Evidence map›Paper›PMID 31340190›Full record

ArticlePharmacological research2019

TRPM8 channel activation triggers relaxation of pudendal artery with increased sensitivity in the hypertensive rats.

Darizy Flavia Silva, Camilla Ferreira Wenceslau, Cameron G Mccarthy, Theodora Szasz, Safia Ogbi, R Clinton Webb

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Article in Pharmacological research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 34% 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

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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

6 citing papers in PubMed, 14 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

6 authors at 3 institutions in 2 countries.

Darizy Flavia SilvaDepartment of Bioregulation, Federal University of Bahia, Salvador, BA, Brazil. Electronic address: darizy@gmail.com.
Camilla Ferreira WenceslauDepartment of Physiology & Pharmacology, University of Toledo College of Medicine and Life Sciences, Toledo, OH, USA.
Cameron G MccarthyDepartment of Physiology & Pharmacology, University of Toledo College of Medicine and Life Sciences, Toledo, OH, USA.
Theodora SzaszDepartment of Physiology, Augusta University, Augusta, GA, USA.
Safia OgbiDepartment of Physiology, Augusta University, Augusta, GA, USA.
R Clinton WebbDepartment of Physiology, Augusta University, Augusta, GA, USA.
Augusta University · USUniversity of Toledo · USUniversidade Federal da Bahia · BR

Funding

Toll-like receptor 9 activation by mitochondrial DNA causes vascular injury in hypertensionP01HL134604 · NHLBI · AUGUSTA UNIVERSITY · PI BRANDS, MICHAEL W. · 2017 to 2021
$9.4M
Intrarenal Arteries Sense Trauma-derived Mitochondrial N-formyl Peptides Leading to Kidney Injury in SIRSK99GM118885 · NIGMS · AUGUSTA UNIVERSITY · PI WENCESLAU, CAMILLA FERREIRA · 2016 to 2017
$162k
NHLBI NIH HHS P01 HL134604NIGMS NIH HHS K99 GM118885
6 · The paper itself

Abstract

introductionErectile dysfunction (ED) is frequently encountered in patients with arterial hypertension and there is a recent functional correlation between the expression of thermoreceptor channels TRPM8 (melastatin 8) and alterations in blood pressure in hypertension. The aim of this study was to investigate the function of cold-sensing TRPM8 channel in internal pudendal artery (IPA) in both normotensive and hypertensive rats.

methodsWe performed experiments integrating physiological, pharmacological, biochemical and cellular techniques.

resultsTRPM8 channels are expressed in the IPA and in vascular smooth muscle cells from IPA. In addition, TRPM8 activation, by both a cooling compound icilin (82.1 ± 3.0%, n = 6) and cold temperature [thermal stimulus, basal tone (25 °C, 41.2 ± 3.4%, n = 5) or pre-contracted tone induced by phenylephrine (25 °C, 87.0 ± 3.6%, n = 7)], induced relaxation in IPA. Furthermore, the results showed that the concentration-response curve to icilin was significantly shifted to the right in different conditions, such as: the absence of the vascular endothelium, in the presence of L-NAME (10

conclusionsThese data demonstrate for the first time, the expression and function of TRPM8 channels in the IPA involving, at least in part, endothelium-derived relaxing factors and ROCK inhibition. Overall, this channel could potentially be a new target for the treatment of hypertension associated-ED.

Indexed as

AnimalsArteriesHypertensionMaleMuscle, Smooth, VascularMyocytes, Smooth MuscleRats, Inbred SHRRats, Sprague-DawleyRats, Wistarrho-Associated Kinasesrho GTP-Binding ProteinsTRPM Cation ChannelsVasodilationRhoA protein, ratrho-Associated Kinasesrho GTP-Binding ProteinsTrpm8 protein, ratTRPM Cation ChannelsEndothelium-derived relaxing factorsInternal pudendal arteryROCKSpontaneously hypertensive ratsTRPM8 channelsVasodilation

Identifiers

PMID31340190
PMCPMC6733625
OpenAlexW2964027066

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Registered trials

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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.