Evidence map›Paper›PMID 42572445›Full record

ArticleDiabetes, obesity & metabolism2026

Systematic Comparison of High-Fat Diet- and Streptozotocin-Induced Prediabetic Obese C57BL/6J Mouse Models: A Sex-Based Protocol Optimization Study.

Min Xu, Chao Ke, Yangkun Liu, Wenying Shi, Yang Cao, Zhengyu Li, Yi Xiao, Wei Zhang

Abstract readComparative Study
In one paragraph

Article in Diabetes, obesity & metabolism, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

8 authors.

Min XuThe First Affiliated Hospital of Hunan University of Chinese Medicine, Changsha, Hunan, China.
Chao KeThe First Affiliated Hospital of Hunan University of Chinese Medicine, Changsha, Hunan, China.
Yangkun LiuThe First Affiliated Hospital of Hunan University of Chinese Medicine, Changsha, Hunan, China.
Wenying ShiThe First Affiliated Hospital of Hunan University of Chinese Medicine, Changsha, Hunan, China.
Yang CaoThe First Affiliated Hospital of Hunan University of Chinese Medicine, Changsha, Hunan, China.
Zhengyu LiThe First Affiliated Hospital of Hunan University of Chinese Medicine, Changsha, Hunan, China.
Yi XiaoThe First Affiliated Hospital of Hunan University of Chinese Medicine, Changsha, Hunan, China.
Wei ZhangThe First Affiliated Hospital of Hunan University of Chinese Medicine, Changsha, Hunan, China.ORCID https://orcid.org/0009-0000-6900-7209

Funding

National Administration of Traditional Chinese Medicine of the People's Republic of China 2019XZZX-ZJ007
6 · The paper itself

Abstract

aimsAnimal models of prediabetes (Pre-DM) are essential for studying metabolic disease and testing therapies, yet high-fat diet (HFD) and HFD-plus-streptozotocin (STZ) protocols vary in feeding duration, STZ dose, and diagnostic criteria and rarely account for sex. We compared five protocols in male and female C57BL/6J mice to find the best balance of duration, cost, and phenotypic stability and to characterize how HFD and HFD-STZ differ in their effects on glucose and lipid metabolism. MATERIALS AND

methodsFive-week-old mice were stratified by sex and assigned to three HFD-only groups (HFD-12w, -16w, -20w) and two STZ groups of differing cumulative dose (HFD-STZ-L, -H). Body weight, food and energy intake, body fat percentage, fasting blood glucose (FBG), OGTT, ITT, fasting insulin, serum lipids, hepatic Oil Red O, histopathology, liver and kidney safety, and per-animal cost were assessed.

resultsHFD induced obesity of equal magnitude in both sexes (non-significant Sex × Diet interactions for body weight and fat mass). Glucose and hepatic-lipid metabolism showed clear sex dimorphism: in males these deteriorated by Week 12, whereas females required 16 weeks to reach the Pre-DM threshold, at a higher preset STZ dose. HFD-STZ-L matched HFD-12w in both sexes within a shorter cycle (overall success 73.3%). Notably, STZ reversed the HFD lipid phenotype, synchronously reducing body fat, serum lipids, and hepatic fat in females.

conclusionsHFD-STZ-L is preferred for glucose and β-cell studies in both sexes; HFD-12w preserves the intact female obesity phenotype; HFD-20w is preferred for MASLD studies. Biological sex must be incorporated into model design and phenotype interpretation.

Indexed as

Diet, High-FatDisease Models, AnimalObesityPrediabetic StateStreptozocinAnimalsBlood GlucoseFemaleLipid MetabolismLiverMaleMiceMice, Inbred C57BLSex FactorsBlood GlucoseStreptozocinC57BL/6J miceglucose intolerancehigh‐fat dietinsulin resistanceMASLDmodel selectionobesityprediabetessex differencesstreptozotocin

Identifiers

PMID42572445
PMCPMC13646350

What Socratic holds

Textmetadata
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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.