Cargando…

OPC-67683, a Nitro-Dihydro-Imidazooxazole Derivative with Promising Action against Tuberculosis In Vitro and In Mice

BACKGROUND: Tuberculosis (TB) is still a leading cause of death worldwide. Almost a third of the world's population is infected with TB bacilli, and each year approximately 8 million people develop active TB and 2 million die as a result. Today's TB treatment, which dates back to the 1970s...

Descripción completa

Detalles Bibliográficos
Autores principales: Matsumoto, Makoto, Hashizume, Hiroyuki, Tomishige, Tatsuo, Kawasaki, Masanori, Tsubouchi, Hidetsugu, Sasaki, Hirofumi, Shimokawa, Yoshihiko, Komatsu, Makoto
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1664607/
https://www.ncbi.nlm.nih.gov/pubmed/17132069
http://dx.doi.org/10.1371/journal.pmed.0030466
_version_ 1782131073805713408
author Matsumoto, Makoto
Hashizume, Hiroyuki
Tomishige, Tatsuo
Kawasaki, Masanori
Tsubouchi, Hidetsugu
Sasaki, Hirofumi
Shimokawa, Yoshihiko
Komatsu, Makoto
author_facet Matsumoto, Makoto
Hashizume, Hiroyuki
Tomishige, Tatsuo
Kawasaki, Masanori
Tsubouchi, Hidetsugu
Sasaki, Hirofumi
Shimokawa, Yoshihiko
Komatsu, Makoto
author_sort Matsumoto, Makoto
collection PubMed
description BACKGROUND: Tuberculosis (TB) is still a leading cause of death worldwide. Almost a third of the world's population is infected with TB bacilli, and each year approximately 8 million people develop active TB and 2 million die as a result. Today's TB treatment, which dates back to the 1970s, is long and burdensome, requiring at least 6 mo of multidrug chemotherapy. The situation is further compounded by the emergence of multidrug-resistant TB (MDR-TB) and by the infection's lethal synergy with HIV/AIDS. Global health and philanthropic organizations are now pleading for new drug interventions that can address these unmet needs in TB treatment. METHODS AND FINDINGS: Here we report OPC-67683, a nitro-dihydro-imidazooxazole derivative that was screened to help combat the unmet needs in TB treatment. The compound is a mycolic acid biosynthesis inhibitor found to be free of mutagenicity and to possess highly potent activity against TB, including MDR-TB, as shown by its exceptionally low minimum inhibitory concentration (MIC) range of 0.006–0.024 μg/ml in vitro and highly effective therapeutic activity at low doses in vivo. Additionally, the results of the post-antibiotic effect of OPC-67683 on intracellular Mycobacterium tuberculosis showed the agent to be highly and dose-dependently active also against intracellular M. tuberculosis H37Rv after a 4-h pulsed exposure, and this activity at a concentration of 0.1 μg/ml was similar to that of the first-line drug rifampicin (RFP) at a concentration of 3 μg/ml. The combination of OPC-67683 with RFP and pyrazinamide (PZA) exhibited a remarkably quicker eradication (by at least 2 mo) of viable TB bacilli in the lung in comparison with the standard regimen consisting of RFP, isoniazid (INH), ethambutol (EB), and PZA. Furthermore, OPC-67683 was not affected by nor did it affect the activity of liver microsome enzymes, suggesting the possibility for OPC-67683 to be used in combination with drugs, including anti-retrovirals, that induce or are metabolized by cytochrome P450 enzymes. CONCLUSIONS: We concluded that based on these properties OPC-67683 has the potential to be used as a TB drug to help combat the unmet needs in TB treatment.
format Text
id pubmed-1664607
institution National Center for Biotechnology Information
language English
publishDate 2006
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-16646072007-06-30 OPC-67683, a Nitro-Dihydro-Imidazooxazole Derivative with Promising Action against Tuberculosis In Vitro and In Mice Matsumoto, Makoto Hashizume, Hiroyuki Tomishige, Tatsuo Kawasaki, Masanori Tsubouchi, Hidetsugu Sasaki, Hirofumi Shimokawa, Yoshihiko Komatsu, Makoto PLoS Med Research Article BACKGROUND: Tuberculosis (TB) is still a leading cause of death worldwide. Almost a third of the world's population is infected with TB bacilli, and each year approximately 8 million people develop active TB and 2 million die as a result. Today's TB treatment, which dates back to the 1970s, is long and burdensome, requiring at least 6 mo