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BRIEF RESEARCH REPORT article

Front. Toxicol.
Sec. Immunotoxicology
Volume 6 - 2024 | doi: 10.3389/ftox.2024.1504508
This article is part of the Research Topic The toxicology of cannabis and cannabis-based products View all 5 articles

The effect of cannabis-derived terpenes on alveolar macrophage function

Provisionally accepted

The final, formatted version of the article will be published soon.

    Cannabis sativa (marijuana) is used by millions of people around the world. C. sativa produces hundreds of secondary metabolites including cannabinoids, flavones and terpenes. Terpenes are a broad class of organic compounds that give cannabis and other plants its aroma. Previous studies have demonstrated that terpenes may exert anti-inflammatory properties on immune cells. However, it is not known whether terpenes derived from cannabis alone or in combination with the cannabinoid ∆ 9 -THC impacts the function of alveolar macrophages, a specialized pulmonary innate immune cell that is important in host defense against pathogens. Therefore, we investigated the immunomodulatory properties of two commercially-available cannabis terpene mixtures on the function of MH-S cells, a murine alveolar macrophage cell line. MH-S cells were exposed to terpene mixtures at sublethal doses and to the bacterial product lipopolysaccharide (LPS). We measured inflammatory cytokine levels using qRT-PCR and multiplex ELISA, as well as phagocytosis of opsonized IgG-coated beads or mCherry-expressing E. coli via flow cytometry. Neither terpene mixture affected inflammatory cytokine production by MH-S cells in response to LPS. Terpenes increased MH-S cell uptake of opsonized beads but had no effect on phagocytosis of E. coli. Addition of ∆ 9 -THC to terpenes did not potentiate cytotoxicity nor phagocytosis. These results suggest that terpenes from cannabis have minimal impact on the function of alveolar macrophages.

    Keywords: Cannabis, Terpenes, Inflammation, Phagocytosis, Macrophages

    Received: 30 Sep 2024; Accepted: 30 Dec 2024.

    Copyright: © 2024 Greiss, Rich, Mackay, Nguyen, Lefsrud, Eidelman and Baglole. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

    * Correspondence: Carolyn J. Baglole, McGill University, Montreal, Canada

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