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脂溶性抗氧化剂泛醇的不稳定性:第二部分——犬类研究。

The Instability of the Lipid-Soluble Antioxidant Ubiquinol: Part 2-Dog Studies.

作者信息

Judy William V

机构信息

Founder and President, SIBR Research.

出版信息

Integr Med (Encinitas). 2021 Oct;20(5):26-30.

PMID:34803537
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8594965/
Abstract

BACKGROUND

Coenzyme Q10 is one of the most widely sold nutritional supplements in the United States. Coenzyme Q10 is available in both its oxidized form (ubiquinone) and its reduced form (ubiquinol). The predominant marketing of Coenzyme Q10 to physicians and patients asserts that the ubiquinol form of Coenzyme Q10 has superior absorption to the ubiquinone form. This study has been designed to compare and contrast the stability and absorption of ubiquinol supplements, as well as the claims made for ubiquinol compared with ubiquinone.Ubiquinol, the reduced state of Coenzyme Q10, is commercially available as a nutritional supplement; however, ubiquinol, by its nature as an electron donor, is much less stable than ubiquinone, the oxidized state of Coenzyme Q10. The absorption, bioavailability and efficacy of ubiquinol products has been much less often tested in clinical trials. Consequently, insufficiently documented marketing claims are being made for ubiquinol supplements.

METHODS

In Part 1 of this report on the instability of the lipid-soluble antioxidant ubiquinol, SIBR Research presented data from lab studies showing that oral ubiquinol is likely to be oxidized to ubiquinone and absorbed as ubiquinone. In this Part 2, SIBR Research conducted a study of the transfer and absorption of orally ingested ubiquinol in large dogs.

RESULTS

In the dog studies, the percentage of ubiquinol converted to ubiquinone increased as the capsule contents passed through the stomach and small intestines and into the lymph system.

CONCLUSIONS

The dog studies demonstrate that oral ubiquinol in commercial nutritional supplements is not stable in the gastrointestinal tract of large dogs. Based on these results, it seems likely that in humans also, most of the ubiquinol from capsules will be oxidized to ubiquinone in the acid profile between the stomach and the small intestines, where there is a wide range of acidity. The ubiquinol from the supplement will be absorbed in the ubiquinone state and will pass into the lymph system as ubiquinone, where it will be reduced back to ubiquinol. It will pass from the lymph system into the blood circulation as ubiquinol.

摘要

背景

辅酶Q10是美国销量最广的营养补充剂之一。辅酶Q10有氧化形式(泛醌)和还原形式(泛醇)两种。向医生和患者进行的辅酶Q10主要营销宣传称,辅酶Q10的泛醇形式比泛醌形式具有更好的吸收性。本研究旨在比较和对比泛醇补充剂的稳定性和吸收情况,以及与泛醌相比泛醇所宣称的优势。泛醇是辅酶Q10的还原态,作为一种营养补充剂在市场上有售;然而,由于其作为电子供体的性质,泛醇比辅酶Q10的氧化态泛醌稳定性要低得多。泛醇产品的吸收、生物利用度和功效在临床试验中的测试要少得多。因此,针对泛醇补充剂的营销宣传缺乏充分的文献记载。

方法

在这份关于脂溶性抗氧化剂泛醇不稳定性报告的第1部分中,SIBR研究公司展示了实验室研究数据,表明口服泛醇很可能被氧化为泛醌并以泛醌形式被吸收。在第2部分中,SIBR研究公司对大型犬口服摄入泛醇的转运和吸收进行了研究。

结果

在犬类研究中,随着胶囊内容物通过胃、小肠并进入淋巴系统,泛醇转化为泛醌的百分比增加。

结论

犬类研究表明,市售营养补充剂中的口服泛醇在大型犬的胃肠道中不稳定。基于这些结果,在人类中似乎也很可能是这样,胶囊中的大多数泛醇在胃和小肠之间酸度范围较宽的酸性环境中会被氧化为泛醌。补充剂中的泛醇将以泛醌状态被吸收,并以泛醌形式进入淋巴系统,在那里它将被还原回泛醇。它将以泛醇形式从淋巴系统进入血液循环。

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引用本文的文献

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J Clin Biochem Nutr. 2023 Mar;72(2):101-106. doi: 10.3164/jcbn.22-91. Epub 2022 Dec 8.
3
Coenzyme Q10 Metabolism: A Review of Unresolved Issues.辅酶 Q10 代谢:未解决问题综述。
Int J Mol Sci. 2023 Jan 30;24(3):2585. doi: 10.3390/ijms24032585.
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The Single-dose Absorption of Different CoQ10 Product Types Into the Lymph Compared to That Transported to the Blood.与转运至血液中的情况相比,不同类型辅酶Q10产品的单剂量吸收进入淋巴的情况。
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本文引用的文献

1
The Instability of the Lipid-Soluble Antioxidant Ubiquinol: Part 1-Lab Studies.脂溶性抗氧化剂泛醇的不稳定性:第一部分——实验室研究
Integr Med (Encinitas). 2021 Aug;20(4):24-28.
2
Bioavailability of Coenzyme Q: An Overview of the Absorption Process and Subsequent Metabolism.辅酶Q的生物利用度:吸收过程及后续代谢概述
Antioxidants (Basel). 2020 May 5;9(5):386. doi: 10.3390/antiox9050386.
3
Bioavailability of coenzyme Q10 supplements depends on carrier lipids and solubilization.辅酶 Q10 补充剂的生物利用度取决于载体脂质和溶解。
Nutrition. 2019 Jan;57:133-140. doi: 10.1016/j.nut.2018.05.020. Epub 2018 Jun 27.
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Coenzyme Q Supplementation in Aging and Disease.衰老与疾病中的辅酶Q补充
Front Physiol. 2018 Feb 5;9:44. doi: 10.3389/fphys.2018.00044. eCollection 2018.
5
Comparison study of plasma coenzyme Q10 levels in healthy subjects supplemented with ubiquinol versus ubiquinone.健康受试者补充泛醇与泛醌的血浆辅酶 Q10 水平比较研究。
Clin Pharmacol Drug Dev. 2014 Jan;3(1):13-7. doi: 10.1002/cpdd.73. Epub 2013 Oct 8.
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CoQ₁₀ Function and Role in Heart Failure and Ischemic Heart Disease.辅酶Q₁₀在心力衰竭和缺血性心脏病中的功能与作用
Annu Rev Nutr. 2015;35:175-213. doi: 10.1146/annurev-nutr-071714-034258. Epub 2015 May 13.
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Statins stimulate atherosclerosis and heart failure: pharmacological mechanisms.他汀类药物会引发动脉粥样硬化和心力衰竭:药理机制。
Expert Rev Clin Pharmacol. 2015 Mar;8(2):189-99. doi: 10.1586/17512433.2015.1011125. Epub 2015 Feb 6.
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Bioenergetic and antioxidant properties of coenzyme Q10: recent developments.辅酶Q10的生物能量学与抗氧化特性:最新进展
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Coenzyme Q(10)--its role as a prooxidant in the formation of superoxide anion/hydrogen peroxide and the regulation of the metabolome.辅酶Q(10)——其在超氧阴离子/过氧化氢形成中作为促氧化剂的作用及代谢组的调节
Mitochondrion. 2007 Jun;7 Suppl:S51-61. doi: 10.1016/j.mito.2007.03.005. Epub 2007 Mar 30.
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Antioxidant defenses in rat intestine and mesenteric lymph.大鼠肠道和肠系膜淋巴中的抗氧化防御系统。
Redox Rep. 1999;4(3):79-87. doi: 10.1179/135100099101534756.