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Novel Split Chest Tube Improves Post-Surgical Thoracic Drainage. 新型开胸管改善术后胸腔引流。
Pub Date : 2014-01-01 DOI: 10.4172/2155-9880.1000321
Albert H Olivencia-Yurvati, Brandon H Cherry, Hunaid A Gurji, Daniel W White, J Tyler Newton, Gary F Scott, Besim Hoxha, Terence Gourlay, Robert T Mallet

Objective: Conventional, separate mediastinal and pleural tubes are often inefficient at draining thoracic effusions.

Description: We developed a Y-shaped chest tube with split ends that divide within the thoracic cavity, permitting separate intrathoracic placement and requiring a single exit port. In this study, thoracic drainage by the split drain vs. that of separate drains was tested.

Methods: After sternotomy, pericardiotomy, and left pleurotomy, pigs were fitted with separate chest drains (n=10) or a split tube prototype (n=9) with internal openings positioned in the mediastinum and in the costo-diaphragmatic recess. Separate series of experiments were conducted to test drainage of D5W or 0.58 M sucrose, an aqueous solution with viscosity approximating that of plasma. One litre of fluid was infused into the thorax, and suction was applied at -20 cm H2O for 30 min.

Results: When D5W was infused, the split drain left a residual volume of 53 ± 99 ml (mean value ± SD) vs. 148 ± 120 for the separate drain (P=0.007), representing a drainage efficiency (i.e. drained vol/[drained + residual vol]) of 95 ± 10% vs. 86 ± 12% for the separate drains (P = 0.011). In the second series, the split drain evacuated more 0.58 M sucrose in the first minute (967 ± 129 ml) than the separate drains (680 ± 192 ml, P<0.001). By 30 min, the split drain evacuated a similar volume of sucrose vs. the conventional drain (1089 ± 72 vs. 1056 ± 78 ml; P = 0.5). Residual volume tended to be lower (25 ± 10 vs. 62 ± 72 ml; P = 0.128) and drainage efficiency tended to be higher (98 ± 1 vs. 95 ± 6%; P = 0.111) with the split drain vs. conventional separate drains.

Conclusion: The split chest tube drained the thoracic cavity at least as effectively as conventional separate tubes. This new device could potentially alleviate postoperative complications.

目的:传统的胸腔和纵隔隔管引流胸腔积液效果不佳。描述:我们开发了一种y形胸管,其分叉端在胸腔内分开,允许单独的胸腔内放置,并且需要一个单独的出口。在本研究中,我们比较了劈开引流管与单独引流管的胸腔引流。方法:猪经胸骨切开、心包切开和左胸膜切开后,分别安装独立胸腔引流管(n=10)或分离式管原型(n=9),其内部开口位于纵隔和肋膈隐窝。分别进行了一系列实验,以测试D5W或0.58 M蔗糖(粘度接近等离子体的水溶液)的排水性。将1升液体注入胸腔,在-20 cm H2O下吸力30 min。结果:D5W输注时,分路引流管剩余容积为53±99 ml(平均值±SD),分路引流管剩余容积为148±120 ml (P=0.007),引流效率(即排出容积/[排出容积+剩余容积])为95±10%,分路引流管剩余容积为86±12% (P= 0.011)。在第二组病例中,劈开胸管第一分钟排出的蔗糖量(967±129 ml)比单独引流多0.58 M(680±192 ml)。结论:劈开胸管对胸腔的引流效果至少与常规单独引流相同。这种新装置有可能减轻术后并发症。
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引用次数: 0
Association between inflammatory markers and liver fat: The Multi-Ethnic Study of Atherosclerosis. 炎症标志物与肝脏脂肪的关系:动脉粥样硬化的多民族研究。
Pub Date : 2014-01-01 DOI: 10.4172/2155-9880.1000344
Yasmin S Hamirani, Ronit Katz, Khurram Nasir, Irfan Zeb, Michael J Blaha, Roger S Blumenthal, Richard N Kronmal, Matthew J Budoff

Background: Nonalcoholic fatty liver disease (NAFLD) is a common liver disease. Data is emerging that an independent association between markers of subclinical atherosclerosis and NAFLD exists and it may be considered as an independent predictor of cardiovascular (CV) outcomes. We aim to better characterize the relationship between NAFLD and inflammatory markers in a multi-ethnic cohort by assessing fatty liver on computed tomography (CT) scans.

