scholarly journals Unified neural pathways that gate affective pain and multisensory innate threat signals to the amygdala

Author(s):  
Sukjae Kang ◽  
Shijia Liu ◽  
Mao Ye ◽  
Dongil Kim ◽  
Jong-Hyun Kim ◽  
...  

Abstract Perception of aversive sensory stimuli such as pain and innate threat cues is essential for animal survival. The amygdala is critical for aversive sensory perception, and it has been suggested that multiple parallel pathways independently relay aversive cues from each sensory modality to the amygdala. However, a convergent pathway that relays multisensory aversive cues to the amygdala has not been identified. Here, we report that neurons expressing calcitonin gene-related peptide (CGRP) in the parvocellular subparafasicular thalamic nucleus (SPFp) are necessary and sufficient for affective-motivational pain perception by forming a spino-thalamo-amygdaloid pain pathway. In addition, we find that this thalamic CGRP pain pathway, together with well-known parabrachio-amygdaloid CGRP pain pathway, relays multisensory innate threat cues to the amygdala. The discovery of unified pathways that collectively gate aversive sensory stimuli from all sensory modalities may provide critical circuit-based insights for developing therapeutic interventions for affective pain- and innate fear-related disorders.

2020 ◽  
Author(s):  
Sukjae Joshua Kang ◽  
Shijia Liu ◽  
Mao Ye ◽  
Dong-Il Kim ◽  
Jong-Hyun Kim ◽  
...  

AbstractPerception of aversive sensory stimuli such as pain and innate threat cues is essential for animal survival. The amygdala is critical for aversive sensory perception, and it has been suggested that multiple parallel pathways independently relay aversive cues from each sensory modality to the amygdala. However, a convergent pathway that relays multisensory aversive cues to the amygdala has not been identified. Here, we report that neurons expressing calcitonin gene-related peptide (CGRP) in the parvocellular subparafasicular thalamic nucleus (SPFp) are necessary and sufficient for affective-motivational pain perception by forming a spino-thalamo-amygdaloid pain pathway. In addition, we find that this thalamic CGRP pain pathway, together with well-known parabrachio-amygdaloid CGRP pain pathway, is critical for the perception of multisensory innate threat cues. The discovery of unified pathways that collectively gate aversive sensory stimuli from all sensory modalities may provide critical circuit-based insights for developing therapeutic interventions for affective pain- and innate fear-related disorders.


2020 ◽  
Vol 21 (16) ◽  
pp. 5929 ◽  
Author(s):  
Edwin Aroke ◽  
Keesha Powell-Roach ◽  
Rosario Jaime-Lara ◽  
Markos Tesfaye ◽  
Abhrarup Roy ◽  
...  

Transient receptor potential (TRP) channels are a superfamily of cation transmembrane proteins that are expressed in many tissues and respond to many sensory stimuli. TRP channels play a role in sensory signaling for taste, thermosensation, mechanosensation, and nociception. Activation of TRP channels (e.g., TRPM5) in taste receptors by food/chemicals (e.g., capsaicin) is essential in the acquisition of nutrients, which fuel metabolism, growth, and development. Pain signals from these nociceptors are essential for harm avoidance. Dysfunctional TRP channels have been associated with neuropathic pain, inflammation, and reduced ability to detect taste stimuli. Humans have long recognized the relationship between taste and pain. However, the mechanisms and relationship among these taste–pain sensorial experiences are not fully understood. This article provides a narrative review of literature examining the role of TRP channels on taste and pain perception. Genomic variability in the TRPV1 gene has been associated with alterations in various pain conditions. Moreover, polymorphisms of the TRPV1 gene have been associated with alterations in salty taste sensitivity and salt preference. Studies of genetic variations in TRP genes or modulation of TRP pathways may increase our understanding of the shared biological mediators of pain and taste, leading to therapeutic interventions to treat many diseases.


