Evidence map›Paper›PMID 41691606›Full record

ArticleActa physiologica (Oxford, England)2026

Alms1 KO Rat: A New Model of Cardiometabolic Syndrome With Spontaneous Hypertension.

Ankita B Jaykumar, Sumit R Monu, Jiang Xu, Mariela Mendez, Xiao-Ping Yang, Nour-Eddine Rhaleb, Pablo A Ortiz

Abstract read
In one paragraph

Article in Acta physiologica (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

  • Update of
    2024
5 · Who and what money

Authors and funding

7 authors.

Ankita B JaykumarDivision of Hypertension and Vascular Research, Henry Ford Hospital, Detroit, Michigan, USA.ORCID https://orcid.org/0000-0002-9396-5850
Sumit R MonuDivision of Hypertension and Vascular Research, Henry Ford Hospital, Detroit, Michigan, USA.
Jiang XuDivision of Hypertension and Vascular Research, Henry Ford Hospital, Detroit, Michigan, USA.
Mariela MendezDivision of Hypertension and Vascular Research, Henry Ford Hospital, Detroit, Michigan, USA.
Xiao-Ping YangDivision of Hypertension and Vascular Research, Henry Ford Hospital, Detroit, Michigan, USA.
Nour-Eddine RhalebDivision of Hypertension and Vascular Research, Henry Ford Hospital, Detroit, Michigan, USA.
Pablo A OrtizDivision of Hypertension and Vascular Research, Henry Ford Hospital, Detroit, Michigan, USA.ORCID https://orcid.org/0000-0002-7512-7255

Funding

Regulation of NKCC2 and renal NaCl transport by protein-protein interactionsR01DK131114 · NIDDK · WAYNE STATE UNIVERSITY · PI Pablo A. Ortiz · 2023 to 2026
$2.2M
Ac-SDKP in the Treatment of Cardiac Dysfunction in Hypertension or Ischemic HeartR01HL136456 · NHLBI · WAYNE STATE UNIVERSITY · PI RHALEB, NOUR-EDDINE · 2018 to 2021
$1.9M
WNK1/OSR1 axis in Hippocampal Insulin Signaling, Glucose Metabolism and Age-related Cognitive DysfunctionK99AG075161 · NIA · UT SOUTHWESTERN MEDICAL CENTER · PI JAYKUMAR, ANKITA BACHHAWAT · 2023 to 2024
$256k
American Heart Association 16PRE27510032NHLBI NIH HHS NIH R01HL136456-A1NHLBI NIH HHS R01 HL136456NIA NIH HHS K99 AG075161NIA NIH HHS NIH K99AG075161NIDDK NIH HHS R01 DK131114NIDDK NIH HHS R01DK131114A1
6 · The paper itself

Abstract

Alström syndrome 1 (ALMS1) is a protein linked to Alström syndrome, a rare genetic disorder characterized by obesity, insulin resistance, hyperinsulinemia, and hypertension. Genetic studies have further associated Alms1 with hypertension in human populations. However, the precise mechanisms by which ALMS1 regulates metabolic and cardiovascular function remain unclear.

aimIn this study, we investigate metabolic and cardiovascular functions regulated by ALMS1.

methodsTo investigate this, we developed and characterized an Alms1 knockout (KO) rat model, which spontaneously develops metabolic syndrome and hypertension.

resultsOur findings reveal that Alms1 KO rats exhibit age-dependent metabolic dysfunction, with hypertension and increased body weight becoming evident by 10-12 weeks of age. Obesity, hyperinsulinemia, and vascular dysfunction emerge later, at 14-16 weeks, suggesting progressive metabolic deterioration. Notably, Alms1 KO rats develop hyperleptinemia as early as 7 weeks, prior to the onset of obesity, implicating ALMS1 in early leptin regulation and metabolic signaling. Moreover, female Alms1 KO rats develop severe metabolic syndrome with hypertension, like males, demonstrating a lack of the typical female cardiovascular protection. Echocardiographic analysis shows progressive cardiac dysfunction, including left ventricular (LV) dilation, increased wall thickness, and impaired contractility. Despite these structural changes, the LV mass/BW ratio remains unchanged, suggesting a shift toward maladaptive eccentric remodeling rather than hypertrophy.

conclusionCollectively, these findings establish the Alms1 KO rat as a robust preclinical model of metabolic syndrome. This model closely mimics human disease and provides a powerful tool for studying the mechanisms of metabolic and cardiovascular dysfunction as well as for testing potential therapeutic interventions.

Indexed as

HypertensionMetabolic SyndromeAnimalsDisease Models, AnimalFemaleGene Knockout TechniquesMaleRatsAlstrom syndromecardiometabolic syndromeendothelial functionhypertension

Identifiers

PMID41691606
PMCPMC12906849

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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.