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Sex differences in mouse Transient Receptor Potential Cation Channel, Subfamily M, Member 8 expressing trigeminal ganglion neurons
The detection of cool temperatures is thought to be mediated by primary afferent neurons that express the cool temperature sensing protein Transient Receptor Potential Cation Channel, Subfamily M, Member 8 (TRPM8). Using mice, this study tested the hypothesis that sex differences in sensitivity to c...
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Published in: | PloS one 2017-05, Vol.12 (5), p.e0176753-e0176753 |
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description | The detection of cool temperatures is thought to be mediated by primary afferent neurons that express the cool temperature sensing protein Transient Receptor Potential Cation Channel, Subfamily M, Member 8 (TRPM8). Using mice, this study tested the hypothesis that sex differences in sensitivity to cool temperatures were mediated by differences in neurons that express TRPM8. Ion currents from TRPM8 expressing trigeminal ganglion (TRG) neurons in females demonstrated larger hyperpolarization-activated cyclic nucleotide-gated currents (Ih) than male neurons at both 30° and 18°C. Additionally, female neurons' voltage gated potassium currents (Ik) were suppressed by cooling, whereas male Ik was not significantly affected. At the holding potential tested (-60mV) TRPM8 currents were not visibly activated in either sex by cooling. Modeling the effect of Ih and Ik on membrane potentials demonstrated that at 30° the membrane potential in both sexes is unstable. At 18°, female TRPM8 TRG neurons develop a large oscillating pattern in their membrane potential, whereas male neurons become highly stable. These findings suggest that the differences in Ih and Ik in the TRPM8 TRG neurons of male and female mice likely leads to greater sensitivity of female mice to the cool temperature. This hypothesis was confirmed in an operant reward/conflict assay. Female mice contacted an 18°C surface for approximately half the time that males contacted the cool surface. At 33° and 10°C male and female mice contacted the stimulus for similar amounts of time. These data suggest that sex differences in the functioning of Ih and Ik in TRPM8 expressing primary afferent neurons leads to differences in cool temperature sensitivity. |
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Using mice, this study tested the hypothesis that sex differences in sensitivity to cool temperatures were mediated by differences in neurons that express TRPM8. Ion currents from TRPM8 expressing trigeminal ganglion (TRG) neurons in females demonstrated larger hyperpolarization-activated cyclic nucleotide-gated currents (Ih) than male neurons at both 30° and 18°C. Additionally, female neurons' voltage gated potassium currents (Ik) were suppressed by cooling, whereas male Ik was not significantly affected. At the holding potential tested (-60mV) TRPM8 currents were not visibly activated in either sex by cooling. Modeling the effect of Ih and Ik on membrane potentials demonstrated that at 30° the membrane potential in both sexes is unstable. At 18°, female TRPM8 TRG neurons develop a large oscillating pattern in their membrane potential, whereas male neurons become highly stable. These findings suggest that the differences in Ih and Ik in the TRPM8 TRG neurons of male and female mice likely leads to greater sensitivity of female mice to the cool temperature. This hypothesis was confirmed in an operant reward/conflict assay. Female mice contacted an 18°C surface for approximately half the time that males contacted the cool surface. At 33° and 10°C male and female mice contacted the stimulus for similar amounts of time. These data suggest that sex differences in the functioning of Ih and Ik in TRPM8 expressing primary afferent neurons leads to differences in cool temperature sensitivity.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0176753</identifier><identifier>PMID: 28472061</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Animals ; Biology and Life Sciences ; Cold ; Cooling ; Cooling effects ; Dentistry ; Experiments ; Female ; Females ; Gender differences ; Health aspects ; Hyperpolarization ; Hypotheses ; Ion currents ; Kinases ; Male ; Males ; Maxillofacial surgery ; Medicine ; Medicine and Health Sciences ; Membrane potential ; Mice ; Mice, Transgenic ; Neurons ; Neurons - metabolism ; Neurosciences ; Operant conditioning ; Orthodontics ; Physical Sciences ; Potassium ; Potassium channels (voltage-gated) ; Potassium currents ; Proteins ; Reinforcement ; Rodents ; Sensitivity ; Sensory neurons ; Sex differences ; Sex differences (Biology) ; Temperature ; Temperature effects ; Transient receptor potential proteins ; Trigeminal ganglion ; Trigeminal Ganglion - cytology ; Trigeminal Ganglion - metabolism ; Trigeminal nerve ; TRPM Cation Channels - genetics ; TRPM Cation Channels - metabolism</subject><ispartof>PloS one, 2017-05, Vol.12 (5), p.e0176753-e0176753</ispartof><rights>COPYRIGHT 2017 Public Library of Science</rights><rights>2017 Caudle et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. 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Using mice, this study tested the hypothesis that sex differences in sensitivity to cool temperatures were mediated by differences in neurons that express TRPM8. Ion currents from TRPM8 expressing trigeminal ganglion (TRG) neurons in females demonstrated larger hyperpolarization-activated cyclic nucleotide-gated currents (Ih) than male neurons at both 30° and 18°C. Additionally, female neurons' voltage gated potassium currents (Ik) were suppressed by cooling, whereas male Ik was not significantly affected. At the holding potential tested (-60mV) TRPM8 currents were not visibly activated in either sex by cooling. Modeling the effect of Ih and Ik on membrane potentials demonstrated that at 30° the membrane potential in both sexes is unstable. At 18°, female TRPM8 TRG neurons develop a large oscillating pattern in their membrane potential, whereas male neurons become highly stable. These findings suggest that the differences in Ih and Ik in the TRPM8 TRG neurons of male and female mice likely leads to greater sensitivity of female mice to the cool temperature. This hypothesis was confirmed in an operant reward/conflict assay. Female mice contacted an 18°C surface for approximately half the time that males contacted the cool surface. At 33° and 10°C male and female mice contacted the stimulus for similar amounts of time. These data suggest that sex differences in the functioning of Ih and Ik in TRPM8 expressing primary afferent neurons leads to differences in cool temperature sensitivity.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>28472061</pmid><doi>10.1371/journal.pone.0176753</doi><tpages>e0176753</tpages><orcidid>https://orcid.org/0000-0002-2394-4114</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animals Biology and Life Sciences Cold Cooling Cooling effects Dentistry Experiments Female Females Gender differences Health aspects Hyperpolarization Hypotheses Ion currents Kinases Male Males Maxillofacial surgery Medicine Medicine and Health Sciences Membrane potential Mice Mice, Transgenic Neurons Neurons - metabolism Neurosciences Operant conditioning Orthodontics Physical Sciences Potassium Potassium channels (voltage-gated) Potassium currents Proteins Reinforcement Rodents Sensitivity Sensory neurons Sex differences Sex differences (Biology) Temperature Temperature effects Transient receptor potential proteins Trigeminal ganglion Trigeminal Ganglion - cytology Trigeminal Ganglion - metabolism Trigeminal nerve TRPM Cation Channels - genetics TRPM Cation Channels - metabolism |
title | Sex differences in mouse Transient Receptor Potential Cation Channel, Subfamily M, Member 8 expressing trigeminal ganglion neurons |
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