4.7 Review

Arthropod toxins and their antinociceptive properties: From venoms to painkillers

Journal

PHARMACOLOGY & THERAPEUTICS
Volume 188, Issue -, Pages 176-185

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.pharmthera.2018.03.007

Keywords

Acid-sensing ion channels; Glutamate; Purinergic receptors; Sodium channels; TRPV receptors; Voltage-dependent calcium channels

Funding

  1. National Council for Scientific and Technological Development (CNPq)
  2. Coordination for the Improvement of Higher Education Personnel (CAPES)
  3. Federal District Research Foundation (FAPDF)

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The complex process of pain control commonly involves the use of systemic analgesics; however, in many cases, a more potent and effective polypharmacological approach is needed to promote clinically significant improvement. Additionally, considering side effects caused by current painkillers, drug discovery is once more turning to nature as a source of more efficient therapeutic alternatives. In this context, arthropod venoms contain a vast array of bioactive substances that have evolved to selectively bind to specific pharmacological targets involved in the pain signaling pathway, playing an important role as pain activators or modulators, the latter serving as promising analgesic agents. The current review explores how the pain pathway works and surveys neuroactive compounds obtained from arthropods' toxins, which function as pain modulators through their interaction with specific ion channels and membrane receptors, emerging as promising candidates for drug design and development. (C) 2018 Elsevier Inc. All rights reserved.

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