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双语推荐:辅酶Q

辅酶Q10是线粒体电子传递链中的一种重要辅酶,也是存在于线粒体中的一种重要脂溶性抗氧化剂。辅酶Q10在医学上的应用十分广泛,主要体现在心血管疾病、高血压、神经系统疾病方面。近些年来研究发现辅酶Q10在高原医学方面也有很大的应用前景,现对其进行综合阐述。
Coenzyme Q10 is not only an important coenzyme in the mitochondrial electron transport chain ,but also one of the important fat-soluble antioxidants existing in the mitochondria .It has been widely used in medicine , especially in cardiovascular diseases ,hypertension ,nervous system diseases ,and etc .Studies have found that coen-zyme Q10 may also have a great application prospect in high altitude medicine ,and this review will give some proof about that .

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通过单因素试验和正交试验对超声波提取辅酶Q10的工艺条件进行了优化,确定了类球红细菌辅酶Q10的最佳提取条件为:输出功率为55%、每次辐射时间为3s、工作总时间为6min、菌液浓度OD为23.4,条件优化后辅酶Q10单位细胞产量达到11.86mg/L。
Coenzyme Q10 ultrasonic extraction conditions were optimized by single factor and orthogonal ex-periments.The optimum extraction conditions Rhodobacter sphaeroides coenzyme Q10 is:55% of the output power,3s of each radiation time,total wording time of 6min,23.4 for the bacterial concentration,after optimi-zation of coenzyme Q10 unit cell production reached 11.86mg/L.

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目的:观察重组人组织型纤溶酶原激酶衍生物(rPa)联合辅酶Q10治疗急性st段抬高型心肌梗死的疗效及安全性。方法选80例符合溶栓治疗指征的急性st段抬高型心肌梗死患者随机分为常规溶栓治疗组和辅酶Q10组,每组各40例;辅酶 Q10组于溶栓治疗同时给予辅酶 Q10治疗。分别于治疗前、治疗后24 h检测2组患者血浆肌钙蛋白 i(ctni)、肌酸激酶同工酶(cK-MB)以及超氧化物歧化酶(sod)活力;所有入选患者2周时行心脏彩超检查,采用 simpson 法测定和计算左室舒张末期内径、左室收缩末期内径、左室射血分数;观察2组治疗后2 周内心血管不良事件发生率。结果(1)辅酶 Q10组血管再通率高于常规溶栓组(65.7%:62.8%),但两组比较差异无统计学意义(P>0.05)。(2)与溶栓治疗前比较,两组治疗后血浆 cK-MB,ctni ,sod 较治疗前明显升高,且 sod 活性升高低于 cK-MB,ctni升高幅度(P<0.05),辅酶 Q10组治疗后血浆 cK-MB ,ctni 升高幅度明显低于常规溶栓组,sod 活性明显高于常规溶栓组(P<0.05)。(3)常规溶栓组左室舒张末期内径、左室收缩末期内径均高于辅酶 Q10钠组,左室射血分数低于辅酶 Q10钠组(分别为56.01±3.48 mm 比50.69±2.99 mm,P<0.05;47.89±4.76 mm 比41.
Objective to observe the effects of recombinant human tissue type plasminogen kinase derivatives (rPa) effect and safety of combined with coenzyme Q10 in the treatment of acute st segment elevation myocardial infarction. Methods 80 patients with acute st syndrome refers to comply with thrombolytic therapy in patients with the segment elevation myocardial infarction were randomly divided into conventional thrombolytic therapy group and coenzyme Q10 group, 40 cases in each group; coenzyme Q10 group in the thrombolytic therapy at the same time give coenzyme Q10 therapy. respectively in the detection of 24h before and after treatment in 2 groups of patients with cardiac troponin i (ctni), creatine kinase isoenzyme MB (cK-MB) and superoxide dismutase (sod) activity; all patients 2 weeks after cardiac ultrasound examination, determination and calculation of left ventricular end diastolic period inside diameter, left ventricular end systolic diameter, left ventricular ejection fract

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利用乙醇提取法从麦麸中分离提取辅酶Q10。结果表明,最佳提取条件为:乙醇浓度95%、料液比1:25(g/mL)、回流温度70℃和回流时间80min。该提取工艺相对比较简单,为麦麸中辅酶Q10的提取分离提供方法。
This experiment extracted and separated coenzyme Q10 from wheat skin using the method of ethanol extraction .The results showed that optimum conditions of ethanol extraction were ethanol concentration 95%, temperature 70 ℃, extraction time 80 min and ratio of material to ethanol 1 ∶ 25, the process is relatively simple,Q10 amount of attaining satisfactory standards. The study aimed to provide scientific method for the extraction and separation of coenzyme Q10 from wheat skin.

