青虾素与黑巧克力共结晶导致中年志愿者氧化标志物的剂量依赖性抑制

Ivan M. Petyaev, Marek Orłowski, V. Klochkov, N. Chalyk, N. Kyle, Ernest Bucior, Y. Bashmakov
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引用次数: 1

摘要

氧化应激和抗氧化剂缺乏是导致衰老、心血管疾病、糖尿病和癌症的因素。研究了含共晶虾青素(lc -DC- astx)的糖苷体黑巧克力(DC)中高生物利用度多酚对生物氧化参数的影响。94名健康中年志愿者(男性48名,女性46名,年龄45 - 65岁)被随机分为4个研究组。第一组被要求摄入常规对照DC (7.5 g),第二组被要求摄入含有4 mg或7 mg虾青素(ASTX)的胶囊,ASTX是一种藻类抗氧化剂。第三组给予DC棒(7.5 g)和ASTX胶囊(4mg)作为两个单独的配方共服。第四组服用含有不同剂量的ASTX (1 mg、2 mg、4 mg或7 mg)与7.5 g DC基质共结晶的LF-DC-ASTX。每种产品每天早餐后服用一次,持续1个月。在研究结束2周和4周后测定血清氧化LDL (ox-LDL)和丙二醛(MDA)水平。无论可可含量(70%、72%或85%)或摄入对照DC的时间长短,血清中ox-LDL或MDA浓度均无显著变化。相比之下,摄入不同剂量的ASTX,作为一个单一的配方,转化为氧化标记物的减少,没有任何剂量依赖性。志愿者分别服用DC和ASTX后,对ox-LDL的抑制作用远远大于单独服用ASTX,这表明DC对脂质氧化参数有一定的加性作用。对这两种氧化标志物的抑制均呈剂量依赖性,反映了DC基质中ASTX的含量。这些结果可能反映了摄入LF-DC-ASTX后可可黄烷醇和ASTX的生物利用度更高,药代动力学得到改善。因此,含有ASTX的DC营养保健品配方可以成功地用于管理与ox-LDL水平升高相关的氧化性疾病。
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Astaxanthin Co-Crystallized With Dark Chocolate Causes a Dose-dependent Inhibition of Oxidation Markers in Middle-aged Volunteers
Oxidative stress and antioxidant deficiency are contributing factors in aging, cardiovascular disease, diabetes and cancer. The effect of highly bioavailable polyphenols of lycosome-formulated dark chocolate (DC) containing co-crystallized astaxanthin (LF-DC-ASTX) on parameters of biological oxidation was investigated in this work. 94 healthy middle-aged volunteers (48 male, 46 female, 45 – 65 years old) were enrolled and randomized into four study groups. The 1st group were instructed to ingest conventional control DC (7.5 g). The 2nd group were asked to ingest capsules containing either 4 mg or 7 mg astaxanthin (ASTX), an algal antioxidant. The 3rd group were given DC bars (7.5 g) and 4 mg ASTX capsules for co-ingestion as two separate formulations. The 4th group were instructed to ingest LF-DC-ASTX containing different amounts of ASTX (1 mg, 2 mg, 4 mg or 7 mg) co-crystallized with 7.5 g of DC matrix. Each product was ingested once daily after breakfast for a period of 1 month. Serum levels of oxidized LDL (ox-LDL) and malonic dialdehyde (MDA) were measured after completion of 2 and 4 weeks of the study. No significant changes were observed in the values for ox-LDL or MDA concentrations in serum irrespective of cocoa content (70%, 72% or 85%) or duration of control DC intake. In contrast, ingestion of different doses of ASTX, as a single formulation, translated into reduction of oxidation markers without any dose-dependency. The inhibition of ox-LDL in volunteers following co-ingestion of DC and ASTX as two separate formulations was far greater than that seen for ASTX alone, revealing some additive effect of DC on lipid oxidation parameters. The inhibition of both oxidative markers was dose-dependent reflecting amount of ASTX in the DC matrix. These results may reflect greater bioavailability and improved pharmacokinetics for cocoa flavanols and ASTX following ingestion of LF-DC-ASTX. Therefore, nutraceutical formulations of DC fortified with ASTX can be successfully used for management of oxidative disorders associated with increased levels of ox-LDL.
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