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...
Autores principales: | , , , , , , , |
---|---|
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 |