Abbas Shafiee1, Maryam Bagheri, Maryam Shekarchi, Mohammad Abdollahi. 1. Department of Medicinal Chemistry, Faculty of Pharmacy, and Laboratory of Chemistry, Pharmaceutical Sciences Research Center, Tehran University of Medical Sciences, Tehran, Iran.
Abstract
PURPOSE: Sympathetic nervous system stimulation, which releases noradrenalin, influences the nociceptive activity that develops after tissue injury. The alpha2-adrenergic agonist, clonidine, produces analgesia through a central mechanism but also inhibits noradrenalin release at terminal nerve fiber endings. METHODS: In this study the effects of some 1-(4-aryl-2-thiazolyl)-3,5-disubstituted-2-pyrazolines (compounds 1a-1e) as analogues of clonidine with some modifications were studied by writhing test, a visceral pain model in mice. RESULTS: Compounds 1a and 1c induced significant reduction in writhing response when compared to control. Regarding the dose-response relationship of compounds 1a and 1c, it is evident that the activity of these compounds is in direct proportion to their dose and all compounds show activities comparable to clonidine. In addition compounds 1a and 1c, having methoxy and nitro groups respectively at para position of 4-aryl showed better antinociception than compounds having similar groups in meta position namely 1b and 1e. This might be due to better interaction of these compounds with the alpha2-receptors. CONCLUSIONS: The antinociceptive properties of these newly synthesized compounds is comparable to clonidine. Further studies are needed to explore the differences in the efficacy and safety of synthesized compounds.
PURPOSE: Sympathetic nervous system stimulation, which releases noradrenalin, influences the nociceptive activity that develops after tissue injury. The alpha2-adrenergic agonist, clonidine, produces analgesia through a central mechanism but also inhibits noradrenalin release at terminal nerve fiber endings. METHODS: In this study the effects of some 1-(4-aryl-2-thiazolyl)-3,5-disubstituted-2-pyrazolines (compounds 1a-1e) as analogues of clonidine with some modifications were studied by writhing test, a visceral pain model in mice. RESULTS: Compounds 1a and 1c induced significant reduction in writhing response when compared to control. Regarding the dose-response relationship of compounds 1a and 1c, it is evident that the activity of these compounds is in direct proportion to their dose and all compounds show activities comparable to clonidine. In addition compounds 1a and 1c, having methoxy and nitro groups respectively at para position of 4-aryl showed better antinociception than compounds having similar groups in meta position namely 1b and 1e. This might be due to better interaction of these compounds with the alpha2-receptors. CONCLUSIONS: The antinociceptive properties of these newly synthesized compounds is comparable to clonidine. Further studies are needed to explore the differences in the efficacy and safety of synthesized compounds.
Authors: Luciane C Lopes; João Ernesto de Carvalho; Marise Kakimore; Débora B Vendramini-Costa; Maria A Medeiros; Humberto M Spindola; Javier Ávila-Román; Ana M Lourenço; Virginia Motilva Journal: Inflammopharmacology Date: 2013-08-09 Impact factor: 4.473
Authors: Humberto M Spindola; Leila Servat; Carina Denny; Rodney A F Rodrigues; Marcos N Eberlin; Elaine Cabral; Ilza M O Sousa; Jorge Y Tamashiro; João E Carvalho; Mary A Foglio Journal: BMC Pharmacol Date: 2010-01-07
Authors: Shyam Sunder A; Satyavati Dhulipala; Sreekanth Thota; Rajeshwar Yerra; Jan Balzarini; Erik De Clercq Journal: J Res Med Sci Date: 2013-03 Impact factor: 1.852