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Opposite Effects of Neuroprotective Cannabinoids, Palmitoylethanolamide, and 2-Arachidonoylglycerol on Function and Morphology of Microglia

Hohmann U, Pelzer M, Kleine J, Hohmann T, Ghadban C, Dehghani F. Front Neurosci. 2019 Nov 7;13:1180.

Laboratory studyOther animalsWith 2-arachidonoylglycerol (2-AG, tested alongside PEA, not as a fixed combination product)

This study tested palmitoylethanolamide together with 2-arachidonoylglycerol (2-AG, tested alongside PEA, not as a fixed combination product). Its results cannot be assigned to palmitoylethanolamide alone. More combination studies.

Design
Laboratory study
Subjects
Organotypic hippocampal slice cultures with excitotoxic lesion, and primary microglial cell cultures stimulated with lipopolysaccharide
Dose used in the study
PEA, 2-AG, or the combination, applied to cultures; concentrations not stated in the abstract
Duration
Not stated in the abstract
What was measured
Number of damaged neurons after excitotoxic lesion; microglial nitric oxide production, ramification index, proliferation and PPAR-alpha distribution.

What the authors reported

PEA or 2-AG alone reduced neuronal damage after excitotoxic lesion, but combining them removed this protective effect, independent of microglial cells. PEA and 2-AG had opposite effects on microglial ramification and nitric oxide production; microglial proliferation and PPAR-alpha expression were unchanged, though PPAR-alpha distribution shifted.

Limits of this study

A cell- and tissue-culture study; it cannot show effect in people or animals. Funding and conflicts not stated in the abstract.

Source

PubMed 31787870 · doi:10.3389/fnins.2019.01180

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.