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Assessing the treatment of cannabidiolic acid methyl ester: a stable synthetic analogue of cannabidiolic acid on c-Fos and NeuN expression in the hypothalamus of rats

  • Eric Murillo-Rodríguez(corresponding author)
    ,
  • Diana Millán-Aldaco
    ,
  • Gloria Arankowsky-Sandoval
    ,
  • Tetsuya Yamamoto
    ,
  • Roger G. Pertwee
    ,
  • Linda Parker
*Corresponding author for this work
  • ,
  • Intercontinental Neuroscience Research Group
    ,
  • Universidad Nacional Autónoma de México
    ,
  • Universidad Autonoma de Yucatan
    ,
  • Tokushima University
    ,
  • University of Aberdeen
Research Output:
Contribution to journal
Article
Peer review

Open Access

Publication Information

Tipo di output

Research Output:
Contribution to journal
Article
Peer review

Lingua originale

English

Numero dell’articolo

31

Rivista (volume, numero edizione)

Journal of Cannabis Research (Volume 3, Edizione 1)

Attività cardine della pubblicazione

  • Published - 01/12/2021

Stato pubblicazione

Published - 01/12/2021

Publication IDs

  • Scopus: 85147136768

Abstract

Background: Cannabidiol (CBD), the non-psychotropic compound from Cannabis sativa, shows positive results on controlling several health disturbances; however, comparable data regarding additional chemical from C. sativa, such as cannabidiolic acid (CBDA), is scarce due to its instability. To address this limitation, a stable CBDA analogue, CBDA methyl ester (HU-580), was synthetized and showed CBDA-like effects. Recently, we described that HU-580 increased wakefulness and wake-related neurochemicals. Objective: To extend the comprehension of HU-580´s properties on waking, the c-Fos and NeuN expression in a wake-linked brain area, the hypothalamus was evaluated. Methods: c-Fos and NeuN expression in hypothalamic sections were analyzed after the injections of HU-580 (0.1 or 100 μg/kg, i.p.). Results: Systemic administrations of HU-580 increased c-Fos and neuronal nuclei (NeuN) expression in hypothalamic nuclei, including the dorsomedial hypothalamic nucleus dorsal part, dorsomedial hypothalamic nucleus compact part, and dorsomedial hypothalamic nucleus ventral part. Conclusion: HU-580 increased c-Fos and NeuN immunoreactivity in hypothalamus nuclei suggesting that this drug might modulate the sleep–wake cycle by engaging the hypothalamus.