Evidence map›Paper›PMID 41793432›Full record

Trial reportEuropean journal of applied physiology2026

Oral phosphodiesterase-5 inhibitor does not augment red blood cell deformability at rest or during handgrip exercise.

Andrew R Steele, Liam A Kightley-Kauser, Jacob McCormick, Nina K Geerts, Brydie Lemkes, Jonah C Dizon, Jay M J R Carr, Philip N Ainslie

Abstract readRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in European journal of applied physiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Andrew R SteeleCentre for Heart, Lung and Vascular Health, School of Health and Exercise Sciences, University of British Columbia-Okanagan, Kelowna, BC, Canada. asteele@ualberta.ca.ORCID http://orcid.org/0000-0003-0557-847X
Liam A Kightley-KauserCentre for Heart, Lung and Vascular Health, School of Health and Exercise Sciences, University of British Columbia-Okanagan, Kelowna, BC, Canada.
Jacob McCormickCentre for Heart, Lung and Vascular Health, School of Health and Exercise Sciences, University of British Columbia-Okanagan, Kelowna, BC, Canada.
Nina K GeertsCentre for Heart, Lung and Vascular Health, School of Health and Exercise Sciences, University of British Columbia-Okanagan, Kelowna, BC, Canada.
Brydie LemkesCentre for Heart, Lung and Vascular Health, School of Health and Exercise Sciences, University of British Columbia-Okanagan, Kelowna, BC, Canada.
Jonah C DizonCentre for Heart, Lung and Vascular Health, School of Health and Exercise Sciences, University of British Columbia-Okanagan, Kelowna, BC, Canada.
Jay M J R CarrInstitute of Mountain Emergency Medicine, Eurac Research, Bolzano, Italy.
Philip N AinslieCentre for Heart, Lung and Vascular Health, School of Health and Exercise Sciences, University of British Columbia-Okanagan, Kelowna, BC, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeRed blood cells (RBCs) rely on deformability for oxygen delivery and capillary transit. Sildenafil citrate, a phosphodiesterase-5 inhibitor (PDE5-i), may enhance RBC deformability via nitric oxide, yet in vivo effects remain unclear.

methodsWe conducted a double-blind, placebo-controlled study to assess the effects of PDE5-i on cerebral blood flow (CBF), brachial artery (BA) blood flow (Q) and shear stress-specific RBC deformability during handgrip exercise (Baseline [BL], 27.5% and 55% of maximal voluntary contraction [MVC]). Fourteen participants (8F; age: 24 ± 6) were tested on separate days, before and 60-min following ingestion of sildenafil citrate (100 mg) or placebo. CBF and BA Q were measured using duplex ultrasound and RBC deformability was assessed with a laser-assisted optical rotational red cell analyzer.

resultsAcute oral administration of PDE5-i had no effect on basal cerebral or BA vascular metrics, including diameter, shear stress, Q, BA shear stress-specific RBC deformability or exercise hyperemia (p > 0.05). Prior to PDE5-i administration, exercise increased RBC deformability [EImax] (BL: 0.55 ± 0.021; 27.5% MVC: 0.57 ± 0.014; 55% MVC: 0.58 ± 0.015 a.u. p < 0.01). However, despite exercise-induced increases in EImax (BL: 0.59 ± 0.018 a.u. p < 0.01), PDE5-i did not further modify this parameter during a subsequent-bout of handgrip exercise (27.5%: 0.59 ± 0.017; 55%: 0.59 ± 0.015 a.u. p > 0.05), a pattern not observed with placebo. EImax did not differ between PDE5-i and placebo at matched exercise intensities post-administration (p > 0.05), indicating no independent effect of PDE5-i on RBC deformability.

conclusionAcute PDE5-i administration does not independently alter RBC deformability or vascular responses, at rest or during handgrip exercise in healthy individuals.

Indexed as

Erythrocyte DeformabilityExerciseHand StrengthPhosphodiesterase 5 InhibitorsSildenafil CitrateAdministration, OralAdultCerebrovascular CirculationDouble-Blind MethodFemaleHumansMaleRestYoung AdultPhosphodiesterase 5 InhibitorsSildenafil CitrateBlood rheologyExercise hyperemiaRed blood cell deformabilitySildenafil citrate

Identifiers

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Textmetadata
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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 Socratic graph.