Evidence map›Paper›PMID 34043767›Full record

ReviewEndocrinology2021

Overcoming Stress, Hunger, and Pain: Cocaine- and Amphetamine-Regulated Transcript Peptide's Promise.

Willis K Samson, Daniela Salvemini, Gina L C Yosten

Open access · bronzeAbstract readReview
In one paragraph

Review in Endocrinology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 44% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. American journal of physiology. Endocrinology and metabolism · 2026
    Article
  4. Review
  5. Article
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

3 authors at 1 institution in 1 country.

Willis K SamsonDepartment of Pharmacology and Physiology and Henry and Amelia Nasrallah Center for Neuroscience Saint Louis University School of Medicine, St Louis, MO 63104, USA.ORCID 0000-0003-0560-4447
Daniela SalveminiDepartment of Pharmacology and Physiology and Henry and Amelia Nasrallah Center for Neuroscience Saint Louis University School of Medicine, St Louis, MO 63104, USA.
Gina L C YostenDepartment of Pharmacology and Physiology and Henry and Amelia Nasrallah Center for Neuroscience Saint Louis University School of Medicine, St Louis, MO 63104, USA.
Saint Louis University · US

Funding

Angiotensin Receptor Regulation By Upstream Short Open Reading FramesR01HL121456 · NHLBI · GEORGETOWN UNIVERSITY · PI SAMSON, WILLIS K., SANDBERG, KATHRYN L · 2014 to 2017
$3.1M
Integrative Physiology of Obesity: Role of GPR160R01DK118340 · NIDDK · SAINT LOUIS UNIVERSITY · PI YOSTEN, GINA L.C. · 2018 to 2022
$2.3M
Isolation of GPR160 for biochemical analysis of the activation mechanism and development of a high throughput screening assay to identify small molecule inhibitorsR01NS113257 · NINDS · SAINT LOUIS UNIVERSITY · PI SALVEMINI, DANIELA, YOSTEN, GINA L.C. · 2019 to 2020
$2.3M
NHLBI NIH HHS R01 HL121456NIDDK NIH HHS R01 DK118340NINDS NIH HHS R01 NS113257
6 · The paper itself

Abstract

Cocaine- and amphetamine-regulated transcript encodes an eponymous peptide, CARTp, which exerts diverse pharmacologic actions in the central and peripheral nervous systems, as well as in several endocrine organs, including pancreas. Here we review those diverse actions, the physiological relevance of which had remained unestablished until recently. With the identification of a CARTp receptor, GPR160, the physiologic importance and therapeutic potential of CARTp or analogs are being revealed. Not only is the CARTp-GPR160 interaction essential for the circadian regulation of appetite and thirst but also for the transmission of nerve injury-induced pain. Molecular approaches now are uncovering additional physiologically relevant actions and the development of acute tissue-specific gene compromise approaches may reveal even more physiologically relevant actions of this pluripotent ligand/receptor pair.

Indexed as

AnimalsCocaine- and Amphetamine-Regulated Transcript ProteinHumansNerve Tissue ProteinsReceptors, G-Protein-CoupledTranslational Research, BiomedicalCocaine- and Amphetamine-Regulated Transcript ProteinGpr160 protein, ratNerve Tissue ProteinsReceptors, G-Protein-Coupledaddictionallodyniaobesitysatiationvagus nerve

Identifiers

PMID34043767
PMCPMC8210821
OpenAlexW3164447007

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.