Comparative Oral Toxicity of Coenzyme Q10 and Its (2Z)-Isomer in Rats: Single and Four-Week Repeated Dose Toxicity Studies
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- HATAKEYAMA Shigeki
- Nisshin Kyorin Pharmaceutical Co., Ltd.
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- KAWASE Shigeo
- Nisshin Kyorin Pharmaceutical Co., Ltd.
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- YOSHIMURA Ikuo
- Nisshin Pharma Inc
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It has been reported that coenzyme Q10 (CoQ10) functions as an electron transfer carrier in mitochondria, and can produce an improvement in heart diseases such as congestive heart failure. Its (2Z)-isomer contains a cis-double bond at the 2-position of the decaprenyl side chain. As the original organic industrial synthesis of CoQ10 resulted in a product that contained a small amount of this isomer, the efficacy and safety of CoQ10 was determined using CoQ10 containing this isomer; however, no toxicity data have been reported for the (2Z)-isomer itself. Thus, we conducted single (2,000 mg/kg) and 4-wk repeated (1,000 mg/kg) oral dose toxicity studies in rats to compare the toxicological profiles of CoQ10 and its (2Z)-isomer. The two compounds displayed similar toxicological profiles, and it was concluded that neither CoQ10 nor its (2Z)-isomer produce toxic effects in rats in single or repeated doses.
収録刊行物
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- Journal of Nutritional Science and Vitaminology
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Journal of Nutritional Science and Vitaminology 52 (1), 9-20, 2006
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詳細情報 詳細情報について
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- CRID
- 1390001206325620736
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- NII論文ID
- 110004656455
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- NII書誌ID
- AA00703822
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- COI
- 1:CAS:528:DC%2BD28XisFKqsLg%3D
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- ISSN
- 18817742
- 03014800
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- NDL書誌ID
- 7834285
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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