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目的通过将他汀类药物联合规律运动应用于冠心病患者治疗,观察冠心病患者血清还原型辅酶Q10、高密度脂蛋白-胆固醇(HDL-C)和低密脂蛋度白-胆固醇(LDL-C)含量变化。方法选择30例入住我院冠心病患者随机分为瑞舒伐他汀组和阿托伐他汀组,分别给予相应药物治疗,同时进行院内无氧锻炼1周和家庭锻炼20周,锻炼计划前后分别检测患者的血脂,辅酶Q10和心肺功能;采用相关性分析患者载脂蛋白A1变化与血清还原型辅酶Q10含量之间的关系。结果两组患者的心肺功能均得到改善,同时LDL-C和甘油三酯下降;两组患者HDL-C和载脂蛋白A1均有不同程度提高,但瑞舒伐他汀组提高幅度明显高于阿托伐他汀组;阿托伐他汀组血清还原型辅酶下降明显,差异有统计学意义;相关性分析显示载脂蛋白A1变化与还原型辅酶Q10呈正相关。结论与阿托伐他汀相比,瑞舒伐他汀联合规律运动能够维持冠心病患者还原型辅酶Q10水平同时使HDL-C上升,对冠心病患者具有更加确切有益的疗效。
Objective To investigate the effects of two statins (rosuvastatin and atorvastatin) combined with exercise on the levels of coenzyme Q10, HDL-C and LDL-C in coronary artery disease(CAD) patients. Methods Af-ter randomizing 30 CAD patients into rosuvastatin (n=14) and atorvastatin (n=14) groups, patients performed week-ly in-hospital aerobic exercise and daily home exercise for 20 weeks. The lipids and ubiquinol in serum and exercise capacity were measured, and the correlation analysis was carried out to explore the relationship between apolipopro-tein A1 (ApoA1) and ubiquinol in patients. Results Both statins equally improved exercise capacity and lowered LDL-C and triglyceride levels. Rosuvastatin significantly increased HDL-C and ApoA1 compared to atorvastatin. Atorvastatin significantly decreased ubiquinol level in serum. There was a significant positive correlation between changes in ubiquinol and ApoA1. Conclusion Compared with atorvastatin, rosuvastatin combined with exercise can

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辅酶Q10产量为指标,对米曲霉2077固体发酵法生产辅酶Q10进行了初步系统性研究.利用配方均匀设计和正交设计方法分别对培养基和培养条件进行优化,建立了相应的数学模型,得到了较优固体培养基为大豆8.20%、麦麸63.53%和谷糠28.27%,确定100 g培养基固体培养条件为:料水比为1、青霉素钠加入量为3mL、发酵温度40℃、发酵时间96 h为较优工艺条件.在此优化培养基和培养条件下得到米曲霉2077产辅酶Q10的最大值为0.947/mg·g-1干培养基.
Based on the yield of coenzyme Q 10 as indicatior , the production of coenzyme Q 10 with solid state fermentation of Aspergillus oryzae 2077 was studied in the paper .The culture medium and conditions were optimized separately by the uniform design of the formulation and the cultivation of the orthogonal design method , and the corresponding mathematical model was established .According to the analysis , the superior solid medium was set at soybean 8 .20%, wheat bran 63 .53% and rice bran 28 .27%, and the optimum conditions of solid fermentation were as following: the atio of material and water was 1, the penicillin sodium addition 3 mL, fermentation temperature 40℃, fermentation time 96 h.On the optimization conditions , the maximum production of coenzyme Q10 was 0.947/mg· g -1 by using Aspergillus oryzae solid fermentation.

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目的观察辅酶Q10对高龄慢性心功能不全的疗效及安全性。方法 70例高龄慢性心功能不全的患者随机分为治疗组和对照组,对照组给以常规治疗,治疗组在常规治疗基础上联合辅酶Q10,两组疗程均为2个月,治疗前后观察两组血浆脑钠肽(BNP)的水平、心功能改善程度。结果两组BNP均下降,但治疗组BNP水平下降明显高于对照组,治疗组心功能不全改善较对照组更明显,差异有显著性(P0.05),且治疗组不良反应发生率很低。结论辅酶Q10对高龄慢性心功能不全的有很好的疗效及安全性。
Objective To observe coenzyme Q 10 for the elderly with chronic heart failure efficacy and safety.Methods 70 ca-ses of elderly patients with chronic heart failure were randomly divided into treatment group and control group ,the control group given conventional treatment group and coenzyme Q 10 in the conventional therapy ,treatment lasted two months ,both before and after treat-ment was observed plasma levels of brain natriuretic peptide ( BNP) ,the degree of improvement in heart function.Results There BNP decreased ,but the treatment group decreased significantly higher BNP , cardiac dysfunction improve the treatment group com-pared with the control group more obvious difference was significant (P<0.05),and a low incidence of adverse reactions treatment groups.Conclusion coenzyme Q10 for the elderly with chronic heart failure have a good efficacy and safety .

