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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
Main Authors: Caudle, Robert M, Caudle, Stephanie L, Jenkins, Alan C, Ahn, Andrew H, Neubert, John K
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Caudle, Stephanie L
Jenkins, Alan C
Ahn, Andrew H
Neubert, John K
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.</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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source Open Access: PubMed Central; Publicly Available Content Database
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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