Side-by-side comparison of mechanisms, dosing, interactions, and stacking potential.
| DHEA (Dehydroepiandrosterone) | Saw Palmetto (Serenoa repens) | |
|---|---|---|
| Category | Supplements | Supplements |
| Standard Dose | 25-50mg daily (men); 10-25mg daily (women) | 320mg daily (standardized to 85-95% fatty acids and sterols) |
| Timing | Morning (mimics natural circadian peak). With food. | With food (fat-soluble lipophilic extract). Morning or evening. |
| Cycle Duration | Ongoing under supervision with regular blood monitoring (DHEA-S, testosterone, estradiol, PSA in men) | Minimum 3 months to assess response; ongoing for maintenance |
| Evidence Level | moderate_human | moderate_human |
DHEA is the most abundant circulating steroid hormone, produced primarily by the adrenal zona reticularis. It serves as a precursor for both androgens (testosterone, DHT via 3beta-HSD and 17beta-HSD) and estrogens (estradiol, estrone via aromatase). DHEA-S (sulfated form) acts as a neurosteroid, positively modulating NMDA receptors and antagonizing GABA-A receptors (cognitive enhancement/alertness). It also modulates immune function (enhances Th1 immunity, IL-2 production), supports bone mineral density via estrogenic metabolites, enhances insulin sensitivity via PPAR-alpha activation, and opposes cortisol's catabolic effects (DHEA:cortisol ratio is a stress/aging biomarker).
25-50mg daily (men); 10-25mg daily (women)
Morning (mimics natural circadian peak). With food.
Ongoing under supervision with regular blood monitoring (DHEA-S, testosterone, estradiol, PSA in men)
Saw palmetto berry extract contains fatty acids (lauric acid, oleic acid, myristic acid) and phytosterols (beta-sitosterol) that inhibit both isoforms of 5-alpha-reductase (types I and II), reducing conversion of testosterone to dihydrotestosterone (DHT). It also exhibits anti-androgenic activity by competing with DHT at androgen receptor binding sites. Additional mechanisms include: inhibition of cyclooxygenase and 5-lipoxygenase (anti-inflammatory in prostate tissue), induction of apoptosis in prostate epithelial cells, and relaxation of bladder smooth muscle via alpha-1 adrenergic receptor antagonism.
320mg daily (standardized to 85-95% fatty acids and sterols)
With food (fat-soluble lipophilic extract). Morning or evening.
Minimum 3 months to assess response; ongoing for maintenance
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