palmitoylethanolamide.com.au
Home › Research › D'Amico 2019

Effects of a new compound containing Palmitoylethanolamide and Baicalein in myocardial ischaemia/reperfusion injury in vivo

D'Amico R, Fusco R, Gugliandolo E, Cordaro M, Siracusa R, Impellizzeri D, Peritore AF, Crupi R, Cuzzocrea S, Di Paola R. Phytomedicine. 2019 Feb 15;54:27-42.

Laboratory studyOther animalsWith baicalein

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

Design
Laboratory study
Subjects
Animals (species not stated in the abstract) with myocardial ischaemia/reperfusion injury from 30 minutes of coronary artery occlusion followed by 2 hours of reperfusion
Dose used in the study
PEA-baicalein composite (9:1), 10 mg/kg, given 5 minutes before the end of ischaemia and again 1 hour after reperfusion
Duration
30 minutes ischaemia plus 2 hours reperfusion
What was measured
Myocardial tissue injury, neutrophil infiltration, mast cell activation markers (chymase, tryptase), cytokines (TNF-alpha, IL-1beta), oxidative stress, and NF-kB and apoptosis pathways

What the authors reported

PEA-baicalein treatment reduced myocardial tissue injury, neutrophil infiltration, chymase and tryptase expression, and TNF-alpha and IL-1beta production. It also reduced oxidative stress and modulated NF-kB and apoptosis pathway activity. PEA-Baicalein (9:1) was given at 10 mg/kg, 5 minutes before the end of ischaemia and again 1 hour after reperfusion.

Limits of this study

An animal model of induced heart injury; it cannot show effect in people. Funding and conflicts not stated in the abstract. PubMed lists an erratum for this paper (Phytomedicine. 2023 Feb;110:154592).

Source

PubMed 30668378 · doi:10.1016/j.phymed.2018.09.191

Entry checked against the abstract on PubMed on 2026-10-19. The dose shown is the dose the researchers used. It is not a recommendation. How to read this page.