Evidence map›Paper›PMID 25409881›Full record

ArticleBritish journal of pharmacology2015

Nuciferine relaxes rat mesenteric arteries through endothelium-dependent and -independent mechanisms.

Xinfeng Wang, Wai San Cheang, Haixia Yang, Lei Xiao, Baochang Lai, Meiqian Zhang, Jiahua Ni, Zhenyu Luo, Zihui Zhang, Yu Huang and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in British journal of pharmacology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

23 citing papers in PubMed, 48 citations in OpenAlex.

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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

11 authors at 3 institutions in 1 country.

Xinfeng WangCardiovascular Research Center, Xi'an Jiaotong University, Xi'an, China.
Wai San CheangInstitute of Vascular Medicine, School of Biomedical Sciences, Chinese University of Hong Kong, Hong Kong, China.
Haixia YangCardiovascular Research Center, Xi'an Jiaotong University, Xi'an, China.
Lei XiaoCardiovascular Research Center, Xi'an Jiaotong University, Xi'an, China.
Baochang LaiCardiovascular Research Center, Xi'an Jiaotong University, Xi'an, China.
Meiqian ZhangCardiovascular Research Center, Xi'an Jiaotong University, Xi'an, China.
Jiahua NiCardiovascular Research Center, Xi'an Jiaotong University, Xi'an, China.
Zhenyu LuoCardiovascular Research Center, Xi'an Jiaotong University, Xi'an, China.
Zihui ZhangCardiovascular Research Center, Xi'an Jiaotong University, Xi'an, China.
Yu HuangInstitute of Vascular Medicine, School of Biomedical Sciences, Chinese University of Hong Kong, Hong Kong, China.
Nanping WangCardiovascular Research Center, Xi'an Jiaotong University, Xi'an, China.
Xi'an Jiaotong University · CNChinese University of Hong Kong · CNPeking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeNuciferine, a constituent of lotus leaf, is an aromatic ring-containing alkaloid, with antioxidative properties. We hypothesize nuciferine might affect vascular reactivity. This study aimed at determining the effects of nuciferine on vasomotor tone and the underlying mechanism EXPERIMENTAL APPROACH: Nuciferine-induced relaxations in rings of rat main mesenteric arteries were measured by wire myographs. Endothelial NOS (eNOS) was determined by immunoblotting. Intracellular NO production in HUVECs and Ca(2+) level in both HUVECs and vascular smooth muscle cells (VSMCs) from rat mesenteric arteries were assessed by fluorescence imaging. KEY

resultsNuciferine induced relaxations in arterial segments pre-contracted by KCl or phenylephrine. Nuciferine-elicited arterial relaxations were reduced by removal of endothelium or by pretreatment with the eNOS inhibitor L-NAME or the NO-sensitive guanylyl cyclase inhibitor ODQ. In HUVECs, the phosphorylation of eNOS at Ser(1177) and increase in cytosolic NO level induced by nuciferine were mediated by extracellular Ca(2+) influx. Under endothelium-free conditions, nuciferine attenuated CaCl2-induced contraction in Ca(2+)-free depolarizing medium. In the absence of extracellular calcium, nuciferine relieved the vasoconstriction induced by phenylephrine and the addition of CaCl2. Nuciferine also suppressed Ca(2+) influx in Ca(2+)-free K(+)-containing solution in VSMCs. CONCLUSIONS AND IMPLICATIONS: Nuciferine has a vasorelaxant effect via both endothelium-dependent and -independent mechanisms. These results suggest that nuciferine may have a therapeutic effect on vascular diseases associated with aberrant vasoconstriction.

Indexed as

AnimalsAporphinesCalciumDose-Response Relationship, DrugEndothelium, VascularFemaleHumansHuman Umbilical Vein Endothelial CellsMesenteric ArteriesMuscle, Smooth, VascularNitric Oxide Synthase Type IIIRatsRats, Sprague-DawleyStructure-Activity RelationshipVasoconstrictionVasodilationAporphinesCalciumNitric Oxide Synthase Type IIInuciferineVasodilator Agents

Identifiers

PMID25409881
PMCPMC4667864
OpenAlexW2153177750

What OpenQuestion holds

Textmetadata
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.