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OX2R-selective orexin agonism is sufficient to ameliorate cataplexy and sleep/wake fragmentation wit...

OX2R-selective orexin agonism is sufficient to ameliorate cataplexy and sleep/wake fragmentation wit...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_2693033755

OX2R-selective orexin agonism is sufficient to ameliorate cataplexy and sleep/wake fragmentation without inducing drug-seeking behavior in mouse model of narcolepsy

About this item

Full title

OX2R-selective orexin agonism is sufficient to ameliorate cataplexy and sleep/wake fragmentation without inducing drug-seeking behavior in mouse model of narcolepsy

Publisher

San Francisco: Public Library of Science

Journal title

PloS one, 2022-07, Vol.17 (7), p.e0271901-e0271901

Language

English

Formats

Publication information

Publisher

San Francisco: Public Library of Science

More information

Scope and Contents

Contents

Acquired loss of hypothalamic orexin (hypocretin)-producing neurons causes the chronic sleep disorder narcolepsy-cataplexy. Orexin replacement therapy using orexin receptor agonists is expected as a mechanistic treatment for narcolepsy. Orexins act on two receptor subtypes, OX1R and OX2R, the latter being more strongly implicated in sleep/wake regu...

Alternative Titles

Full title

OX2R-selective orexin agonism is sufficient to ameliorate cataplexy and sleep/wake fragmentation without inducing drug-seeking behavior in mouse model of narcolepsy

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_plos_journals_2693033755

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_2693033755

Other Identifiers

ISSN

1932-6203

E-ISSN

1932-6203

DOI

10.1371/journal.pone.0271901

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