Inhibition of α 1 -Adrenergic, Non-Adrenergic and Neurogenic Human Prostate Smooth Muscle Contraction and of Stromal Cell Growth by the Isoflavones Genistein and Daidzein.
Ru HuangYuhan LiuSheng HuAlexander TamalunasRaphaela WaidelichFrank StrittmatterChristian G StiefMartin HennenbergPublished in: Nutrients (2022)
Isoflavone-rich legumes, including soy, are used for food production, as dietary supplements and in traditional medicine. Soy consumption correlates negatively with benign prostatic hyperplasia (BPH) and voiding symptoms. However, isoflavone effects on the prostate are hardly known. Here, we examined the effects on human prostate smooth muscle contractions and stromal cell growth, which are driving factors of voiding symptoms in BPH. Smooth muscle contractions were induced in prostate tissues from radical prostatectomy. Growth-related functions were studied in cultured stromal cells (WPMY-1). Neurogenic, α1-adrenergic and non-adrenergic contractions were strongly inhibited with 50 µM and by around 50% with 10 µM genistein. Daidzein inhibited neurogenic contractions using 10 and 100 µM. Agonist-induced contractions were inhibited by 100 µM but not 10 µM daidzein. A combination of 6 µM genistein with 5 µM daidzein still inhibited neurogenic and agonist-induced contractions. Proliferation of WPMY-1 cells was inhibited by genistein (>50%) and daidzein (<50%). Genistein induced apoptosis and cell death (by seven-fold relative to controls), while daidzein induced cell death (6.4-fold) without apoptosis. Viability was reduced by genistein (maximum: 87%) and daidzein (62%). In conclusion, soy isoflavones exert sustained effects on prostate smooth muscle contractions and stromal cell growth, which may explain the inverse relationships between soy-rich nutrition, BPH and voiding symptoms.
Keyphrases
- smooth muscle
- benign prostatic hyperplasia
- lower urinary tract symptoms
- prostate cancer
- induced apoptosis
- cell death
- high glucose
- endothelial cells
- radical prostatectomy
- cell cycle arrest
- diabetic rats
- spinal cord injury
- endoplasmic reticulum stress
- oxidative stress
- signaling pathway
- bone marrow
- drug induced
- gene expression
- induced pluripotent stem cells
- cell proliferation
- physical activity
- climate change
- pluripotent stem cells
- depressive symptoms