Abstract
Background: Chronic pain is an urgent medical problem worldwide, resulting in long-term sick leave, low quality of life, and high socioeconomic costs. Despite the physiological, emotional, and financial burden of chronic pain, there is still a lack of efficient treatments. In this context, toxins isolated from arthropods are considered powerful tools because they have targets that are compatible with the impulse transmission of pain and can provide an interesting alternative in the development of more efficient analgesic treatments. Wasps are arthropods with potent venom that contains a complex mixture of compounds, including biogenic amines, proteins, and peptides. For decades, chemical identification and biological characterization of wasp venom peptides have accumulated considerable attention from researchers. Objective: The objective of this work was to evaluate the antinociceptive activity of the peptide fraction (Fpep) from low-molecular-weight compounds (LMWCs) from the venom of the Brazilian social wasp Pseudopolybia vespiceps testacea. Materials and Methods: P. vespiceps females were collected, and after euthanasia by freezing (−20°C), a total of 148 venom sacs were used to acquire only compounds with LMWCs. The antinociceptive effect of the Fpepfrom LMWCs was observed by two thermal tests: tail flick and hot plate measured in male Swiss mice. Results: Fpepshowed dose-dependent antinociceptive activity in mice submitted to intracerebroventricular injection in two different models. Conclusion: These results revealed the significant potential impact of the LMWCs of the venom of Pseudopolybia vespiceps testacea, including neuroactive peptides that can be used as pharmacological resources for antinociceptive drug research. Abbreviations used: ACN/H2O: Acetonitrile/deionized water; CEUA: Committee for Ethics in Animal Use; CNS: Central nervous system; Fpep: Peptide fraction; i.c.v: Intracerebroventricular; LMWCs: Low-molecular-weight compounds; P. vespiceps: Pseudopolybia vespiceps testacea.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
Details
1 Department of Physiological Sciences, Neuropharmacology Laboratory, Institute of Biological Sciences, University of Brasília, Brasília