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Middleton, S. J., Perini, I., Themistocleous, A. C., Weir, G. A., McCann, K., Barry, A. M., . . . Bennett, D. L. (2022). Na(v)1.7 is required for normal C-low threshold mechanoreceptor function in humans and mice. Brain, 1145(10), 3637-3653
Öppna denna publikation i ny flik eller fönster >>Na(v)1.7 is required for normal C-low threshold mechanoreceptor function in humans and mice
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2022 (Engelska)Ingår i: Brain, ISSN 0006-8950, E-ISSN 1460-2156, Vol. 1145, nr 10, s. 3637-3653Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Middleton, Perini et al. show that the role of Na(v)1.7 extends beyond pain perception. Using a multidisciplinary, cross-species approach, they show that Na(v)1.7 is also essential for C-low threshold mechanoreceptor function in mice and humans, regulating pleasant touch, punctate discrimination and sensitivity to cooling. Patients with bi-allelic loss of function mutations in the voltage-gated sodium channel Nav1.7 present with congenital insensitivity to pain (CIP), whilst low threshold mechanosensation is reportedly normal. Using psychophysics (n = 6 CIP participants and n = 86 healthy controls) and facial electromyography (n = 3 CIP participants and n = 8 healthy controls), we found that these patients also have abnormalities in the encoding of affective touch, which is mediated by the specialized afferents C-low threshold mechanoreceptors (C-LTMRs). In the mouse, we found that C-LTMRs express high levels of Nav1.7. Genetic loss or selective pharmacological inhibition of Nav1.7 in C-LTMRs resulted in a significant reduction in the total sodium current density, an increased mechanical threshold and reduced sensitivity to non-noxious cooling. The behavioural consequence of loss of Nav1.7 in C-LTMRs in mice was an elevation in the von Frey mechanical threshold and less sensitivity to cooling on a thermal gradient. Nav1.7 is therefore not only essential for normal pain perception but also for normal C-LTMR function, cool sensitivity and affective touch.

Ort, förlag, år, upplaga, sidor
OXFORD UNIV PRESS, 2022
Nyckelord
affective touch; C-low threshold mechanoreceptors; congenital insensitivity to pain; Na(v)1; 7
Nationell ämneskategori
Klinisk laboratoriemedicin
Identifikatorer
urn:nbn:se:liu:diva-187747 (URN)10.1093/brain/awab482 (DOI)000839656800001 ()34957475 (PubMedID)
Anmärkning

Funding Agencies|Wellcome Trust [102645/Z/13/Z]; UK Medical Research Council [MR/T020113/1]; NIHR Cambridge Clinical Research Facility; NIHR Eastern Clinical Research; Swedish Research Council [2015-02684]; ALF Grants; Region Ostergotland; Knut and Alice Wallenberg Foundation; Wellcome [202747/Z/16/Z]

Tillgänglig från: 2022-08-30 Skapad: 2022-08-30 Senast uppdaterad: 2023-02-16Bibliografiskt granskad
Morrison, I. (2016). ALE meta-analysis reveals dissociable networks for affective and discriminative aspects of touch. Human Brain Mapping, 37(4), 1308-1320
Öppna denna publikation i ny flik eller fönster >>ALE meta-analysis reveals dissociable networks for affective and discriminative aspects of touch
2016 (Engelska)Ingår i: Human Brain Mapping, ISSN 1065-9471, E-ISSN 1097-0193, Vol. 37, nr 4, s. 1308-1320Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Emotionally-laden tactile stimulationsuch as a caress on the skin or the feel of velvetmay represent a functionally distinct domain of touch, underpinned by specific cortical pathways. In order to determine whether, and to what extent, cortical functional neuroanatomy supports a distinction between affective and discriminative touch, an activation likelihood estimate (ALE) meta-analysis was performed. This meta-analysis statistically mapped reported functional magnetic resonance imaging (fMRI) activations from 17 published affective touch studies in which tactile stimulation was associated with positive subjective evaluation (n=291, 34 experimental contrasts). A separate ALE meta-analysis mapped regions most likely to be activated by tactile stimulation during detection and discrimination tasks (n=1,075, 91 experimental contrasts). These meta-analyses revealed dissociable regions for affective and discriminative touch, with posterior insula (PI) more likely to be activated for affective touch, and primary somatosensory cortices (SI) more likely to be activated for discriminative touch. Secondary somatosensory cortex had a high likelihood of engagement by both affective and discriminative touch. Further, meta-analytic connectivity (MCAM) analyses investigated network-level co-activation likelihoods independent of task or stimulus, across a range of domains and paradigms. Affective-related PI and discriminative-related SI regions co-activated with different networks, implicated in dissociable functions, but sharing somatosensory co-activations. Taken together, these meta-analytic findings suggest that affective and discriminative touch are dissociable both on the regional and network levels. However, their degree of shared activation likelihood in somatosensory cortices indicates that this dissociation reflects functional biases within tactile processing networks, rather than functionally and anatomically distinct pathways.

