دورية أكاديمية

Kv3.1 Voltage-gated Potassium Channels Modulate Anxiety-like Behaviors in Female Mice.

التفاصيل البيبلوغرافية
العنوان: Kv3.1 Voltage-gated Potassium Channels Modulate Anxiety-like Behaviors in Female Mice.
المؤلفون: Page CE; Department of Neuroscience, The Ohio State University, Columbus, OH, United States., Coutellier L; Department of Neuroscience, The Ohio State University, Columbus, OH, United States; Department of Psychology, The Ohio State University, Columbus, OH, United States. Electronic address: Coutellier.8@osu.edu.
المصدر: Neuroscience [Neuroscience] 2024 Feb 06; Vol. 538, pp. 68-79. Date of Electronic Publication: 2023 Dec 28.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: Elsevier Science Country of Publication: United States NLM ID: 7605074 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1873-7544 (Electronic) Linking ISSN: 03064522 NLM ISO Abbreviation: Neuroscience Subsets: MEDLINE
أسماء مطبوعة: Publication: [New York?] : Elsevier Science
Original Publication: Oxford, Elmsford, N. Y., Pergamon Press
مواضيع طبية MeSH: Potassium Channels, Voltage-Gated*/metabolism, Male ; Mice ; Female ; Animals ; Neurons/metabolism ; Interneurons/metabolism ; Brain/metabolism ; Anxiety/metabolism ; Shaw Potassium Channels/metabolism
مستخلص: Inhibitory parvalbumin (PV) interneurons regulate the activity of neural circuits within brain regions involved in emotional processing, including the prefrontal cortex (PFC). Recently, rodent studies have implicated a stress-induced increase in prefrontal PV neuron activity in the development of anxiety behaviors, particularly in females. However, the mechanisms through which stress increases activity of prefrontal PV neurons remain unknown. The fast-spiking properties of PV neurons in part come from their expression of voltage-gated potassium (K+) ion channels, particularly Kv3.1 channels. We therefore suggest that stress-induced changes in Kv3.1 channels contribute to the appearance of an anxious phenotype following chronic stress in female mice. Here, we first showed that unpredictable chronic mild stress (UCMS) increased expression of Kv3.1 channels on prefrontal PV neurons in female mice, a potential mechanism underlying the previously observed hyperactivity of these neurons after stress. We then showed that female mice deficient in Kv3.1 channels displayed resilience to UCMS-induced anxiety-like behaviors. Altogether, our findings implicate Kv3.1 channels in the development of anxiety-like behaviors following UCMS, particularly in females, providing a novel mechanism to understand sex-specific vulnerabilities to stress-induced psychopathologies.
(Copyright © 2023 IBRO. Published by Elsevier Inc. All rights reserved.)
References: Front Neural Circuits. 2018 May 16;12:37. (PMID: 29867371)
J Neurosci. 2016 Mar 16;36(11):3322-35. (PMID: 26985040)
Trends Neurosci. 2001 Sep;24(9):517-26. (PMID: 11506885)
Neurosci Biobehav Rev. 2019 Oct;105:39-51. (PMID: 31377218)
Biol Psychiatry. 2020 Sep 1;88(5):405-414. (PMID: 32331822)
Neuropharmacology. 2017 May 15;118:102-112. (PMID: 28242439)
