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Multi targets of cannabidiol (CBD) on skeletal mammalian and avian neuromuscular preparations.
Castro-da-Silva, Maria Luiza Rodrigues de; Farias-de-França, Anna Paula; Ravazoli, Isabella; Oliveira, Karollyna Corrêa; Orsi, Valéria de Campos; Yoshida, Edson Hideaki; Tavares, Renata Vasques da Silva; Oshima-Franco, Yoko.
Afiliação
  • Castro-da-Silva MLR; Pharmacy Course, University of Sorocaba (UNISO), Sorocaba, Brazil.
  • Farias-de-França AP; Pharmacy Course, University of Sorocaba (UNISO), Sorocaba, Brazil.
  • Ravazoli I; Pharmacy Course, University of Sorocaba (UNISO), Sorocaba, Brazil.
  • Oliveira KC; Post-Graduate Program in Pharmaceutical Sciences, University of Sorocaba (UNISO), Sorocaba, Brazil.
  • Orsi VC; Post-Graduate Program in Pharmaceutical Sciences, University of Sorocaba (UNISO), Sorocaba, Brazil.
  • Yoshida EH; Post-Graduate Program in Pharmaceutical Sciences, University of Sorocaba (UNISO), Sorocaba, Brazil.
  • Tavares RVDS; Pharmacy Course, University of Sorocaba (UNISO), Sorocaba, Brazil.
  • Oshima-Franco Y; Post-Graduate Program in Pharmaceutical Sciences, University of Sorocaba (UNISO), Sorocaba, Brazil.
Nat Prod Res ; : 1-10, 2023 Dec 06.
Article em En | MEDLINE | ID: mdl-38054804
ABSTRACT
Cannabidiol (CBD) has been used in diseases that affect the central nervous system. Its effects on the peripheral synapses are of great interest, since endocannabinoid receptors are expressed in muscles. CBD (0.3 mM) was analysed using mammalian and avian neuromuscular preparations, through myographic techniques in complementary protocols. Mammalian cells were examined by light microscopy while exogenous acetylcholine (40 µM) and potassium chloride (100 mM) were added into avian preparations, before and at the end of experiments. Pharmacological tools such as atropine (2 µM), polyethylene glycol (PEG 400, 20 µM), Ca2+ (1.8 mM), F55-6 (20 µg/mL), and nifedipine (1.3 mM) were assessed with CBD. In mice, CBD causes a facilitatory effect and paralysis, whereas in avian, paralysis. Concluding, CBD is responsible for activated or inhibited channels, for ACh release via muscarinic receptor modulation, and by the inhibition of nicotinic receptors leading to neuromuscular blockade, with no damage to striated muscle cells.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article