Evidence map›Paper›PMID 27689971›Full record

ArticleMolecules (Basel, Switzerland)2016

Glycyrrhizic Acid Reduces Heart Rate and Blood Pressure by a Dual Mechanism.

Kailash Singh, Aung Moe Zaw, Revathi Sekar, Ahuja Palak, Ahmed A Allam, Jamaan Ajarem, Billy K C Chow

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2016. 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
0.9field-weighted citation impact, top 20% 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, 16 citations in OpenAlex.

  1. Review
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  6. Propranolol suppresses gastric cancer cell growth by regulating proliferation and apoptosis.Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association · 2021
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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

7 authors at 3 institutions in 3 countries.

Kailash SinghSchool of Biological Sciences, The University of Hong Kong, Pokfulam Road, Hong Kong SAR, China. kailash@connect.hku.hk.
Aung Moe ZawSchool of Biological Sciences, The University of Hong Kong, Pokfulam Road, Hong Kong SAR, China. moezaw@connect.hku.hk.
Revathi SekarSchool of Biological Sciences, The University of Hong Kong, Pokfulam Road, Hong Kong SAR, China. revathis@hku.hk.
Ahuja PalakSchool of Biological Sciences, The University of Hong Kong, Pokfulam Road, Hong Kong SAR, China. palak@hku.hk.
Ahmed A AllamDepartment of Zoology, College of Science, King Saud University, Riyadh 11451, Saudi Arabia. aallam@ksu.edu.sa.
Jamaan AjaremDepartment of Zoology, College of Science, King Saud University, Riyadh 11451, Saudi Arabia. jajarem@KSU.EDU.SA.
Billy K C ChowSchool of Biological Sciences, The University of Hong Kong, Pokfulam Road, Hong Kong SAR, China. bkcc@hku.hk.
University of Hong Kong · HKBeni-Suef University · EGKing Saud University · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Beta adrenergic receptors are crucial for their role in rhythmic contraction of heart along with their role in the pathological conditions such as tachycardia and high risk of heart failure. Studies report that the levels of beta-1 adrenergic receptor tend to decrease by 50%, whereas, the levels of beta-2 adrenergic receptor remains constant during the risk of heart failure. Beta blockers-the antagonistic molecules for beta-adrenergic receptors, function by slowing the heart rate, which thereby allows the left ventricle to fill completely during tachycardia incidents and hence helps in blood pumping capacity of heart and reducing the risk of heart failure. In the present study, we investigate the potential of glycyrrhizic acid (GA) as a possible principal drug molecule for cardiac arrhythmias owing to its ability to induce reduction in the heart rate and blood pressure. We use in vitro and in silico approach to study GA's effect on beta adrenergic receptor along with an in vivo study to examine its effect on heart rate and blood pressure. Additionally, we explore GA's proficiency in eliciting an increase in the plasma levels of vasoactive intestinal peptide, which by dilating the blood vessel consequently, can be a crucial aid during the occurrence of a potential heart attack. Therefore, we propose GA as a potential principal drug molecule via its potential in modulating heart rate and blood pressure.

Indexed as

adrenergic receptorsglycyrrhizic acidtachycardiavasoactive-intestinal peptide

Identifiers

PMID27689971
PMCPMC6274536
OpenAlexW2525313554

What OpenQuestion holds

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LicenceCC BY
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.