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Design, Synthesis and Biological Evaluation of Two Opioid Agonist and Ca v 2.2 Blocker Multitarget Ligands

2014; Wiley; Volume: 86; Issue: 2 Linguagem: Inglês

10.1111/cbdd.12479

1747-0285

Adriano Mollica, Roberto Costante, Ettore Novellino, Azzurra Stefanucci, Stefano Pieretti, Ferenc Zádor, Reza Samavati, Anna Borsodi, Sándor Benyhe, Irina Vetter, Richard J. Lewis,

Neuropeptides and Animal Physiology

N-type voltage-dependent Ca(2+) channels (CaV 2.2) are located at nerve endings in the central and peripheral nervous systems and are strongly associated with the pathological processes of cerebral ischaemia and neuropathic pain. CaV 2.2 blockers such as the ω-conotoxin MVIIA (Prialt) are analgesic and have opioid-sparing effects. With the aim to develop new multitarget analgesic compounds, we designed the first ω-conotoxin/opioid peptidomimetics based on the enkephalin-like sequence Tyr-D-Ala-Gly-Phe (for the opioid portion) and two fragments derived from the loop-2 pharmacophore of ω-conotoxin MVIIA. Antinociceptive activity evaluated in vitro and in vivo revealed differential affinity for CaV 2.2 and opioid receptors and no significant synergistic activity.