Evidence map›Paper›PMID 21913902›Full record

ArticleBritish journal of pharmacology2012

Inhibitory effect of bufalin and cinobufagin on steroidogenesis via the activation of ERK in human adrenocortical cells.

Mei-Mei Kau, Jiing-Rong Wang, Shiow-Chwen Tsai, Ching-Han Yu, Paulus S Wang

Open access · bronzeAbstract read
In one paragraph

Article in British journal of pharmacology, 2012. 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
0.4field-weighted citation impact, top 37% 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, 19 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

5 authors at 3 institutions in 1 country.

Mei-Mei KauCenter of General Education, National Taipei University of Nursing and Health Sciences, Taipei, TaiwanDepartment of Pathology and Laboratory Medicine, Shin Kong Wu Ho-Su Memorial Hospital, Taipei, TaiwanGraduate Institute of Transition and Leisure Education for Individuals with Disabilities, Taipei Physical Education College, Taipei, TaiwanDepartment of Physiology, School of Medicine, Chung Shan Medical University, Taichung, TaiwanDepartment of Physiology, School of Medicine, National Yang-Ming University, Taipei, Taiwan.
Jiing-Rong WangCenter of General Education, National Taipei University of Nursing and Health Sciences, Taipei, TaiwanDepartment of Pathology and Laboratory Medicine, Shin Kong Wu Ho-Su Memorial Hospital, Taipei, TaiwanGraduate Institute of Transition and Leisure Education for Individuals with Disabilities, Taipei Physical Education College, Taipei, TaiwanDepartment of Physiology, School of Medicine, Chung Shan Medical University, Taichung, TaiwanDepartment of Physiology, School of Medicine, National Yang-Ming University, Taipei, Taiwan.
Shiow-Chwen TsaiCenter of General Education, National Taipei University of Nursing and Health Sciences, Taipei, TaiwanDepartment of Pathology and Laboratory Medicine, Shin Kong Wu Ho-Su Memorial Hospital, Taipei, TaiwanGraduate Institute of Transition and Leisure Education for Individuals with Disabilities, Taipei Physical Education College, Taipei, TaiwanDepartment of Physiology, School of Medicine, Chung Shan Medical University, Taichung, TaiwanDepartment of Physiology, School of Medicine, National Yang-Ming University, Taipei, Taiwan.
Ching-Han YuCenter of General Education, National Taipei University of Nursing and Health Sciences, Taipei, TaiwanDepartment of Pathology and Laboratory Medicine, Shin Kong Wu Ho-Su Memorial Hospital, Taipei, TaiwanGraduate Institute of Transition and Leisure Education for Individuals with Disabilities, Taipei Physical Education College, Taipei, TaiwanDepartment of Physiology, School of Medicine, Chung Shan Medical University, Taichung, TaiwanDepartment of Physiology, School of Medicine, National Yang-Ming University, Taipei, Taiwan.
Paulus S WangCenter of General Education, National Taipei University of Nursing and Health Sciences, Taipei, TaiwanDepartment of Pathology and Laboratory Medicine, Shin Kong Wu Ho-Su Memorial Hospital, Taipei, TaiwanGraduate Institute of Transition and Leisure Education for Individuals with Disabilities, Taipei Physical Education College, Taipei, TaiwanDepartment of Physiology, School of Medicine, Chung Shan Medical University, Taichung, TaiwanDepartment of Physiology, School of Medicine, National Yang-Ming University, Taipei, Taiwan.
Chung Shan Medical University · TWNational Taipei University of Nursing and Health Science · TWNational Yang Ming Chiao Tung University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeBufalin and cinobufagin exhibit cardiotonic and natriuretic activities. The aim of this study was to evaluate the effects of bufalin and cinobufagin on aldosterone and cortisol secretion and their mechanisms of action in human adrenocortical cells (NCI-H295). EXPERIMENTAL APPROACH: H295 cells were incubated with bufalin or cinobufagin in the presence or absence of angiotensin II (Ang II), forskolin, 8-Br-cAMP, corticosterone or deoxycortisol. The role of ERK1/2 was studied by use of the inhibitor of MEK (U0126). The binding of transcription factor steroidogenic factor 1 (SF-1) to steroidogenic acute regulatory (StAR) gene promoter was analysed by EMSA. KEY

resultsBufalin and cinobufagin markedly inhibited basal, Ang II-, forskolin- or 8-Br-cAMP-stimulated aldosterone and cortisol secretion, and the conversions of corticosterone to aldosterone and deoxycortisol to cortisol. Bufalin and cinobufagin also inhibited StAR protein expression and SF-1 binding to StAR gene promoter. They both increased phosphorylation of ERK1/2, and U0126 fully abolished these effects on ERK1/2 in H295 cells. Furthermore, U0126 reversed the inhibitory effects of bufalin and cinobufagin on StAR protein expression and the binding of SF-1 to StAR gene promoter. However, U0126 did not completely reverse their inhibitory effects on aldosterone and cortisol release. CONCLUSIONS AND IMPLICATIONS: The inhibitory effects of bufalin and cinobufagin on steroidogenesis of aldosterone and cortisol were associated with inhibition of aldosterone synthase and 11β-hydroxylase, as well as the suppression of StAR protein expression and SF-1 binding to StAR promoter via the phosphorylation of ERK1/2 in H295 cells.

Indexed as

Adrenal CortexAldosteroneAngiotensin IIBufanolidesButadienesCardiotonic AgentsCell LineCholesterol Side-Chain Cleavage EnzymeCorticosteroneEnzyme InhibitorsHumansHydrocortisoneMAP Kinase Signaling SystemMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3NitrilesAldosteroneAngiotensin IIbufalinBufanolidesButadienesCardiotonic AgentsCholesterol Side-Chain Cleavage EnzymecinobufaginCorticosteroneEnzyme InhibitorsHydrocortisoneMAPK1 protein, humanMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3NitrilesPhosphoproteinsSteroidogenic Acute Regulatory ProteinSteroidogenic Factor 1U 0126

Identifiers

PMID21913902
PMCPMC3372836
OpenAlexW1840745895

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.