Evidence map›Paper›PMID 25009703›Full record

ArticleBiomolecules & therapeutics2014

Cordycepin-Enriched WIB801C from Cordyceps militaris Inhibits Collagen-Induced [Ca(2+)]i Mobilization via cAMP-Dependent Phosphorylation of Inositol 1, 4, 5-Trisphosphate Receptor in Human Platelets.

Dong-Ha Lee, Hyun-Hong Kim, Hyun-Jeong Cho, Young-Bin Yu, Hyo-Chan Kang, Jong-Lae Kim, Jong-Jin Lee, Hwa-Jin Park

Abstract read
In one paragraph

Article in Biomolecules & therapeutics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.3field-weighted citation impact, top 14% 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

7 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Anticancer Efficacy ofEvidence-based complementary and alternative medicine : eCAM · 2017
    Article
  5. Article
  6. Article
  7. 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 4 institutions in 1 country.

Dong-Ha LeeDepartment of Biomedical Laboratory Science, College of Biomedical Science and Engineering, Inje University, Gimhae 621-749.
Hyun-Hong KimDepartment of Biomedical Laboratory Science, College of Biomedical Science and Engineering, Inje University, Gimhae 621-749.
Hyun-Jeong ChoDepartment of Biomedical Laboratory Science, College of Medical Science, Konyang University, Daejeon 302-718.
Young-Bin YuDepartment of Biomedical Laboratory Science, College of Medical Science, Konyang University, Daejeon 302-718.
Hyo-Chan KangDepartment of Medical Laboratory Science, Dong-Eui Institute of Technology, Busan 614-715.
Jong-Lae KimBioscience & Biotechnology Team, Central Research Center, Whanin Pharm. Co., Ltd., Suwon 443-766, Republic of Korea.
Jong-Jin LeeBioscience & Biotechnology Team, Central Research Center, Whanin Pharm. Co., Ltd., Suwon 443-766, Republic of Korea.
Hwa-Jin ParkDepartment of Biomedical Laboratory Science, College of Biomedical Science and Engineering, Inje University, Gimhae 621-749.
Inje University · KRDong Wha Pharm (South Korea) · KRKonyang University · KRDong-Eui University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this study, we prepared cordycepin-enriched (CE)-WIB801C, a n-butanol extract of Cordyceps militaris-hypha, and investigated the effect of CE-WIB801C on collagen-induced human platelet aggregation. CE-WIB801C dose-dependently inhibited collagen-induced platelet aggregation, and its IC50 value was 175 μg/ml. CE-WIB801C increased cAMP level more than cGMP level, but inhibited collagen-elevated [Ca(2+)]i mobilization and thromboxane A2 (TXA2) production. cAMP-dependent protein kinase (A-kinase) inhibitor Rp-8-Br-cAMPS increased the CE-WIB801C-downregulated [Ca(2+)]i level in a dose dependent manner, and strongly inhibited CE-WIB801C-induced inositol 1, 4, 5-trisphosphate receptor (IP3R) phosphorylation. These results suggest that the inhibition of [Ca(2+)]i mobilization by CE-WIB801C is resulted from the cAMP/A-kinase-dependent phosphorylation of IP3R. CE-WIB801C suppressed TXA2 production, but did not inhibit the activities of cyclooxygenase-1 (COX-1) and TXA2 synthase (TXAS). These results suggest that the inhibition of TXA2 production by WIB801C is not resulted from the direct inhibition of COX-1 and TXAS. In this study, we demonstrate that CE-WIB801C with cAMP-dependent Ca(2+)-antagonistic antiplatelet effects may have preventive or therapeutic potential for platelet aggregation-mediated diseases, such as thrombosis, myocardial infarction, atherosclerosis, and ischemic cerebrovascular disease.

Indexed as

Ca2+cAMPCE-WIB801CIP3RTXA2

Identifiers

PMID25009703
PMCPMC4060073
OpenAlexW1988952685

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.