Permixon®, hexane-extracted Serenoa repens, inhibits human prostate and bladder smooth muscle contraction and exerts growth-related functions in human prostate stromal cells.
Actins
/ metabolism
Adrenergic Agents
/ pharmacology
Endothelin-1
/ metabolism
Hexanes
/ metabolism
Humans
Male
Methacholine Chloride
/ metabolism
Muscle Contraction
Muscle, Smooth
Phalloidine
/ metabolism
Plant Extracts
/ therapeutic use
Prostate
/ metabolism
Prostatic Hyperplasia
/ drug therapy
Serenoa
Sincalide
/ metabolism
Stromal Cells
/ metabolism
Thromboxanes
/ metabolism
Urinary Bladder
/ metabolism
Lower urinary tract symptoms
Overactive bladder
Phytotherapy
Plant extracts
Prostatic hyperplasia
Smooth muscle contraction
Journal
Life sciences
ISSN: 1879-0631
Titre abrégé: Life Sci
Pays: Netherlands
ID NLM: 0375521
Informations de publication
Date de publication:
01 Nov 2022
01 Nov 2022
Historique:
received:
22
07
2022
revised:
25
08
2022
accepted:
01
09
2022
pubmed:
10
9
2022
medline:
7
10
2022
entrez:
9
9
2022
Statut:
ppublish
Résumé
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 α Our 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
Identifiants
pubmed: 36084760
pii: S0024-3205(22)00631-2
doi: 10.1016/j.lfs.2022.120931
pii:
doi:
Substances chimiques
Actins
0
Adrenergic Agents
0
Endothelin-1
0
Hexanes
0
Plant Extracts
0
Thromboxanes
0
Methacholine Chloride
0W5ETF9M2K
Phalloidine
17466-45-4
n-hexane
2DDG612ED8
saw palmetto extract
J7WWH9M8QS
Sincalide
M03GIQ7Z6P
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
120931Informations de copyright
Copyright © 2022 Elsevier Inc. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of competing interest Thomas Kolben holds stock of Roche AG and a relative is employed at Roche AG. The other authors have no conflict of interest to declare.