Pesquisa | SciELO

Abstract Background: Medications currently used to treat pain are frequently associated with serious adverse effects and rapid development of tolerance. Thus, there is a need to develop more effective, and safer medicines for the population. Blocking NMDA receptors (NMDAR) has shown to be a promising target for the development of new drugs. That statement is due to NMDAR activation and glutamate release in the spinal cord which affects chronic pain modulation. Therefore, the aim of this study was to evaluate the possible spinal antinociceptive activity of PnTx4(5-5) toxin. The peptide is purified from the venom of the spider P. nigriventer and its affinity for NMDAR and sodium channels Nav1.2-1.6 has already been established. Methods: We compared its effect and safety with MK-801 (NMDAR antagonist) and evaluated its influence on glutamate and reactive oxygen species (ROS) levels in CSF. PnTx4(5-5) was administered intrathecally in the Formalin test and co-administered with NMDA in the Spontaneous pain test. After three minutes of observation, mice cerebrospinal fluid was collected to measure glutamate and ROS levels. Results: The spider peptide inhibited nociception as post-treatment in the inflammatory phase of the Formalin test. Furthermore, it inhibited spontaneous nociception induced by NMDA, being more potent and effective than MK-801 in both models tested. A glutamate rise level in the CSF of mice was significantly reduced by the toxin, but ROS increase was not affected. The animals’ motor skills were not affected by the tested doses of NMDAR inhibitors. Conclusion: In conclusion, the results suggest PnTx4(5-5) may mediate its antinociceptive effect in the spinal cord not only by inhibiting postsynaptic receptors but probably also by acting on autoreceptors. This effect does not affect the motricity of mice at the highest dose tested, which suggests that it has therapeutic potential and safety for use as a painkiller. Background tolerance Thus population drugs modulation Therefore PnTx455 PnTx PnTx4 5 PnTx4(5-5 toxin P Nav1.21.6 Nav1216 Nav Nav1.2 1.6 Nav1 2 1 6 Nav1.2-1. established Methods MK801 MK 801 MK-80 antagonist (ROS coadministered co observation Results posttreatment post treatment Furthermore animals inhibitors Conclusion conclusion autoreceptors painkiller PnTx45 PnTx4(5- 21 Nav1.21. Nav121 Nav12 Nav1. 16 1. Nav1.2-1 MK80 80 MK-8 PnTx4(5 Nav1.21 Nav1.2- MK8 8 MK- PnTx4(

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