Evidence map›Paper›PMID 36213756›Full record

ArticleFrontiers in neuroscience2022

Developmental or adult-onset deletion of neurotensin receptor-1 from dopamine neurons differentially reduces body weight.

Patricia Perez-Bonilla, Jariel Ramirez-Virella, Pooja Menon, Eva Troyano-Rodriguez, Sydney K Arriaga, Anna Makela, Raluca Bugescu, Michael J Beckstead, Gina M Leinninger

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neuroscience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 41% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. 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

9 authors at 3 institutions in 1 country.

Patricia Perez-BonillaNeuroscience Graduate Program, Michigan State University, East Lansing, MI, United States.
Jariel Ramirez-VirellaNeuroscience Graduate Program, Michigan State University, East Lansing, MI, United States.
Pooja MenonDepartment of Physiology, Michigan State University, East Lansing, MI, United States.
Eva Troyano-RodriguezAging and Metabolism Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, United States.
Sydney K ArriagaDepartment of Physiology, Michigan State University, East Lansing, MI, United States.
Anna MakelaDepartment of Physiology, Michigan State University, East Lansing, MI, United States.
Raluca BugescuDepartment of Physiology, Michigan State University, East Lansing, MI, United States.
Michael J BecksteadAging and Metabolism Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, United States.
Gina M LeinningerDepartment of Physiology, Michigan State University, East Lansing, MI, United States.
Michigan State University · USOklahoma City VA Medical Center · USOklahoma Medical Research Foundation · US

Funding

Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Mehboob A Hussain · 2013 to 2026
$24.3M
Role of Lateral Hypothalamic Neurotensin Neurons in Energy BalanceR01DK103808 · NIDDK · MICHIGAN STATE UNIVERSITY · PI Gina Marie Leinninger · 2014 to 2026
$4.8M
Integrative Pharmacological Sciences Training Program (IPSTP)T32GM142521 · NIGMS · MICHIGAN STATE UNIVERSITY · PI ANNE M. DORRANCE, Gina Marie Leinninger · 2021 to 2026
$2.4M
Effects of dietary restriction on age-related neurophysiological adaptations: frombehavior to single dopaminergic neuronsR01AG052606 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI BECKSTEAD, MICHAEL J · 2016 to 2020
$2.1M
BLRD VA I01 BX005396NIA NIH HHS R01 AG052606NIDDK NIH HHS P30 DK020572NIDDK NIH HHS R01 DK103808NIGMS NIH HHS T32 GM142521
6 · The paper itself

Abstract

Central neurotensin signaling via neurotensin receptor-1 (NtsR1) modulates various aspects of physiology, including suppressing feeding and promoting locomotor activity that can support weight loss. However, it remains unclear when and where NtsR1 expression contributes to control of body weight vs. other effects. We previously showed that activating ventral tegmental area (VTA) dopamine (DA) neurons that express NtsR1 promotes weight loss. We therefore hypothesized that deleting NtsR1 from DA neurons would promote weight gain by increasing food intake and decreasing physical activity. In contrast, developmental deletion of NtsR1 from DA neurons (by crossing

Indexed as

energy balancefeedinglocomotor activityobesityventral tegmental area (VTA)

Identifiers

PMID36213756
PMCPMC9537700
OpenAlexW4297003870

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.