Evidence map›Paper›PMID 30060151›Full record

ArticleSleep2018

Optical probing of orexin/hypocretin receptor antagonists.

Shi-Bin Li, Natalie Nevárez, William J Giardino, Luis de Lecea

Open access · bronzeAbstract read
In one paragraph

Article in Sleep, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. A Distinct Subpopulation of Extended Amygdala Neurons Drives Food Intake.Biological psychiatry global open science · 2026
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  5. Article
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  7. A Distinct Subpopulation of Extended Amygdala Neurons Drives Food Intake.bioRxiv : the preprint server for biology · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Shi-Bin LiDepartment of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, CA.
Natalie NevárezDepartment of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, CA.
William J GiardinoDepartment of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, CA.
Luis de LeceaDepartment of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, CA.
Stanford University · US

Funding

VECTOR COREP30NS069375 · NINDS · STANFORD UNIVERSITY · PI SHAMLOO, MEHRDAD · 2011 to 2019
$6.3M
Optogenetic interrogation of sleep circuits during agingR01AG047671 · NIA · STANFORD UNIVERSITY · PI DE LECEA, LUIS, WYSS-CORAY, TONY · 2014 to 2018
$2.1M
Neuronal mapping of anxiety and panicR01MH102638 · NIMH · STANFORD UNIVERSITY · PI DE LECEA, LUIS · 2014 to 2018
$2.0M
Alcohol-related sleep disturbances and circuit dynamics of arousal neuropeptidesK99AA025677 · NIAAA · STANFORD UNIVERSITY · PI GIARDINO, WILLIAM J · 2018 to 2020
$442k
NIAAA NIH HHS K99 AA025677NIA NIH HHS R01 AG047671NIMH NIH HHS R01 MH102638NINDS NIH HHS P30 NS069375
6 · The paper itself

Abstract

Study Objectives: The present study investigated the function of Hypocretin (Hcrt or Orexin/OX) receptor antagonists in sleep modulation and memory function with optical methods in transgenic mice. Methods: We used Hcrt-IRES-Cre knock-in mice and AAV vectors expressing channelrhodopsin-2 (ChR2) to render Hcrt neurons sensitive to blue light stimulation. We optogenetically stimulated Hcrt neurons and measured latencies to wakefulness in the presence or absence of OX1/2R antagonists and Zolpidem. We also examined endogenous Hcrt neuronal activity with fiber photometry. Changes in memory after optogenetic sleep disruption were evaluated by the novel object recognition test (NOR) and compared for groups treated with vehicle, OX1/2R antagonists, or Zolpidem. We also analyzed electroencephalogram (EEG) power spectra of wakefulness, rapid eye movement (REM) sleep, and non-REM (NREM) sleep following the injections of vehicle, OX1/2R antagonists, and Zolpidem in young adult mice. Results: Acute optogenetic stimulation of Hcrt neurons at different frequencies resulted in wakefulness. Treatment with dual OX1/2R antagonists (DORAs) DORA12 and MK6096, as well as selective OX2R antagonist MK1064 and Zolpidem, but not selective OX1R antagonist 1SORA1, significantly reduced the bout length of optogenetic stimulation-evoked wakefulness episode. Fiber photometry recordings of GCaMP6f signals showed that Hcrt neurons are active during wakefulness, even in the presence of OXR antagonists. Treatment with dual OX1/2R antagonists improved memory function despite optogenetic sleep fragmentation caused impaired memory function in a NOR test. Conclusions: Our results show DORAs and selective OX2R antagonists stabilize sleep and improve sleep-dependent cognitive processes even when challenged by optogenetic stimulation mimicking highly arousing stimuli.

Indexed as

AnimalsElectroencephalographyMaleMemoryMiceMice, Inbred C57BLMice, TransgenicNeuronsOrexin Receptor AntagonistsPhotic StimulationSleepWakefulnessZolpidemOrexin Receptor AntagonistsZolpidem

Identifiers

PMID30060151
PMCPMC6454482
OpenAlexW2883649457

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.