2007 ◽  
Vol 21 (8) ◽  
pp. 1615-1629 ◽  
Author(s):  
Ramona Kenntner-Mabiala ◽  
Peter Weyers ◽  
Paul Pauli

2017 ◽  
Vol 41 (S1) ◽  
pp. S412-S413
Author(s):  
M. Martin ◽  
S. Chapman

IntroductionTheoretical controversy surrounds the issue of the extent to which cognitive processes can be identified which are characteristic of patients with irritable Bowel syndrome (IBS). The issue is important because particular patterns of idiosyncrasies would suggest tailored therapeutic interventions.ObjectivesTo map the processing of pain information in IBS and healthy participants in relation to physical and social threat, using latency as well as frequency metrics.MethodsParticipants (20 with IBS and 33 controls) were tested in an extended exogenous cuing paradigm whose derived measures included assessments of bias, engagement and disengagement. They also completed a battery of health and illness activity tests.ResultsThere was a significant interaction between bias in processing of pain (physical threat) and of neutral stimuli, as shown on Fig. 1. Further significant idiosyncrasies were observed in the relations between measures of attention and levels both of symptoms and of illness behaviour.ConclusionsDetailed evidence was obtained of anomalies in attention in IBS. The results may be interpreted in terms of interactive feedback between pain perception in relation to the gut, pain-specific attentional processes, and health behaviour. It will be discussed how mindfulness based cognitive therapy can be used as an intervention to disrupt this feedback.Disclosure of interestThe authors have not supplied their declaration of competing interest.Fig. 1Attentional bias in IBS and healthy groups with pain and neutral stimuli. Target in the same (valid) or different (invalid) position as the cue, bias = (RT invalid − RT valid).


Psychology ◽  
2019 ◽  
Author(s):  
Emily E. Perszyk ◽  
Bob Stewart ◽  
Haley R. Roland

The word taste commonly evokes the experience of a robust California red wine, a perfectly seasoned and roasted duck breast, or a decadent Belgian chocolate. In fact, the perceptual experience that accompanies ingestion of food is most correctly termed flavor. Flavor comprises combined elements of olfactory (i.e., retronasal odor), somatosensory (e.g., texture and temperature), and gustatory sensations that attend ingestion. In contrast, taste refers exclusively to the perceptions and behaviors that arise when chemical components of food stimulate the gustatory apparatus of the oral cavity, namely taste receptor cells found within taste buds. Consequent neural activity in taste nerves and taste-related areas of the brain lead to gustatory sensation and perception. There is general agreement that activation of the taste system results in the perception of five unique taste qualities, or basic tastes, in humans: sweet, sour, salty, bitter, and umami. It has long been appreciated that perception of these tastes plays a pivotal role in feeding by providing the organism with an appraisal of food nutrient value and/or potential toxicity. Though much remains unknown, our understanding of the gustatory system has burgeoned since 2000. Advances in molecular genetic techniques, for example, provided the launchpad for explosive growth in our understanding of the basic molecular and cellular physiology of taste receptor cells. This information, in turn, has stimulated theoretical, conceptual, and experimental reappraisal of long-standing ideas about the neuroanatomical and neurophysiological bases of taste stimulus coding and perception. Simultaneously, progress in functional brain-imaging technologies permitted non-invasive investigation of the neural pathways and processes involved in taste perception in humans. Results from functional imaging studies have confirmed, extended, and clarified findings from previous psychophysical studies in healthy participants and in patients with peripheral and central nervous system lesions. These studies have also revealed neural correlates of flavor, taste and flavor hedonics, and food-related reward. Combined molecular, behavioral, psychophysical, and imaging data suggest that taste can influence and be influenced by disease. Taste modulates metabolism and contributes to diseases such as obesity, diabetes, and hypertension. Various diseases and the drugs used to treat them can have strong negative impacts on taste, which can lead to impaired nutrition and diminished quality of life. The reciprocal influences of disease and taste signal the importance of considering this sensory modality in health, nutrition, and food industry policies and practice.


