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Exploring the Cardiovascular Impacts of Agmatine: A Systematic Review
Oana-Mădălina Manole1,2, Gabriela Rusu-Zota3,4, Amin Bazyani5
1Internal Medicine Department, Faculty of Medicine, "Grigore T. Popa" University of Medicine and Pharmacy, 700115 Iasi, Romania.
Agmatine (AG), an endogenous neurotransmitter, exhibits dual cardiovascular effects, influencing blood pressure and heart rate. Its specific impact depends on dosage, administration route, and targeted receptors.
Area of Science:
- Neuroscience
- Pharmacology
- Cardiovascular Research
Background:
- Agmatine (AG) is an endogenous neurotransmitter with diverse receptor interactions, including imidazoline and N-methyl-D-aspartate receptors.
- AG exhibits neuroprotective, anxiolytic, antidepressant, anticonvulsant, and anti-inflammatory properties.
- Cardiovascular effects of AG were investigated following the demonstration of clonidine's hypotensive effects.
Purpose of the Study:
- To systematically review and consolidate findings on agmatine's cardiovascular effects from preclinical studies.
- To understand the modulatory role of agmatine in cardiovascular function.
Main Methods:
- A systematic literature search was conducted across PubMed, Cochrane, and Embase databases.
- Keywords used included "agmatine" combined with "cardiac" or "vascular."
- Sixty preclinical studies were identified and included in the analysis.
Main Results:
- Agmatine, initially known as Clonidine Displacing Substance (CDS), demonstrated dose-dependent dual effects on cardiovascular parameters.
- Studies showed that AG can either increase or decrease blood pressure.
- AG also exhibited variable effects on heart rate, either increasing or decreasing it.
Conclusions:
- The cardiovascular effects of agmatine are complex and context-dependent.
- Dosage and route of administration significantly influence AG's impact on the cardiovascular system.
- The specific receptors targeted and the pathophysiological pathways involved dictate the observed cardiovascular outcomes of AG.
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