Skip to main content

EDITORIAL article

Front. Aging Neurosci., 04 January 2023
Sec. Cellular and Molecular Mechanisms of Brain-aging
This article is part of the Research Topic Targeting the Endocannabinoidome in Neurodegenerative Disorders View all 5 articles

Editorial: Targeting the endocannabinoidome in neurodegenerative disorders

  • 1Department of Neuropsychiatry, Graduate School of Medicine, University of Yamanashi, Chuo, Japan
  • 2Department of Clinical Genetics, Graduate School of Medicine, University of Yamanashi, Chuo, Japan

Current studies have unveiled the important roles of the endocannabinoid system (ECS) in multiple aspects of neural functions, including motor coordination, learning and memory, emotion and motivation, and psychiatric disorders such as mood disorders (de Melo Reis et al., 2021). ECS is composed of the two canonical receptor subtypes: type-1 cannabinoid (CB1R) and type 2 receptor (CB2R), as well as endocannabinoids (eCBs) and enzymes responsible for the synthesis and degradation of eCBs. Many studies have focused on each molecule of ECS using cannabinoid receptor ligands, such as CBD, to discover the role that ECS might play in psychiatric and neurodegenerative disorders. CB2R in particular became known as a major regulator of the activity of microglia, which is upregulated under inflammatory conditions (Komorowska-Müller et al., 2021). ECS could potentially be involved in those disorders by regulating monoamine systems (Mendiguren et al., 2021; Peters and Naneix, 2022) and GABAergic and cholinergic neurons.

In addition, expanded ECS, called “endocannabinoidome,” has been recognized to understand the molecular mechanism underlying various diseases and to develop novel therapeutics for them. The endocannabinoidome potentially includes hundreds of lipid mediators, more than 20 biosynthetic or inactivating enzymes, and more than 20 molecular targets, such as many previously identified nuclear receptors, ligand-activated ion channels, and orphan GPCRs (Veilleux et al., 2019; Morris et al., 2021). For example, N-Oleoyl-glycine is a lipid mediator that belongs to endocannabinoidome, which has recently gained attention for its protective effects in a mouse model of mild traumatic brain injury (Shahen-Zoabi et al., 2022). Besides, recent studies have also indicated an interaction between orexinergic and ECS, such as in addiction and fear (Deli et al., 2022; Ten-Blanco et al., 2022), while orexin's role in stress regulation and memory remains to be elucidated.

From a clinical perspective, depression varies in its clinical phenotypes at different onset ages. Our studies indicated the association of CB2R with patients with depression who had been diagnosed with major depressive disorders and had experienced a single episode of depression up until halfway through their lives but they did not include recurrent depression and bipolar disorders depression in the elderly (Onaivi et al., 2008), nor stress-related disorders in animal models (Ishiguro et al., 2018). ECS and related neural systems are needed to define the different phenotypes of depression. Since the early stages of Alzheimer's Disease (AD) and Parkinson's Disease (PD) are known to show a depressive phenotype, new perspectives regarding neuroinflammation and neuroprogression by endocannabinoidome could help unravel the molecular brain function underlying AD and PD.

While AD is characterized by an abnormal accumulation of β-amyloid (Aβ), eCBs have been shown to decrease Aβ-induced microglia activation and neuroinflammation (Vázquez et al., 2015; Schmöle et al., 2018). CB2R levels were significantly elevated in animal models of PD and postmortem studies of PD patients, and this increase correlated significantly with an increase in microglial activation, indicating the possible role of CB2Rs in PD (Concannon et al., 2015; Gómez-Gálvez et al., 2016).

This Research Topic focuses on neurodegenerative diseases and the comprehensive elucidation of endocannabinoidome in neurodegenerative disorders. It includes two original research projects: one brief research report and one review. In brief, each research piece indicates the role of CB2R in microglia and astroglia in AD-related cerebral amyloidosis as a suitable target for imaging neuro-inflammation and the role of the orexin system as endocannabinoidome in mild-to-moderate, age-related cognitive decline. Considering orexin's role as a stress regulator, it is also interesting to understand its potential role in the aforementioned different types of depression. A review summarizes the role of psychological and cellular stress on protein homeostasis via ECS, as a part of the neuro-immune system and the HPA axis, in degenerative conditions underlying AD. Another piece of original research shows that N-Oleoyl-glycine, which is known as a lipoamino acid that stimulates adipogenesis associated with the activation of CB1R, could have a promising therapeutic effect on PD. Hence, these carefully selected articles on this topic could point us toward understanding endocannabinoidome and the development of therapeutics for neurodegenerative disorders.

Author contributions

The author confirms being the sole contributor of this work and has approved it for publication.

Conflict of interest

The author declares that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher's note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

Concannon, R. M., Okine, B. N., Finn, D. P., and Dowd, E. (2015). Differential upregulation of the cannabinoid CB2 receptor in neurotoxic and inflammation-driven rat models of Parkinson's disease. Exp. Neurol. 269, 133–141. doi: 10.1016/j.expneurol.04.007

PubMed Abstract | CrossRef Full Text | Google Scholar

de Melo Reis, R. A., Isaac, A. R., Freitas, H. R., de Almeida, M. M., Schuck, P. F., Ferreira, G. C., et al. (2021). Quality of life and a surveillant endocannabinoid system. Front. Neurosci. 15, 47229. doi: 10.3389/fnins.2021.747229

