1. Design, synthesis, and characterization of high-affinity, systemically-active galanin analogues with potent anticonvulsant activities
- Author
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Marianna Dorota Sochanska, Hee Kyoung Lee, Sean P. Flynn, Liuyin Zhang, Grzegorz Bulaj, Timothy H. Pruess, Misty D. Smith, Erika A. Scholl, Brad R. Green, Karen White, Charles R. Robertson, and H. Steve White
- Subjects
medicine.medical_treatment ,Chemistry, Pharmaceutical ,Amino Acid Motifs ,Molecular Conformation ,Neuropeptide ,Galanin receptor ,Peptide ,Galanin ,Ligands ,chemistry.chemical_compound ,Mice ,In vivo ,Drug Discovery ,Peptide synthesis ,medicine ,Animals ,Receptor ,chemistry.chemical_classification ,Epilepsy ,Brain ,Kinetics ,Anticonvulsant ,chemistry ,Biochemistry ,Models, Chemical ,Blood-Brain Barrier ,Drug Design ,Molecular Medicine ,Anticonvulsants - Abstract
Galanin is an endogenous neuropeptide that modulates seizures in the brain. Because this neuropeptide does not penetrate the blood-brain barrier, we designed truncated galanin analogues in which nonessential amino acid residues were replaced by cationic and/or lipoamino acid residues. The analogues prevented seizures in the 6 Hz mouse model of epilepsy following intraperitoneal administration. The most active analogue, Gal-B2 (NAX 5055), contained the -Lys-Lys-Lys(palmitoyl)-Lys-NH(2) motif and exhibited high affinity for galanin receptors (K(i) = 3.5 nM and 51.5 nM for GalR1 and GalR2, respectively), logD = 1.24, minimal helical conformation and improved metabolic stability. Structure-activity-relationship analysis suggested that cationization combined with position-specific lipidization was critical for improving the systemic activity of the analogues. Because the anticonvulsant activity of galanin is mediated by the receptors located in hippocampus and other limbic brain structures, our data suggest that these analogues penetrate into the brain. Gal-B2 may lead to development of first-in-class antiepileptic drugs.
- Published
- 2008