Arturo Coaviche-Yoval, Héctor Luna, Ricardo Tovar-Miranda, Marvin Antonio Soriano-Ursúa and José G. Trujillo-Ferrara* Pages 77 - 86 ( 10 )
Background: Benzofurans are heterocyclic compounds with neurotropic activity. Some have been developed for the treatment of acute and degenerative neuronal injuries. Objective: The study aimed to evaluate the in silico binding of some promising benzofurans on the GABA receptors, and the in vivo neurotropic activity of benzofuran analogues (BZF 6-10) of gamma-aminobutyric acid (GABA) on a seizure model.
Methods: The ligands with the best physicochemical attributes were docked on two GABA receptors (the alpha-1 subunit of GABAA-R and GBR1 subunit of GABAB-R). Selected benzofuran derivatives were synthesized by a multistep procedure and characterized. To examine the neurotropic effects, mice were pretreated with different concentrations of the compounds prior to PTZ- or 4- AP-induced seizures. We assessed acute toxicity, motor behavior, and the effects on seizures.
Results: The tested ligands that complied with Lipinski’s rule of five were tested in silico with GABAA-R (ΔG = -5.51 to -5.84 kcal/mol) at the allosteric site for benzodiazepines. They bound to a similar cluster of residues as the reference compound (gaboxadol, ΔG = -5.51 kcal/mol). Synthesis was achieved with good overall yields (42-9.7%). Two compounds were selected for biological tests (BZF-7 and rac-BZF-10) on a mouse model of seizures, induced by pentylenetetrazol (PTZ) or 4-aminopyridine (4-AP). PTZ-induced seizures are associated with GABA receptors, and those 4-AP-induced with the blockage of the delayed rectifier-type potassium channel, which promotes the release of the NMDA-sensitive glutamatergic ionotropic receptor and other neurotransmitters. The biological assays demonstrated that BZF-7 and rac-BZF-10 do not protect against seizures. Indeed, BZF-7 increased the number of PTZ-induced seizures and decreased latency time. The 4-AP model apparently showed a potentiation of seizure effects after administration of the BZF-analogues, evidenced by the incidence and severity of the seizures and reduced latency time.
Conclusion: The results suggest that the test compounds are GABAergic antagonists with stimulatory activity on the CNS.
2, 3-disubstituted benzofurans (BZF), molecular docking, GABA receptor (GABA-R), seizures, pentylenetetrazol (PTZ), 4-aminopyridine (4-AP).
Departamento de Sistemas Biologicos, Universidad Autonoma Metropolitana – Campus Xochimilco. Calzada del Hueso 1100, Col. Villa Quietud, Coyoacan, C.P. 04960, Mexico City, Departamento de Sistemas Biologicos, Universidad Autonoma Metropolitana – Campus Xochimilco. Calzada del Hueso 1100, Col. Villa Quietud, Coyoacan, C.P. 04960, Mexico City, Instituto de Ciencias Basicas, Universidad Veracruzana, Av. Dr. Luis Castelazo Ayala s/n Col. Industrial Animas, 91190 Xalapa, Veracruz, Escuela Superior de Medicina, Instituto Politecnico Nacional, Plan de San Luis y Diaz Miron s/n Col. Casco de Santo Tomas, Del. Miguel Hidalgo, 11340, Mexico City, Escuela Superior de Medicina, Instituto Politecnico Nacional, Plan de San Luis y Diaz Miron s/n Col. Casco de Santo Tomas, Del. Miguel Hidalgo, 11340, Mexico City