Sedative and muscle relaxant activities of diterpenoids from Phlomidoschema parviflorum

• Autor(a) principal: Rauf,Abdur
• Data de Publicação: 2017
• Outros Autores: Farooq,Umar, Khan,Ajmal, Hadda,Taibi Ben, Naz,Sadia, Ibrar,Aliya, Jehan,Noor, Cerón-Carrasco,José P., Haan,Helena den, Peña-García,Jorge, Pérez-Sánchez,Horacio, Khan,Haroon, Ramadan,Mohamed Fawzy, Abu-Izneid,Tareq, Bawazeer,Saud
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Revista Brasileira de Farmacognosia (Online)
• Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-695X2017000500636
• topic: Rosane diterpenoids; Stachysrosane; Sedative; Skeleton muscle relaxant activity; Molecular docking

Abstract Phlomidoschema parviflorum (Benth.) Vved. (Basionym: Stachys parviflora Benth.) Lamiaceae, have significance medicinal importance as it is used in number of health disorders including diarrhea, fever, sore mouth and throat, internal bleeding, weaknesses of the liver and heart genital tumors, sclerosis of the spleen, inflammatory tumors and cancerous ulcers. The present contribution deals with the sedative and muscle relaxant like effects of diterpenoids trivially named stachysrosane and stachysrosane, isolated from the ethyl acetate soluble fraction of P. parviflorum. Both compounds (at 5, 10 and 15 mg/kg, i.p) were assessed for their in vivo sedative and muscle relaxant activity in open field and inclined plane test, respectively. The geometries of both compounds were optimized with density functional theory. The molecular docking of both compounds were performed with receptor gamma aminobutyric acid. Both compounds showed marked activity in a dose dependent manner. The docking studies showed that both compounds interact strongly with important residues in receptor gamma aminobutyric acid. The reported data demonstrate that both compounds exhibited significant sedative and muscle relaxant-like effects in animal models, which opens a door for novel therapeutic applications.