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
- ,
- Intercontinental Neuroscience Research Group,
- Universidad Nacional Autónoma de México,
- Universidad Autonoma de Yucatan,
- Tokushima University,
- University of Aberdeen
Open Access
Publication Information
Tipo di output
Lingua originale
EnglishNumero dell’articolo
31Rivista (volume, numero edizione)
Journal of Cannabis Research (Volume 3, Edizione 1)Attività cardine della pubblicazione
- Published - 01/12/2021
Stato pubblicazione
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.
