Evidence map›Paper›PMID 42749977›Full record

ArticleGeroScience2026

Age-dependent changes in lipid droplet distribution and vascularization in naked mole rat vs. mouse hippocampus.

Liv S Krogstad, Markus Augustin Teppen, Harald S Mjønes, Jonathan R Brewer, Thomas Park, Samuel Geiseler, Cecilie Morland

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Article in GeroScience, 2026. 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

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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

7 authors.

Liv S KrogstadSection for Pharmacology, and Pharmaceutical Biosciences, Department of Pharmacy, The Faculty of Mathematics and Natural Sciences, University of Oslo, Blindern 0316, Oslo, 1068, Norway.ORCID http://orcid.org/0000-0002-5312-6526
Markus Augustin TeppenSection for Pharmacology, and Pharmaceutical Biosciences, Department of Pharmacy, The Faculty of Mathematics and Natural Sciences, University of Oslo, Blindern 0316, Oslo, 1068, Norway.ORCID http://orcid.org/0009-0007-6239-8092
Harald S MjønesSection for Pharmacology, and Pharmaceutical Biosciences, Department of Pharmacy, The Faculty of Mathematics and Natural Sciences, University of Oslo, Blindern 0316, Oslo, 1068, Norway.ORCID http://orcid.org/0009-0003-6638-0675
Jonathan R BrewerDepartment of Biochemistry and Molecular Biology, University of Southern Denmark, Odense, Denmark.ORCID http://orcid.org/0000-0002-3444-1715
Thomas ParkDepartment of Biological Sciences, University of Illinois Chicago, 840 W Taylor St, Chicago, IL, 60607, USA.ORCID http://orcid.org/0000-0002-2447-2948
Samuel Geiseler *Section for Pharmacology, and Pharmaceutical Biosciences, Department of Pharmacy, The Faculty of Mathematics and Natural Sciences, University of Oslo, Blindern 0316, Oslo, 1068, Norway.ORCID http://orcid.org/0000-0002-1332-3816
Cecilie Morland *Section for Pharmacology, and Pharmaceutical Biosciences, Department of Pharmacy, The Faculty of Mathematics and Natural Sciences, University of Oslo, Blindern 0316, Oslo, 1068, Norway. Cecilie.morland@farmasi.uio.no.ORCID http://orcid.org/0000-0002-1776-1821

Funding

National Science Foundation 2201647
6 · The paper itself

Abstract

The accumulation of lipid droplets in microglia has been reported to increase in response to ageing and age-related diseases like Alzheimer's disease. The present study investigates changes in lipid droplet dynamics with increasing age in the mouse and the similarly sized long-lived rodent, the naked mole rat (Heterocephalus glaber). We show that the naked mole rat contains large amounts of microglial lipid droplets in the CA1 and CA3 region of the hippocampus with an age-dependent increase in the CA3 region. Neuronal lipid droplet size is unaffected by age in the naked mole rat. The mouse hippocampus contains fewer microglial lipid droplets and shows no age-dependent change. However, neuronal lipid droplet size increases with age in the CA3 region in mice. These results could indicate two different ways of regulating lipid accumulation in the brain, where the naked mole rat shuttles their lipids from neurons to microglia to prevent neuronal lipotoxicity and neurodegeneration, while this does not seem to happen in mice. This shuttling of lipids between cells could be a protective mechanism contributing to the high resilience against diseases and damages to the brain seen in the naked mole rat. Additionally, we show that the brain of the naked mole rat has a lower vascularization than the mouse in the dentate hilus, stratum radiatum, and sensory/motor cortex. This could be coupled to the naked mole rats' low metabolism and conforms with its ability to live with low concentrations of oxygen without damage to the brain.

Indexed as

AgeingConfocal microscopyHippocampusLipid dropletMicrogliaNaked mole ratVascularization

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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.