Evidence map›Paper›PMID 26047506›Full record

ArticlePloS one2015

The Orphan G Protein-Coupled Receptor Gene GPR178 Is Evolutionary Conserved and Altered in Response to Acute Changes in Food Intake.

Vanni Caruso, Madeleine Le Grevés, Shahrzad Shirazi Fard, Tatjana Haitina, Pawel K Olszewski, Johan Alsiö, Helgi B Schiöth, Robert Fredriksson

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. 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
0.6field-weighted citation impact, top 38% 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, 13 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

8 authors at 1 institution in 2 countries.

Vanni CarusoDepartment of Neuroscience, Unit of Functional Pharmacology, Uppsala University, Uppsala, Sweden.
Madeleine Le GrevésDepartment of Neuroscience, Unit of Functional Pharmacology, Uppsala University, Uppsala, Sweden.
Shahrzad Shirazi FardDepartment of Neuroscience, Unit of Functional Pharmacology, Uppsala University, Uppsala, Sweden.
Tatjana HaitinaDepartment of Neuroscience, Unit of Functional Pharmacology, Uppsala University, Uppsala, Sweden.
Pawel K OlszewskiDepartment of Neuroscience, Unit of Functional Pharmacology, Uppsala University, Uppsala, Sweden; Department of Biological Sciences, University of Waikato, Hamilton, New Zealand.
Johan AlsiöDepartment of Neuroscience, Unit of Functional Pharmacology, Uppsala University, Uppsala, Sweden.
Helgi B SchiöthDepartment of Neuroscience, Unit of Functional Pharmacology, Uppsala University, Uppsala, Sweden.
Robert FredrikssonDepartment of Neuroscience, Unit of Functional Pharmacology, Uppsala University, Uppsala, Sweden.
Uppsala University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

G protein-coupled receptors (GPCRs) are a class of integral membrane proteins mediating physiological functions fundamental for survival, including energy homeostasis. A few years ago, an amino acid sequence of a novel GPCR gene was identified and named GPR178. In this study, we provide new insights regarding the biological significance of Gpr178 protein, investigating its evolutionary history and tissue distribution as well as examining the relationship between its expression level and feeding status. Our phylogenetic analysis indicated that GPR178 is highly conserved among all animal species investigated, and that GPR178 is not a member of a protein family. Real-time PCR and in situ hybridization revealed wide expression of Gpr178 mRNA in both the brain and periphery, with high expression density in the hypothalamus and brainstem, areas involved in the regulation of food intake. Hence, changes in receptor expression were assessed following several feeding paradigms including starvation and overfeeding. Short-term starvation (12-48h) or food restriction resulted in upregulation of Gpr178 mRNA expression in the brainstem, hypothalamus and prefrontal cortex. Conversely, short-term (48h) exposure to sucrose or Intralipid solutions downregulated Gpr178 mRNA in the brainstem; long-term exposure (10 days) to a palatable high-fat and high-sugar diet resulted in a downregulation of Gpr178 in the amygdala but not in the hypothalamus. Our results indicate that hypothalamic Gpr178 gene expression is altered during acute exposure to starvation or acute exposure to palatable food. Changes in gene expression following palatable diet consumption suggest a possible involvement of Gpr178 in the complex mechanisms of feeding reward.

Indexed as

EatingAmygdalaAnimalsBiological EvolutionBrainHypothalamusIn Situ HybridizationMaleMiceMice, Inbred C57BLPhylogenyPrefrontal CortexRatsRats, Sprague-DawleyReal-Time Polymerase Chain ReactionReceptors, G-Protein-CoupledReceptors, G-Protein-CoupledRNA, Messenger

Identifiers

PMID26047506
PMCPMC4457792
OpenAlexW1809179277

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.