Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/99985
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dc.contributorDepartment of Biomedical Engineeringen_US
dc.creatorMurugappan, SKen_US
dc.creatorXie, Len_US
dc.creatorWong, HYen_US
dc.creatorIqbal, Zen_US
dc.creatorLei, Zen_US
dc.creatorRamkrishnan, ASen_US
dc.creatorLi, Yen_US
dc.date.accessioned2023-07-26T05:49:39Z-
dc.date.available2023-07-26T05:49:39Z-
dc.identifier.issn1661-6596en_US
dc.identifier.urihttp://hdl.handle.net/10397/99985-
dc.language.isoenen_US
dc.publisherMDPIen_US
dc.rights© 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).en_US
dc.rightsThe following publication Murugappan SK, Xie L, Wong HY, Iqbal Z, Lei Z, Ramkrishnan AS, Li Y. Suppression of Pain in the Late Phase of Chronic Trigeminal Neuropathic Pain Failed to Rescue the Decision-Making Deficits in Rats. International Journal of Molecular Sciences. 2021; 22(15):7846 is available at https://doi.org/10.3390/ijms22157846.en_US
dc.subjectAnterior cingulate cortexen_US
dc.subjectTrigeminal neuropathic painen_US
dc.subjectDecision makingen_US
dc.subjectEarly or late phaseen_US
dc.subjectTetrodotoxinen_US
dc.subjectSynaptic plasticityen_US
dc.subjectTheta oscillationsen_US
dc.subjectCognitive deficitsen_US
dc.subjectChronic constriction injuryen_US
dc.subjectRiluzoleen_US
dc.titleSuppression of pain in the late phase of chronic trigeminal neuropathic pain failed to rescue the decision‐making deficits in ratsen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume22en_US
dc.identifier.issue15en_US
dc.identifier.doi10.3390/ijms22157846en_US
dcterms.abstractTrigeminal neuropathic pain (TNP) led to vital cognitive functional deficits such as impaired decision-making abilities in a rat gambling task. Chronic TNP caused hypomyelination in the anterior cingulate cortex (ACC) associated with decreased synchronization between ACC spikes and basal lateral amygdala (BLA) theta oscillations. The aim of this study was to investigate the effect of pain suppression on cognitive impairment in the early or late phases of TNP. Blocking afferent signals with a tetrodotoxin (TTX)-ELVAX implanted immediately following nerve lesion suppressed the allodynia and rescued decision-making deficits. In contrast, the TTX used at a later phase could not suppress the allodynia nor rescue decision-making deficits. Intra-ACC administration of riluzole reduced the ACC neural sensitization but failed to restore ACC-BLA spike-field phase synchrony during the late stages of chronic neuropathic pain. Riluzole suppressed allodynia but failed to rescue the decision-making deficits during the late phase of TNP, suggesting that early pain relief is important for recovering from pain-related cognitive impairments. The functional disturbances in ACC neural circuitry may be relevant causes for the deficits in decision making in the chronic TNP state.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationInternational journal of molecular sciences, Aug. 2021, v. 22, no. 15, 7846en_US
dcterms.isPartOfInternational journal of molecular sciencesen_US
dcterms.issued2021-08-
dc.identifier.scopus2-s2.0-85111006665-
dc.identifier.pmid34360612-
dc.identifier.eissn1422-0067en_US
dc.identifier.artn7846en_US
dc.description.validate202307 bcchen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_Scopus/WOS-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextCentre for Biosystems, Neuroscience, and Nanotechnology; City University of Hong Kong Neuroscience Research Infrastructure; Innovation and Tech; Innovation and Technology Fund Hong Kong; Shenzhen Fundamental Research Institutions; Shenzhen—Hong Kong Institute of Brain Science—Shenzhen Fundamental Research Institutions; National Natural Science Foundation of China; Health and Medical Research Funden_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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