Methods: The Multi-Ethnic Study of Atherosclerosis (MESA) is a longitudinal, population-based study from four ethnic groups free of CV disease at baseline. The inflammatory markers studied include: C-reactive protein (CRP) and interleukin 6 (IL-6). On CT scans liver-to-spleen ratio (LSR: Hounsfield Units (HU) of the liver divided by HU of spleen) of <1 and liver attenuation of <40 HU were used as criteria for fatty liver. Unadjusted and adjusted multivariate linear and logistic regression analysis was performed.

Results: 4038 participants amongst 6814 MESA population with visible spleen on the CT scan, available CRP and IL-6 levels and no reported liver cirrhosis were included. The average age was 61 +/- 10 years, 37% Caucasians and 45% were males. Mean CRP and IL-6 were 2.36 mg/dl and 1.37 pg/ml respectively. 696 participants (17%) had LSR of <1 and 253 (6%) had liver attenuation of <40 HU. When using LSR <1 as a continuous variable, the correlation (adjusted odds ratio (OR)) with CRP >2.0 was 0.037 (95% CI: 0.02-0.054) and with IL-6 was 0.014 (95% CI: 0.004-0.023). On the other hand when presence and absence of LSR <1 was considered, higher ORs for association with CRP >2: 1.41 (95% CI: 1.16 to 1.73) and IL6:1.18 (95% CI: 1.05 to 1.31) were found. Similarly, the adjusted association of per unit decrease in liver attenuation with CRP>2 was 1.92 (95% CI: 1.20 to 2.63) while for IL-6 was 1.08 (95% CI: 0.69 to 1.47). When considering presence and absence of liver attenuation <40 HU the OR for CRP >2 was 2.27 (95% CI: 1.62 to 3.16) and for IL-6 was 1.33 (95% CI: 1.13 to 1.58).

Conclusion: CRP and IL-6 levels were found to be significantly associated with liver fat assessed on CT scan after adjusting for other risk factors for atherosclerosis.

背景:非酒精性脂肪肝(NAFLD)是一种常见的肝脏疾病。数据显示,亚临床动脉粥样硬化和NAFLD标志物之间存在独立关联,并且可能被认为是心血管(CV)结局的独立预测因子。我们的目标是通过在计算机断层扫描(CT)上评估脂肪肝,更好地表征多种族队列中NAFLD和炎症标志物之间的关系。方法:动脉粥样硬化多民族研究(MESA)是一项纵向、基于人群的研究,来自基线时无心血管疾病的四个民族。研究的炎症标志物包括:c反应蛋白(CRP)和白细胞介素6 (IL-6)。CT扫描肝脾比(LSR:肝脏的Hounsfield单位(HU)除以脾脏的HU)结果:6814名MESA人群中有4038名参与者,CT扫描上可见脾脏,可用的CRP和IL-6水平,未报告肝硬化。平均年龄61±10岁,白种人占37%,男性占45%。平均CRP和IL-6分别为2.36 mg/dl和1.37 pg/ml。696名参与者(17%)的LSR为2.0,分别为0.037 (95% CI: 0.02-0.054)和0.014 (95% CI: 0.004-0.023)。另一方面,当发现存在和不存在LSR 2: 1.41 (95% CI: 1.16至1.73)和IL6:1.18 (95% CI: 1.05至1.31)时。同样,每单位肝衰减与CRP>2的校正相关性为1.92 (95% CI: 1.20至2.63),而与IL-6的校正相关性为1.08 (95% CI: 0.69至1.47)。当考虑肝衰减是否存在时,2为2.27 (95% CI: 1.62至3.16),IL-6为1.33 (95% CI: 1.13至1.58)。结论:在校正动脉粥样硬化的其他危险因素后,发现CT扫描评估的CRP和IL-6水平与肝脏脂肪有显著相关性。
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引用次数: 0
Coronary Revascularization Using Bilateral Internal Thoracic Arteries: Safe with Skeletonization? 双侧胸内动脉冠脉血运重建术:与骨骼化相比安全吗?
Pub Date : 2013-11-20 DOI: 10.4172/2155-9880.S7-007
Brody Wehman, Bradley Taylor

Substantial evidence exists to support a long-term survival benefit with bilateral internal thoracic artery (BITA) revascularization in coronary artery bypass grafting. However, this technique remains grossly underutilized worldwide and especially in the United States. In this review, we discuss evidence for the advantages of BITA grafting as well as the associated the risk of sternal wound complications. We then review a growing body of literature that suggests 'skeletonization' of the internal thoracic artery during harvest confers a protective benefit against sternal wound infection in patients receiving BITA.

