Evidence map›Paper›PMID 29996693›Full record

ArticleThe Journal of international medical research2018

Tetramethylpyrazine protects against high glucose-induced vascular smooth muscle cell injury through inhibiting the phosphorylation of JNK, p38MAPK, and ERK.

Yutao Liu, Xu Li, Shanling Jiang, Quanli Ge

Open access · goldAbstract read
In one paragraph

Article in The Journal of international medical research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
3.8field-weighted citation impact, top 8% 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

9 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Total Panax notoginseng saponin inhibits balloon injury-induced neointimal hyperplasia in rat carotid artery models by suppressing pERK/p38 MAPK pathways.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2020
    Article
  5. Skimmin Improves Insulin ResistanceFrontiers in pharmacology · 2020
    Article
  6. Article
  7. Article
  8. Article
  9. 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

4 authors at 3 institutions in 1 country.

Yutao Liu1 Department of Pharmacy, Yantaishan Hospital, Yantai, Shandong, China.
Xu Li2 Department of Pharmacy, Yantai Hospital of Infectious Diseases, Yantai, Shandong, China.
Shanling Jiang3 Department of Pharmacy, The Affiliated Yantai Yuhuangding Hospital, Qingdao University, Yantai, Shandong, China.
Quanli Ge1 Department of Pharmacy, Yantaishan Hospital, Yantai, Shandong, China.ORCID https://orcid.org/0000-0001-5455-0663
Yantaishan Hospital · CNQingdao University · CNYantai Infectious Diseases Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives High glucose-induced alterations in vascular smooth muscle cell behavior have not been fully characterized. We explored the protective mechanism of tetramethylpyrazine (TMP) on rat smooth muscle cell injury induced by high glucose via the mitogen-activated protein kinase (MAPK) signaling pathway. Methods Vascular smooth muscle cells (VSMCs) isolated from rat thoracic aortas were divided into control, high glucose (HG), and pre-hatching TMP groups. The effect of different glucose concentrations on cell viability and on the migration activity of VSMC cells was examined using MTT analysis and the wound scratch assay, respectively. Superoxide dismutase (SOD) and malondialdehyde (MDA) levels were measured using enzyme-linked immunoassays. The levels of extracellular signal-regulated kinase (ERK), c-Jun N-terminal kinase (JNK), and p38MAPK, and MAPK phosphorylation were assessed by western blotting. Results Cell proliferation was remarkably increased by increased glucose concentrations. Compared with the HG group, the migratory ability of VSMC cells was reduced in the presence of TMP. TMP also decreased the MDA content in the supernatant, but significantly increased the SOD activity. Western blotting showed that TMP inhibited the phosphorylation of JNK, p38MAPK, and ERK. Conclusions TMP appears to protect against HG-induced VSMC injury through inhibiting reactive oxygen species overproduction, and p38MAPK/JNK/ERK phosphorylation.

Indexed as

AnimalsAorta, ThoracicCells, CulturedExtracellular Signal-Regulated MAP KinasesGlucoseHyperglycemiaJNK Mitogen-Activated Protein KinasesMAP Kinase Signaling SystemMuscle, Smooth, VascularMuscular DiseasesMyocytes, Smooth Musclep38 Mitogen-Activated Protein KinasesPhosphorylationPyrazinesRatsSignal TransductionExtracellular Signal-Regulated MAP KinasesGlucoseJNK Mitogen-Activated Protein Kinasesp38 Mitogen-Activated Protein KinasesPyrazinestetramethylpyrazineVasodilator Agentshigh glucosep38MAPK signalingreactive oxygen speciesTetramethylpyrazinetraditional Chinese medicinevascular smooth muscle cells

Identifiers

PMID29996693
PMCPMC6134667
OpenAlexW2869164078

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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 OpenQuestion graph.