Evidence mapPaperPMID 31011149Full record

ArticleMedical science monitor : international medical journal of experimental and clinical research2019

Effect of Cyclocarya Paliurus on Hypoglycemic Effect in Type 2 Diabetic Mice.

Lichun Zhao, Xue Wang, Junxiu Li, Xiaoming Tan, Lanlan Fan, Zhenwei Zhang, Jing Leng

Open access · hybridAbstract read
In one paragraph

Article in Medical science monitor : international medical journal of experimental and clinical research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 19% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 32 citations in OpenAlex.

  1. Effects ofFrontiers in nutrition · 2020
    Pooled it
  2. Trial
  3. Article
  4. Article
  5. Review
  6. Review
  7. Anti-Hyperglycemic Effects of Refined Fractions fromMolecules (Basel, Switzerland) · 2021
    Article
  8. Review
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 at 2 institutions in 1 country.

Lichun ZhaoCollege of Pharmacy, Guangxi University of Chinese Medicine, Nanning, Guangxi, China (mainland).
Xue WangCollege of Pharmacy, Guangxi University of Chinese Medicine, Nanning, Guangxi, China (mainland).
Junxiu LiCollege of Pharmacy, Guangxi University of Chinese Medicine, Nanning, Guangxi, China (mainland).
Xiaoming TanCollege of Pharmacy, Guangxi University of Chinese Medicine, Nanning, Guangxi, China (mainland).
Lanlan FanCollege of Pharmacy, Guangxi University of Chinese Medicine, Nanning, Guangxi, China (mainland).
Zhenwei ZhangCollege of Pharmacy, Guangxi University of Chinese Medicine, Nanning, Guangxi, China (mainland).
Jing LengCollege of Pharmacy, Guangxi University of Chinese Medicine, Nanning, Guangxi, China (mainland).
Guangxi University · CNGuangxi University of Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND The aim of this study was to assess the hypoglycemic effect of Cyclocarya paliurus extract (CPE) on diabetes mellitus (DM) mice. MATERIAL AND METHODS A DM mouse model was established to test FBG, TC, and TG. The DM mice were divided into 3 groups: a DM group, a DM+CPE (0.5 g/Kg) group, and a DM+CPE (1.0 g/Kg) group. The FBG and body weight were measured. The glucose tolerance ability was determined by OGTT test. FINS was measured to calculate ISI and IRI. Serum MDA, SOD, and GSH-Px levels were detected. NIT-1 cells were cultured in vitro and divided into 4 groups: a control group, a STZ group, a STZ+CPE (80 μg/mL) group, and a STZ+CPE (160 μg/mL) group. Cell apoptosis and ROS content were assessed by flow cytometry. Cell proliferation was detected by EdU staining. RESULTS Compared with the control group, FBG, TC, and TG were significantly increased in the DM group. CPE gavage obviously reduced FBG level, increased body weight, enhanced glucose tolerance, elevated FINS level and ISI, and reduced IRI, all in a dose-dependent manner. CPE gavage reduced serum MDA content and increased SOD and GSH-Px enzyme activities in DM mice. STZ markedly enhanced ROS production, induced apoptosis, and inhibited proliferation in NIT-1 cells. CPE treatment clearly reduced ROS production and apoptosis, enhanced cell proliferation, and alleviated STZ damage to NIT-1 cells. CONCLUSIONS CPE has the effects of decreasing blood glucose and insulin resistance, and enhancing glucose tolerance in DM mice, which may be related to its effects of reducing oxidation and reduced apoptosis, and relieving STZ in pancreatic beta cell injury.

Indexed as

AnimalsAntioxidantsBlood GlucoseCholesterolDiabetes Mellitus, ExperimentalDiabetes Mellitus, Type 2Disease Models, AnimalFemaleHypoglycemic AgentsInsulinInsulin ResistanceInsulin-Secreting CellsJuglandaceaeLipid MetabolismLiverMaleAntioxidantsBlood GlucoseCholesterolHypoglycemic AgentsInsulinPlant ExtractsTriglycerides

Identifiers

PMID31011149
PMCPMC6492607
OpenAlexW2942179360

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.