# A Multi-Target Phytotherapeutic Approach to Benign Prostatic Hyperplasia: Preclinical Characterization of a PhytoBPH-Mix

**Authors:** Chiara Amante, Chiara De Soricellis, Maria Rosaria Sellitto, Giovanni Falcone, Luigi Luccheo, Gianni Luccheo, Pasquale Del Gaudio

PMC · DOI: 10.3390/nu18040650 · 2026-02-16

## TL;DR

A new plant-based mixture shows promise in treating benign prostatic hyperplasia by targeting multiple causes with fewer side effects.

## Contribution

The study introduces and evaluates a novel multi-component phytocomplex for BPH treatment with multi-target effects.

## Key findings

- The mixture significantly inhibited 5α-reductase activity in vitro.
- It reduced the release of pro-inflammatory cytokines IL-6 and TNF-α.
- The formulation showed antibacterial effects against E. coli.

## Abstract

Background: Benign prostatic hyperplasia (BPH) is a prevalent condition affecting over 50% of men aged 60 and above, often leading to lower urinary tract symptoms that significantly impact quality of life. Current pharmacological treatments, including α-adrenergic receptor antagonists and 5α-reductase inhibitors, are associated with adverse effects, prompting the exploration of alternative therapies. This study investigates the potential role of a novel multi-component phytocomplex (PhytoBPH-Mix) comprising Serenoa repens, Pygeum africanum, Urtica dioica, Epilobium angustifolium L., Protium heptaphyllum, lycopene, Vitamin E, zinc, and selenium. Methods: The anti-androgenic, anti-inflammatory, and antimicrobial properties of the mixture were evaluated in vitro. Results: The formulation significantly inhibited 5α-reductase activity, reduced the release of pro-inflammatory cytokines (IL-6 and TNF-α), and exhibited antibacterial effects against E. coli compared to individual extracts. Conclusions: These findings suggest that this specific mixture offers a promising natural alternative or an adjuvant for managing BPH by targeting multiple pathological mechanisms with minimal side effects and could also serve as an effective adjuvant in conventional therapy.

## Linked entities

- **Chemicals:** lycopene (PubChem CID 446925), Vitamin E (PubChem CID 14985), zinc (PubChem CID 23994), selenium (PubChem CID 6326970)
- **Diseases:** Benign prostatic hyperplasia (MONDO:0010811)
- **Species:** Serenoa repens (taxon 4722), Urtica dioica (taxon 3501), Protium heptaphyllum (taxon 246847)

## Full-text entities

- **Genes:** IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}
- **Diseases:** oncological diseases (MESH:D000072716), hyperplasia (MESH:D006965), retrograde ejaculation (MESH:D061686), nocturia (MESH:D053158), Prostatic (MESH:D011472), chronic (MESH:D002908), gynecomastia (MESH:D006177), LUTS (MESH:D059411), impotence (MESH:D007172), BPH (MESH:D011470), cytotoxic (MESH:D064420), urinary tract infections (MESH:D014552), prostate cancer (MESH:D011471), fibrosis (MESH:D005355), bacterial inflammation (MESH:D007249), injury to (MESH:D014947)
- **Chemicals:** DHT (MESH:D013196), reactive oxygen species (MESH:D017382), flavonoids (MESH:D005419), oenothein B. (MESH:C080077), DMSO (MESH:D004121), glucose (MESH:D005947), ethanol (MESH:D000431), L-glutamine (MESH:D005973), steroid (MESH:D013256), citrate (MESH:D019343), CO2 (MESH:D002245), Polyphenols (MESH:D059808), ellagitannins (MESH:D047348), lycopene (MESH:D000077276), alpha-tocopherol (MESH:D024502), resin (MESH:D012116), sterol (MESH:D013261), silodosin (MESH:C095285), dutasteride (MESH:D000068538), lipid (MESH:D008055), phenolic acids (MESH:C017616), Testosterone (MESH:D013739), LPS (MESH:D008070), beta-sitosterol (MESH:C025473), Vitamin E (MESH:D014810), dihydrocortisone (MESH:D006854), prostaglandins (MESH:D011453), lignans (MESH:D017705), 3,3',5,5'-tetramethylbenzidine (MESH:C021758), E2 (MESH:D004958), polysaccharides (MESH:D011134), Selenium (MESH:D012643), fatty acid (MESH:D005227), phytosterols (MESH:D010840), streptomycin (MESH:D013307), tannins (MESH:D013634), triterpenes (MESH:D014315), tamsulosin (MESH:D000077409), saline (MESH:D012965), MHB (-), finasteride (MESH:D018120), penicillin (MESH:D010406), salicylic acid (MESH:D020156), Zinc (MESH:D015032), phosphate (MESH:D010710), acids (MESH:D000143)
- **Species:** Pygeum (genus) [taxon 401066], Chamaenerion angustifolium (fireweed, species) [taxon 13055], Mycoplasma (genus) [taxon 2093], Escherichia coli O111:B4 (no rank) [taxon 1090940], Protium heptaphyllum (species) [taxon 246847], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Prunus africana (species) [taxon 379279], Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606], Urtica dioica (great nettle, species) [taxon 3501], Serenoa repens (saw palmetto, species) [taxon 4722], Solanum lycopersicum (tomato, species) [taxon 4081], Escherichia coli (E. coli, species) [taxon 562]
- **Cell lines:** ATCC 15221 — Homo sapiens (Human), Transformed cell line (CVCL_5W51), RAW 264.7 — Mus musculus (Mouse), Mouse leukemia, Cancer cell line (CVCL_0493), THP-1 — Homo sapiens (Human), Childhood acute monocytic leukemia, Cancer cell line (CVCL_0006), VCaP — Homo sapiens (Human), Prostate carcinoma, Cancer cell line (CVCL_2235), CRL-2876 — Homo sapiens (Human), Turner syndrome, Transformed cell line (CVCL_9L40)

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12943485/full.md

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Source: https://tomesphere.com/paper/PMC12943485