Dataset Information

Linear Integration of Tactile and Non-tactile Inputs Mediates Estimation of Fingertip Relative Position.

ABSTRACT: While skin, joints and muscles receptors alone provide lower level information about individual variables (e.g., exerted limb force and limb displacement), the distance between limb endpoints (i.e., relative position) has to be extracted from high level integration of somatosensory and motor signals. In particular, estimation of fingertip relative position likely involves more complex sensorimotor transformations than those underlying hand or arm position sense: the brain has to estimate where each fingertip is relative to the hand and where fingertips are relative to each other. It has been demonstrated that during grasping, feedback of digit position drives rapid adjustments of fingers force control. However, it has been shown that estimation of fingertips' relative position can be biased by digit forces. These findings raise the question of how the brain combines concurrent tactile (i.e., cutaneous mechanoreceptors afferents induced by skin pressure and stretch) and non-tactile (i.e., both descending motor command and joint/muscle receptors signals associated to muscle contraction) digit force-related inputs for fingertip distance estimation. Here we addressed this question by quantifying the contribution of tactile and non-tactile force-related inputs for the estimation of fingertip relative position. We asked subjects to match fingertip vertical distance relying only on either tactile or non-tactile inputs from the thumb and index fingertip, and compared their performance with the condition where both types of inputs were combined. We found that (a) the bias in the estimation of fingertip distance persisted when tactile inputs and non-tactile force-related signals were presented in isolation; (b) tactile signals contributed the most to the estimation of fingertip distance; (c) linear summation of the matching errors relying only on either tactile or non-tactile inputs was comparable to the matching error when both inputs were simultaneously available. These findings reveal a greater role of tactile signals for sensing fingertip distance and suggest a linear integration mechanism with non-tactile inputs for the estimation of fingertip relative position.

SUBMITTER: Toma S

PROVIDER: S-EPMC6378372 | biostudies-literature | 2019

REPOSITORIES: biostudies-literature

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Linear Integration of Tactile and Non-tactile Inputs Mediates Estimation of Fingertip Relative Position.

Toma Simone S Shibata Daisuke D Chinello Francesco F Prattichizzo Domenico D Santello Marco M

Frontiers in neuroscience 20190211

While skin, joints and muscles receptors alone provide lower level information about individual variables (e.g., exerted limb force and limb displacement), the distance between limb endpoints (i.e., relative position) has to be extracted from high level integration of somatosensory and motor signals. In particular, estimation of fingertip relative position likely involves more complex sensorimotor transformations than those underlying hand or arm position sense: the brain has to estimate where e ...[more]

PMID: 30804743

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Project description:Morphine and related compounds are the first line of therapy in the treatment of moderate to severe pain. Over time, individuals taking opioids can develop an increasing sensitivity to noxious stimuli, even evolving into a painful response to previously non-noxious stimuli (opioid-induced hyperalgesia; OIH). The mechanism underlying OIH is not well understood although complex intracellular neural mechanisms, including opioid receptor desensitization and down-regulation, are believed to be major mechanisms underlying OIH. However, OIH may also be associated with changes in gene expression. A growing body of evidence suggests that cellular exposure to mu agonists upregulate chemokines/receptors and recent work from our laboratory implicates chemokine upregulation in a variety of neuropathic pain behaviors. Here we characterized the degree to which chemokines/receptors signaling is increased in primary afferent neurons of the dorsal root ganglion (DRG) following chronic morphine sulfate treatment and correlated these changes with tactile hyperalgesic behavior in rodents. We demonstrate that mRNA expression of the chemokine, stromal-derived factor-1 (SDF1/CXCL12) is upregulated following morphine treatment in sensory neurons of the rat. The release of SDF1 was found to be constitutive when compared with the activity dependent release of the C-C chemokine, monocyte chemoattractant protein-1 (MCP1/CCL2) in a line of F11 neuroblastoma-sensory neuron hybrid cells. We further determined that there is pronounced CXCR4 expression in satellite glial cells and following morphine treatment, increased functional CXCR4 expression in sensory neurons of the DRG. Moreover, intraperitoneal administration of the specific CXCR4 antagonist, AMD3100, completely reversed OIH in the rat. Taken together; the data suggest that opioid-induced SDF1/CXCR4 signaling is central to the development of long lasting OIH and that receptor antagonists represent a promising novel approach to the management of the side effects associated with the use of opioids for chronic pain management.

Dataset Information

Linear Integration of Tactile and Non-tactile Inputs Mediates Estimation of Fingertip Relative Position.

Publications

Linear Integration of Tactile and Non-tactile Inputs Mediates Estimation of Fingertip Relative Position.

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