Evidence map›Paper›PMID 36928850›Full record

ArticleAdvances in neurobiology2023

Discovery of New Transmitter Systems and Hence New Drug Targets.

Tiffany Schwasinger-Schmidt, Sheldon H Preskorn

Abstract read
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In one paragraph

Article in Advances in neurobiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

2 authors at 2 institutions in 1 country.

Tiffany Schwasinger-SchmidtDepartment of Internal Medicine, University of Kansas School of Medicine-Wichita, Wichita, KS, USA. tschwasinger-schmidt@kumc.edu.
Sheldon H PreskornDepartment of Psychiatry and Behavioral Science, University of Kansas School of Medicine-Wichita, Wichita, KS, USA.
University of Kansas · USWichita State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The development of medications used to treat psychiatric conditions has largely proceeded through serendipity, where a potential drug to treat mental illness is identified by chance. This approach is based on a limited understanding of the underlying pathophysiology of mental illness and brain disorders. Identification of novel neurotransmitter systems has allowed for new molecular-based approaches for drug development that identify specific receptor targets to treat a specific symptom. An example of this approach includes the development of suvorexant, which is a dual orexin receptor antagonist FDA approved in 2014 for the treatment of insomnia. This chapter will discuss challenges in psychiatric drug development; the importance of identifying discrete neurotransmitter systems that target a specific symptom, not a syndrome; the orexin pathway and targets within this pathway that can be used to modulate sleep; and a high-throughput approach to streamlining drug development.

Indexed as

Brain DiseasesSleep Initiation and Maintenance DisordersDrug DiscoveryHumansOrexin Receptor AntagonistsOrexin Receptor AntagonistsDual orexin receptor antagonistsOrexin neurotransmittersPsychiatric drug developmentSuvorexantTargeted drug development

Identifiers

PMID36928850
OpenAlexW4327654123

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.