Evidence map›Paper›PMID 25910805›Full record

ArticleAmerican journal of physiology. Heart and circulatory physiology2015

Regulation of myogenic tone and structure of parenchymal arterioles by hypertension and the mineralocorticoid receptor.

Paulo W Pires, William F Jackson, Anne M Dorrance

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Heart and circulatory physiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 1 pooled it
3.6field-weighted citation impact, top 7% 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

46 citing papers in PubMed, 1 synthesis or guideline pooled it, 73 citations in OpenAlex.

  1. Prevalence of mild cognitive impairment in patients with hypertension: a systematic review and meta-analysis.Hypertension research : official journal of the Japanese Society of Hypertension · 2021
    Pooled it
  2. Review
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  9. Review
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  11. Role ofbioRxiv : the preprint server for biology · 2023
    Article
  12. Endothelial KAmerican journal of physiology. Heart and circulatory physiology · 2023
    Article
  13. Article
  14. Article
  15. Oxidative Regulation of Vascular CaAntioxidants (Basel, Switzerland) · 2022
    Review
  16. Cerebral arteriolar and neurovascular dysfunction after chemically induced menopause in mice.American journal of physiology. Heart and circulatory physiology · 2022
    Article
  17. Article
  18. Review
  19. Myogenic Vasoconstriction Requires Canonical GJournal of the American Heart Association · 2022
    Article
  20. 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

3 authors at 2 institutions in 1 country.

Paulo W PiresDepartment of Pharmacology and Toxicology, Michigan State University, East Lansing, Michigan; and Department of Pharmacology, University of Nevada School of Medicine, Reno, Nevada.
William F JacksonDepartment of Pharmacology and Toxicology, Michigan State University, East Lansing, Michigan; and.
Anne M DorranceDepartment of Pharmacology and Toxicology, Michigan State University, East Lansing, Michigan; and dorranc3@msu.edu.
Michigan State University · USUniversity of Nevada, Reno · US

Funding

SIGNALING MECHANISMS IN ARTERIES AND VEINS IN HYPERTENSIONP01HL070687 · NHLBI · MICHIGAN STATE UNIVERSITY · PI WATTS, STEPHANIE W · 2003 to 2019
$22.8M
NHLBI NIH HHS P01 HL070687NHLBI NIH HHS P01-HL-070687
6 · The paper itself

Abstract

Proper perfusion is vital for maintenance of neuronal homeostasis and brain function. Changes in the function and structure of cerebral parenchymal arterioles (PAs) could impair blood flow regulation and increase the risk of cerebrovascular diseases, including dementia and stroke. Hypertension alters the structure and function of large cerebral arteries, but its effects on PAs remain unknown. We hypothesized that hypertension increases myogenic tone and induces inward remodeling in PAs; we further proposed that antihypertensive therapy or mineralocorticoid receptor (MR) blockade would reverse the effects of hypertension. PAs from 18-wk-old stroke-prone spontaneously hypertensive rats (SHRSP) were isolated and cannulated in a pressure myograph. At 50-mmHg intraluminal pressure, PAs from SHRSP showed higher myogenic tone (%tone: 39.1 ± 1.9 vs. 28.7 ± 2.5%, P < 0.01) and smaller resting luminal diameter (34.7 ± 1.9 vs. 46.2 ± 2.4 μm, P < 0.01) than those from normotensive Wistar-Kyoto rats, through a mechanism that seems to require Ca(2+) influx through L-type voltage-gated Ca(2+) channels. PAs from SHRSP showed inward remodeling (luminal diameter at 60 mmHg: 55.2 ± 1.4 vs. 75.7 ± 5.1 μm, P < 0.01) and a paradoxical increase in distensibility and compliance. Treatment of SHRSP for 6 wk with antihypertensive therapy reduced PAs' myogenic tone, increased their resting luminal diameter, and prevented inward remodeling. In contrast, treatment of SHRSP for 6 wk with an MR antagonist did not reduce blood pressure or myogenic tone, but prevented inward remodeling. Thus, while hypertensive remodeling of PAs may involve the MR, myogenic tone seems to be independent of MR activity.

Indexed as

AnimalsAntihypertensive AgentsArteriolesCalciumCalcium Channel BlockersCalcium Channels, L-TypeCerebrovascular CirculationCerebrumComplianceEplerenoneHydralazineHydrochlorothiazideHypertensionMiddle Cerebral ArteryMineralocorticoid Receptor AntagonistsMuscle, Smooth, VascularAntihypertensive AgentsCalciumCalcium Channel BlockersCalcium Channels, L-TypeEplerenoneHydralazineHydrochlorothiazideMineralocorticoid Receptor AntagonistsNifedipineReceptors, MineralocorticoidReserpineSpironolactonecerebral parenchymal arterioleshypertensioninward remodelingmineralocorticoid receptormyogenic tone

Identifiers

PMID25910805
PMCPMC4491521
OpenAlexW2321920894

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.