Evidence map›Paper›PMID 32182221›Full record

ArticleJCI insight2020

Leptin receptor-expressing nucleus tractus solitarius neurons suppress food intake independently of GLP1 in mice.

Wenwen Cheng, Ermelinda Ndoka, Chelsea Hutch, Karen Roelofs, Andrew MacKinnon, Basma Khoury, Jack Magrisso, Ki Suk Kim, Christopher J Rhodes, David P Olson and 3 more

Abstract read
In one paragraph

Article in JCI insight, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
–field-weighted citation impact
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

55 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Cellular coding of ingestion in the caudal brainstem.bioRxiv : the preprint server for biology · 2026
    Article
  6. Article
  7. GLP-1 physiology and pharmacology along the gut-brain axis.The Journal of clinical investigation · 2026
    Review
  8. Article
  9. Central leptin pathways in metabolic homeostasis.Clinical science (London, England : 1979) · 2025
    Review
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Role of epicardial adipose tissue in heart failure with preserved ejection fraction: An emerging molecular mechanism and therapeutic potential.Obesity reviews : an official journal of the International Association for the Study of Obesity · 2025
    Review
  17. Article
  18. Review
  19. Review
  20. 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

13 authors.

Wenwen ChengDepartment of Internal Medicine and.
Ermelinda NdokaDepartment of Internal Medicine and.
Chelsea HutchDepartment of Surgery, University of Michigan, Ann Arbor, Michigan, USA.
Karen RoelofsDepartment of Surgery, University of Michigan, Ann Arbor, Michigan, USA.
Andrew MacKinnonDepartment of Internal Medicine and.
Basma KhouryDepartment of Surgery, University of Michigan, Ann Arbor, Michigan, USA.
Jack MagrissoDepartment of Surgery, University of Michigan, Ann Arbor, Michigan, USA.
Ki Suk KimDepartment of Surgery, University of Michigan, Ann Arbor, Michigan, USA.
Christopher J RhodesAstraZenica Inc., Gaithersburg, Maryland, USA.
David P OlsonDepartment of Pediatrics and.
Randy J SeeleyDepartment of Surgery, University of Michigan, Ann Arbor, Michigan, USA.
Darleen SandovalDepartment of Surgery, University of Michigan, Ann Arbor, Michigan, USA.
Martin G MyersDepartment of Internal Medicine and.

Funding

Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Mehboob A Hussain · 2013 to 2026
$24.3M
University of Michigan Center for Gastrointestinal ResearchP30DK034933 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI OWYANG, CHUNG · 1986 to 2021
$22.5M
Pilot and Feasibility (P and F) ProgramP30DK089503 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Joyce Lee · 2010 to 2026
$20.3M
Project 3: Neural mediators in the metabolic effects of Vertical Sleeve GastrectomyP01DK117821 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SANDOVAL, DARLEEN A. · 2019 to 2023
$9.3M
Unique Roles for Defined PVH Neurons in the Control of Energy BalanceR01DK104999 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI OLSON, DAVID P · 2016 to 2020
$2.5M
Role of GDF15 and its receptor in the CNS regulation of food intake and body weightR01DK119188 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SEELEY, RANDY J · 2019 to 2022
$1.9M
Role of Glucokinase in GLP-1 Regulation of Energy and Glucose HomeostasisR01DK082480 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SANDOVAL, DARLEEN A. · 2010 to 2014
$1.7M
Unique Roles for Defined PVH Neurons in the Control of Energy BalanceR56DK104999 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI OLSON, DAVID P · 2015 to 2015
$156k
NIDDK NIH HHS P01 DK117821NIDDK NIH HHS P30 DK020572NIDDK NIH HHS P30 DK034933NIDDK NIH HHS P30 DK089503NIDDK NIH HHS R01 DK082480NIDDK NIH HHS R01 DK104999NIDDK NIH HHS R01 DK119188NIDDK NIH HHS R56 DK104999
6 · The paper itself

Abstract

Leptin receptor-expressing (LepRb-expressing) neurons of the nucleus tractus solitarius (NTS; LepRbNTS neurons) receive gut signals that synergize with leptin action to suppress food intake. NTS neurons that express preproglucagon (Ppg) (and that produce the food intake-suppressing PPG cleavage product glucagon-like peptide-1 [GLP1]) represent a subpopulation of mouse LepRbNTS cells. Using Leprcre, Ppgcre, and Ppgfl mouse lines, along with Designer Receptors Exclusively Activated by Designer Drugs (DREADDs), we examined roles for Ppg in GLP1NTS and LepRbNTS cells for the control of food intake and energy balance. We found that the cre-dependent ablation of NTS Ppgfl early in development or in adult mice failed to alter energy balance, suggesting the importance of pathways independent of NTS GLP1 for the long-term control of food intake. Consistently, while activating GLP1NTS cells decreased food intake, LepRbNTS cells elicited larger and more durable effects. Furthermore, while the ablation of NTS Ppgfl blunted the ability of GLP1NTS neurons to suppress food intake during activation, it did not impact the suppression of food intake by LepRbNTS cells. While Ppg/GLP1-mediated neurotransmission plays a central role in the modest appetite-suppressing effects of GLP1NTS cells, additional pathways engaged by LepRbNTS cells dominate for the suppression of food intake.

Indexed as

EatingGene Expression RegulationAnimalsGlucagon-Like Peptide 1MiceMice, KnockoutNeuronsReceptors, LeptinSolitary NucleusGlucagon-Like Peptide 1leptin receptor, mouseReceptors, LeptinEndocrinologyLeptinMetabolismObesityPeptides

Identifiers

PMID32182221
PMCPMC7205255

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.