Evidence map›Paper›PMID 31025261›Full record

ArticleEndocrine2019

Phenotypic characterization of a novel type 2 diabetes animal model in a SHANXI MU colony of Chinese hamsters.

Lu Wang, Chenyang Wang, Ruihu Zhang, Yu Liu, Chunfang Wang, Guohua Song, Jingjing Yu, Zhaoyang Chen

Abstract read
PubMed Publisher
In one paragraph

Article in Endocrine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 28% of its field
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

6 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Bile acid metabolism in type 2 diabetes mellitus.Nature reviews. Endocrinology · 2025
    Review
  3. Review
  4. Article
  5. Review
  6. 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 at 1 institution in 1 country.

Lu WangLaboratory Animal Center of Shanxi Medical University, Shanxi Province, China.
Chenyang WangLaboratory Animal Center of Shanxi Medical University, Shanxi Province, China.
Ruihu ZhangLaboratory Animal Center of Shanxi Medical University, Shanxi Province, China.
Yu LiuDepartment of Pharmacology, Shanxi Medical University, Shanxi Province, China.
Chunfang WangLaboratory Animal Center of Shanxi Medical University, Shanxi Province, China.
Guohua SongLaboratory Animal Center of Shanxi Medical University, Shanxi Province, China.
Jingjing YuLaboratory Animal Center of Shanxi Medical University, Shanxi Province, China.
Zhaoyang ChenLaboratory Animal Center of Shanxi Medical University, Shanxi Province, China. ccytycn@163.com.ORCID 0000-0002-6811-6945
Shanxi Medical University · CN

Funding

Shanxi Medical University Youth Fund Project of China NO. 02201317Shanxi Province Experimental Animal Resources Service Platform of China NO. 201605D121019Shanxi Scholarship Council of China NO. 2015-054
6 · The paper itself

Abstract

purposeDeveloping animal models for human diseases is critical for studying complex diseases such as type 2 diabetes mellitus (T2DM). Since inbred colonies of Chinese hamsters tend toward spontaneous development of diabetes, we investigated them as a possible model.

methodsWe regarded individuals with fasting blood glucose (FBG) higher than 6.0 mmol/L and post-prandial blood glucose (PBG) higher than 7.0 mmol/L as diabetic based on the mean and 95% frequency distribution values of FBG and PBG. Diabetic hamsters were characterized based on metabolic profiles, histopathological features, and changes in the expression of genes involved in glucose and lipid metabolism.

resultsMetabolic analyses showed that diabetic hamsters exhibited mild hyperglycemia, hypertriglyceridemia, glucose intolerance, and insulin resistance. Histopathological analysis revealed that cell nuclei migrated inward in skeletal muscle and obvious partial liver lipid deposition and focal necrosis was found. We additionally observed mild injury, atrophy, and occasional vacuolization in islet cells. Changes in the expression of several genes related to glucose and lipid metabolism were observed. Decreased expression of adiponectin and GLUT4 and increased expression of PPARγ, Akt, and leptin was observed in skeletal muscle. Decreased expression of adiponectin with increased expression of PPARγ and leptin was observed in the liver.

conclusionsThese results indicate that we have established a spontaneous diabetic hamster line that closely mimics human T2DM, which may hold potential for further research on the pathogenesis and treatment of this disease.

Indexed as

CricetulusDisease Models, AnimalAnimalsBlood GlucoseCricetinaeDiabetes Mellitus, ExperimentalDiabetes Mellitus, Type 2FemaleGene Expression RegulationGlucose IntoleranceHumansInsulin ResistanceMalePhenotypeBlood GlucoseChinese hamsterDifferentially expressed genesGlucose intoleranceInsulin resistanceType 2 diabetes mellitus

Identifiers

PMID31025261
OpenAlexW2941320637

What Socratic holds

Textmetadata
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.