of multidrug chemotherapy. The situation is further compounded by the emergence of multidrug-resistant TB (MDR-TB) and by the infection's lethal synergy with HIV/AIDS. Global health and philanthropic organizations are now pleading for new drug interventions that can address these unmet needs in TB treatment. METHODS AND FINDINGS: Here we report OPC-67683, a nitro-dihydro-imidazooxazole derivative that was screened to help combat the unmet needs in TB treatment. The compound is a mycolic acid biosynthesis inhibitor found to be free of mutagenicity and to possess highly potent activity against TB, including MDR-TB, as shown by its exceptionally low minimum inhibitory concentration (MIC) range of 0.006–0.024 μg/ml in vitro and highly effective therapeutic activity at low doses in vivo. Additionally, the results of the post-antibiotic effect of OPC-67683 on intracellular Mycobacterium tuberculosis showed the agent to be highly and dose-dependently active also against intracellular M. tuberculosis H37Rv after a 4-h pulsed exposure, and this activity at a concentration of 0.1 μg/ml was similar to that of the first-line drug rifampicin (RFP) at a concentration of 3 μg/ml. The combination of OPC-67683 with RFP and pyrazinamide (PZA) exhibited a remarkably quicker eradication (by at least 2 mo) of viable TB bacilli in the lung in comparison with the standard regimen consisting of RFP, isoniazid (INH), ethambutol (EB), and PZA. Furthermore, OPC-67683 was not affected by nor did it affect the activity of liver microsome enzymes, suggesting the possibility for OPC-67683 to be used in combination with drugs, including anti-retrovirals, that induce or are metabolized by cytochrome P450 enzymes. CONCLUSIONS: We concluded that based on these properties OPC-67683 has the potential to be used as a TB drug to help combat the unmet needs in TB treatment. Public Library of Science 2006-11 2006-11-28 /pmc/articles/PMC1664607/ /pubmed/17132069 http://dx.doi.org/10.1371/journal.pmed.0030466 Text en © 2006 Matsumoto 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
Matsumoto, Makoto
Hashizume, Hiroyuki
Tomishige, Tatsuo
Kawasaki, Masanori
Tsubouchi, Hidetsugu
Sasaki, Hirofumi
Shimokawa, Yoshihiko
Komatsu, Makoto
OPC-67683, a Nitro-Dihydro-Imidazooxazole Derivative with Promising Action against Tuberculosis In Vitro and In Mice
title OPC-67683, a Nitro-Dihydro-Imidazooxazole Derivative with Promising Action against Tuberculosis In Vitro and In Mice
title_full OPC-67683, a Nitro-Dihydro-Imidazooxazole Derivative with Promising Action against Tuberculosis In Vitro and In Mice
title_fullStr OPC-67683, a Nitro-Dihydro-Imidazooxazole Derivative with Promising Action against Tuberculosis In Vitro and In Mice
title_full_unstemmed OPC-67683, a Nitro-Dihydro-Imidazooxazole Derivative with Promising Action against Tuberculosis In Vitro and In Mice
title_short OPC-67683, a Nitro-Dihydro-Imidazooxazole Derivative with Promising Action against Tuberculosis In Vitro and In Mice
title_sort opc-67683, a nitro-dihydro-imidazooxazole derivative with promising action against tuberculosis in vitro and in mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1664607/
https://www.ncbi.nlm.nih.gov/pubmed/17132069
http://dx.doi.org/10.1371/journal.pmed.0030466
work_keys_str_mv AT matsumotomakoto opc67683anitrodihydroimidazooxazolederivativewithpromisingactionagainsttuberculosisinvitroandinmice
AT hashizumehiroyuki opc67683anitrodihydroimidazooxazolederivativewithpromisingactionagainsttuberculosisinvitroandinmice
AT tomishigetatsuo opc67683anitrodihydroimidazooxazolederivativewithpromisingactionagainsttuberculosisinvitroandinmice
AT kawasakimasanori opc67683anitrodihydroimidazooxazolederivativewithpromisingactionagainsttuberculosisinvitroandinmice
AT tsubouchihidetsugu opc67683anitrodihydroimidazooxazolederivativewithpromisingactionagainsttuberculosisinvitroandinmice
AT sasakihirofumi opc67683anitrodihydroimidazooxazolederivativewithpromisingactionagainsttuberculosisinvitroandinmice
AT shimokawayoshihiko opc67683anitrodihydroimidazooxazolederivativewithpromisingactionagainsttuberculosisinvitroandinmice
AT komatsumakoto opc67683anitrodihydroimidazooxazolederivativewithpromisingactionagainsttuberculosisinvitroandinmice