PubMed Abstract | CrossRef Full Text | Google Scholar

Deli, S. B., Bonab, S. I., Khakpay, R., Khakpai, F., and Feyzi, M. H. (2022). An interaction between basolateral amygdala orexinergic and endocannabinoid systems in inducing anti-nociception in the rat formalin test. Psychopharmacology 239, 3171–3184. doi: 10.1007/s00213-022-06199-1

PubMed Abstract | CrossRef Full Text | Google Scholar

Gómez-Gálvez, Y., Palomo-Garo, C., Fernández-Ruiz, J., and García, C. (2016). Potential of the cannabinoid CB2 receptor as a pharmacological target against inflammation in Parkinson's disease. Prog. Neuropsychopharmacol. Biol. Psychiatry 64, 200–208. doi: 10.1016/j.pnpbp.03.017

PubMed Abstract | CrossRef Full Text | Google Scholar

Ishiguro, H., Horiuchi, Y., Tabata, K., Liu, Q. R., Arinami, T., Onaivi, E. S., et al. (2018). Cannabinoid CB2 receptor gene and environmental interaction in the development of psychiatric disorders. Molecules 23, 1836. doi: 10.3390/molecules23081836

PubMed Abstract | CrossRef Full Text | Google Scholar

Komorowska-Müller, J. A., Rana, T., Olabiyi, B. F., Zimmer, A., and Schmöle, A. C. (2021). Cannabinoid receptor 2 alters social memory and microglial activity in an age-dependent manner. Molecules 26, 5984. doi: 10.3390/molecules26195984

PubMed Abstract | CrossRef Full Text | Google Scholar

Mendiguren, A., Aostri, E., and Pineda, J. (2021). Modulation of noradrenergic and serotonergic systems by cannabinoids: electrophysiological, neurochemical and behavioral evidence. Adv. Exp. Med. Biol. 1297, 111–132. doi: 10.1007/978-3-030-61663-2_8

PubMed Abstract | CrossRef Full Text | Google Scholar

Morris, G., Walder, K., Kloiber, S., Amminger, P., Berk, M., Bortolasci, C. C., et al. (2021). The endocannabinoidome in neuropsychiatry: opportunities and potential risks. Pharmacol. Res. 170, 105729. doi: 10.1016/j.phrs.2021.105729

PubMed Abstract | CrossRef Full Text | Google Scholar

Onaivi, E. S., Ishiguro, H., Gong, J. P., Patel, S., Meozzi, P. A., Myers, L., et al. (2008). Brain neuronal CB2 cannabinoid receptors in drug abuse and depression: from mice to human subjects. PLoS ONE 3, e1640. doi: 10.1371/journal.pone.0001640

PubMed Abstract | CrossRef Full Text | Google Scholar

Peters, K. Z., and Naneix, F. (2022). The role of dopamine and endocannabinoid systems in prefrontal cortex development: adolescence as a critical period. Front. Neural Circ. 16, 939235. doi: 10.3389/fncir.2022.939235

PubMed Abstract | CrossRef Full Text | Google Scholar

Schmöle, A. C., Lundt, R., Toporowski, G., Hansen, J. N., Beins, E., Halle, A., et al. (2018). Cannabinoid receptor 2-deficiency ameliorates disease symptoms in a mouse model with Alzheimer's disease-like pathology. J. Alzheimers Dis. 64, 379–392. doi: 10.3233/JAD-180230

PubMed Abstract | CrossRef Full Text | Google Scholar

Shahen-Zoabi, S., Smoum, R., Beiser, T., Nemirovski, A., Mechoulam, R., Yaka, R., et al. (2022). N-Oleoyl glycine and its derivatives attenuate the acquisition and expression of cocaine-induced behaviors. Cannabis Cannabinoid Res. doi: 10.1089/can.2022.0005. [Epub ahead of print].

PubMed Abstract | CrossRef Full Text | Google Scholar

Ten-Blanco, M., Flores, Á., Pereda-Pérez, I., Piscitelli, F., Izquierdo-Luengo, C., Cristino, L., et al. (2022). Amygdalar CB2 cannabinoid receptor mediates fear extinction deficits promoted by orexin-A/hypocretin-1. Biomed. Pharmacother. 149, 112925. doi: 10.1016/j.biopha.2022.112925

PubMed Abstract | CrossRef Full Text | Google Scholar

Vázquez, C., Tolón, R. M., Grande, M. T., Caraza, M., Moreno, M., Koester, E. C., et al. (2015). Endocannabinoid regulation of amyloid-induced neuroinflammation. Neurobiol. Aging 36, 3008–3019. doi: 10.1016/j.neurobiolaging.08.003

PubMed Abstract | CrossRef Full Text | Google Scholar

Veilleux, A., Di Marzo, V., and Silvestri, C. (2019). the expanded endocannabinoid system/endocannabinoidome as a potential target for treating diabetes mellitus. Curr. Diab. Rep. 19, 117. doi: 10.1007/s11892-019-1248-9

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: endocannabinoid, expanded endocannabinoid system, cannabinoid CB2 receptor, Alzheimer's Disease, Parkinson's Disease, N-Oleoyl-glycine, orexin

Citation: Ishiguro H (2023) Editorial: Targeting the endocannabinoidome in neurodegenerative disorders. Front. Aging Neurosci. 14:1116635. doi: 10.3389/fnagi.2022.1116635

Received: 05 December 2022; Accepted: 09 December 2022;
Published: 04 January 2023.

Edited and reviewed by: Thomas Wisniewski, Grossman School of Medicine, New York University, United States

Copyright © 2023 Ishiguro. 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) and the copyright owner(s) 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: Hiroki Ishiguro, yes hishiguro@yamanashi.ac.jp

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.