Evidence map›Paper›PMID 23848055›Full record

ArticleBritish journal of pharmacology2014

Orexin/hypocretin receptor signalling: a functional perspective.

C S Leonard, J P Kukkonen

Open access · bronzeAbstract readComment
In one paragraph

Article in British journal of pharmacology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed, 2 pooled it
5.0field-weighted citation impact, top 4% 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

61 citing papers in PubMed, 2 syntheses or guidelines pooled it, 133 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Review
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  12. Article
  13. A molecular network map of orexin-orexin receptor signaling system.Journal of cell communication and signaling · 2023
    Article
  14. Antagonization of OXInternational journal of molecular sciences · 2022
    Article
  15. Physiological Role of Orexinergic System for Health.International journal of environmental research and public health · 2022
    Review
  16. Review
  17. Article
  18. Review
  19. Article
  20. Article

1 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 2 institutions in 2 countries.

C S LeonardDepartment of Physiology, New York Medical College, Valhalla, NY, USA.
J P Kukkonen
New York Medical College · USUniversity of Helsinki · FI

Funding

"Synaptic Modulation of Mesopontine Cholingergic Neurons"R01NS027881 · NINDS · NEW YORK UNIVERSITY · PI LEONARD, CHRISTOPHER S · 1992 to 2022
$7.1M
K+-CHANNELS REGULATING REM-RELATED CHOLINGERGIC NEURONSR01HL064150 · NHLBI · NEW YORK MEDICAL COLLEGE · PI LEONARD, CHRISTOPHER S · 1999 to 2011
$2.6M
SYNAPTIC MODULATION OF MESOPONTINE CHOLINERGIC NEURONSR55NS027881 · NINDS · NEW YORK UNIVERSITY · PI LEONARD, CHRISTOPHER S · 1991 to 1991
–
NHLBI NIH HHS HL064150NHLBI NIH HHS R01 HL064150NINDS NIH HHS NS027881NINDS NIH HHS R01 NS027881
6 · The paper itself

Abstract

Multiple homeostatic systems are regulated by orexin (hypocretin) peptides and their two known GPCRs. Activation of orexin receptors promotes waking and is essential for expression of normal sleep and waking behaviour, with the sleep disorder narcolepsy resulting from the absence of orexin signalling. Orexin receptors also influence systems regulating appetite/metabolism, stress and reward, and are found in several peripheral tissues. Nevertheless, much remains unknown about the signalling pathways and targets engaged by native receptors. In this review, we integrate knowledge about the orexin receptor signalling capabilities obtained from studies in expression systems and various native cell types (as presented in Kukkonen and Leonard, this issue of British Journal of Pharmacology) with knowledge of orexin signalling in different tissues. The tissues reviewed include the CNS, the gastrointestinal tract, the pituitary gland, pancreas, adrenal gland, adipose tissue and the male reproductive system. We also summarize the findings in different native and recombinant cell lines, especially focusing on the different cascades in CHO cells, which is the most investigated cell line. This reveals that while a substantial gap exists between what is known about orexin receptor signalling and effectors in recombinant systems and native systems, mounting evidence suggests that orexin receptor signalling is more diverse than originally thought. Moreover, rather than being restricted to orexin receptor 'overexpressing' cells, this signalling diversity may be utilized by native receptors in a site-specific manner.

Indexed as

AnimalsHumansOrexin ReceptorsSignal TransductionOrexin Receptorsadipose tissueadrenal glandcell deathdepolarizationhormone releasehypocretinneuronorexinplasticitysecond messenger

Identifiers

PMID23848055
PMCPMC3904253
OpenAlexW1671441783

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.