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分别以33.5、67.0、134.0mg/kg·BW(相当于人体推荐用量5、10、20倍)剂量的辅酶Q10软胶囊给小鼠连续灌胃30 d,分别测定ConA诱导的小鼠淋巴细胞转化功能、小鼠的迟发型变态反应、小鼠抗体生成和溶血素水平、单核-巨噬细胞碳廓清能力、腹腔巨噬细胞吞噬鸡红细胞能力以及NK细胞活性。结果显示辅酶Q10软胶囊能促进小鼠的脾淋巴细胞增殖、转化作用,促进小鼠的抗体生成细胞增殖,提高小鼠的血清溶血素水平,促进小鼠的迟发型变态反应及其单核-巨噬细胞的吞噬功能,因此,可判定辅酶Q10软胶囊具有增强小鼠免疫力的作用。
Coenzyme Q10 soft capsule were consecutively orally given to mice with the doses of 33.5, 67, 134 mg/kg·bw (5,10,20 times to the recommended human dosage) for 30 d. The spleen lymphocyte transformation efficiency, delayed type hypersensitivity, antibody-producing, Monocyte-macrophage carbon clearance ability, Peritoneal macrophage phagocytic capacity and the activity of natural killer ( NK )were determined. The results showed that Coenzyme Q10 soft capsule can promote the proliferation of mouse spleen lymphocytes and transformation of mice''S spleen lymphocytes and the proliferation of antibody-producing cells in mice, increased levels of serum hemolysin in mice, promote delayed hypersensitivity and its monocyte-macrophage phagocytosis. Therefore, Coenzyme Q10 soft capsule can be determined in mice with enhanced immunity.

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研究生脉饮对病毒性心肌炎心肌细胞凋亡作用的影响。方法:用柯萨奇B病毒建立感染的心肌细胞模型,在感染后24小时将细胞分为正常对照组、病理模型组、生脉饮组和辅酶Q10组。4组分别在不同时间点观察细胞形态,并采用TUNEL法进行细胞凋亡的检测。结果:在48小时点开始检测,正常对照组无细胞凋亡,生脉饮组及辅酶Q10组均有凋亡,生脉饮组凋亡率低于辅酶Q10组(P0.05),病理模型组随着时间的推移,凋亡率增加,72小时点明显高于48小时点(P0.01),与药物干预组比较差异具有统计学意义(P0.05)。结论:生脉饮能够有效抑制病毒性心肌炎心肌细胞的凋亡,且应该早期干预。
Objective:To study the effect of pulse-activating decoction compound preparation in myocardial apoptosis effect of viral myocarditis.Methods:Using coxsackie B virus established infectious myocardial cell model.In 24 hours after infection,the cells were divided into four groups:the normal control group,the pathological model group,the pulse-activating decoction group and the coenzyme Q10 group.The cellular morphology of four groups of cells were observed at different time points.The apoptosis was detected by TUNEL method.Results:Begin testing at 48 hours,the normal control group had no apoptosis;the pulse-activating decoction group and the coenzyme Q10 group all had apoptosis;the apoptosis rate of the pulse-activating decoction group was lower than that of the coenzyme Q10 group(P<0.05).In the pathological model group,the apoptosis rate was increased as time goes on.72 hours point was obviously higher than 48 hours point(P<0.01).There had statistically significant compared with the drug

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目的探讨胸闷患者的常见病因,并评价辅酶Q10对缓解胸闷症状治疗效果。方法选择2010年9月~2013年1月间住院的无心肺病史胸闷患者206例,随机分为治疗组和对照组,在常规治疗基础上,对照组患者口服维生素C片、治疗组口服辅酶Q10治疗。对患者临床表现及检查结果进行分析。结果胸闷患者的病因主要有:冠脉慢血流现象、慢性阻塞性肺疾病、支气管哮喘、冠心病、气胸、急性上呼吸道感染、胸腔积液、肺炎、心律失常、肺癌、心肌炎等。治疗组胸闷症状明显改善(Z=2.197,P=0.028)。结论无心肺病史胸闷患者发病主要原因为冠脉慢血流现象及慢性阻塞性肺疾病,在诊断明确前辅酶Q10有助于安全缓解症状。
Objective Investigate the etiology of patients with chest tightness, and evaluation the effect of coenzyme Q10 on chest tightness. Methods Single blind placebo study was adopted in this study.206 cases of hospitalized patients with chest tightness were selected in Wuhan No.1 Hospital without history of heart or lung diseases from 2010 September to 2013 January, and randomly divided into treatment group and control group. On the basis of routine treatment, patients in the control group gave oral Vitamin C Tablets, treatment group with oral coenzyme Q10 therapy. The clinical manifestations and examination results were recorded. Results The etiology of these patients were:coronary slow flow phenomenon, chronic obstructive pulmonary disease, asthma, coronary heart disease, acute upper respiratory tract infection, pneumothorax, pleural effusion, pneumonia, lung cancer, cardiac arrhythmias, myocarditis. In the treatment group chest symptoms were alleviated significantly(Z=2.197, P=0.028). Co

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