Evidence map›Paper›PMID 42099265›Full record

ArticleHistology and histopathology2026

Efficient sampling of liver tissue for histological analysis of rodent MASLD/MASH models.

Jenny Norlin, Sara T Hjuler, Kasper Almholt, Rikke K Kirk, Henning Hvid

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Article in Histology and histopathology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Jenny NorlinGlobal Research, Novo Nordisk A/S, Novo Nordisk Park, Maaloer, Denmark.
Sara T HjulerGlobal Research, Novo Nordisk A/S, Novo Nordisk Park, Maaloer, Denmark.
Kasper AlmholtGlobal Research, Novo Nordisk A/S, Novo Nordisk Park, Maaloer, Denmark.
Rikke K KirkGlobal Research, Novo Nordisk A/S, Novo Nordisk Park, Maaloer, Denmark.
Henning HvidGlobal Research, Novo Nordisk A/S, Novo Nordisk Park, Maaloer, Denmark. hhvd@novonordisk.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mouse and rat models of MASLD/MASH can provide valuable information about the effects of potential new treatments on liver histopathology. Liver samples for histology must therefore be representative of the entire organ, but it is also important that they can be collected efficiently. In rodent toxicity studies, it is recommended to collect samples for histopathology from the left lateral liver lobe (LLL), the right medial lobe (RML), and the caudate lobe (CL). Samples collected from multiple lobes provide a representative overview of the entire liver, but at the same time, increase the workload in the histology laboratory. The aim of the present study was to explore whether the number of histology samples per animal could be reduced and still provide the same information about treatment effects on quantitative histology endpoints. This was examined in different mouse and rat MASH models, where fibrosis (marker: picrosirius red), stellate-cell activation (marker: smooth muscle actin), and inflammation (marker: CD45) were quantified by image analysis of the three recommended liver lobes. Results determined in a single lobe, as well as combined analysis of the LLL and RML, revealed the same relative treatment effects as analysis of all three lobes combined. Results from single lobes tended to have slightly higher variation than results based on the analysis of three lobes, with the CL being the most variable. In conclusion, sampling of the LLL and/or the RML provides information about treatment effects comparable to sampling of three lobes and allows for efficient processing of histology samples in the laboratory.

Indexed as

LiverAnimalsDisease Models, AnimalMaleMiceRats

Identifiers

PMID42099265

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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.