PetCaseFinder

Peer-reviewed veterinary case report

In vitro inhibition of 5-α reductase and in vivo suppression of benign prostatic hyperplasia by Physalis angulata ethyl acetate extract.

Journal:
Fitoterapia
Year:
2024
Authors:
Nguyen, Ngoc Phuc et al.
Affiliation:
Department of Pharmacology
Species:
rodent

Abstract

The inhibitory effect against 5-&#x3b1; reductase of the ethyl acetate (EA) extract from Physalis angulata was evaluated in vitro using mouse prostate homogenates, and the suppression of benign prostatic hyperplasia (BPH) was assessed in a mouse model of testosterone-induced BPH. The EA extract exhibited a potentially inhibitory effect on 5-&#x3b1; reductase with an ICof 197&#xa0;&#x3bc;g/ml. In BPH mice, the EA extract at a dose of 12&#xa0;mg/kg was comparable to finasteride 5&#xa0;mg/kg in suppressing BPH in terms of reducing absolute enlarged prostate weight (p&#xa0;<&#xa0;0.05 vs. BPH group) and mitigating the hypertrophy of glandular elements and prostate connective tissue. Identification of chemical ingredients in the EA extract by UPLC-QTOF-MS revealed 37 substances belonging chiefly to flavonoids and physalins. Further quantification of the EA extract by HPLC-PDA methods revealed that chlorogenic acid, and rutin were the main components. Molecular docking studies of chlorogenic acid and rutin on 5-&#x3b1; reductase showed their high affinity to the enzyme with binding energies of -9.3 and&#xa0;-&#xa0;9.2&#xa0;kcal/mol, respectively compared with finasteride (- 10.3&#xa0;kcal/mol). Additionally, chlorogenic acid inhibited 5-&#x3b1; reductase with an ICof 12.07 &#xb5;M while rutin did not. The presence of chlorogenic acid in the EA extract may explain the inhibitory effects of the EA extract on 5-&#x3b1; reductase, and thus the suppression of BPH.

Find similar cases for your pet

PetCaseFinder finds other peer-reviewed reports of pets with the same symptoms, plus a plain-English summary of what was tried across them.

Search related cases →

Original publication: https://pubmed.ncbi.nlm.nih.gov/38599338/