Evidence map›Paper›PMID 41105609›Full record

ArticlePloS one2025

Partial removal of visceral epididymal white adipose tissue in obese Ldlr-/-.Leiden mice impacts adipokine secretion, plasma free fatty acids, and improves cerebrovascular health.

Florine Seidel, Martine C Morrison, Ilse Arnoldussen, Vivienne Verweij, Simon Ebert, Joline Attema, Christa de Ruiter, Wim van Duyvenvoorde, Jessica Snabel, Bram Geenen and 6 more

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

16 authors.

Florine SeidelDepartment Medical Imaging, Anatomy, Preclinical Imaging Center, Radboud Alzheimer Center, Donders Institute for Brain, Cognition, and Behavior, Radboud university medical center, Nijmegen, The Netherlands.
Martine C MorrisonDepartment of Metabolic Health Research, Netherlands Organisation for Applied Scientific Research (TNO), Leiden, The Netherlands.
Ilse ArnoldussenDepartment Medical Imaging, Anatomy, Preclinical Imaging Center, Radboud Alzheimer Center, Donders Institute for Brain, Cognition, and Behavior, Radboud university medical center, Nijmegen, The Netherlands.
Vivienne VerweijDepartment Medical Imaging, Anatomy, Preclinical Imaging Center, Radboud Alzheimer Center, Donders Institute for Brain, Cognition, and Behavior, Radboud university medical center, Nijmegen, The Netherlands.
Simon EbertDivision of Vascular Biology, Institute for Stroke and Dementia Research (ISD), LMU Klinikum, Ludwig Maximilian University (LMU) Munich, Munich, Germany.ORCID https://orcid.org/0009-0004-5776-2089
Joline AttemaDepartment of Metabolic Health Research, Netherlands Organisation for Applied Scientific Research (TNO), Leiden, The Netherlands.
Christa de RuiterDepartment of Metabolic Health Research, Netherlands Organisation for Applied Scientific Research (TNO), Leiden, The Netherlands.
Wim van DuyvenvoordeDepartment of Metabolic Health Research, Netherlands Organisation for Applied Scientific Research (TNO), Leiden, The Netherlands.
Jessica SnabelDepartment of Metabolic Health Research, Netherlands Organisation for Applied Scientific Research (TNO), Leiden, The Netherlands.
Bram GeenenDepartment Medical Imaging, Anatomy, Preclinical Imaging Center, Radboud Alzheimer Center, Donders Institute for Brain, Cognition, and Behavior, Radboud university medical center, Nijmegen, The Netherlands.ORCID https://orcid.org/0000-0001-7838-3097
Ayla FrancoDepartment Medical Imaging, Anatomy, Preclinical Imaging Center, Radboud Alzheimer Center, Donders Institute for Brain, Cognition, and Behavior, Radboud university medical center, Nijmegen, The Netherlands.
Eveline GartDepartment of Metabolic Health Research, Netherlands Organisation for Applied Scientific Research (TNO), Leiden, The Netherlands.
Jürgen BernhagenDivision of Vascular Biology, Institute for Stroke and Dementia Research (ISD), LMU Klinikum, Ludwig Maximilian University (LMU) Munich, Munich, Germany.ORCID https://orcid.org/0000-0003-2996-2652
Maximilian WiesmannDepartment Medical Imaging, Anatomy, Preclinical Imaging Center, Radboud Alzheimer Center, Donders Institute for Brain, Cognition, and Behavior, Radboud university medical center, Nijmegen, The Netherlands.
Robert KleemannDepartment of Metabolic Health Research, Netherlands Organisation for Applied Scientific Research (TNO), Leiden, The Netherlands.
Amanda J KiliaanDepartment Medical Imaging, Anatomy, Preclinical Imaging Center, Radboud Alzheimer Center, Donders Institute for Brain, Cognition, and Behavior, Radboud university medical center, Nijmegen, The Netherlands.ORCID https://orcid.org/0000-0002-2158-6210

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Visceral white adipose tissue (WAT) dysfunction may contribute to obesity-related brain impairments but causal relationship has not been demonstrated. We herein investigated the impact of visceral epididymal WAT (eWAT) lipectomy on brain health and obesity-associated comorbidities (liver steatosis, atherosclerosis, WAT dysfunction) in obese Ldlr-/-.Leiden mice. High-fat diet (HFD)-fed obese mice underwent sham surgery or partial removal (~70%) of eWAT. A separate group of mice was kept on chow diet (control). Liver disease, atherosclerosis and three WAT depots were examined histologically, and WAT biopsies were also cultured ex vivo. Brain structure and function were monitored longitudinally using cognitive tests and neuroimaging, paralleled by histological analysis of brain pathology and hippocampal RNA-sequencing. In ex vivo WAT culture, the surgically removed eWAT portion secreted many adipokines and pro-inflammatory factors. Histological analyses at the end of the study showed that eWAT-lipectomy did not affect liver disease and atherosclerosis development, but reduced the number of severely hypertrophic adipocytes in the residual-eWAT. This was consistent with reduced secretion of adipokines (e.g., leptin, adiponectin) and pro-inflammatory mediators (e.g., PAI-1, MIP-1α/CCL3, IL-17) from the residual-eWAT in the ex vivo culturing experiments. Importantly, lipectomy alleviated HFD-induced adverse effects on hippocampal vasoreactivity, increased cortico-hippocampal (resting-state) functional connectivity and prevented the development of sedentary behavior. Lipectomy did not significantly affect histological neuroinflammation or circulating cytokines/chemokines, but increased specific free fatty acids (e.g., eicosatrienoic acid and docosahexaenoic acid, known to have anti-inflammatory and vaso-protective properties). Hence, partial eWAT lipectomy in mice with manifest obesity partly prevents hippocampal cerebrovascular disturbances, demonstrating a causal involvement of visceral WAT in obesity-associated brain impairments. The beneficial effects of eWAT lipectomy may, at least partly, be mediated by anti-inflammatory free fatty acids, and possible changes in release of adipokines and inflammatory mediators.

Indexed as

AdipokinesAdipose Tissue, WhiteEpididymisIntra-Abdominal FatObesityReceptors, LDLAnimalsDiet, High-FatHippocampusMaleMiceMice, KnockoutMice, ObeseAdipokinesReceptors, LDL

Identifiers

PMID41105609
PMCPMC12533877

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Registered trials

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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.