palmitoylethanolamide.com.au
HomeResearchRosanna 2016

Co-micronized Palmitoylethanolamide/Polydatin Treatment Causes Endometriotic Lesion Regression in a Rodent Model of Surgically Induced Endometriosis

Rosanna Di Paola, Roberta Fusco, Enrico Gugliandolo, Rosalia Crupi, Maurizio Evangelista, Roberta Granese, Salvatore Cuzzocrea. Front Pharmacol. 2016 Oct 14;7:382.

Laboratory studyOther animalsWith polydatin

This study tested palmitoylethanolamide together with polydatin. Its results cannot be assigned to palmitoylethanolamide alone. More combination studies.

Design
Laboratory study
Subjects
Female Wistar albino rats with surgically induced endometriosis (10 per group)
Dose used in the study
Co-micronised PEA/polydatin 10 mg/kg/day, oral
Duration
28 days
What was measured
Endometrioma volume, fibrosis, mast cell number, VEGF, nerve growth factor, ICAM, matrix metalloproteinase-9, lymphocyte accumulation, and oxidative/inflammatory markers

What the authors reported

Treated rats had smaller endometriotic cyst diameter, better fibrosis scores and fewer mast cells. PEA/polydatin reduced VEGF, nerve growth factor, ICAM and MMP-9 expression, lymphocyte accumulation, peroxynitrite formation, PARP activation and NF-kB nuclear translocation.

Limits of this study

A rat model of surgically induced endometriosis; it cannot show effect in people. Funding and conflicts not stated in the abstract; the group has used Epitech-linked co-micronised PEA formulations before.

Source

PubMed 27790149 · doi:10.3389/fphar.2016.00382

Entry checked against the abstract on PubMed on 2026-09-22. The dose shown is the dose the researchers used. It is not a recommendation. How to read this page.