Ort, förlag, år, upplaga, sidor
WILEY-BLACKWELL, 2016
Nyckelord
affective touch; discriminative touch; posterior insula; secondary somatosensory cortex; activation likelihood estimate; meta-analytic connectivity modeling
Nationell ämneskategori
Klinisk medicin
Identifikatorer
urn:nbn:se:liu:diva-127043 (URN)10.1002/hbm.23103 (DOI)000372296500003 ()26873519 (PubMedID)
Anmärkning

Funding Agencies|Templeton Positive Neuroscience award; Swedish Research Council [FYF-2013-687]

Tillgänglig från: 2016-04-13 Skapad: 2016-04-13 Senast uppdaterad: 2017-11-30
Perini, I., Morrison, I. & Olausson, H. (2015). Seeking pleasant touch: neural correlates of behavioral preferences for skin stroking. Frontiers in Behavioral Neuroscience, 9(8)
Öppna denna publikation i ny flik eller fönster >>Seeking pleasant touch: neural correlates of behavioral preferences for skin stroking
2015 (Engelska)Ingår i: Frontiers in Behavioral Neuroscience, E-ISSN 1662-5153, Vol. 9, nr 8Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Affective touch is a dynamic process. In this fMRI study we investigated affective touch by exploring its effects on overt behavior. Arm and palm skin were stroked with a soft brush at five different velocities (0.3, 1, 10, 3, and 30 cm s(-1)), using a novel feedback-based paradigm. Following stimulation in each trial, participants actively chose whether the caress they would receive in the next trial would be the same speed ("repeat") or different ("change"). Since preferred stroking speeds should be sought with greater frequency than non-preferred speeds, this paradigm provided a measure of such preferences in the form of active choices. The stimulation velocities were implemented with respect to the differential subjective pleasantness ratings they elicit in healthy subjects, with intermediate velocities (1, 10, and 3 cm s(-1)) considered more pleasant than very slow or very fast ones. Such pleasantness ratings linearly correlate with changes in mean firing rates of unmyelinated low-threshold C-tactile (CT) afferent nerves in the skin. Here, gentle, dynamic stimulation optimal for activating CT-afferents not only affected behavioral choices, but engaged brain regions involved in reward-related behavior and decision-making. This was the case for both hairy skin of the arm, where CTs are abundant, and glabrous skin of the palm, where CTs are absent. These findings provide insights on central and behavioral mechanisms underlying the perception of affective touch, and indicate that seeking affective touch involves value-based neural processing that is ultimately reflected in behavioral preferences.

Ort, förlag, år, upplaga, sidor
Frontiers, 2015
Nyckelord
fMRI; CT afferents; affective touch; seeking behavior; interoception
Nationell ämneskategori
Klinisk medicin
Identifikatorer
urn:nbn:se:liu:diva-114564 (URN)10.3389/fnbeh.2015.00008 (DOI)000348851300001 ()25698948 (PubMedID)
Anmärkning

Funding Agencies|Templeton Positive Neuroscience Award; Swedish Research Council Distinguished Young Researcher grant [FF-2013-687]

Tillgänglig från: 2015-03-02 Skapad: 2015-02-26 Senast uppdaterad: 2024-07-04
Organisationer
Identifikatorer
ORCID-id: ORCID iD iconorcid.org/0000-0002-7992-0306

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