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Antihypertensive mechanisms of spermidine

Antihypertensive mechanisms of spermidine

Mahmoud Gaber Salaheldin Abdellatif (ORCID: 0000-0002-5042-9054)
  • Grant DOI 10.55776/P34926
  • Funding program Principal Investigator Projects
  • Status ongoing
  • Start October 1, 2022
  • End February 28, 2026
  • Funding amount € 281,169
  • Project website
  • E-mail

Disciplines

Clinical Medicine (70%); Medical-Theoretical Sciences, Pharmacy (30%)

Keywords

    Spermidine, Autophagy, Hypertension

Abstract

The incidence of cardiovascular disease increases exponentially with aging. In Austria, almost a fifth of the general population is above 65 years, and thus novel medical therapies that extend healthy aging are needed more than ever. In their recently FWF-funded project, Dr. Abdellatif and his colleagues aim to achieve this goal. Specifically, they aim to study vascular stiffening and increased blood pressure, which affects a majority of elderly individuals and is considered the single leading cause of death worldwide. The research team located at the Department of Cardiology, Medical University of Graz will examine the use of spermidine, a natural compound that mimics the benefits of fasting without reducing food intake. The rationale behind this is that caloric restriction (ie, reduced caloric intake without malnutrition) has been shown to reduce high blood pressure and lower the risk of cardiovascular disease, but because fasting is hard to adhere to and might cause undesirable side effects on bone density and immunity, to which the elderly individuals are particularly vulnerable, safe and effective pharmaceutical alternatives are urgently needed. Towards this end, the researchers will employ state-of-the-art tools and techniques to decipher novel mechanisms regulating vascular health both experimentally and clinically with the aim to promote healthy aging and provide novel effective treatments that can be applied on on a whole population level.

Research institution(s)
  • Medizinische Universität Graz - 100%
Project participants
  • Sasa Frank, Medizinische Universität Graz , national collaboration partner
International project participants
  • Guido Kroemer, INSERM U1138 - France

Research Output

  • 269 Citations
  • 14 Publications
Publications
  • 2025
    Title Autophagy is required for the therapeutic effects of the NAD+ precursor nicotinamide in obesity-related heart failure with preserved ejection fraction
    DOI 10.1093/eurheartj/ehaf062
    Type Journal Article
    Author Abdellatif M
    Journal European Heart Journal
    Pages 1863-1866
    Link Publication
  • 2025
    Title Caloric restriction and its mimetics in heart failure with preserved ejection fraction: mechanisms and therapeutic potential
    DOI 10.1186/s12933-024-02566-8
    Type Journal Article
    Author Fuerlinger A
    Journal Cardiovascular Diabetology
    Pages 21
    Link Publication
  • 2024
    Title Mechanisms of myocardial reverse remodelling and its clinical significance: A scientific statement of the ESC Working Group on Myocardial Function
    DOI 10.1002/ejhf.3264
    Type Journal Article
    Author Falcão-Pires I
    Journal European Journal of Heart Failure
    Pages 1454-1479
    Link Publication
  • 2024
    Title Risks and Benefits of Intermittent Fasting for the Aging Cardiovascular System
    DOI 10.1016/j.cjca.2024.02.004
    Type Journal Article
    Author Ozcan M
    Journal Canadian Journal of Cardiology
    Pages 1445-1457
    Link Publication
  • 2025
    Title Mitochondrial targets in ischaemic heart disease and heart failure, and their potential for a more efficient clinical translation. A scientific statement of the ESC Working Group on Cellular Biology of the Heart and the ESC Working Group on Myocardia
    DOI 10.1002/ejhf.3674
    Type Journal Article
    Author Paillard M
    Journal European Journal of Heart Failure
    Link Publication
  • 2022
    Title DBI/ACBP is a targetable autophagy checkpoint involved in aging and cardiovascular disease
    DOI 10.1080/15548627.2022.2160565
    Type Journal Article
    Author Montégut L
    Journal Autophagy
    Pages 2166-2169
    Link Publication
  • 2022
    Title High plasma concentrations of acyl-coenzyme A binding protein (ACBP) predispose to cardiovascular disease: Evidence for a phylogenetically conserved proaging function of ACBP
    DOI 10.1111/acel.13751
    Type Journal Article
    Author Montégut L
    Journal Aging Cell
    Link Publication
  • 2024
    Title Targeting organ-specific mitochondrial dysfunction to improve biological aging
    DOI 10.1016/j.pharmthera.2024.108710
    Type Journal Article
    Author Madreiter-Sokolowski C
    Journal Pharmacology & Therapeutics
    Pages 108710
    Link Publication
  • 2024
    Title Anti-ageing interventions for the treatment of cardiovascular disease
    DOI 10.1093/cvr/cvae177
    Type Journal Article
    Author Abdellatif M
    Journal Cardiovascular Research
    Link Publication
  • 2023
    Title Hallmarks of cardiovascular ageing
    DOI 10.1038/s41569-023-00881-3
    Type Journal Article
    Author Abdellatif M
    Journal Nature Reviews Cardiology
    Pages 754-777
  • 2023
    Title Acyl coenzyme A binding protein (ACBP): An aging- and disease-relevant “autophagy checkpoint”
    DOI 10.1111/acel.13910
    Type Journal Article
    Author Montégut L
    Journal Aging Cell
    Link Publication
  • 2024
    Title A surge in endogenous spermidine is essential for rapamycin-induced autophagy and longevity
    DOI 10.1080/15548627.2024.2396793
    Type Journal Article
    Author Hofer S
    Journal Autophagy
    Pages 2824-2826
    Link Publication
  • 2023
    Title Metabolic control of mitophagy
    DOI 10.1111/eci.14138
    Type Journal Article
    Author Zimmermann A
    Journal European Journal of Clinical Investigation
    Link Publication
  • 2023
    Title Antagonistic pleiotropy: the example of cardiac insulin-like growth factor signaling, which is essential in youth but detrimental in age
    DOI 10.1080/14728222.2023.2178420
    Type Journal Article
    Author Abdellatif M
    Journal Expert Opinion on Therapeutic Targets
    Pages 87-90
    Link Publication

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