2011 ◽  
Vol 106 (6) ◽  
pp. 3216-3229 ◽  
Author(s):  
L. Hu ◽  
M. Liang ◽  
A. Mouraux ◽  
R. G. Wise ◽  
Y. Hu ◽  
...  

Across-trial averaging is a widely used approach to enhance the signal-to-noise ratio (SNR) of event-related potentials (ERPs). However, across-trial variability of ERP latency and amplitude may contain physiologically relevant information that is lost by across-trial averaging. Hence, we aimed to develop a novel method that uses 1) wavelet filtering (WF) to enhance the SNR of ERPs and 2) a multiple linear regression with a dispersion term (MLRd) that takes into account shape distortions to estimate the single-trial latency and amplitude of ERP peaks. Using simulated ERP data sets containing different levels of noise, we provide evidence that, compared with other approaches, the proposed WF+MLRd method yields the most accurate estimate of single-trial ERP features. When applied to a real laser-evoked potential data set, the WF+MLRd approach provides reliable estimation of single-trial latency, amplitude, and morphology of ERPs and thereby allows performing meaningful correlations at single-trial level. We obtained three main findings. First, WF significantly enhances the SNR of single-trial ERPs. Second, MLRd effectively captures and measures the variability in the morphology of single-trial ERPs, thus providing an accurate and unbiased estimate of their peak latency and amplitude. Third, intensity of pain perception significantly correlates with the single-trial estimates of N2 and P2 amplitude. These results indicate that WF+MLRd can be used to explore the dynamics between different ERP features, behavioral variables, and other neuroimaging measures of brain activity, thus providing new insights into the functional significance of the different brain processes underlying the brain responses to sensory stimuli.


2002 ◽  
Vol 19 (4) ◽  
pp. 207-219 ◽  
Author(s):  
Eynat Gal ◽  
Murray Dyck ◽  
Anne Passmore

AbstractThis study was designed to test whether there is a functional relationship between sensory stimulation and stereotyped movements (SM). Four children with autism and intellectual disability (according to DSM-IV criteria) who showed stereotyped movements were studied. The Short Sensory Profile was used to define whether a child perceived stimulation within each sensory modality as aversive, attractive, or neutral. The Stereotyped and Self-Injurious Movements Interview was used to identify each child's repetitive movements. Children were then exposed to sensory stimuli that were neutral, aversive or attractive. Results indicate that children: (a) initiate or increase stereotyped movements immediately following the onset of an aversive stimulus, (b) terminate or decrease stereotyped movements following the onset of an attractive stimulus and (c) initiate or increase stereotyped movements during periods of neutral stimulation. We conclude that stereotyped movements are functionally related to sensory stimulation; individuals who frequently engage in stereotyped movements may do so in order to cope with under-stimulation and aversive over-stimulation.


2021 ◽  
Vol 15 ◽  
Author(s):  
Irene Togoli ◽  
Roberto Arrighi

Humans and other species share a perceptual mechanism dedicated to the representation of approximate quantities that allows to rapidly and reliably estimate the numerosity of a set of objects: an Approximate Number System (ANS). Numerosity perception shows a characteristic shared by all primary visual features: it is susceptible to adaptation. As a consequence of prolonged exposure to a large/small quantity (“adaptor”), the apparent numerosity of a subsequent (“test”) stimulus is distorted yielding a robust under- or over-estimation, respectively. Even if numerosity adaptation has been reported across several sensory modalities (vision, audition, and touch), suggesting the idea of a central and a-modal numerosity processing system, evidence for cross-modal effects are limited to vision and audition, two modalities that are known to preferentially encode sensory stimuli in an external coordinate system. Here we test whether numerosity adaptation for visual and auditory stimuli also distorts the perceived numerosity of tactile stimuli (and vice-versa) despite touch being a modality primarily coded in an internal (body-centered) reference frame. We measured numerosity discrimination of stimuli presented sequentially after adaptation to series of either few (around 2 Hz; low adaptation) or numerous (around 8 Hz; high adaptation) impulses for all possible combinations of visual, auditory, or tactile adapting and test stimuli. In all cases, adapting to few impulses yielded a significant overestimation of the test numerosity with the opposite occurring as a consequence of adaptation to numerous stimuli. The overall magnitude of adaptation was robust (around 30%) and rather similar for all sensory modality combinations. Overall, these findings support the idea of a truly generalized and a-modal mechanism for numerosity representation aimed to process numerical information independently from the sensory modality of the incoming signals.


