Evidence map›Paper›PMID 23604714›Full record

ArticleAmerican journal of physiology. Heart and circulatory physiology2013

Smooth muscle-selective CPI-17 expression increases vascular smooth muscle contraction and blood pressure.

Wen Su, Zhongwen Xie, Shu Liu, Lindsay E Calderon, Zhenheng Guo, Ming C Gong

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Heart and circulatory physiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

21 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Article
  3. Possible roles of N- and C-terminal unstructured tails of CPI-17 in regulating CaJournal of smooth muscle research = Nihon Heikatsukin Gakkai kikanshi · 2022
    Article
  4. Regulation of myosin light-chain phosphorylation and its roles in cardiovascular physiology and pathophysiology.Hypertension research : official journal of the Japanese Society of Hypertension · 2022
    Review
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  19. Neural programming of mesenteric and renal arteries.American journal of physiology. Heart and circulatory physiology · 2014
    Article
  20. Review
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

6 authors at 1 institution in 1 country.

Wen SuDepartment of Physiology, University of Kentucky Medical Center, Lexington, KY, USA.
Zhongwen Xie
Shu Liu
Lindsay E Calderon
Zhenheng Guo
Ming C Gong
University of Kentucky · US

Funding

A Novel Mechanism by which iPLA2 Links Diabetes to Cardiovascular DiseasesR01HL088389 · NHLBI · UNIVERSITY OF KENTUCKY · PI GUO, ZHENHENG · 2008 to 2012
$2.1M
Vascular Smooth Muscle Hyper-contractility/HypertensionR01HL082791 · NHLBI · UNIVERSITY OF KENTUCKY · PI GONG, MING C · 2006 to 2010
$1.6M
NHLBI NIH HHS HL-082791NHLBI NIH HHS HL-088389NHLBI NIH HHS HL-088389-02S1
6 · The paper itself

Abstract

Recent data revealed that protein kinase C-potentiated myosin phosphatase inhibitor of 17 kDa (CPI-17), a myosin phosphatase inhibitory protein preferentially expressed in smooth muscle, is upregulated/activated in several diseases but whether this CPI-17 increase plays a causal role in pathologically enhanced vascular smooth muscle contractility and blood pressure remains unclear. To address this possibility, we generated a smooth muscle-specific CPI-17 transgenic mouse model (CPI-17-Tg) and demonstrated that the CPI-17 transgene was selectively expressed in smooth muscle-enriched tissues, including mesenteric arteries. The isometric contractions in the isolated second-order branch of mesenteric artery helical strips from CPI-17-Tg mice were significantly enhanced compared with controls in response to phenylephrine, U-46619, serotonin, ANG II, high potassium, and calcium. The perfusion pressure increases in isolated perfused mesenteric vascular beds in response to norepinephrine were also enhanced in CPI-17-Tg mice. The hypercontractility was associated with increased phosphorylation of CPI-17 and 20-kDa myosin light chain under basal and stimulated conditions. Surprisingly, the protein levels of rho kinase 2 and protein kinase Cα/δ were significantly increased in CPI-17-Tg mouse mesenteric arteries. Radiotelemetry measurements demonstrated that blood pressure was significantly increased in CPI-17-Tg mice. However, no vascular remodeling was detected by morphometric analysis. Taken together, our results demonstrate that increased CPI-17 expression in smooth muscle promotes vascular smooth muscle contractility and increases blood pressure, implicating a pathological significant role of CPI-17 upregulation.

Indexed as

Blood Pressure15-Hydroxy-11 alpha,9 alpha-(epoxymethano)prosta-5,13-dienoic AcidAngiotensin IIAnimalsCalciumIntracellular Signaling Peptides and ProteinsIsometric ContractionMesenteric ArteriesMiceMice, Inbred C57BLMice, TransgenicMuscle ProteinsMuscle, Smooth, VascularPhenylephrinePhosphoproteinsPotassium15-Hydroxy-11 alpha,9 alpha-(epoxymethano)prosta-5,13-dienoic AcidAngiotensin IICalciumIntracellular Signaling Peptides and ProteinsMuscle ProteinsPhenylephrinePhosphoproteinsPotassiumPpp1r14a protein, mouseSerotoninVasoconstrictor Agentshypercontractilityphosphatase inhibitory proteinprotein kinase C-potentiated myosin phosphatase inhibitor of 17 kilodaltons

Identifiers

PMID23604714
PMCPMC3727105
OpenAlexW2168772784

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.