Evidence map›Paper›PMID 24168917›Full record

ArticleAmerican journal of hypertension2014

Amlodipine increased endothelial nitric oxide and decreased nitroxidative stress disproportionately to blood pressure changes.

R Preston Mason, Robert F Jacob, J Jose Corbalan, Roman Kaliszan, Tadeusz Malinski

Open access · bronzeAbstract read
In one paragraph

Article in American journal of hypertension, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

13 citing papers in PubMed, 30 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Review
  5. The effect of amlodipin, a calcium channel blocker, on tendon healing: an experimental study in rat model of Achilles tendon injury.European journal of trauma and emergency surgery : official publication of the European Trauma Society · 2025
    Article
  6. Article
  7. Article
  8. Article
  9. The wHole Story About Fenestrations in LSEC.Frontiers in physiology · 2021
    Review
  10. Manipulating fenestrations in young and old liver sinusoidal endothelial cells.American journal of physiology. Gastrointestinal and liver physiology · 2019
    Article
  11. Pleiotropic effects of calcium channel blockers.Hypertension research : official journal of the Japanese Society of Hypertension · 2018
    Article
  12. Effect of amlodipine, lisinopril and allopurinol on acetaminophen-induced hepatotoxicity in rats.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2016
    Article
  13. 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

5 authors at 3 institutions in 2 countries.

R Preston MasonCardiovascular Division, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
Robert F Jacob
J Jose Corbalan
Roman Kaliszan
Tadeusz Malinski
Ohio University · USBeverly Hospital · USHarvard University · US

Funding

RENOVATION OF BIOCHEMISTRY LABORATORIESC06RR014575 · NCRR · OHIO UNIVERSITY ATHENS · PI FLEMMING, LESLIE A · 1999 to 1999
–
NCRR NIH HHS C06 RR014575NCRR NIH HHS C06 RR-014575-01
6 · The paper itself

Abstract

backgroundClinical trials have shown that amlodipine reduces cardiovascular events at a rate that is not predicted by changes in brachial arterial pressure alone. These findings may be explained, in part, by the pleiotropic effects of amlodipine on endothelial cell (EC) function. In this study, we elucidated the effect of amlodipine on nitric oxide (NO) bioavailability and cytotoxic peroxynitrite (ONOO(-)) and blood pressure (BP).

methodsSpontaneously hypertensive rats (SHRs) were treated with vehicle or amlodipine (5 mg/kg/day) for 8 weeks and compared with untreated, baseline rats. NO and ONOO(-) release from aortic and glomerular ECs were measured ex vivo using amperometric nanosensors following maximal stimulation with calcium ionophore. BP was measured using the tail-cuff method.

resultsAs compared with baseline, vehicle treatment had reduced aortic endothelial NO release from 157 ± 11 nM to 55 ± 6 nM and increased ONOO(-) from 69 ± 7 nM to 156 ± 19 nM. The NO/ONOO(-) ratio, a comprehensive measurement of eNOS function, decreased from 2.3 ± 0.3 to 0.3 ± 0.1. Compared with vehicle, amlodipine treatment restored NO to 101 ± 3 nM, decreased ONOO(-) to 50 ± 4 nM, and increased the NO/ONOO(-) ratio to 2.0 ± 0.2, a level similar to baseline. Similar changes were observed for glomerular ECs. Mean arterial blood pressure increased from 149 ± 3 mm Hg (baseline) to 174 ± 1 mm Hg (vehicle). Amlodipine slightly, but significantly, decreased mean arterial blood pressure to 167 ± 3 mm Hg vs. vehicle treatment.

conclusionsAmlodipine increased NO bioavailability and decreased nitroxidative stress in SHRs with EC dysfunction disproportionately to BP changes. These direct, vascular effects of amlodipine on EC function may contribute to reduced risk for atherothrombotic events as observed in clinical trials.

Indexed as

AmlodipineAnimalsAntihypertensive AgentsAortaBlood PressureDisease Models, AnimalEndothelial CellsHypertensionKidney GlomerulusMaleNitric OxideNitric Oxide Synthase Type IIIOxidative StressPeroxynitrous AcidRatsRats, Inbred SHRAmlodipineAntihypertensive AgentsNitric OxideNitric Oxide Synthase Type IIINos3 protein, ratPeroxynitrous Acidamlodipineblood pressureendothelial cellshypertensionnitric oxideperoxynitritespontaneously hypertensive rats.

Identifiers

PMID24168917
PMCPMC3915743
OpenAlexW2116752330

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.