Evidence map›Paper›PMID 26838069›Full record

ArticleActa pharmacologica Sinica2016

Ophiopogonin D maintains Ca2+ homeostasis in rat cardiomyocytes in vitro by upregulating CYP2J3/EETs and suppressing ER stress.

Wen-ting You, Tao Zhou, Zeng-chun Ma, Qian-de Liang, Cheng-rong Xiao, Xiang-lin Tang, Hong-ling Tan, Bo-li Zhang, Yu-guang Wang, Yue Gao

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Acta pharmacologica Sinica, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.5field-weighted citation impact, top 13% 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

18 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
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  5. Differential lipid signaling from CD4Frontiers in immunology · 2024
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  13. Liriopogons (GeneraFrontiers in pharmacology · 2021
    Review
  14. Article
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  16. Review
  17. Review
  18. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 1 country.

Wen-ting YouDepartment of Pharmacology, Anhui Medical University, Hefei 230032, China.
Tao ZhouDepartment of Pharmacology and Toxicology, Beijing Institute of Radiation Medicine, Beijing 100850, China.
Zeng-chun MaDepartment of Pharmacology and Toxicology, Beijing Institute of Radiation Medicine, Beijing 100850, China.
Qian-de LiangDepartment of Pharmacology and Toxicology, Beijing Institute of Radiation Medicine, Beijing 100850, China.
Cheng-rong XiaoDepartment of Pharmacology and Toxicology, Beijing Institute of Radiation Medicine, Beijing 100850, China.
Xiang-lin TangDepartment of Pharmacology and Toxicology, Beijing Institute of Radiation Medicine, Beijing 100850, China.
Hong-ling TanDepartment of Pharmacology and Toxicology, Beijing Institute of Radiation Medicine, Beijing 100850, China.
Bo-li ZhangTianjin University of Traditional Chinese Medicine, Tianjin 300193, China.
Yu-guang WangDepartment of Pharmacology and Toxicology, Beijing Institute of Radiation Medicine, Beijing 100850, China.
Yue GaoDepartment of Pharmacology and Toxicology, Beijing Institute of Radiation Medicine, Beijing 100850, China.
Beijing Radiation Center · CNAnhui Medical University · CNGuangxi Medical University · CNTianjin University of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimCYP2J3 in myocardium metabolizes arachidonic acid to 4 regioisomeric epoxyeicosatrienoic acids (EETs), which have diverse biological activities in rat heart. In this study we examined whether CYP2J3 was involved in cardioprotective effects of ophiopogonin D (OPD), a steroidal glycoside isolated from Chinese herb Radix ophiopogonis.

methodsRat cardiomyoblast cell line (H9c2 cells) was tested. Intracellular Ca(2+) concentrations ([Ca(2+)]i) were measured using Fluo-4/AM. The expression of calcium-regulating molecules and ER stress signaling molecules was measured with qRT-PCR and Western blot analyses. Cell apoptosis was quantified with Hoechst 33258 staining and TUNEL assay. The level of 14,15-DHET, a stable metabolite of 14,15-EET, was assessed with ELISA.

resultsAngiotensin II (10(-6) mol/L) significantly decreased the expression of calcium-regulating molecules (SERCA2a, PLB, RyR2 and FKBP12.6), and elevated [Ca(2+)]i in H9c2 cells. Furthermore, angiotensin II markedly increased the expression of ER stress signaling molecules (GRP78, CHOP, p-JNK and cleaved caspase-12) and ER stress-mediated apoptosis. OPD (100, 250 and 500 nmol/L) dose-dependently increased CYP2J3 expression and 14,15-DHET levels in normal H9c2 cells. Pretreatment of H9c2 cells with OPD suppressed angiotensin II-induced abnormalities in Ca(2+) homeostasis, ER stress responses and apoptosis. Overexpression of CYP2J3 or addition of exogenous 14,15-EET also prevented angiotensin II-induced abnormalities in Ca(2+) homeostasis, whereas transfection with CYP2J3 siRNA diminished the effects of OPD on Ca(2+) homeostasis. Furthermore, the intracellular Ca(2+) chelator BAPTA suppressed angiotensin II-induced ER stress responses and apoptosis in H9c2 cells.

conclusionOPD is a novel CYP2J3 inducer that may offer a therapeutic benefit in treatment of cardiovascular diseases related to disturbance of Ca(2+) homeostasis and ER stress.

Indexed as

AnimalsApoptosisCalciumCardiotonic AgentsCell LineCytochrome P-450 Enzyme SystemEndoplasmic Reticulum StressHomeostasisMyocytes, CardiacRatsSaponinsSpirostansUp-RegulationCalciumCardiotonic AgentsCyp2j3 protein, ratCytochrome P-450 Enzyme Systemophiopogonin DSaponinsSpirostans

Identifiers

PMID26838069
PMCPMC4775850
OpenAlexW2320955057

What OpenQuestion 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 OpenQuestion graph.