Evidence map›Paper›PMID 41508103›Full record

ArticleBiology of sex differences2026

The impact of testosterone on paraventricular nucleus gene expression in male and female spontaneously hypertensive rats.

Alex Paterson, Su-Yi Loh, Shadi Kadijeh Gholami, Mark F Rogers, Dharmani Devi Murugan, Lam Sau-Kuen, Mohammad Rais Mustafa, Benjamin P Ott, Prusha Balaratnam, Andre S Mecawi and 2 more

Abstract read
In one paragraph

Article in Biology of sex differences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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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

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5 · Who and what money

Authors and funding

12 authors.

Alex PatersonBristol Medical School: Translational Health Sciences, Dorothy Hodgkin Building, University of Bristol, Bristol, BS1 3NY, England.
Su-Yi LohDepartment of Physiology, Faculty of Medicine, Universiti Malaya, Kuala Lumpur, 50603, Malaysia.
Shadi Kadijeh GholamiDepartment of Physiology, Faculty of Medicine, Universiti Malaya, Kuala Lumpur, 50603, Malaysia.
Mark F RogersBristol Medical School: Translational Health Sciences, Dorothy Hodgkin Building, University of Bristol, Bristol, BS1 3NY, England.
Dharmani Devi MuruganDepartment of Pharmacology, Faculty of Medicine, Universiti Malaya, Kuala Lumpur, 50603, Malaysia.
Lam Sau-KuenDepartment of Physiology, Faculty of Medicine, Universiti Malaya, Kuala Lumpur, 50603, Malaysia.
Mohammad Rais MustafaDepartment of Pharmacology, Faculty of Medicine, Universiti Malaya, Kuala Lumpur, 50603, Malaysia.
Benjamin P OttDepartment of Medicine, School of Medicine, Queen's University, Kingston, K7L 3N6, ON, Canada.
Prusha BalaratnamDepartment of Medicine, School of Medicine, Queen's University, Kingston, K7L 3N6, ON, Canada.
Andre S MecawiDepartment of Physiology, Faculty of Medicine, Universiti Malaya, Kuala Lumpur, 50603, Malaysia.
David MurphyBristol Medical School: Translational Health Sciences, Dorothy Hodgkin Building, University of Bristol, Bristol, BS1 3NY, England. d.murphy@bristol.ac.uk.ORCID 0000-0003-2946-0353
Charles C T HindmarchBristol Medical School: Translational Health Sciences, Dorothy Hodgkin Building, University of Bristol, Bristol, BS1 3NY, England. c.hindmarch@queensu.ca.ORCID 0000-0002-6036-1292

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHypertension is a polygenic, complex disease that impacts men and women differently; whilst the incidence of high blood pressure (BP) is roughly equal over a lifetime, men typically are at higher risk of developing the disease earlier in life, before 50 years of age. There is adequate evidence that the brain is critical for the BP setpoint. The paraventricular nucleus (PVN) of the hypothalamus is an integrative structure that can influence not only neurohumoral responses to blood pressure changes, but also sympathetic drive. Here we manipulate the androgenic status of both male and female spontaneously hypertensive rats (SHRs) to determine how this changes gene expression within the PVN of these animals.

methodsSHR (8-weeks old) were either sham-operated or orchiectomized, whereas all females were oophorectomized, half of which received 10 mg testosterone propionate subcutaneously. Mean arterial pressure (MAP) and testosterone (T) were measured by carotid cannulation and ELISA respectively. Sequencing was performed on hand-punched PVN sections and subjected to robust bioinformatic analysis.

resultsin total, 6,571 differentially regulated genes (DRGs) are regulated in the PVN of male and female rats. High T (endogenous or replaced) correlates with higher MAP in both sexes. Orchidectomy-induced T depletion resulted in the significant regulation of 5,104 genes, involved in thousands of biological roles, including ones related to hormone and sex-hormone signalling. In the female SHR, testosterone replacement in oophorectomized animals induced the regulation of 1,727 genes, sharing many biological functions with those in the high T males. We validated key genes by qPCR to determine false discovery rate.

conclusionsT status in hypertensive rats correlates with MAP, and consistent changes in PVN transcriptome.

Indexed as

Gene Expression RegulationParaventricular Hypothalamic NucleusTestosteroneAnimalsBlood PressureFemaleHypertensionMaleOrchiectomyOvariectomyRatsRats, Inbred SHRSex CharacteristicsTestosteroneAndrogenAngiotensin II (ANGII)Epoxyhydrolase 2 (Ephx2)EstrogenParaventricular nucleus (PVN)RNAsequencingSexSpontaneously hypertensive rat (SHR)Testosterone (T)

Identifiers

PMID41508103
PMCPMC12870226

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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.