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LASSBio-1135: A Dual TRPV1 Antagonist and Anti-TNF-Alpha Compound Orally Effective in Models of Inflammatory and Neuropathic Pain

LASSBio-1135 is an imidazo[1,2-a]pyridine derivative with high efficacy in screening models of nociception and inflammation, presumed as a weak COX-2 inhibitor. In order to tease out its mechanism of action, we investigated others possible target for LASSBio-1135, such as TNF-α and TRPV1, to better...

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Autores principales: Lima, Cleverton K. F., Silva, Rafael M., Lacerda, Renata B., Santos, Bruna L. R., Silva, Rafaela V., Amaral, Luciana S., Quintas, Luís E. M., Fraga, Carlos A. M., Barreiro, Eliezer J., Guimaraes, Marília Z. P., Miranda, Ana L. P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4062389/
https://www.ncbi.nlm.nih.gov/pubmed/24941071
http://dx.doi.org/10.1371/journal.pone.0099510
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author Lima, Cleverton K. F.
Silva, Rafael M.
Lacerda, Renata B.
Santos, Bruna L. R.
Silva, Rafaela V.
Amaral, Luciana S.
Quintas, Luís E. M.
Fraga, Carlos A. M.
Barreiro, Eliezer J.
Guimaraes, Marília Z. P.
Miranda, Ana L. P.
author_facet Lima, Cleverton K. F.
Silva, Rafael M.
Lacerda, Renata B.
Santos, Bruna L. R.
Silva, Rafaela V.
Amaral, Luciana S.
Quintas, Luís E. M.
Fraga, Carlos A. M.
Barreiro, Eliezer J.
Guimaraes, Marília Z. P.
Miranda, Ana L. P.
author_sort Lima, Cleverton K. F.
collection PubMed
description LASSBio-1135 is an imidazo[1,2-a]pyridine derivative with high efficacy in screening models of nociception and inflammation, presumed as a weak COX-2 inhibitor. In order to tease out its mechanism of action, we investigated others possible target for LASSBio-1135, such as TNF-α and TRPV1, to better characterize it as a multitarget compound useful in the treatment of chronic pain. TRPV1 modulation was assessed in TRPV1-expressing Xenopus oocytes against capsaicin and low pH-induced current. Modulation of TNF-α production was evaluated in culture of macrophages stimulated with LPS. In vivo efficacy of LASSBio-1135 was investigated in carrageenan and partial sciatic ligation-induced thermal hyperalgesia and mechanical allodynia. Corroborating its previous demonstration of efficacy in a model of capsaicin-induced hyperalgesia, LASSBio-1135 blocks capsaicin-elicited currents in a non-competitive way with an IC(50) of 580 nM as well as low pH-induced current at 50 µM. As an additional action, LASSBio-1135 inhibited TNF-α release in these cells stimulated by LPS with an IC(50) of 546 nM by reducing p38 MAPK phosphorilation. Oral administration of 100 µmol.Kg(−1) LASSBio-1135 markedly reduced thermal hyperalgesia induced by carrageenan, however at 10 µmol.Kg(−1) only a partial reduction was observed at the 4(th) h. Neutrophil recruitment and TNF-α production after carrageenan stimulus was also inhibited by the treatment with LASSBio-1135. Modulating TRPV1 and TNF-α production, two key therapeutic targets of neuropathic pain, 100 µmol.Kg(−1) LASSBio-1135 was orally efficacious in reversing thermal hyperalgesia and mechanical allodynia produced by partial sciatic ligation 7–11 days after surgery without provoking hyperthermia, a common side effect of TRPV1 antagonists. In conclusion LASSBio-1135, besides being a weak COX-2 inhibitor, is a non-competitive TRPV1 antagonist and a TNF-α inhibitor. As a multitarget compound, LASSBio-1135 is orally efficacious in a model of neuropathic pain without presenting hyperthermia.
