دورية أكاديمية

The Changes of Intrinsic Excitability of Pyramidal Neurons in Anterior Cingulate Cortex in Neuropathic Pain.

التفاصيل البيبلوغرافية
العنوان: The Changes of Intrinsic Excitability of Pyramidal Neurons in Anterior Cingulate Cortex in Neuropathic Pain.
المؤلفون: Yang Z; Department of Anesthesiology, First Affiliated Hospital, Anhui Medical University, Hefei, China., Tan Q; Department of Anesthesiology, First Affiliated Hospital, Anhui Medical University, Hefei, China., Cheng D; Department of Anesthesiology, First Affiliated Hospital, Anhui Medical University, Hefei, China., Zhang L; Department of Anesthesiology, First Affiliated Hospital, Anhui Medical University, Hefei, China., Zhang J; Department of Anesthesiology, First Affiliated Hospital, Anhui Medical University, Hefei, China., Gu EW; Department of Anesthesiology, First Affiliated Hospital, Anhui Medical University, Hefei, China., Fang W; Department of Anesthesiology, First Affiliated Hospital, Anhui Medical University, Hefei, China., Lu X; Department of Anesthesiology, First Affiliated Hospital, Anhui Medical University, Hefei, China., Liu X; Department of Anesthesiology, First Affiliated Hospital, Anhui Medical University, Hefei, China.
المصدر: Frontiers in cellular neuroscience [Front Cell Neurosci] 2018 Nov 21; Vol. 12, pp. 436. Date of Electronic Publication: 2018 Nov 21 (Print Publication: 2018).
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101477935 Publication Model: eCollection Cited Medium: Print ISSN: 1662-5102 (Print) Linking ISSN: 16625102 NLM ISO Abbreviation: Front Cell Neurosci Subsets: PubMed not MEDLINE
أسماء مطبوعة: Original Publication: Lausanne, Switzerland : Frontiers Research Foundation, 2007-
مستخلص: To find satisfactory treatment strategies for neuropathic pain syndromes, the cellular mechanisms should be illuminated. Central sensitization is a generator of pain hypersensitivity, and is mainly reflected in neuronal hyperexcitability in pain pathway. Neuronal excitability depends on two components, the synaptic inputs and the intrinsic excitability. Previous studies have focused on the synaptic plasticity in different forms of pain. But little is known about the changes of neuronal intrinsic excitability in neuropathic pain. To address this question, whole-cell patch clamp recordings were performed to study the synaptic transmission and neuronal intrinsic excitability 1 week after spared nerve injury (SNI) or sham operation in male C57BL/6J mice. We found increased spontaneous excitatory postsynaptic currents (sEPSC) frequency in layer II/III pyramidal neurons of anterior cingulate cortex (ACC) from mice with neuropathic pain. Elevated intrinsic excitability of these neurons after nerve injury was also picked up, which was reflected in gain of input-output curve, inter-spike interval (ISI), spike threshold and Refractory period (RP). Besides firing rate related to neuronal intrinsic excitability, spike timing also plays an important role in neural information processing. The precision of spike timing measured by standard deviation of spike timing (SDST) was decreased in neuropathic pain state. The electrophysiological studies revealed the elevated intrinsic excitation in layer II/III pyramidal neurons of ACC in mice with neuropathic pain, which might contribute to central excitation.
References: Oncotarget. 2017 Aug 1;8(42):72424-72437. (PMID: 29069799)
Neuroscience. 2016 Dec 3;338:220-229. (PMID: 27530697)
Nat Neurosci. 1999 Nov;2(11):947-57. (PMID: 10526332)
Neurology. 2002 Sep 24;59(6):816-24. (PMID: 12297560)
Pflugers Arch. 2010 Jul;460(2):249-63. (PMID: 20101409)
J Neurosci. 2014 Aug 6;34(32):10675-87. (PMID: 25100600)
