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Silicon-Containing GABA Derivatives, Silagaba Compounds, as Orally Effective Agents for Treating Neuropathic Pain without Central-Nervous-System-Related Side Effects
[Image: see text] Neuropathic pain is a chronic condition resulting from neuronal damage. Pregabalin, the (S)-isomer of 3-isobutyl-γ-aminobutyric acid (GABA), is widely used to treat neuropathic pain, despite the occurrence of central nervous system (CNS)-related side effects such as dizziness and s...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4102965/ https://www.ncbi.nlm.nih.gov/pubmed/24738473 http://dx.doi.org/10.1021/cn500053d |
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author | Fukasawa, Hiroshi Muratake, Hideaki Ito, Ai Suzuki, Hideyuki Amano, Yohei Nagae, Marina Sugiyama, Kiyoshi Shudo, Koichi |
author_facet | Fukasawa, Hiroshi Muratake, Hideaki Ito, Ai Suzuki, Hideyuki Amano, Yohei Nagae, Marina Sugiyama, Kiyoshi Shudo, Koichi |
author_sort | Fukasawa, Hiroshi |
collection | PubMed |
description | [Image: see text] Neuropathic pain is a chronic condition resulting from neuronal damage. Pregabalin, the (S)-isomer of 3-isobutyl-γ-aminobutyric acid (GABA), is widely used to treat neuropathic pain, despite the occurrence of central nervous system (CNS)-related side effects such as dizziness and somnolence. Here we describe the pharmacology of novel GABA derivatives containing silicon–carbon bonds, silagaba compounds. Silagaba131, 132, and 161 showed pregabalin-like analgesic activities in animal models of neuropathic pain, but in contrast to pregabalin they did not impair neuromuscular coordination in rotarod tests. Pharmacokinetic studies showed that brain exposure to silagaba compounds was lower than that to pregabalin. Surprisingly, despite their potent analgesic action in vivo, silagaba compounds showed only weak binding to α2-δ protein. These compounds may be useful to study mechanisms of neuropathic pain. Our results also indicate that silagaba132 and 161 are candidates for orally effective treatment of neuropathic pain without CNS-related side effects. |
format | Online Article Text |
id | pubmed-4102965 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-41029652015-07-16 Silicon-Containing GABA Derivatives, Silagaba Compounds, as Orally Effective Agents for Treating Neuropathic Pain without Central-Nervous-System-Related Side Effects Fukasawa, Hiroshi Muratake, Hideaki Ito, Ai Suzuki, Hideyuki Amano, Yohei Nagae, Marina Sugiyama, Kiyoshi Shudo, Koichi ACS Chem Neurosci [Image: see text] Neuropathic pain is a chronic condition resulting from neuronal damage. Pregabalin, the (S)-isomer of 3-isobutyl-γ-aminobutyric acid (GABA), is widely used to treat neuropathic pain, despite the occurrence of central nervous system (CNS)-related side effects such as dizziness and somnolence. Here we describe the pharmacology of novel GABA derivatives containing silicon–carbon bonds, silagaba compounds. Silagaba131, 132, and 161 showed pregabalin-like analgesic activities in animal models of neuropathic pain, but in contrast to pregabalin they did not impair neuromuscular coordination in rotarod tests. Pharmacokinetic studies showed that brain exposure to silagaba compounds was lower than that to pregabalin. Surprisingly, despite their potent analgesic action in vivo, silagaba compounds showed only weak binding to α2-δ protein. These compounds may be useful to study mechanisms of neuropathic pain. Our results also indicate that silagaba132 and 161 are candidates for orally effective treatment of neuropathic pain without CNS-related side effects. American Chemical Society 2014-04-16 /pmc/articles/PMC4102965/ /pubmed/24738473 http://dx.doi.org/10.1021/cn500053d Text en Copyright © 2014 American Chemical Society Terms of Use (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) |
spellingShingle | Fukasawa, Hiroshi Muratake, Hideaki Ito, Ai Suzuki, Hideyuki Amano, Yohei Nagae, Marina Sugiyama, Kiyoshi Shudo, Koichi Silicon-Containing GABA Derivatives, Silagaba Compounds, as Orally Effective Agents for Treating Neuropathic Pain without Central-Nervous-System-Related Side Effects |
title | Silicon-Containing GABA Derivatives, Silagaba Compounds,
as Orally Effective Agents for Treating Neuropathic Pain without Central-Nervous-System-Related
Side Effects |
title_full | Silicon-Containing GABA Derivatives, Silagaba Compounds,
as Orally Effective Agents for Treating Neuropathic Pain without Central-Nervous-System-Related
Side Effects |
title_fullStr | Silicon-Containing GABA Derivatives, Silagaba Compounds,
as Orally Effective Agents for Treating Neuropathic Pain without Central-Nervous-System-Related
Side Effects |
title_full_unstemmed | Silicon-Containing GABA Derivatives, Silagaba Compounds,
as Orally Effective Agents for Treating Neuropathic Pain without Central-Nervous-System-Related
Side Effects |
title_short | Silicon-Containing GABA Derivatives, Silagaba Compounds,
as Orally Effective Agents for Treating Neuropathic Pain without Central-Nervous-System-Related
Side Effects |
title_sort | silicon-containing gaba derivatives, silagaba compounds,
as orally effective agents for treating neuropathic pain without central-nervous-system-related
side effects |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4102965/ https://www.ncbi.nlm.nih.gov/pubmed/24738473 http://dx.doi.org/10.1021/cn500053d |
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