Evidence map›Paper›PMID 28757640›Full record

ArticleInternational journal of obesity (2005)2017

Effects of peripheral administration of a Neuromedin U receptor 2-selective agonist on food intake and body weight in obese mice.

T Kaisho, H Nagai, T Asakawa, N Suzuki, H Fujita, K Matsumiya, N Nishizawa, Y Kanematsu-Yamaki, K Dote, J-I Sakamoto and 2 more

Abstract read
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In one paragraph

Article in International journal of obesity (2005), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 25% 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

6 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Crosstalk of Brain and Bone-Clinical Observations and Their Molecular Bases.International journal of molecular sciences · 2020
    Review
  5. Article
  6. 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

12 authors at 1 institution in 1 country.

T KaishoResearch, Takeda Pharmaceutical Company Limited, Fujisawa, Japan.
H NagaiResearch, Takeda Pharmaceutical Company Limited, Fujisawa, Japan.
T AsakawaResearch, Takeda Pharmaceutical Company Limited, Fujisawa, Japan.
N SuzukiResearch, Takeda Pharmaceutical Company Limited, Fujisawa, Japan.
H FujitaResearch, Takeda Pharmaceutical Company Limited, Fujisawa, Japan.
K MatsumiyaResearch, Takeda Pharmaceutical Company Limited, Fujisawa, Japan.
N NishizawaResearch, Takeda Pharmaceutical Company Limited, Fujisawa, Japan.
Y Kanematsu-YamakiResearch, Takeda Pharmaceutical Company Limited, Fujisawa, Japan.
K DoteResearch, Takeda Pharmaceutical Company Limited, Fujisawa, Japan.
J-I SakamotoResearch, Takeda Pharmaceutical Company Limited, Fujisawa, Japan.
T AsamiResearch, Takeda Pharmaceutical Company Limited, Fujisawa, Japan.
S TakekawaResearch, Takeda Pharmaceutical Company Limited, Fujisawa, Japan.
Takeda (Japan) · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNeuromedin U (NMU) is a neuropeptide with various physiological functions, including regulation of smooth-muscle contraction, blood pressure, stress responses and feeding behaviors. NMU activates two distinct receptors, NMUR1 and NMUR2, which are predominantly expressed in peripheral tissues and the central nervous system (CNS), respectively. It is reported that the NMU signaling system regulates food intake (FI) and body weight (BW) via NMUR2, suggesting that an NMUR2 agonist exhibiting anorectic effects would be a potential therapy for obesity.

methodsAntiobesity effects of NMUR2 activation were assessed using a recently developed, novel NMUR2-selective agonist, NMU-7005 (a polyethylene glycolated octapeptide). Here we assessed cumulative FI and BW loss after peripheral administration of NMU-7005 in NMUR2 knockout and diet-induced obese mice. To gain mechanistic insights, we performed immunohistochemical analysis of c-Fos-like protein expression in the brain.

resultsWe found that NMU-7005 was a NMUR2-selective agonist with little activity toward NMUR1. The anorectic effect of NMU-7005 was completely abrogated in NMUR2 knockout mice. Repeated subcutaneous administration of NMU-7005 showed a potent antiobesity effect with FI inhibition (P<0.025) in diet-induced obese mice. NMU-7005 in combination with the glucagon-like peptide-1 receptor (GLP-1R) agonist liraglutide showed an additive antiobesity effect, suggesting that NMUR2-mediated anorectic action is different from that of GLP-1R agonists. NMU-7005 also elicited a minimal conditioned taste-aversive effect, while the effect of liraglutide was significant. As c-Fos expression was upregulated in the hypothalamus and the medulla oblongata in NMU-7005-administered mice, the pharmacological effects of NMU-7005 appeared to be mediated via activation of the CNS.

conclusionOur results demonstrated that a novel NMUR2-selective agonist, NMU-7005, is a beneficial tool for the elucidation of NMUR2-mediated physiological functions, which is a promising therapeutic strategy for treating obesity.

Indexed as

AnimalsAnti-Obesity AgentsBody WeightDisease Models, AnimalEatingFeeding BehaviorImmunohistochemistryLiraglutideMiceMice, ObeseNeuropeptidesObesityReceptors, NeurotransmitterAnti-Obesity AgentsLiraglutideneuromedin Uneuromedin U receptorNeuropeptidesReceptors, Neurotransmitter

Identifiers

PMID28757640
OpenAlexW2739858130

What OpenQuestion holds

Texttitle and abstract
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.