Evidence map›Paper›PMID 24800210›Full record

ArticleBioMed research international2014

Characterization of imidazoline receptors in blood vessels for the development of antihypertensive agents.

Mei-Fen Chen, Jo-Ting Tsai, Li-Jen Chen, Tung-Pi Wu, Jia-Jang Yang, Li-Te Yin, Yu-Lin Yang, Tai-An Chiang, Han-Lin Lu, Ming-Chang Wu

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 22% 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, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
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  3. Article
  4. Article
  5. Article
  6. 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

10 authors at 5 institutions in 1 country.

Mei-Fen ChenDepartment of Food Science, National Pingtung University of Science and Technology, Neipu, Pingtung 91201, Taiwan ; College of Medicine and Life Science, Chung Hwa University of Medical Technology, Rende District, Tainan City 71703, Taiwan.
Jo-Ting TsaiDepartment of Radiation Oncology, Taipei Medical University-Shuang Ho Hospital, and College of Medicine, Taipei Medical University, Taipei City 10361, Taiwan.ORCID 0000-0001-7745-1131
Li-Jen ChenInstitute of Basic Medical Sciences, College of Medicine, National Cheng Kung University, Tainan City 70101, Taiwan.
Tung-Pi WuDepartment of Obs/Gyn, Tainan Sin-Lau Hospital, The Presbyterian Church in Taiwan, Tainan City 70142, Taiwan.
Jia-Jang YangCollege of Medicine and Life Science, Chung Hwa University of Medical Technology, Rende District, Tainan City 71703, Taiwan.
Li-Te YinCollege of Medicine and Life Science, Chung Hwa University of Medical Technology, Rende District, Tainan City 71703, Taiwan.
Yu-Lin YangCollege of Medicine and Life Science, Chung Hwa University of Medical Technology, Rende District, Tainan City 71703, Taiwan.
Tai-An ChiangCollege of Medicine and Life Science, Chung Hwa University of Medical Technology, Rende District, Tainan City 71703, Taiwan.
Han-Lin LuDepartment of Chinese Medicine, Tainan Sin-Lau Hospital, The Presbyterian Church in Taiwan, Tainan City 70142, Taiwan.
Ming-Chang WuDepartment of Food Science, National Pingtung University of Science and Technology, Neipu, Pingtung 91201, Taiwan.
Chung Hwa University of Medical Technology · TWSin-Lau Christian Hospital · TWNational Cheng Kung University · TWNational Pingtung University of Science and Technology · TWTaipei Medical University-Shuang Ho Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It has been indicated that activation of peripheral imidazoline I2-receptor (I-2R) may reduce the blood pressure in spontaneously hypertensive rats (SHRs). Also, guanidinium derivatives show the ability to activate imidazoline receptors. Thus, it is of special interest to characterize the I-2R using guanidinium derivatives in blood vessels for development of antihypertensive agent(s). Six guanidinium derivatives including agmatine, amiloride, aminoguanidine, allantoin, canavanine, and metformin were applied in this study. Western blot analysis was used for detecting the expression of imidazoline receptor in tissues of Wistar rats. The isometric tension of aortic rings isolated from male rats was also estimated. The expression of imidazoline receptor on rat aorta was identified. However, guanidinium derivatives for detection of aortic relaxation were not observed except agmatine and amiloride which induced a marked relaxation in isolated aortic rings precontracted with phenylephrine or KCl. Both relaxations induced by agmatine and amiloride were attenuated by glibenclamide at concentration enough to block ATP-sensitive potassium (KATP) channels. Meanwhile, only agmatine-induced relaxation was abolished by BU224, a selective antagonist of imidazoline I2-receptors. Taken together, we suggest that agmatine can induce vascular relaxation through activation of peripheral imidazoline I2-receptor to open KATP channels. Thus, agmatine-like compound has the potential to develop as a new therapeutic agent for hypertension in the future.

Indexed as

AnimalsAntihypertensive AgentsAortaGuanidineHypertensionImidazoline ReceptorsMaleRatsRats, WistarTissue DistributionTreatment OutcomeVasodilationAntihypertensive AgentsGuanidineImidazoline Receptors

Identifiers

PMID24800210
PMCPMC3996295
OpenAlexW2109693245

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.