THIRTEEN-WEEK REPEATED DOSE ORAL TOXICITY STUDY OF COENZYME Q10 IN RATS
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- HONDA Kumiko
- Department of Toxicology, Panapharm Laboratories Co., Ltd.
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- TOMINAGA Sayumi
- Department of Toxicology, Panapharm Laboratories Co., Ltd.
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- OSHIKATA Takafumi
- Department of Toxicology, Panapharm Laboratories Co., Ltd.
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- KAMIYA Kouichi
- Department of Toxicology, Panapharm Laboratories Co., Ltd.
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- HAMAMURA Masao
- Department of Toxicology, Panapharm Laboratories Co., Ltd.
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- KAWASAKI Tsuneshirou
- Asahi Kasei Pharma Corporation
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- WAKIGAWA Kouichi
- Asahi Kasei Pharma Corporation
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As part of a safety evaluation of Coenzyme Q10, a subchronic toxicology study was conducted. Coenzyme Q10 was repeatedly administered orally to male and female Crl:CD(SD) rats at daily dose levels of 300, 600 and 1200 mg/kg for 13 weeks. Neither death nor any toxicological signs were observed in any group during the administration period. No change related to the test substance administered was observed in any group with regard to body weight, food consumption, ophthalmoscopy, hematology, blood biochemistry, necropsy, organ weights or histopathology. Based on these results, the non-observed-adverse-effect level (NOAEL) of Coenzyme Q10 was considered to be 1200 mg/kg/day for male and female rats under these study conditions.<br>
収録刊行物
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- The Journal of Toxicological Sciences
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The Journal of Toxicological Sciences 32 (4), 437-448, 2007
一般社団法人 日本毒性学会
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詳細情報 詳細情報について
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- CRID
- 1390282679877281024
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- NII論文ID
- 110006420619
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- NII書誌ID
- AN00002808
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- ISSN
- 18803989
- 03881350
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- NDL書誌ID
- 8981738
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- NDL
- Crossref
- CiNii Articles
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- 抄録ライセンスフラグ
- 使用不可