Temperature modulates PVN pre-sympathetic neurones via transient receptor potential ion channels

The paraventricular nucleus (PVN) of the hypothalamus plays a vital role in maintaining homeostasis and modulates cardiovascular function via autonomic pre-sympathetic neurones. We have previously shown that coupling between transient receptor potential cation channel subfamily V Member 4 (Trpv4) an...

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Main Authors: Fiona O’Brien, Claire H. Feetham, Caroline A. Staunton, Kathryn Hext, Richard Barrett-Jolley
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-10-01
Series:Frontiers in Pharmacology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fphar.2023.1256924/full
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author Fiona O’Brien
Claire H. Feetham
Caroline A. Staunton
Kathryn Hext
Richard Barrett-Jolley
author_facet Fiona O’Brien
Claire H. Feetham
Caroline A. Staunton
Kathryn Hext
Richard Barrett-Jolley
author_sort Fiona O’Brien
collection DOAJ
description The paraventricular nucleus (PVN) of the hypothalamus plays a vital role in maintaining homeostasis and modulates cardiovascular function via autonomic pre-sympathetic neurones. We have previously shown that coupling between transient receptor potential cation channel subfamily V Member 4 (Trpv4) and small-conductance calcium-activated potassium channels (SK) in the PVN facilitate osmosensing, but since TRP channels are also thermosensitive, in this report we investigated the temperature sensitivity of these neurones.Methods: TRP channel mRNA was quantified from mouse PVN with RT-PCR and thermosensitivity of Trpv4-like PVN neuronal ion channels characterised with cell-attached patch-clamp electrophysiology. Following recovery of temperature-sensitive single-channel kinetic schema, we constructed a predictive stochastic mathematical model of these neurones and validated this with electrophysiological recordings of action current frequency.Results: 7 thermosensitive TRP channel genes were found in PVN punches. Trpv4 was the most abundant of these and was identified at the single channel level on PVN neurones. We investigated the thermosensitivity of these Trpv4-like channels; open probability (Po) markedly decreased when temperature was decreased, mediated by a decrease in mean open dwell times. Our neuronal model predicted that PVN spontaneous action current frequency (ACf) would increase as temperature is decreased and in our electrophysiological experiments, we found that ACf from PVN neurones was significantly higher at lower temperatures. The broad-spectrum channel blocker gadolinium (100 µM), was used to block the warm-activated, Ca2+-permeable Trpv4 channels. In the presence of gadolinium (100 µM), the temperature effect was largely retained. Using econazole (10 µM), a blocker of Trpm2, we found there were significant increases in overall ACf and the temperature effect was inhibited.Conclusion: Trpv4, the abundantly transcribed thermosensitive TRP channel gene in the PVN appears to contribute to intrinsic thermosensitive properties of PVN neurones. At physiological temperatures (37°C), we observed relatively low ACf primarily due to the activity of Trpm2 channels, whereas at room temperature, where most of the previous characterisation of PVN neuronal activity has been performed, ACf is much higher, and appears to be predominately due to reduced Trpv4 activity. This work gives insight into the fundamental mechanisms by which the body decodes temperature signals and maintains homeostasis.
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spelling doaj.art-cacd86674d08480587384cc6e30983022023-10-18T07:04:13ZengFrontiers Media S.A.Frontiers in Pharmacology1663-98122023-10-011410.3389/fphar.2023.12569241256924Temperature modulates PVN pre-sympathetic neurones via transient receptor potential ion channelsFiona O’BrienClaire H. FeethamCaroline A. StauntonKathryn HextRichard Barrett-JolleyThe paraventricular nucleus (PVN) of the hypothalamus plays a vital role in maintaining homeostasis and modulates cardiovascular function via autonomic pre-sympathetic neurones. We have previously shown that coupling between transient receptor potential cation channel subfamily V Member 4 (Trpv4) and small-conductance calcium-activated potassium channels (SK) in the PVN facilitate osmosensing, but since TRP channels are also thermosensitive, in this report we investigated the temperature sensitivity of these neurones.Methods: TRP channel mRNA was quantified from mouse PVN with RT-PCR and thermosensitivity of Trpv4-like PVN neuronal ion channels characterised with cell-attached patch-clamp electrophysiology. Following recovery of temperature-sensitive single-channel kinetic schema, we constructed a predictive stochastic mathematical model of these neurones and validated this with electrophysiological recordings of action current frequency.Results: 7 thermosensitive TRP channel genes were found in PVN punches. Trpv4 was the most abundant of these and was identified at the single channel level on PVN neurones. We investigated the thermosensitivity of these Trpv4-like channels; open probability (Po) markedly decreased when temperature was decreased, mediated by a decrease in mean open dwell times. Our neuronal model predicted that PVN spontaneous action current frequency (ACf) would increase as temperature is decreased and in our electrophysiological experiments, we found that ACf from PVN neurones was significantly higher at lower temperatures. The broad-spectrum channel blocker gadolinium (100 µM), was used to block the warm-activated, Ca2+-permeable Trpv4 channels. In the presence of gadolinium (100 µM), the temperature effect was largely retained. Using econazole (10 µM), a blocker of Trpm2, we found there were significant increases in overall ACf and the temperature effect was inhibited.Conclusion: Trpv4, the abundantly transcribed thermosensitive TRP channel gene in the PVN appears to contribute to intrinsic thermosensitive properties of PVN neurones. At physiological temperatures (37°C), we observed relatively low ACf primarily due to the activity of Trpm2 channels, whereas at room temperature, where most of the previous characterisation of PVN neuronal activity has been performed, ACf is much higher, and appears to be predominately due to reduced Trpv4 activity. This work gives insight into the fundamental mechanisms by which the body decodes temperature signals and maintains homeostasis.https://www.frontiersin.org/articles/10.3389/fphar.2023.1256924/fullPVNPVHthermoregulationion channelTRPV4computational model
spellingShingle Fiona O’Brien
Claire H. Feetham
Caroline A. Staunton
Kathryn Hext
Richard Barrett-Jolley
Temperature modulates PVN pre-sympathetic neurones via transient receptor potential ion channels
Frontiers in Pharmacology
PVN
PVH
thermoregulation
ion channel
TRPV4
computational model
title Temperature modulates PVN pre-sympathetic neurones via transient receptor potential ion channels
title_full Temperature modulates PVN pre-sympathetic neurones via transient receptor potential ion channels
title_fullStr Temperature modulates PVN pre-sympathetic neurones via transient receptor potential ion channels
title_full_unstemmed Temperature modulates PVN pre-sympathetic neurones via transient receptor potential ion channels
title_short Temperature modulates PVN pre-sympathetic neurones via transient receptor potential ion channels
title_sort temperature modulates pvn pre sympathetic neurones via transient receptor potential ion channels
topic PVN
PVH
thermoregulation
ion channel
TRPV4
computational model
url https://www.frontiersin.org/articles/10.3389/fphar.2023.1256924/full
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AT carolineastaunton temperaturemodulatespvnpresympatheticneuronesviatransientreceptorpotentialionchannels
AT kathrynhext temperaturemodulatespvnpresympatheticneuronesviatransientreceptorpotentialionchannels
AT richardbarrettjolley temperaturemodulatespvnpresympatheticneuronesviatransientreceptorpotentialionchannels