日本薬理学会年会要旨集
Online ISSN : 2435-4953
WCP2018 (The 18th World Congress of Basic and Clinical Pharmacology)
セッションID: WCP2018_PO3-1-65
会議情報

Poster session
Optogenetic manipulation of dorsal raphe serotonergic neurons modulates emotional behaviors in rodents
Naoya NishitaniNozomi AsaokaHiroyuki KawaiNorihiro ShibuiYuma NagaiChihiro AndohKazuki NagayasuHisashi ShirakawaTakayuki NakagawaShuji Kaneko
著者情報
キーワード: serotonin, optogenetics, viral vector
会議録・要旨集 オープンアクセス

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抄録

Serotonergic neurons are thought to play an important role in the control of the emotional states. Optogenetics using channelrhodopsin-2 (ChR2), a light activated cation channel, and archaerhodopsin (eArchT), a light-activated proton pump, have been widely used for the accurate control of the neuronal activity by light. Specifically, importance of the activity of serotonergic neurons in the control of anxiety has been shown by optogenetic analyses in transgenic mice. However, elucidation of the behavioral differences among mice strains and the animal species necessitates the tools for selective control of serotonergic neurons across the strains and the species. Here, we made a lentiviral vector (LVV) capable of optogenetic control of serotonergic neurons in mice and rats. In the dorsal raphe nucleus (DRN), one of the serotonergic nucleus, of mouse and rat injected with the LVV, transgenes were selectively expressed in tryptophan hydroxylase (TPH)-positive, serotonergic neurons. In whole-cell recordings from ChR2-positive and eArchT-positive neurons in acute DRN slice, photostimulation evoked action potentials and inhibited neuronal firing, respectively. Optogenetic stimulation of the mouse DRN serotonergic neurons decreased immobility duration in the tail suspension test, whereas it had no effect on the locomotor activity and anxiety-like behaviors in open field test and elevated plus maze test. Moreover, Optogenetic stimulation of the rat DRN serotonergic neurons decreased immobility duration in the forced swim test, while optogenetic inhibition of them enhanced anxiety-like behaviors in elevated plus maze test. These results demonstrate that selective activation of DRN serotonergic neurons is sufficient to elicit antidepressant-like effect in mice and rats, and that these new vectors pave the way towards selective manipulation of serotonergic neural circuits in rats to which transgenic technology cannot be easily applied.

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© 2018 The Authors(s)
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