Arthropod toxins and their antinociceptive properties: From venoms to painkillers

被引:10
|
作者
Monge-Fuentes, Victoria [1 ]
Arenas, Claudia [1 ]
Galante, Priscilla [1 ]
Goncalves, Jacqueline Coimbra [1 ]
Mortari, Marcia Renata [1 ]
Schwartz, Elisabeth Ferroni [1 ]
机构
[1] Univ Brasilia, Inst Biol Sci, Lab Neuropharmacol, Dept Physiol Sci, BR-70910900 Brasilia, DF, Brazil
关键词
Acid-sensing ion channels; Glutamate; Purinergic receptors; Sodium channels; TRPV receptors; Voltage-dependent calcium channels; SPIDER PHONEUTRIA-NIGRIVENTER; BUTHUS-MARTENSII KARSCH; GATED SODIUM-CHANNEL; OMEGA-AGATOXIN IVA; FUNNEL-WEB SPIDER; GLUTAMATE RECEPTORS; CALCIUM-CHANNELS; NEUROPATHIC PAIN; SPINAL-CORD; AGELENOPSIS-APERTA;
D O I
10.1016/j.pharmthera.2018.03.007
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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.
引用
收藏
页码:176 / 185
页数:10
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