Abstract

Background and Objectives: Neuroinflammation is associated with many neurodegenerative diseases, including amyotrophic lateral sclerosis (ALS). In this study, we investigate the anti-inflammatory, anti-oxidant, and anti-apoptotic properties of two non-psychoactive phytocannabinoids, cannabigerol (CBG) and cannabidiol (CBD). Materials and Methods: The motoneuron-like cell line NSC-34 differentiated by serum deprivation and with the additional treatment of all-trans retinoic acid (RA) is a valid model to investigate molecular events linked to neurodegeneration in ALS. Results: Pre-treatment with CBG (at 2.5 and 5 µM doses) alone and in combination with CBD (at 2.5 and 5 µM doses) was able to reduce neuroinflammation induced by a culture medium of LPS-stimulated macrophages. In particular, the pre-treatment with CBD at a 5 µM dose decreased TNF-α levels and increased IL10 and IL-37 expression. CBG–CBD association at a 5 µM dose also reduced NF-kB nuclear factor activation with low degradation of the inhibitor of kappaB alpha (IkBα). CBG and CBD co-administered at a 5 µM dose decreased iNOS expression and increased Nrf2 levels. Furthermore, the pre-treatment with the association of two non-psychoactive cannabinoids downregulated Bax protein expression and upregulated Bcl-2 expression. Our data show the anti-inflammatory, anti-oxidant, and anti-apoptotic effects PPARγ-mediated. Conclusions: Our results provide preliminary support on the potential therapeutic application of a CBG–CBD combination for further preclinical studies.

Highlights

  • Neuroinflammation is a key pathological event associated with many neurodegenerative diseases, including amyotrophic lateral sclerosis (ALS)

  • In differentiated NSC-34 cells, we evaluated by an MTT assay the possible toxicity on motoneurons of serial concentrations (2.5, 5, 10, 20, 40, and 80 μM) of CBG and CBD alone and in association with a 1:1 ratio

  • We analyzed NSC-34 cells incubated with dimethyl sulfoxide (DMSO < 0.1%), and no cytotoxicity was observed in line with our previous study reporting a normal morphological evaluation and nothing was altered in the transcriptome analysis of cells treated with DMSO [25]

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Summary

Introduction

Neuroinflammation is a key pathological event associated with many neurodegenerative diseases, including amyotrophic lateral sclerosis (ALS). Neuroinflammation is associated with many neurodegenerative diseases, including amyotrophic lateral sclerosis (ALS). We investigate the anti-inflammatory, anti-oxidant, and anti-apoptotic properties of two non-psychoactive phytocannabinoids, cannabigerol (CBG) and cannabidiol (CBD). Materials and Methods: The motoneuron-like cell line NSC-34 differentiated by serum deprivation and with the additional treatment of all-trans retinoic acid (RA) is a valid model to investigate molecular events linked to neurodegeneration in ALS. Results: Pre-treatment with CBG (at 2.5 and 5 μM doses) alone and in combination with CBD (at 2.5 and 5 μM doses) was able to reduce neuroinflammation induced by a culture medium of LPS-stimulated macrophages. The pre-treatment with CBD at a 5 μM dose decreased TNF-α levels and increased IL10 and IL-37 expression. Conclusions: Our results provide preliminary support on the potential therapeutic application of a CBG–CBD combination for further preclinical studies

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