Pharmacological modulation of hyperalgesia induced by Bothrops asper (terciopelo) snake venom

The ability of Bothrops asper snake venom to cause hyperalgesia was investigated in rats, using the paw pressure test. Intraplantar injection of the venom (5–15 μg/paw) caused a dose and time-related hyperalgesia, which peaked 2 h after venom injection. Bothrops asper venom-induced hyperalgesia was...

Full description

Bibliographic Details
Authors: Chacur, Marucia; Picolo, Gisele; Gutiérrez, José María; Teixeira, Catarina de Fátima; Cury, Yara
Format: Article
Publication date:2001
Country:Costa Rica
Institution:UCR
Repository:Kérwá
OAI Identifier:oai:kerwa.ucr.ac.cr:10669/29476
Online Access:http://www.sciencedirect.com/science/article/pii/S0041010100002543
https://hdl.handle.net/10669/29476
Access Level:Embargoed access
Keyword:Bothrops asper venom
Hyperalgesia
Bradykinin
Leukotrienes
Snake venom
_version_ 1878655259571650560
author Chacur, Marucia
author2 Picolo, Gisele
Gutiérrez, José María
Teixeira, Catarina de Fátima
Cury, Yara
author2_role author
author
author
author
author_browse Chacur, Marucia
Cury, Yara
Gutiérrez, José María
Picolo, Gisele
Teixeira, Catarina de Fátima
author_facet Chacur, Marucia
Picolo, Gisele
Gutiérrez, José María
Teixeira, Catarina de Fátima
Cury, Yara
author_role author
bitstream_url_str_mv https://www.kerwa.ucr.ac.cr/bitstreams/5fd3ccae-a91e-4d8c-9b0a-2974f2514a06/download
https://www.kerwa.ucr.ac.cr/bitstreams/4af7c6ed-6efb-4ab1-8843-11431a5258e6/download
https://www.kerwa.ucr.ac.cr/bitstreams/505f7db6-2a27-499a-b338-66f0eea14fcb/download
https://www.kerwa.ucr.ac.cr/bitstreams/a987ad17-4564-4a41-b47b-b1580c011fe5/download
collection Kérwá
description The ability of Bothrops asper snake venom to cause hyperalgesia was investigated in rats, using the paw pressure test. Intraplantar injection of the venom (5–15 μg/paw) caused a dose and time-related hyperalgesia, which peaked 2 h after venom injection. Bothrops asper venom-induced hyperalgesia was blocked by the bradykinin B2 receptor antagonist HOE 140 and attenuated by dexamethasone, an inhibitor of phospholipase A2. Inhibition of the lipoxygenase pathway by NDGA abrogated the algogenic phenomenon. The hyperalgesic response was not modified by pretreatment with indomethacin, an inhibitor of the cyclo-oxygenase pathway, by meloxicam, an inhibitor of the type 2 cyclo-oxygenase pathway, by the PAF receptor antagonist BN52021 or by anti-TNF-α or anti-interleukin 1 antibodies. Intraplantar injection of the venom also caused an oedematogenic response which was not modified by any of these pharmacological treatments. These results suggest that hyperalgesia induced by Bothrops asper venom is, at least partially, mediated by bradykinin, phospholipase A2 activity and leukotrienes. Distinct mechanisms are involved in the development of hyperalgesia and oedema induced by the venom.
eu_rights_str_mv embargoedAccess
format article
id CR_96d6500a8fe9bd1b3f4c77cd1c1efcda
identifier_str_mv 10.1016/S0041-0101(00)00254-3
institution UCR
instname_str Universidad de Costa Rica
network_acronym_str CR
network_name_str Costa Rica
oai_identifier_str oai:kerwa.ucr.ac.cr:10669/29476
publishDate 2001
publishDateSort 2001
reponame_str Kérwá
spelling Pharmacological modulation of hyperalgesia induced by Bothrops asper (terciopelo) snake venom Chacur, Marucia Picolo, Gisele Gutiérrez, José María Teixeira, Catarina de Fátima Cury, Yara Bothrops asper venom Hyperalgesia Bradykinin Leukotrienes Snake venom The ability of Bothrops asper snake venom to cause hyperalgesia was investigated in rats, using the paw pressure test. Intraplantar injection of the venom (5–15 μg/paw) caused a dose and time-related hyperalgesia, which peaked 2 h after venom injection. Bothrops asper venom-induced hyperalgesia was blocked by the bradykinin B2 receptor antagonist HOE 140 and attenuated by dexamethasone, an inhibitor of phospholipase A2. Inhibition of the lipoxygenase pathway by NDGA abrogated the algogenic phenomenon. The hyperalgesic response was not modified by pretreatment with indomethacin, an inhibitor of the cyclo-oxygenase pathway, by meloxicam, an inhibitor of the type 2 cyclo-oxygenase pathway, by the PAF receptor antagonist BN52021 or by anti-TNF-α or anti-interleukin 1 antibodies. Intraplantar injection of the venom also caused an oedematogenic response which was not modified by any of these pharmacological treatments. These results suggest that hyperalgesia induced by Bothrops asper venom is, at least partially, mediated by bradykinin, phospholipase A2 activity and leukotrienes. Distinct mechanisms are involved in the development of hyperalgesia and oedema induced by the venom. Fundação de Amparo à Pesquisa do Estado de São Paulo/[98/00257-0]/FAPESP/Brasil Instituto Butantan///Brasil Universidad de Costa Rica//UCR/Costa Rica UCR::Vicerrectoría de Investigación::Unidades de Investigación::Ciencias de la Salud::Instituto Clodomiro Picado (ICP) http://www.sciencedirect.com/science/article/pii/S0041010100002543 0041-0101 https://hdl.handle.net/10669/29476 10.1016/S0041-0101(00)00254-3 11306127
spellingShingle Pharmacological modulation of hyperalgesia induced by Bothrops asper (terciopelo) snake venom
Chacur, Marucia
Bothrops asper venom
Hyperalgesia
Bradykinin
Leukotrienes
Snake venom
title Pharmacological modulation of hyperalgesia induced by Bothrops asper (terciopelo) snake venom
title_full Pharmacological modulation of hyperalgesia induced by Bothrops asper (terciopelo) snake venom
title_fullStr Pharmacological modulation of hyperalgesia induced by Bothrops asper (terciopelo) snake venom
title_full_unstemmed Pharmacological modulation of hyperalgesia induced by Bothrops asper (terciopelo) snake venom
title_short Pharmacological modulation of hyperalgesia induced by Bothrops asper (terciopelo) snake venom
title_sort Pharmacological modulation of hyperalgesia induced by Bothrops asper (terciopelo) snake venom
topic Bothrops asper venom
Hyperalgesia
Bradykinin
Leukotrienes
Snake venom
topic_facet Bothrops asper venom
Hyperalgesia
Bradykinin
Leukotrienes
Snake venom
url http://www.sciencedirect.com/science/article/pii/S0041010100002543
https://hdl.handle.net/10669/29476