2021 ◽  
Vol 14 ◽  
Author(s):  
Zhiyun Zhang ◽  
Dongsheng Xu ◽  
Jia Wang ◽  
Jingjing Cui ◽  
Shuang Wu ◽  
...  

Objective: To investigate the sensory and sympathetic innervations associated with both acupoint “Shenshu” (BL23) and kidney in the rat for insight into the neuronal correlation between the Back-Shu Point and its corresponding visceral organ.Methods: The BL23 and kidney were selected as the representative acupoint and visceral organ in this study, in which their local nerve fibers were examined by using double fluorescent immunohistochemistry with calcitonin gene-related peptide (CGRP) and tyrosine hydroxylase (TH). Meanwhile, their neuronal correlation in the dorsal root ganglia (DRGs), spinal cord, and sympathetic (paravertebral) chain were investigated using a double fluorescent neural tracing technique with Alexa Fluor 488 and 594 conjugates with cholera toxin subunit B (AF488/594-CTB).Results: The local tissue of acupoint BL23 and the fibrous capsule of kidney distributed abundantly with CGRP- and TH-positive nerve fibers, corresponding to their sensory and sympathetic innervation. On the other hand, the sensory neurons associated with acupoint BL23 and kidney were labeled with AF488/594-CTB and distributed from thoracic (T) 11 to lumbar (L) 3 DRGs and from T10 to L2 DRGs, respectively, in which some of them in T12-T13 DRGs were simultaneously labeled with both AF488/594-CTB. Also, postganglionic neurons associated with both acupoint BL23 and kidney were found in the sympathetic chain at the same spinal segments but separately labeled with AF488-CTB and AF594-CTB.Conclusion: Our study demonstrates the neural characteristics of the acupoint BL23 and kidney in the rat from the perspective of neurochemistry and neural pathways, providing an example for understanding the neuronal correlation between the Back-Shu Points and their corresponding visceral organs. These results suggest that the stimulation of the Back-Shu Points may regulate the activities of the target-organs via the periphery sensory and sympathetic pathways.


2019 ◽  
Vol 9 (3) ◽  
pp. 68 ◽  
Author(s):  
Emily Kilroy ◽  
Lisa Aziz-Zadeh ◽  
Sharon Cermak

Abnormal sensory-based behaviors are a defining feature of autism spectrum disorders (ASD). Dr. A. Jean Ayres was the first occupational therapist to conceptualize Sensory Integration (SI) theories and therapies to address these deficits. Her work was based on neurological knowledge of the 1970’s. Since then, advancements in neuroimaging techniques make it possible to better understand the brain areas that may underlie sensory processing deficits in ASD. In this article, we explore the postulates proposed by Ayres (i.e., registration, modulation, motivation) through current neuroimaging literature. To this end, we review the neural underpinnings of sensory processing and integration in ASD by examining the literature on neurophysiological responses to sensory stimuli in individuals with ASD as well as structural and network organization using a variety of neuroimaging techniques. Many aspects of Ayres’ hypotheses about the nature of the disorder were found to be highly consistent with current literature on sensory processing in children with ASD but there are some discrepancies across various methodological techniques and ASD development. With additional characterization, neurophysiological profiles of sensory processing in ASD may serve as valuable biomarkers for diagnosis and monitoring of therapeutic interventions, such as SI therapy.


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