Evidence map›Paper›PMID 39300303›Full record

ArticleHypertension research : official journal of the Japanese Society of Hypertension2024

Investigation of synergistic interaction of sinensetin, eupatorin, and 3'-hydroxy-5,6,7,4'-tetramethoxyflavone in vasodilation efficacy.

Mun Fei Yam, Wan Yin Tew, Chu Shan Tan, Qiyue Qiu, Ruixian Zhou, Xuye Wang, Yau Pin Yap, Wei Xu, Wen Xu, Lai Kuan Teh

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Article in Hypertension research : official journal of the Japanese Society of Hypertension, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

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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

1 citing paper in PubMed.

  1. 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.

Mun Fei YamCollege of Pharmacy, Fujian University of Traditional Chinese Medicine, Fuzhou, Fujian, China. yammunfei@yahoo.com.
Wan Yin TewDepartment of Pharmacology, School of Pharmaceutical Sciences, Universiti Sains Malaysia, Minden, Pulau Pinang, Malaysia.
Chu Shan TanMaterial Characterization and Inorganic Spectroscopy, Perkin Elmer Sdn Bhd, Wisma Academy, Petaling Jaya, Selangor, Malaysia.
Qiyue QiuDepartment of Pharmacology, School of Pharmaceutical Sciences, Universiti Sains Malaysia, Minden, Pulau Pinang, Malaysia.
Ruixian ZhouDepartment of Acupuncture and Moxibustion, Affiliated Hospital of Guizhou Medical University, Guiyang, China.
Xuye WangDepartment of Pharmacology, School of Pharmaceutical Sciences, Universiti Sains Malaysia, Minden, Pulau Pinang, Malaysia.
Yau Pin YapDepartment of Chinese Medicine, M Kandiah Faculty of Medicine & Health Sciences, Universiti Tunku Abdul Rahman, Kajang, Selangor, Malaysia.
Wei XuCollege of Pharmacy, Fujian University of Traditional Chinese Medicine, Fuzhou, Fujian, China.
Wen XuCollege of Pharmacy, Fujian University of Traditional Chinese Medicine, Fuzhou, Fujian, China. 2012029@fjtcm.edu.cn.
Lai Kuan TehDepartment of Allied Health Sciences, Faculty of Science, Universiti Tunku Abdul Rahman, Kampar, Perak, Malaysia. tehlk@utar.edu.my.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Modern medicines often follow a "single-compound, single-target" paradigm, which may not be effective against complex diseases with multifactorial causes. Medicinal plants, such as Orthosiphon stamineus-widely used in Southeast Asia for its significant vasodilatory and antihypertensive properties-offer an alternative. These effects are largely attributed to the synergistic actions of sinensetin, eupatorin, and 3'-hydroxy-5,6,7,4'- tetramethoxyflavone (TMF). The present study was designed to explore the interactions among these compounds and their collective impact on vasodilation. The current investigation utilized in vitro aortic ring assays and an orthogonal stimulus-response compatibility approach to unveil the synergistic interactions of sinensetin, eupatorin, and TMF in specific combination ratios within compatibility groups. The current results showed that G2, G7, G27, and G28 achieved vasodilatory efficacies exceeding 100%, with recorded efficacies of 190%, 148%, 117.6%, and 116.25%, respectively. Conversely, formulation F1 exhibited only additive effects with an efficacy of 88.02%. The dose-response study revealed G28 exhibited the strongest concentration-dependent vasodilatory responses, with a maximum response (R

Indexed as

Drug SynergismFlavonesFlavonoidsVasodilationVasodilator AgentsAnimalsMaleOrthosiphonRatsRats, Sprague-DawleyeupatorinFlavonesFlavonoidssinensetinVasodilator Agents3′-hydroxy-5,6,7,4′-tetramethoxyflavoneEupatorineOrthogonal stimulus-response compatibilitySinensetinVasodilation

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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.