J Vis Exp. 2013 Dec 19;(82):e51212. (PMID: 24378519)
Nat Rev Neurosci. 2008 May;9(5):357-69. (PMID: 18425090)
Nat Rev Neurosci. 2013 Jul;14(7):502-11. (PMID: 23719569)
Proc Natl Acad Sci U S A. 2001 Jul 3;98(14):8077-82. (PMID: 11416168)
Neuron. 2007 Aug 2;55(3):449-63. (PMID: 17678857)
Nat Neurosci. 2013 Aug;16(8):1032-41. (PMID: 23852113)
Pain. 2016 Aug;157(8):1599-606. (PMID: 27115670)
Neuron. 2007 Sep 20;55(6):930-41. (PMID: 17880896)
Pain. 2013 Aug;154(8):1170-80. (PMID: 23622763)
PLoS One. 2015 Jun 17;10(6):e0130250. (PMID: 26083350)
Mol Pain. 2013 Nov 29;9:61. (PMID: 24286165)
Neuroscience. 2016 Sep 7;331:206-20. (PMID: 27343829)
Science. 1997 Aug 15;277(5328):968-71. (PMID: 9252330)
J Neurosci. 2006 Sep 6;26(36):9084-97. (PMID: 16957065)
Nat Rev Neurosci. 2016 Aug;17(8):485-96. (PMID: 27307118)
Neuron. 2005 Sep 15;47(6):859-72. (PMID: 16157280)
Biochemistry. 2004 Aug 3;43(30):9866-76. (PMID: 15274641)
Philos Trans R Soc Lond B Biol Sci. 2013 Dec 02;369(1633):20130146. (PMID: 24298148)
Trends Cogn Sci. 2000 Jun;4(6):215-222. (PMID: 10827444)
J Neurosurg. 1962 Feb;19:89-100. (PMID: 13893868)
Ann Neurol. 2000 Jun;47(6):729-38. (PMID: 10852538)
J Physiol. 2013 Jul 1;591(13):3215-32. (PMID: 23551945)
Neuron. 2003 Feb 6;37(3):513-23. (PMID: 12575957)
Anesth Analg. 2014 Mar;118(3):554-62. (PMID: 24557103)
J Neurosci. 2011 Nov 30;31(48):17637-48. (PMID: 22131424)
Exp Neurol. 2016 Nov;285(Pt A):82-95. (PMID: 27639636)
Neurosci Lett. 2014 May 7;568:29-34. (PMID: 24686190)
Neural Comput. 1998 Oct 1;10(7):1679-703. (PMID: 9744892)
Biochem Biophys Res Commun. 2006 Feb 3;340(1):151-7. (PMID: 16343428)
Pain. 2000 Aug;87(2):149-58. (PMID: 10924808)
Nature. 2009 Jun 4;459(7247):698-702. (PMID: 19396159)
J Neurosci. 2011 Mar 9;31(10):3880-93. (PMID: 21389243)
Neurobiol Aging. 2011 Nov;32(11):2109.e1-14. (PMID: 21794952)
J Pain. 2003 Oct;4(8):465-70. (PMID: 14622667)
Neuropharmacology. 2017 Jan;112(Pt A):228-234. (PMID: 27543416)
J Neurosci. 2008 Dec 10;28(50):13649-61. (PMID: 19074038)
Neuroscience. 2010 Dec 29;171(4):1314-25. (PMID: 20951771)
Biochem Biophys Res Commun. 2006 Jul 21;346(1):281-7. (PMID: 16756951)
Science. 1995 Jun 9;268(5216):1503-6. (PMID: 7770778)
Pain. 2011 Mar;152(3 Suppl):S2-15. (PMID: 20961685)
Science. 1996 Dec 6;274(5293):1724-6. (PMID: 8939866)
J Pain. 2009 Sep;10(9):895-926. (PMID: 19712899)
Exp Neurol. 2006 Jan;197(1):22-30. (PMID: 15996657)
J Neurophysiol. 2008 Jun;99(6):2985-97. (PMID: 18400958)
Neurology. 2010 Oct 19;75(16):1454-8. (PMID: 20956790)
PeerJ. 2016 Nov 15;4:e2702. (PMID: 27896032)
Mol Pain. 2009 Dec 16;5:73. (PMID: 20015370)
Nat Rev Neurosci. 2008 Feb;9(2):97-107. (PMID: 18200026)
J Physiol. 2005 Jul 15;566(Pt 2):379-94. (PMID: 15878946)
J Neurosci. 2007 Mar 21;27(12):3274-84. (PMID: 17376988)
J Neurosci. 2014 Oct 1;34(40):13505-15. (PMID: 25274827)
Electroencephalogr Clin Neurophysiol. 1960 May;12:455-66. (PMID: 13821598)
Sci Rep. 2017 Oct 6;7(1):12743. (PMID: 28986567)
J Neurosci. 2006 Aug 30;26(35):8923-30. (PMID: 16943548)
Mol Pain. 2010 Sep 28;6:62. (PMID: 20920185)
Mol Brain. 2014 Jan 02;7:1. (PMID: 24382121)
J Neurosci. 2013 Jun 5;33(23):9644-54. (PMID: 23739961)
Nat Neurosci. 2013 Mar;16(3):259-63. (PMID: 23434978)
Exp Brain Res. 1997 Apr;114(2):329-38. (PMID: 9166922)
فهرسة مساهمة: Keywords: anterior cingulate cortex; intrinsic excitability; neuropathic pain; refractory period; spike threshold; spontaneous excitatory postsynaptic currents
تواريخ الأحداث: Date Created: 20181207 Latest Revision: 20201001
رمز التحديث: 20231215
مُعرف محوري في PubMed: PMC6258991
DOI: 10.3389/fncel.2018.00436
PMID: 30519160
قاعدة البيانات: MEDLINE
الوصف
تدمد:1662-5102
DOI:10.3389/fncel.2018.00436