Evidence map›Paper›PMID 41251447›Full record

ReviewClinical science (London, England : 1979)2025

Central leptin pathways in metabolic homeostasis.

Yuying Zhao, Connor Laule, Kamal Rahmouni

Abstract readReview
In one paragraph

Review in Clinical science (London, England : 1979), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–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

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Review
  4. 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

3 authors.

Yuying Zhao *Department of Neuroscience and Pharmacology, University of Iowa Carver College of Medicine, Iowa City, Iowa.
Connor Laule *Department of Neuroscience and Pharmacology, University of Iowa Carver College of Medicine, Iowa City, Iowa.
Kamal RahmouniDepartment of Neuroscience and Pharmacology, University of Iowa Carver College of Medicine, Iowa City, Iowa.ORCID 0000-0001-5136-6748

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Obesity continues to be a major global health crisis, contributing to the rising prevalence of metabolic disorders such as type 2 diabetes, cardiovascular disease, and certain cancers. Central to the regulation of energy homeostasis is the adipocyte-derived hormone leptin, which serves as a key afferent signal to the central nervous system to suppress food intake, enhance energy expenditure, and maintain glucose balance. Since its discovery over three decades ago, a wealth of research has illuminated the molecular, cellular, and physiological mechanisms through which leptin exerts its metabolic effects. These foundational studies have delineated the neural circuits, particularly within the hypothalamus and brainstem, that integrate leptin signaling to co-ordinate complex metabolic responses. This review provides a comprehensive synthesis of the current understanding of leptin's metabolic actions, with an emphasis on the intracellular signaling cascades that mediate leptin receptor activation. We also highlight the diverse neuronal populations and brain regions that contribute to leptin's regulatory roles.

Indexed as

Energy MetabolismHomeostasisLeptinAnimalsHumansHypothalamusObesityReceptors, LeptinSignal TransductionLeptinReceptors, Leptinenergy balanceglucose homeostasishypothalamusneural circuitsobesity

Identifiers

PMID41251447
PMCPMC12751087

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.