不同辅酶Q10产物类型在淋巴中的单剂量吸收与输送到血液中的相比。

Q3 Medicine Integrative medicine Pub Date : 2022-11-01
William V Judy
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引用次数: 0

摘要

背景:辅酶Q10在吸收到血液中之前和之后的代谢科学是众所周知的。关于辅酶Q10在淋巴中的吸收,几乎一无所知。目的:本研究旨在测量和比较三种辅酶Q10产品配方无晶体泛醌、结晶泛醌醇和干粉泛醌在腹部淋巴管中的单剂量吸收与在血液循环中的吸收。设计:研究人员设计了一个动物研究。动物:动物是六只大型犬(>50公斤)。干预:通过胃灌胃,给狗服用100 mg剂量的无晶体泛醌(Q-Best)、晶体泛醌醇(Qnol)或干粉泛醌,并收集淋巴和静脉样本(5 ml)。结果测量:三种辅酶Q10产品类型的主要终点测量是浓度(Cmax)、Cmax时间(Tmax)以及吸收到淋巴和输送到血液中的辅酶Q10总量。结果:在干粉和结晶泛醌醇制剂中发现辅酶Q10晶体。在无晶体制剂中未发现晶体。在小肠食糜中发现了结晶和干粉制剂中的结晶。在摄入100mg剂量的CoQ10制剂后,所有三种制剂在2小时内对淋巴的组平均吸收达到峰值,在6小时内在血液中出现峰值(Cmax)。与在淋巴和血浆中测量的结晶和干粉制剂相比,无结晶制剂的吸收显著更大(P≤.001)。结论:这些数据表明,无晶体制剂的吸收优于其他两种制剂。这些结果表明,辅酶Q10晶体是导致辅酶Q10吸收不良的原因。延迟出现在血液中是由于缓慢的淋巴流将辅酶Q10输送到血液中。CoQ10的吸收可能不像文献中描述的那样差。
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The Single-dose Absorption of Different CoQ10 Product Types Into the Lymph Compared to That Transported to the Blood.

Context: The science of the metabolism of CoQ10 before and after its absorption into the blood is well known. Almost nothing is known about the absorption of CoQ10 into the lymph.

Objective: The study intended to measure and compare the single-dose absorption of three CoQ10 product formulations-crystal-free ubiquinone, crystalline ubiquinol, and a dry-powder ubiquinone-into the abdominal lymph duct as compared to their absorption into the blood circulation.

Design: The researcher designed an animal study.

Animals: The animals were six large dogs (>50 Kg).

Intervention: By gastric gavage, the dogs were given a 100-mg dose of either crystal-free ubiquinone (Q-Best), crystalline ubiquinol (Qunol), or dry-powder ubiquinone, and lymph and venous samples (5 ml) were collected.

Outcome measures: The primary end-point measurements for three CoQ10 product types were the concentration (Cmax), time of Cmax (Tmax), and total CoQ10 absorbed into the lymph and that transported to the blood.

Results: Coenzyme Q10 (CoQ10) crystals were found in the dry powder and crystalline ubiquinol formulations. No crystals were found in the crystal-free formulation. Crystals from both the crystalline and dry-powder formulations were found in the small intestine's chyme. After ingestion of a 100-mg dose of CoQ10 formulation, the group mean absorption into the lymph peaked in 2 hours for all three formulations, and the peak appearance (Cmax) in the blood occurred at 6 hours. The absorption was significantly (P ≤ .001) greater for the crystal-free formulation compared to that of the crystalline and dry-powder formulations measured in the lymph and plasma.

Conclusions: These data show that the crystal-free formulation's absorption is superior to that found for the other two formulations. These results show that CoQ10 crystals are the causative factor for the poor absorption of CoQ10. The delayed appearance in the blood is due to the slow lymph flow delivering CoQ10 to the blood. The absorption of CoQ10 may not be as poor as described in the literature.

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来源期刊
Integrative medicine
Integrative medicine Medicine-Complementary and Alternative Medicine
CiteScore
1.10
自引率
0.00%
发文量
21
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