Evidence map›Paper›PMID 24810608›Full record

ArticlePloS one2014

Add-on effect of probucol in atherosclerotic, cholesterol-fed rabbits treated with atorvastatin.

Yuka Keyamura, Chifumi Nagano, Masayuki Kohashi, Manabu Niimi, Masanori Nozako, Takashi Koyama, Reiko Yasufuku, Ayako Imaizumi, Hiroyuki Itabe, Tomohiro Yoshikawa

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. 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
1.5field-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

6 citing papers in PubMed, 18 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Article
  6. 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

10 authors at 2 institutions in 1 country.

Yuka KeyamuraFree Radical Research Project, Otsuka Pharmaceutical Co., Ltd., Tokushima, Japan; Division of Biological Chemistry, Department of Molecular Biology, Showa University School of Pharmacy, Tokyo, Japan.
Chifumi NaganoFree Radical Research Project, Otsuka Pharmaceutical Co., Ltd., Tokushima, Japan.
Masayuki KohashiFree Radical Research Project, Otsuka Pharmaceutical Co., Ltd., Tokushima, Japan.
Manabu NiimiFree Radical Research Project, Otsuka Pharmaceutical Co., Ltd., Tokushima, Japan.
Masanori NozakoFree Radical Research Project, Otsuka Pharmaceutical Co., Ltd., Tokushima, Japan.
Takashi KoyamaFree Radical Research Project, Otsuka Pharmaceutical Co., Ltd., Tokushima, Japan.
Reiko YasufukuFree Radical Research Project, Otsuka Pharmaceutical Co., Ltd., Tokushima, Japan.
Ayako ImaizumiFree Radical Research Project, Otsuka Pharmaceutical Co., Ltd., Tokushima, Japan.
Hiroyuki ItabeDivision of Biological Chemistry, Department of Molecular Biology, Showa University School of Pharmacy, Tokyo, Japan.
Tomohiro YoshikawaFree Radical Research Project, Otsuka Pharmaceutical Co., Ltd., Tokushima, Japan.
Otsuka (Japan) · JPShowa University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveLowering the blood concentration of low-density lipoprotein (LDL) cholesterol is the primary strategy employed in treating atherosclerotic disorders; however, most commonly prescribed statins prevent cardiovascular events in just 30% to 40% of treated patients. Therefore, additional treatment is required for patients in whom statins have been ineffective. In this study of atherosclerosis in rabbits, we examined the effect of probucol, a lipid-lowering drug with potent antioxidative effects, added to treatment with atorvastatin. METHODS AND

resultsAtherosclerosis was induced by feeding rabbits chow containing 0.5% cholesterol for 8 weeks. Probucol 0.1%, atorvastatin 0.001%, and atorvastatin 0.003% were administered solely or in combination for 6 weeks, beginning 2 weeks after the start of atherosclerosis induction. Atorvastatin decreased the plasma concentration of non-high-density lipoprotein cholesterol (non-HDLC) dose-dependently; atorvastatin 0.003% decreased the plasma concentration of non-HDLC by 25% and the area of atherosclerotic lesions by 21%. Probucol decreased the plasma concentration of non-HDLC to the same extent as atorvastatin (i.e., by 22%) and the area of atherosclerotic lesions by 41%. Probucol with 0.003% atorvastatin decreased the plasma concentration of non-HDLC by 38% and the area of atherosclerotic lesions by 61%. Co-administration of probucol with atorvastatin did not affect the antioxidative effects of probucol, which were not evident on treatment with atorvastatin alone, such as prevention of in vitro LDL-oxidation, increase in paraoxonase-1 activity of HDL, and decreases in plasma and plaque levels of oxidized-LDL in vivo.

conclusionsProbucol has significant add-on anti-atherosclerotic effects when combined with atorvastatin treatment; suggesting that this combination might be beneficial for treatment of atherosclerosis.

Indexed as

AnimalsAnticholesteremic AgentsAntioxidantsAtherosclerosisAtorvastatinBiomarkersCholesterolC-Reactive ProteinDrug SynergismHeptanoic AcidsProbucolPyrrolesRabbitsAnticholesteremic AgentsAntioxidantsAtorvastatinBiomarkersCholesterolC-Reactive ProteinHeptanoic AcidsProbucolPyrroles

Identifiers

PMID24810608
PMCPMC4014602
OpenAlexW2091656297

What OpenQuestion holds

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Registered trials

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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.