J Neurosci. 2003 Feb 15;23(4):1133-41. (PMID: 12598601)
Cerebellum. 2009 Sep;8(3):323-33. (PMID: 19247732)
Neuropsychopharmacology. 2014 Aug;39(9):2252-62. (PMID: 24690741)
Nat Commun. 2023 May 22;14(1):2912. (PMID: 37217515)
J Neurosci. 2000 Dec 15;20(24):9071-85. (PMID: 11124984)
Mol Psychiatry. 2014 May;19(5):573-9. (PMID: 23628987)
J Neurosci. 1996 Jan 15;16(2):506-18. (PMID: 8551335)
Cell. 2017 Oct 5;171(2):456-469.e22. (PMID: 28985566)
J Neurophysiol. 2002 Jul;88(1):394-408. (PMID: 12091563)
Nat Commun. 2015 Dec 17;6:10173. (PMID: 26673941)
J Neurosci Methods. 2011 Apr 15;197(1):21-31. (PMID: 21277897)
Korean J Physiol Pharmacol. 2018 Jan;22(1):71-80. (PMID: 29302214)
J Biosci. 2018 Mar;43(1):85-95. (PMID: 29485117)
Neurobiol Stress. 2022 Sep 22;21:100492. (PMID: 36532368)
Am J Med Genet A. 2021 Nov;185(11):3384-3389. (PMID: 34448338)
Neuroscience. 2022 Feb 1;482:87-99. (PMID: 34902495)
Schizophr Bull. 2006 Apr;32(2):259-73. (PMID: 16221997)
J Clin Psychiatry. 1999;60 Suppl 22:18-22. (PMID: 10634351)
Proc Natl Acad Sci U S A. 1997 Feb 18;94(4):1533-8. (PMID: 9037088)
Nat Commun. 2019 Nov 1;10(1):4994. (PMID: 31676823)
Neuropsychopharmacology. 2018 Apr;43(5):1099-1106. (PMID: 28862251)
Mol Psychiatry. 2023 Sep;28(9):3994-4010. (PMID: 37833406)
Trends Neurosci. 2017 Nov;40(11):667-679. (PMID: 28916130)
J Clin Psychiatry. 2004;65 Suppl 5:29-33. (PMID: 15078116)
J Neurophysiol. 1999 Nov;82(5):2476-89. (PMID: 10561420)
Prog Neuropsychopharmacol Biol Psychiatry. 2023 Dec 20;127:110829. (PMID: 37451593)
Neuropsychopharmacology. 2018 Jan;43(2):435-444. (PMID: 28857068)
J Pharmacol Sci. 2008 Jan;106(1):38-45. (PMID: 18187934)
Proc Natl Acad Sci U S A. 2015 Jun 30;112(26):8106-11. (PMID: 26056286)
Neuroscience. 2016 Sep 22;332:1-12. (PMID: 27365172)
Nat Commun. 2015 Jul 16;6:7660. (PMID: 26179626)
J Pharmacol Exp Ther. 2015 Sep;354(3):251-60. (PMID: 26085652)
Front Cell Dev Biol. 2022 Oct 26;10:998009. (PMID: 36393851)
Elife. 2021 Jun 28;10:. (PMID: 34180393)
Int J Methods Psychiatr Res. 2012 Sep;21(3):169-84. (PMID: 22865617)
Behav Brain Res. 2021 Sep 10;413:113468. (PMID: 34274375)
J Neurosci. 1999 Nov 1;19(21):9332-45. (PMID: 10531438)
J Physiol. 2020 Sep;598(17):3711-3725. (PMID: 32638407)
Biol Psychiatry. 2015 Feb 1;77(3):276-284. (PMID: 24673881)
Biol Psychiatry. 2018 Jan 1;83(1):18-28. (PMID: 28651788)
Nature. 2013 Dec 12;504(7479):272-6. (PMID: 24336286)
eNeuro. 2023 Mar 2;10(3):. (PMID: 36808099)
Physiol Rev. 2017 Oct 1;97(4):1431-1468. (PMID: 28904001)
Neuron. 2016 Jul 20;91(2):260-92. (PMID: 27477017)
معلومات مُعتمدة: R21 MH119090 United States MH NIMH NIH HHS
فهرسة مساهمة: Keywords: anxiety; chronic stress; parvalbumin neurons; potassium channels
المشرفين على المادة: 0 (Potassium Channels, Voltage-Gated)
0 (Shaw Potassium Channels)
تواريخ الأحداث: Date Created: 20231229 Date Completed: 20240205 Latest Revision: 20240218
رمز التحديث: 20240218
مُعرف محوري في PubMed: PMC10872248
DOI: 10.1016/j.neuroscience.2023.12.011
PMID: 38157976
قاعدة البيانات: MEDLINE
الوصف
تدمد:1873-7544
DOI:10.1016/j.neuroscience.2023.12.011