Evidence mapPaperPMID 40679600Full record

ArticlePhysiological genomics2025

Dynamic rewiring of microRNA networks in the brainstem autonomic control circuits during hypertension development in the female spontaneously hypertensive rat.

Alison Moss, Ankita Srivastava, Lakshmi Kuttippurathu, James S Schwaber, Rajanikanth Vadigepalli

Abstract read
In one paragraph

Article in Physiological genomics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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.

Alison MossDepartment of Pathology and Genomic Medicine, Daniel Baugh Institute for Functional Genomics and Computational Biology, Thomas Jefferson University, Philadelphia, Pennsylvania, United States.ORCID 0000-0002-7907-8796
Ankita SrivastavaDepartment of Pathology and Genomic Medicine, Daniel Baugh Institute for Functional Genomics and Computational Biology, Thomas Jefferson University, Philadelphia, Pennsylvania, United States.ORCID 0000-0002-1221-1353
Lakshmi KuttippurathuDepartment of Pathology and Genomic Medicine, Daniel Baugh Institute for Functional Genomics and Computational Biology, Thomas Jefferson University, Philadelphia, Pennsylvania, United States.ORCID 0000-0001-6612-9040
James S SchwaberDepartment of Pathology and Genomic Medicine, Daniel Baugh Institute for Functional Genomics and Computational Biology, Thomas Jefferson University, Philadelphia, Pennsylvania, United States.ORCID 0000-0003-0598-7345
Rajanikanth VadigepalliDepartment of Pathology and Genomic Medicine, Daniel Baugh Institute for Functional Genomics and Computational Biology, Thomas Jefferson University, Philadelphia, Pennsylvania, United States.ORCID 0000-0002-8405-1037

Funding

Molecular Neurogenetics of the Brainstem Neuronal Source of Cardioprotective Vagal OutflowR01HL161696 · THOMAS JEFFERSON UNIVERSITY · 2025 to 2025
$571k
NHLBI NIH HHS R01 HL161696NHLBI NIH HHS U01 HL133360NIH HHS OT2 OD030534ODCDC CDC HHS OT2 OD030534
6 · The paper itself

Abstract

We describe global microRNA (miRNA) changes in the central autonomic control circuits during the development of neurogenic hypertension. Using the female spontaneously hypertensive rat (SHR) and the normotensive Wistar Kyoto (WKY), we analyzed the dynamic miRNA expression changes in three brainstem regions-the nucleus of the solitary tract, caudal ventrolateral medulla, and rostral ventrolateral medulla-as a time series beginning at 8 wk of age before hypertension onset through to extended chronic hypertension. Our analysis yielded nine miRNAs that were significantly differentially regulated in all three regions between SHR and WKY over time. We collated computationally predicted gene targets of these nine miRNAs in pathways related to neuronal plasticity and autonomic regulation to construct a putative miRNA-target gene network involved in the development of neurogenic hypertension. We analyzed the dynamic correlations between the miRNAs and their putative targets to identify the regulatory interactions shifting between WKY and SHR. Comparing the results with previously published data in male SHR and WKY identified miRNA network dynamics specific to female SHR during hypertension development. Collectively, our results point to distinct rewiring of the miRNA regulatory networks governing angiotensin signaling and homeostasis, neuronal plasticity, and inflammatory processes contributing to the development of hypertension in female SHR.

Indexed as

Autonomic Nervous SystemBrain StemGene Regulatory NetworksHypertensionMicroRNAsAnimalsFemaleMaleRatsRats, Inbred SHRRats, Inbred WKYMicroRNAsautonomic control circuitsmicroRNA networksmicroRNA profilingneurogenic hypertensionspontaneously hypertensive rat

Identifiers

PMID40679600
PMCPMC12341004

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.