Evidence map›Paper›PMID 40429740›Full record

ArticleInternational journal of molecular sciences2025

Effects of Combination Treatment with Leptin and Liraglutide on Glucose Metabolism in Insulin-Dependent Diabetic Mice.

Linlin Fu, Mariko Sugiyama, Shahriar Kamal, Tsubasa Ide, Tadashi Takeda, Mitsuhiro Kuno, Hiroshi Takagi, Teruhiko Koike, Hiroshi Arima, Ryoichi Banno

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Central leptin pathways in metabolic homeostasis.Clinical science (London, England : 1979) · 2025
    Review
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

10 authors.

Linlin FuResearch Center of Health, Physical Fitness and Sports, Nagoya University, Fro-cho, Chikusa-ku, Nagoya 464-8601, Aichi, Japan.
Mariko SugiyamaDepartment of Endocrinology and Diabetes, Graduate School of Medicine, Nagoya University, 65 Tsurumai-Cho, Showa-ku, Nagoya 466-8560, Aichi, Japan.ORCID 0000-0001-6289-1249
Shahriar KamalResearch Center of Health, Physical Fitness and Sports, Nagoya University, Fro-cho, Chikusa-ku, Nagoya 464-8601, Aichi, Japan.ORCID 0009-0009-9583-0472
Tsubasa IdeDepartment of Endocrinology and Diabetes, Graduate School of Medicine, Nagoya University, 65 Tsurumai-Cho, Showa-ku, Nagoya 466-8560, Aichi, Japan.
Tadashi TakedaDepartment of Endocrinology and Diabetes, Graduate School of Medicine, Nagoya University, 65 Tsurumai-Cho, Showa-ku, Nagoya 466-8560, Aichi, Japan.
Mitsuhiro KunoDepartment of Endocrinology and Diabetes, Graduate School of Medicine, Nagoya University, 65 Tsurumai-Cho, Showa-ku, Nagoya 466-8560, Aichi, Japan.
Hiroshi TakagiDepartment of Endocrinology and Diabetology, Nagoya City University East Medical Center, 1-2-23 Wakamizu, Chikusa-ku, Nagoya 464-8547, Aichi, Japan.
Teruhiko KoikeResearch Center of Health, Physical Fitness and Sports, Nagoya University, Fro-cho, Chikusa-ku, Nagoya 464-8601, Aichi, Japan.ORCID 0000-0003-3809-499X
Hiroshi ArimaDepartment of Endocrinology and Diabetes, Graduate School of Medicine, Nagoya University, 65 Tsurumai-Cho, Showa-ku, Nagoya 466-8560, Aichi, Japan.ORCID 0000-0003-3746-1997
Ryoichi BannoResearch Center of Health, Physical Fitness and Sports, Nagoya University, Fro-cho, Chikusa-ku, Nagoya 464-8601, Aichi, Japan.

Funding

a grant from the Japan IDDM Network NAa Grant-in Aid for Scientific Research (C) from the Japanese Society for Promotion of Science 24K10033JST SPRING JPMJSP2125
6 · The paper itself

Abstract

We investigated whether the peripheral co-administration of leptin and liraglutide (a glucagon-like peptide-1 receptor agonist) improved glucose metabolism in a mouse model of insulin-dependent diabetes mellitus (IDDM). Twelve-week-old male C57BL/6J mice were injected intraperitoneally with a high dose of streptozotocin to induce IDDM or vehicle-treated. Mice with IDDM were divided into four groups: leptin treatment alone (LEP), liraglutide treatment alone (LIRA), co-administration of leptin and liraglutide treatment (LEP+LIRA), untreated mice (UNT). Vehicle-treated mice were the healthy controls (HC). The blood glucose (BG) levels were measured, and a glucose tolerance test (GTT) was performed to compare the five groups. Leptin was administered peripherally at 20 μg/day using an osmotic pump, while liraglutide was administered subcutaneously at 1000 μg/kg/day. Monotherapy with leptin or liraglutide significantly improved glucose metabolism, as assessed by comparing BG levels and GTTs with those of the UNT group. Mice in the LEP+LIRA group showed even greater improvements in glucose metabolism than the monotherapy groups. Notably, glucose metabolism in the LEP+LIRA group improved comparably with the HC group. Thus, the peripheral co-administration of leptin and liraglutide effectively improved glucose metabolism in mice with IDDM without the use of insulin.

Indexed as

Diabetes Mellitus, ExperimentalDiabetes Mellitus, Type 1GlucoseHypoglycemic AgentsLeptinLiraglutideAnimalsBlood GlucoseDrug Therapy, CombinationGlucose Tolerance TestInsulinMaleMiceMice, Inbred C57BLBlood GlucoseGlucoseHypoglycemic AgentsInsulinLeptinLiraglutideglucagon-like peptide-1 receptor agonistglucose metabolismIDDMleptinliraglutide

Identifiers

PMID40429740
PMCPMC12111290

What Socratic 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 Socratic graph.