Box ◽  
Control Element ◽  
Control Mechanisms ◽  
Severity Of Disease ◽  
The Brain ◽  
Specific Control ◽  
Central Level ◽  
Shed Light

It is generally held that the role of a specific control element can only be understood within its physiological environment. The reviewed studies make it clear that there is a potent interplay between locally produced substances such as adenosine, nitric oxide, prostaglandins, and various others all interacting with the central level of control. This can occur at central sites (e.g., nitric oxide in the brain) or in the periphery (e.g., neural influence on autoregulation). The interactions are more or less pronounced during specific physiological challenges. Furthermore, several of these interactions are altered under pathological circumstances, and in some cases, the interactions seem to maintain or even augment the severity of disease. When more than three parameters participate in an interaction, the resulting regulation may become extremely complex. If these parameters are nonlinearly coupled with each other, the only way to shed light onto the nature of control network is by treating it as a black box. With the use of spectral analysis or nonlinear methods, it is possible to disentangle the fundamental nature of the system in terms of the complexity and stability. Therefore, modern developments in cardiovascular physiology utilizing these techniques, some of which are derived from the "chaos theory," are reviewed.

Dream science 2000: A response to commentaries on Dreaming and the brain

2000 ◽  
Vol 23 (6) ◽  
pp. 1019-1035 ◽  
Author(s):  
J. Allan Hobson ◽  
Edward F. Pace-Schott ◽  
Robert Stickgold
Keyword(s):  
Learning And Memory ◽  
Emerging Technologies ◽  
Mental Activity ◽  
Control Mechanisms ◽  
Dream Research ◽  
The Brain ◽  
Formal Features

Definitions of dreaming are not required to map formal features of mental activity onto brain measures. While dreaming occurs during all stages of sleep, intense dreaming is largely confined to REM. Forebrain structures and many neurotransmitters can contribute to sleep and dreaming without negating brainstem and aminergic-cholinergic control mechanisms. Reductionism is essential to science and AIM has considerable heuristic value. Recent findings support sleep's role in learning and memory. Emerging technologies may address long-standing issues in sleep and dream research.

scholarly journals Mapping the common and distinct neural correlates of visual, rule and motor conflict

2020 ◽  
Author(s):  
Bryony Goulding Mew ◽  
Darije Custovic ◽  
Eyal Soreq ◽  
Romy Lorenz ◽  
Ines Violante ◽  
...  
Keyword(s):  
Region Of Interest ◽  
Neural Correlates ◽  
Brain Regions ◽  
Control Mechanisms ◽  
Activation Patterns ◽  
The Common ◽  
Full Factorial ◽  
The Brain ◽  
Categorical Scale ◽  
Conflict Types

AbstractFlexible behaviour requires cognitive-control mechanisms to efficiently resolve conflict between competing information and alternative actions. Whether a global neural resource mediates all forms of conflict or this is achieved within domainspecific systems remains debated. We use a novel fMRI paradigm to orthogonally manipulate rule, response and stimulus-based conflict within a full-factorial design. Whole-brain voxelwise analyses show that activation patterns associated with these conflict types are distinct but partially overlapping within Multiple Demand Cortex (MDC), the brain regions that are most commonly active during cognitive tasks. Region of interest analysis shows that most MDC sub-regions are activated for all conflict types, but to significantly varying levels. We propose that conflict resolution is an emergent property of distributed brain networks, the functional-anatomical components of which place on a continuous, not categorical, scale from domain-specialised to domain general. MDC brain regions place towards one end of that scale but display considerable functional heterogeneity.

A Case Report on Heart Rate Variability Biofeedback and Postconcussion Syndrome: Healing the Autonomic Nervous System

Biofeedback ◽  
2021 ◽  
Vol 49 (4) ◽  
pp. 86-88
Author(s):  
Leah M. Lagos
Keyword(s):  
Heart Rate ◽  
Heart Rate Variability ◽  
High Amplitude ◽  
Regulatory Control ◽  
Control Mechanisms ◽  
Postconcussion Syndrome ◽  
Heart Rate Variability Biofeedback ◽  
The Mind ◽  
The Brain ◽  
Cardiovascular Functions

Postconcussion syndrome is a devastating condition of the mind, body, and even personality. Mounting research demonstrates that heart rate variability biofeedback can help the concussed individual in three critical ways: (a) eliciting high amplitude oscillations in cardiovascular functions and thereby strengthening self-regulatory control mechanisms; (b) restoring autonomic balance; and (c) increasing the afferent impulse stream from the baroreceptors to restore balance between inhibitory and excitatory processes in the brain.

scholarly journals Re-membering the body: applications of computational neuroscience to the top-down control of regeneration of limbs and other complex organs

2015 ◽  
Vol 7 (12) ◽  
pp. 1487-1517 ◽  
Author(s):  
G. Pezzulo ◽  
M. Levin
Keyword(s):  
Information Processing ◽  
Pattern Formation ◽  
Computational Neuroscience ◽  
Memory System ◽  
The Body ◽  
Signaling Networks ◽  
Control Mechanisms ◽  
Top Down ◽  
The Brain

How do regenerating bodies know when to stop remodeling? Bioelectric signaling networks guide pattern formation and may implement a somatic memory system. Deep parallels may exist between information processing in the brain and morphogenetic control mechanisms.

Significance of neuro-cardiac control mechanisms governed by higher regions of the brain

2016 ◽  
Vol 199 ◽  
pp. 54-65 ◽  
Author(s):  
Peter Taggart ◽  
Hugo Critchley ◽  
Stefan van Duijvendoden ◽  
Pier D. Lambiase
Keyword(s):  
Control Mechanisms ◽  
Cardiac Control ◽  
The Brain

scholarly journals Sex Differences in the Epigenome: A Cause or Consequence of Sexual Differentiation of the Brain?

Genes ◽  
2019 ◽  
Vol 10 (6) ◽  
pp. 432 ◽  
Author(s):  
Bruno Gegenhuber ◽  
Jessica Tollkuhn
Keyword(s):  
Gene Expression ◽  
Sex Differences ◽  
Sexual Differentiation ◽  
Hormone Receptors ◽  
Neurological Diseases ◽  
Activity Patterns ◽  
Regulatory Elements ◽  
The Body ◽  
Epigenetic Mechanism ◽  
The Brain

Females and males display differences in neural activity patterns, behavioral responses, and incidence of psychiatric and neurological diseases. Sex differences in the brain appear throughout the animal kingdom and are largely a consequence of the physiological requirements necessary for the distinct roles of the two sexes in reproduction. As with the rest of the body, gonadal steroid hormones act to specify and regulate many of these differences. It is thought that transient hormonal signaling during brain development gives rise to persistent sex differences in gene expression via an epigenetic mechanism, leading to divergent neurodevelopmental trajectories that may underlie sex differences in disease susceptibility. However, few genes with a persistent sex difference in expression have been identified, and only a handful of studies have employed genome-wide approaches to assess sex differences in epigenomic modifications. To date, there are no confirmed examples of gene regulatory elements that direct sex differences in gene expression in the brain. Here, we review foundational studies in this field, describe transcriptional mechanisms that could act downstream of hormone receptors in the brain, and suggest future approaches for identification and validation of sex-typical gene programs. We propose that sexual differentiation of the brain involves self-perpetuating transcriptional states that canalize sex-specific development.

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