Evidence map›Paper›PMID 35651628›Full record

ArticleFrontiers in neuroscience2022

Renal Nerve Activity and Arterial Depressor Responses Induced by Neuromodulation of the Deep Peroneal Nerve in Spontaneously Hypertensive Rats.

Maria Alejandra Gonzalez-Gonzalez, Kevin Romero, John Beitter, David Lloyd, Danny V Lam, Ana Guadalupe Hernandez-Reynoso, Aswini Kanneganti, Han-Kyul Kim, Caroline K Bjune, Scott Smith and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neuroscience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. 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

12 authors at 4 institutions in 1 country.

Maria Alejandra Gonzalez-GonzalezDepartment of Biomedical Engineering and Biomedical Sciences, University of Houston, Houston, TX, United States.
Kevin RomeroDepartment of Biomedical Engineering and Biomedical Sciences, University of Houston, Houston, TX, United States.
John BeitterDepartment of Biomedical Engineering, The University of Texas at Dallas, Dallas, TX, United States.
David LloydDepartment of Biomedical Engineering and Biomedical Sciences, University of Houston, Houston, TX, United States.
Danny V LamDepartment of Biomedical Engineering, The University of Texas at Dallas, Dallas, TX, United States.
Ana Guadalupe Hernandez-ReynosoDepartment of Biomedical Engineering, The University of Texas at Dallas, Dallas, TX, United States.
Aswini KannegantiDepartment of Biomedical Engineering, The University of Texas at Dallas, Dallas, TX, United States.
Han-Kyul KimHypertension Section, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, United States.
Caroline K BjuneDraper Laboratory, Boston, MA, United States.
Scott SmithHypertension Section, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, United States.
Wanpen VongpatanasinHypertension Section, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, United States.
Mario I Romero-OrtegaDepartment of Biomedical Engineering and Biomedical Sciences, University of Houston, Houston, TX, United States.
The University of Texas at Dallas · USUniversity of Houston · USThe University of Texas Southwestern Medical Center · USDraper Laboratory · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hypertension is a main cause of death in the United States with more than 103 million adults affected. While pharmacological treatments are effective, blood pressure (BP) remains uncontrolled in 50-60% of resistant hypertensive subjects. Using a custom-wired miniature electrode, we previously reported that deep peroneal nerve stimulation (DPNS) elicited acute cardiovascular depressor responses in anesthetized spontaneously hypertensive rats (SHRs). Here, we further study this effect by implementing a wireless system and exploring different stimulation parameters to achieve a maximum depressor response. Our results indicate that DPNS consistently induces a reduction in BP and suggests that renal sympathetic nerve activity (RSNA) is altered by this bioelectronic treatment. To test the acute effect of DPNS in awake animals, we developed a novel miniaturized wireless microchannel electrode (w-μCE), with a Z-shaped microchannel through which the target nerves slide and lock into the recording/stimulation chamber. Animals implanted with w-μCE and BP telemetry systems for 3 weeks showed an average BP of 150 ± 14 mmHg, which was reduced significantly by an active DPNS session to 135 ± 8 mmHg (

Indexed as

deep peroneal nervehypertensionneuromodulationrenal nerve activityspontaneously hypertensive rats

Identifiers

PMID35651628
PMCPMC9149221
OpenAlexW4280590975

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.