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First Evidence of the Protective Effects of 2-Pentadecyl-2-Oxazoline (PEA-OXA) in In Vitro Models of Acute Lung Injury

Aniello Schiano Moriello, Fiorentina Roviezzo, Fabio Arturo Iannotti, Giuseppina Rea, Marco Allarà, Rosa Camerlingo, Roberta Verde, Vincenzo Di Marzo, Stefania Petrosino. Biomolecules. 2022 Dec 24;13(1):33.

Laboratory studyHumansWith PEA-OXA (2-pentadecyl-2-oxazoline, a PEA analogue, tested alongside ultramicronised PEA)

This study tested palmitoylethanolamide together with PEA-OXA (2-pentadecyl-2-oxazoline, a PEA analogue, tested alongside ultramicronised PEA). Its results cannot be assigned to palmitoylethanolamide alone. More combination studies.

Design
Laboratory study
Subjects
Human lung epithelial A549 cells activated by poly-(I:C) or TGF-beta
Dose used in the study
PEA-OXA or ultramicronised palmitoylethanolamide added to cell culture; concentrations not stated in the abstract
Duration
Not stated in the abstract
What was measured
IL-6 release by ELISA; epithelial-mesenchymal transition by immunofluorescence; endogenous anandamide, 2-AG and PEA levels

What the authors reported

This in vitro study found:

  • Both PEA-OXA and PEA reduced poly-(I:C)-induced IL-6 release and reversed TGF-beta-induced epithelial-mesenchymal transition.
  • PEA raised anandamide and 2-AG levels, while PEA-OXA raised only endogenous PEA.
  • PEA-OXA was described as superior to PEA in protective effect.

Limits of this study

A human cell-line study; it cannot show effect in people. Three authors are employees of Epitech Group SpA, and two hold patents on adelmidrol or PEA.

Source

PubMed 36671418 · doi:10.3390/biom13010033

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.