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Safety Assessment of Bangle (Zingiber purpureum Rosc.) Rhizome Extract: Acute and Chronic Studies in Rats and Clinical Studies in Human
[Image: see text] Bangle (Zingiber purpureum Rosc.) rhizome extract (BRE) contains phenylbutenoid dimers (banglenes), which exert neurotrophic effects and possess the potential capability to regenerate hippocampal neurons in mice. The acute and chronic oral toxicities of BRE powder were evaluated in...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6288899/ https://www.ncbi.nlm.nih.gov/pubmed/30556016 http://dx.doi.org/10.1021/acsomega.8b02485 |
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author | Kato, Eishin Kubo, Miwa Okamoto, Yasuko Matsunaga, Yoichi Kyo, Hoko Suzuki, Nobutaka Uebaba, Kazuo Fukuyama, Yoshiyasu |
author_facet | Kato, Eishin Kubo, Miwa Okamoto, Yasuko Matsunaga, Yoichi Kyo, Hoko Suzuki, Nobutaka Uebaba, Kazuo Fukuyama, Yoshiyasu |
author_sort | Kato, Eishin |
collection | PubMed |
description | [Image: see text] Bangle (Zingiber purpureum Rosc.) rhizome extract (BRE) contains phenylbutenoid dimers (banglenes), which exert neurotrophic effects and possess the potential capability to regenerate hippocampal neurons in mice. The acute and chronic oral toxicities of BRE powder were evaluated in Sprague–Dawley rats. A dose of BRE powder was estimated to be higher than 2000 mg/kg containing BRE 534 mg/kg as minimum lethal dose in a single-dose oral toxicity study. The no-observed-adverse-effect-level for the BRE powder was 1000 mg/kg/day (BRE 267 mg/kg) in the 90 day oral toxicity study. Four week clinical studies of BRE tablets in humans suggested that the ingestion of BRE tablets within 850 mg/man/day (BRE 227 mg/man/day) was safe for at least 1 month and in a usual manner. The C(max), t(max), and AUC of cis- and trans-(E)-3-(3,4-dimethoxyphenyl)-4-[(E)-3,4-dimethoxystyryl]cyclohex-1-enes (c- and t-banglenes) were calculated after the ingestion of BRE tablets (BRE 227 mg) and were 17.73 and 22.61 ng/mL, 1.8 and 1.8 h, and 71.47 and 95.53 ng/mL/h, respectively. |
format | Online Article Text |
id | pubmed-6288899 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-62888992018-12-12 Safety Assessment of Bangle (Zingiber purpureum Rosc.) Rhizome Extract: Acute and Chronic Studies in Rats and Clinical Studies in Human Kato, Eishin Kubo, Miwa Okamoto, Yasuko Matsunaga, Yoichi Kyo, Hoko Suzuki, Nobutaka Uebaba, Kazuo Fukuyama, Yoshiyasu ACS Omega [Image: see text] Bangle (Zingiber purpureum Rosc.) rhizome extract (BRE) contains phenylbutenoid dimers (banglenes), which exert neurotrophic effects and possess the potential capability to regenerate hippocampal neurons in mice. The acute and chronic oral toxicities of BRE powder were evaluated in Sprague–Dawley rats. A dose of BRE powder was estimated to be higher than 2000 mg/kg containing BRE 534 mg/kg as minimum lethal dose in a single-dose oral toxicity study. The no-observed-adverse-effect-level for the BRE powder was 1000 mg/kg/day (BRE 267 mg/kg) in the 90 day oral toxicity study. Four week clinical studies of BRE tablets in humans suggested that the ingestion of BRE tablets within 850 mg/man/day (BRE 227 mg/man/day) was safe for at least 1 month and in a usual manner. The C(max), t(max), and AUC of cis- and trans-(E)-3-(3,4-dimethoxyphenyl)-4-[(E)-3,4-dimethoxystyryl]cyclohex-1-enes (c- and t-banglenes) were calculated after the ingestion of BRE tablets (BRE 227 mg) and were 17.73 and 22.61 ng/mL, 1.8 and 1.8 h, and 71.47 and 95.53 ng/mL/h, respectively. American Chemical Society 2018-11-21 /pmc/articles/PMC6288899/ /pubmed/30556016 http://dx.doi.org/10.1021/acsomega.8b02485 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Kato, Eishin Kubo, Miwa Okamoto, Yasuko Matsunaga, Yoichi Kyo, Hoko Suzuki, Nobutaka Uebaba, Kazuo Fukuyama, Yoshiyasu Safety Assessment of Bangle (Zingiber purpureum Rosc.) Rhizome Extract: Acute and Chronic Studies in Rats and Clinical Studies in Human |
title | Safety Assessment of Bangle (Zingiber
purpureum Rosc.) Rhizome Extract: Acute and Chronic
Studies in Rats and Clinical Studies in Human |
title_full | Safety Assessment of Bangle (Zingiber
purpureum Rosc.) Rhizome Extract: Acute and Chronic
Studies in Rats and Clinical Studies in Human |
title_fullStr | Safety Assessment of Bangle (Zingiber
purpureum Rosc.) Rhizome Extract: Acute and Chronic
Studies in Rats and Clinical Studies in Human |
title_full_unstemmed | Safety Assessment of Bangle (Zingiber
purpureum Rosc.) Rhizome Extract: Acute and Chronic
Studies in Rats and Clinical Studies in Human |
title_short | Safety Assessment of Bangle (Zingiber
purpureum Rosc.) Rhizome Extract: Acute and Chronic
Studies in Rats and Clinical Studies in Human |
title_sort | safety assessment of bangle (zingiber
purpureum rosc.) rhizome extract: acute and chronic
studies in rats and clinical studies in human |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6288899/ https://www.ncbi.nlm.nih.gov/pubmed/30556016 http://dx.doi.org/10.1021/acsomega.8b02485 |
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