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Chronic Stress Decreases Cerebrovascular Responses During Rat Hindlimb Electrical Stimulation

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dc.contributor.authorSohee Lee-
dc.contributor.authorBok-Man Kang-
dc.contributor.authorMin-Kyoo Shin-
dc.contributor.authorJiwoong Min-
dc.contributor.authorChaejeong Heo-
dc.contributor.authorYubu Lee-
dc.contributor.authorEunha Baeg-
dc.contributor.authorMinah Suh-
dc.date.available2016-06-22T08:13:58Z-
dc.date.created2016-01-22-
dc.date.issued2015-12-
dc.identifier.issn1662-453X-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/2561-
dc.description.abstractRepeated stress is one of the major risk factors for cerebrovascular disease, including stroke, and vascular dementia. However, the functional alterations in the cerebral hemodynamic response induced by chronic stress have not been clarified. Here, we investigated the in vivo cerebral hemodynamic changes and accompanying cellular and molecular changes in chronically stressed rats. After 3 weeks of restraint stress, the elicitation of stress was verified by behavioral despair in the forced swimming test and by physical indicators of stress. The evoked changes in the cerebral blood volume and pial artery responses following hindpaw electrical stimulation were measured using optical intrinsic signal imaging. We observed that, compared to the control group, animals under chronic restraint stress exhibited a decreased hemodynamic response, with a smaller pial arterial dilation in the somatosensory cortex during hindpaw electrical stimulation. The effect of chronic restraint stress on vasomodulator enzymes, including neuronal nitric oxide synthase (nNOS) and heme oxygenase-2 (HO-2), was assessed in the somatosensory cortex. Chronic restraint stress downregulated nNOS and HO-2 compared to the control group. In addition, we examined the subtypes of cells that can explain the environmental changes due to the decreased vasomodulators. The expression of parvalbumin in GABAergic interneurons and glutamate receptor-1 in neurons were decreased, whereas the microglial activation was increased. Our results suggest that the chronic stress-induced alterations in cerebral vascular function and the modulations of the cellular expression in the neuro-vasomodulatory system may be crucial contributing factors in the development of various vascular-induced conditions in the brain. Copyright©2015Lee,Kang,Shin,Min,Heo,Lee,BaegandSuh.Thisis anopen- accessarticledistributedunderthetermsoftheCreativeCommonsAttribution License(CCBY).Theuse,distributionorreproductioninotherforumsispermitted, providedtheoriginalauthor(s)orlicensorarecreditedand thattheoriginal publicationinthisjournaliscited,inaccordancewithacceptedacademicpractice. Nouse,distributionorreproductionispermittedwhichdoes notcomplywiththese terms.-
dc.description.uri1-
dc.language영어-
dc.publisherFRONTIERS MEDIA SA-
dc.subjectchronic stress-
dc.subjectsensory stimulation-
dc.subjectneurovascular coupling-
dc.subjectoptical intrinsic signals-
dc.subjectrestraint stress-
dc.subjectsomatosensory cortex-
dc.titleChronic Stress Decreases Cerebrovascular Responses During Rat Hindlimb Electrical Stimulation-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000367099900001-
dc.identifier.scopusid2-s2.0-84954510971-
dc.identifier.rimsid22091-
dc.date.tcdate2018-10-01-
dc.contributor.affiliatedAuthorSohee Lee-
dc.contributor.affiliatedAuthorBok-Man Kang-
dc.contributor.affiliatedAuthorChaejeong Heo-
dc.contributor.affiliatedAuthorYubu Lee-
dc.contributor.affiliatedAuthorEunha Baeg-
dc.contributor.affiliatedAuthorMinah Suh-
dc.identifier.doi10.3389/fnins.2015.00462-
dc.identifier.bibliographicCitationFRONTIERS IN NEUROSCIENCE, v.9, pp.462-
dc.citation.titleFRONTIERS IN NEUROSCIENCE-
dc.citation.volume9-
dc.citation.startPage462-
dc.date.scptcdate2018-10-01-
dc.description.wostc2-
dc.description.scptc3-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.subject.keywordPlusNITRIC-OXIDE SYNTHASE-
dc.subject.keywordPlusCEREBRAL-BLOOD-FLOW-
dc.subject.keywordPlusMAJOR DEPRESSIVE DISORDER-
dc.subject.keywordPlusENDOTHELIAL FUNCTION-
dc.subject.keywordPlusISCHEMIC-STROKE-
dc.subject.keywordPlusMENTAL STRESS-
dc.subject.keywordPlusDENTATE GYRUS-
dc.subject.keywordPlusBRAIN-BARRIER-
dc.subject.keywordPlusSOCIAL STRESS-
dc.subject.keywordPlusCELL-DEATH-
dc.subject.keywordAuthorchronic stress-
dc.subject.keywordAuthorsensory stimulation-
dc.subject.keywordAuthorneurovascular coupling-
dc.subject.keywordAuthoroptical intrinsic signals-
dc.subject.keywordAuthorrestraint stress-
dc.subject.keywordAuthorsomatosensory cortex-
Appears in Collections:
Center for Neuroscience Imaging Research (뇌과학 이미징 연구단) > 1. Journal Papers (저널논문)
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