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      Identification of Molecular Fingerprints in Human Heat Pain Thresholds by Use of an Interactive Mixture Model R Toolbox (AdaptGauss)

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          Abstract

          Biomedical data obtained during cell experiments, laboratory animal research, or human studies often display a complex distribution. Statistical identification of subgroups in research data poses an analytical challenge. Here were introduce an interactive R-based bioinformatics tool, called “AdaptGauss”. It enables a valid identification of a biologically-meaningful multimodal structure in the data by fitting a Gaussian mixture model (GMM) to the data. The interface allows a supervised selection of the number of subgroups. This enables the expectation maximization (EM) algorithm to adapt more complex GMM than usually observed with a noninteractive approach. Interactively fitting a GMM to heat pain threshold data acquired from human volunteers revealed a distribution pattern with four Gaussian modes located at temperatures of 32.3, 37.2, 41.4, and 45.4 °C. Noninteractive fitting was unable to identify a meaningful data structure. Obtained results are compatible with known activity temperatures of different TRP ion channels suggesting the mechanistic contribution of different heat sensors to the perception of thermal pain. Thus, sophisticated analysis of the modal structure of biomedical data provides a basis for the mechanistic interpretation of the observations. As it may reflect the involvement of different TRP thermosensory ion channels, the analysis provides a starting point for hypothesis-driven laboratory experiments.

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            TRP channels as cellular sensors.

            TRP channels are the vanguard of our sensory systems, responding to temperature, touch, pain, osmolarity, pheromones, taste and other stimuli. But their role is much broader than classical sensory transduction. They are an ancient sensory apparatus for the cell, not just the multicellular organism, and they have been adapted to respond to all manner of stimuli, from both within and outside the cell.
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              Impaired nociception and pain sensation in mice lacking the capsaicin receptor.

              The capsaicin (vanilloid) receptor VR1 is a cation channel expressed by primary sensory neurons of the "pain" pathway. Heterologously expressed VR1 can be activated by vanilloid compounds, protons, or heat (>43 degrees C), but whether this channel contributes to chemical or thermal sensitivity in vivo is not known. Here, we demonstrate that sensory neurons from mice lacking VR1 are severely deficient in their responses to each of these noxious stimuli. VR1-/- mice showed normal responses to noxious mechanical stimuli but exhibited no vanilloid-evoked pain behavior, were impaired in the detection of painful heat, and showed little thermal hypersensitivity in the setting of inflammation. Thus, VR1 is essential for selective modalities of pain sensation and for tissue injury-induced thermal hyperalgesia.
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                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                Int J Mol Sci
                Int J Mol Sci
                ijms
                International Journal of Molecular Sciences
                MDPI
                1422-0067
                28 October 2015
                October 2015
                : 16
                : 10
                : 25897-25911
                Affiliations
                [1 ]DataBionics Research Group, University of Marburg, Hans-Meerwein-Straße, Marburg 35032, Germany; E-Mails: ultsch@ 123456informatik.uni-marburg.de (A.U.); mthrun@ 123456informatik.uni-marburg.de (M.C.T.)
                [2 ]Institute of Clinical Pharmacology, Goethe-University, Theodor-Stern-Kai 7, Frankfurt am Main 60590, Germany; E-Mail: Hansen-Goos@ 123456med.uni-frankfurt.de
                [3 ]Fraunhofer Institute for Molecular Biology and Applied Ecology IME, Project Group Translational Medicine and Pharmacology TMP, Theodor-Stern-Kai 7, Frankfurt am Main 60590, Germany
                Author notes
                [* ]Author to whom correspondence should be addressed; E-Mail: j.loetsch@ 123456em.uni-frankfurt.de ; Tel.: +49-69-6301-4589; Fax: +49-69-6301-4354.
                Article
                ijms-16-25897
                10.3390/ijms161025897
                4632832
                26516852
                f285db16-5283-440d-82ab-2a6644a4725c
                © 2015 by the authors; licensee MDPI, Basel, Switzerland.

                This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 19 August 2015
                : 21 October 2015
                Categories
                Article

                Molecular biology
                pain,r software,bioinformatics,data modeling,molecular mechanisms
                Molecular biology
                pain, r software, bioinformatics, data modeling, molecular mechanisms

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