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spelling pubmed-40623892014-06-24 LASSBio-1135: A Dual TRPV1 Antagonist and Anti-TNF-Alpha Compound Orally Effective in Models of Inflammatory and Neuropathic Pain Lima, Cleverton K. F. Silva, Rafael M. Lacerda, Renata B. Santos, Bruna L. R. Silva, Rafaela V. Amaral, Luciana S. Quintas, Luís E. M. Fraga, Carlos A. M. Barreiro, Eliezer J. Guimaraes, Marília Z. P. Miranda, Ana L. P. PLoS One Research Article LASSBio-1135 is an imidazo[1,2-a]pyridine derivative with high efficacy in screening models of nociception and inflammation, presumed as a weak COX-2 inhibitor. In order to tease out its mechanism of action, we investigated others possible target for LASSBio-1135, such as TNF-α and TRPV1, to better characterize it as a multitarget compound useful in the treatment of chronic pain. TRPV1 modulation was assessed in TRPV1-expressing Xenopus oocytes against capsaicin and low pH-induced current. Modulation of TNF-α production was evaluated in culture of macrophages stimulated with LPS. In vivo efficacy of LASSBio-1135 was investigated in carrageenan and partial sciatic ligation-induced thermal hyperalgesia and mechanical allodynia. Corroborating its previous demonstration of efficacy in a model of capsaicin-induced hyperalgesia, LASSBio-1135 blocks capsaicin-elicited currents in a non-competitive way with an IC(50) of 580 nM as well as low pH-induced current at 50 µM. As an additional action, LASSBio-1135 inhibited TNF-α release in these cells stimulated by LPS with an IC(50) of 546 nM by reducing p38 MAPK phosphorilation. Oral administration of 100 µmol.Kg(−1) LASSBio-1135 markedly reduced thermal hyperalgesia induced by carrageenan, however at 10 µmol.Kg(−1) only a partial reduction was observed at the 4(th) h. Neutrophil recruitment and TNF-α production after carrageenan stimulus was also inhibited by the treatment with LASSBio-1135. Modulating TRPV1 and TNF-α production, two key therapeutic targets of neuropathic pain, 100 µmol.Kg(−1) LASSBio-1135 was orally efficacious in reversing thermal hyperalgesia and mechanical allodynia produced by partial sciatic ligation 7–11 days after surgery without provoking hyperthermia, a common side effect of TRPV1 antagonists. In conclusion LASSBio-1135, besides being a weak COX-2 inhibitor, is a non-competitive TRPV1 antagonist and a TNF-α inhibitor. As a multitarget compound, LASSBio-1135 is orally efficacious in a model of neuropathic pain without presenting hyperthermia. Public Library of Science 2014-06-18 /pmc/articles/PMC4062389/ /pubmed/24941071 http://dx.doi.org/10.1371/journal.pone.0099510 Text en © 2014 Lima et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Lima, Cleverton K. F.
Silva, Rafael M.
Lacerda, Renata B.
Santos, Bruna L. R.
Silva, Rafaela V.
Amaral, Luciana S.
Quintas, Luís E. M.
Fraga, Carlos A. M.
Barreiro, Eliezer J.
Guimaraes, Marília Z. P.
Miranda, Ana L. P.
LASSBio-1135: A Dual TRPV1 Antagonist and Anti-TNF-Alpha Compound Orally Effective in Models of Inflammatory and Neuropathic Pain
title LASSBio-1135: A Dual TRPV1 Antagonist and Anti-TNF-Alpha Compound Orally Effective in Models of Inflammatory and Neuropathic Pain
title_full LASSBio-1135: A Dual TRPV1 Antagonist and Anti-TNF-Alpha Compound Orally Effective in Models of Inflammatory and Neuropathic Pain
title_fullStr LASSBio-1135: A Dual TRPV1 Antagonist and Anti-TNF-Alpha Compound Orally Effective in Models of Inflammatory and Neuropathic Pain
title_full_unstemmed LASSBio-1135: A Dual TRPV1 Antagonist and Anti-TNF-Alpha Compound Orally Effective in Models of Inflammatory and Neuropathic Pain
title_short LASSBio-1135: A Dual TRPV1 Antagonist and Anti-TNF-Alpha Compound Orally Effective in Models of Inflammatory and Neuropathic Pain
title_sort lassbio-1135: a dual trpv1 antagonist and anti-tnf-alpha compound orally effective in models of inflammatory and neuropathic pain
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4062389/
https://www.ncbi.nlm.nih.gov/pubmed/24941071
http://dx.doi.org/10.1371/journal.pone.0099510
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