Permixon®, hexane-extracted Serenoa repens, inhibits human prostate and bladder smooth muscle contraction and exerts growth-related functions in human prostate stromal cells
Autor: | Alexander, Tamalunas, Amin, Wendt, Florian, Springer, Victor, Vigodski, Anna, Ciotkowska, Beata, Rutz, Ruixiao, Wang, Ru, Huang, Yuhan, Liu, Heiko, Schulz, Stephan, Ledderose, Thomas, Kolben, Giuseppe, Magistro, Christian G, Stief, Martin, Hennenberg |
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Rok vydání: | 2022 |
Předmět: |
Male
Endothelin-1 Phalloidine Plant Extracts Urinary Bladder Prostate Prostatic Hyperplasia Thromboxanes Muscle Smooth General Medicine Actins Sincalide General Biochemistry Genetics and Molecular Biology Adrenergic Agents Serenoa Hexanes Humans Stromal Cells General Pharmacology Toxicology and Pharmaceutics Methacholine Chloride Muscle Contraction |
Zdroj: | Life Sciences. 308:120931 |
ISSN: | 0024-3205 |
DOI: | 10.1016/j.lfs.2022.120931 |
Popis: | Recently, the European Association of Urology recommended hexane-extracted fruit of Serenoa repens (HESr) in their guidelines on management of non-neurogenic male lower urinary tracts symptoms (LUTS). Despite previously lacking recommendations, Permixon® is the most investigated HESr in clinical trials, where it proved effective for male LUTS. In contrast, underlying mechanisms were rarely addressed and are only marginally understood. We therefore investigated effects of Permixon® on human prostate and detrusor smooth muscle contraction and on growth-related functions in prostate stromal cells.Permixon® capsules were dissolved using n-hexane. Contractions of human prostate and detrusor tissues were induced in organ bath. Proliferation (EdU assay), growth (colony formation), apoptosis and cell death (flow cytometry), viability (CCK-8) and actin organization (phalloidin staining) were studied in cultured human prostate stromal cells (WPMY-1).Permixon® inhibited αOur results provide a novel basis that allows, for the first time, to fully explain the ubiquitous beneficial effects of HESr in clinical trials. HESr may inhibit at least neurogenic, α |
Databáze: | OpenAIRE |
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