4.0 Article

A new class of peptides from wasp venom: a pathway to antiepileptic/neuroprotective drugs

Journal

BRAIN COMMUNICATIONS
Volume 5, Issue 1, Pages -

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/braincomms/fcad016

Keywords

Wasp venoms; neuropeptides; antiepileptic drug; neuroprotection; epilepsy

Funding

  1. CNPq (National Council for Scientific and Technological Development) [470532/ 2011-4, 407625/2013-5, 4289008/2018-7]
  2. FAPDF (Federal District Research Support Foundation) [193.000.539/2009, 0193.000.494/2015, 00193-00001343/2019-53, 0193.001.200/2016]
  3. CAPES (Coordination for the Improvement of Higher Education Personnel) finance graduate student scholarship

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This study reports a new wasp venom-derived peptide that can protect against seizures in both acute and chronic models, providing a unique platform for the development of innovative epilepsy treatments.
Mortari et al. report a new wasp venom-derived peptide capable of protecting against seizures induced in both acute and chronic models. This peptide provides a unique platform for the development of innovative treatments for epilepsy. The ability of venom-derived peptides to disrupt physiological processes in mammals provides an exciting source for pharmacological development. Our research group has identified a new class of neuroactive peptides from the venom of a Brazilian social wasp, Polybia occidentalis, with the potential pharmacological profile to treat epilepsies. The study was divided into five phases: Phase 1 concerned the extraction, isolation and purification of Occidentalin-1202(n) from the crude venom, followed by the synthesis of an identical analogue peptide, named Occidentalin-1202(s). In Phase 2, we described the effects of both peptides in two acute models of epilepsy-kainic acid and pentylenetetrazole-induced model of seizures-and measured estimated ED50 and therapeutic index values, electroencephalographic studies and C-fos evaluation. Phase 3 was a compilation of advanced tests performed with Occidentalin-1202(s) only, reporting histopathological features and its performance in the pilocarpine-induced status epilepticus. After the determination of the antiepileptic activity of Occidentalin-1202(s), Phase 4 consisted of evaluating its potential adverse effects, after chronic administration, on motor coordination (Rotarod) and cognitive impairment (Morris water maze) tests. Finally, in Phase 5, we proposed a mechanism of action using computational models with kainate receptors. The new peptide was able to cross the blood-brain barrier and showed potent antiseizure effects in acute (kainic acid and pentylenetetrazole) and chronic (temporal lobe epilepsy model induced by pilocarpine) models. Motor and cognitive behaviour were not adversely affected, and a potential neuroprotective effect was observed. Occidentalin-1202 can be a potent blocker of the kainate receptor, as assessed by computational analysis, preventing glutamate and kainic acid from binding to the receptor's active site. Occidentalin-1202 is a peptide with promising applicability to treat epilepsy and can be considered an interesting drug model for the development of new medicines.

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