有大量证据支持双侧胸内动脉(BITA)血管重建术在冠状动脉搭桥术中的长期生存获益。然而,这项技术在世界范围内,特别是在美国,仍未得到充分利用。在这篇综述中,我们讨论了BITA移植的优势以及相关的胸骨伤口并发症的风险。然后,我们回顾了越来越多的文献,这些文献表明,在收获期间“骨骼化”胸内动脉对接受BITA的患者的胸骨伤口感染具有保护作用。
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引用次数: 6
Myocardial Mitochondria at the Intersection of Health and Disease 心肌线粒体在健康和疾病的交叉点
Pub Date : 2013-03-16 DOI: 10.4172/2155-9880.1000E123
Edwards Jg
The air that we breathe and the food that we eat reach their confluency in the mitochondria to derive the energy that the cell is dependent upon. The heart is the most aerobic of organs and has little anaerobic reserve compared to the constant demands placed upon it. At rest the arterial-venous oxygen extraction from the blood is the greatest from the heart and this only goes up with exercise. Common to all cell types residing in the heart is the need for energy and mitochondrial dysfunction is a significant contributor to cell death across the spectrum of cardiac disorders. Mitochondrial failure within any one cell type creates varying complications that eventually manifest as heart failure.
我们呼吸的空气和吃的食物在线粒体中汇合,产生细胞赖以生存的能量。心脏是最需氧的器官,与它所承受的持续需求相比,它几乎没有无氧储备。在休息时,从血液中提取的动静脉氧是最大的,这只有在锻炼时才会增加。居住在心脏中的所有细胞类型都需要能量,线粒体功能障碍是导致心脏疾病范围内细胞死亡的重要因素。任何一种细胞类型的线粒体衰竭都会产生各种并发症,最终表现为心力衰竭。
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引用次数: 1
Nutritional Supplement-5 with a Combination of Proteasome Inhibitors (Resveratrol, Quercetin, δ-Tocotrienol) Modulate Age-Associated Biomarkers and Cardiovascular Lipid Parameters in Human Subjects. 结合蛋白酶体抑制剂(白藜芦醇、槲皮素、δ-生育三烯醇)的营养补充剂-5调节人类受试者年龄相关的生物标志物和心血管脂质参数。
Pub Date : 2013-03-02 DOI: 10.4172/2155-9880.1000238
Asaf A Qureshi, Dilshad A Khan, Wajiha Mahjabeen, Christopher J Papasian, Nilofer Qureshi

Background: Age-associated altered redox imbalances and dysregulated immune function, contribute to the development of a variety of age associated diseases. Inflammatory markers and lipid profiles are useful prognostic indicators of a variety of age-associated and cardiovascular diseases. We have previously studied the impact of several proteasome inhibitors on several markers of inflammation and lipid profiles in vitro, in vivo, in cell lines, animal models, and in human subjects. The current study represents an extension of this work. Our main hypothesis is that a combination of various naturally-occurring proteasome inhibitors, which inhibits nitric oxide (NO), and C-reactive protein (CRP) mediated inflammation, will have better efficacy in the prevention and treatment of age-associated disorders including cardiovascular disease.

Methods: Two double blind, randomized, placebo-controlled cross-over trials were conducted to determine the impact of a mixture of NS-5 (resveratrol, pterostilbene, quercetin, δ-tocotrienol, nicotinic acid) on serum NO, CRP, γ-glutamyl-transferase (γ-GT) activity, total antioxidant status (TAS), total cholesterol, LDL-cholesterol, HDL-cholesterol and triglycerides levels. Healthy seniors (Group-1; n = 32) free-living (A, B; 16/group), and hypercholesterolemic (Group-2; n = 64) subjects on AHA-Step-1-diet were divided into two groups (C, D; 32/group). Baseline levels were established for parameters as mentioned above. Groups A, C were administered 4-capsules/d of NS-5 and groups B, D, placebo (starch) for 6-weeks. Groups were crossed-over, followed by a 2-week wash-out period. Groups A, C were given 4-capsules/d of placebo and groups B, D, 4-capsules/d of NS-5 for 6-weeks. Groups C, D were continued on AHA-Step-1-diet.

Results: All the subjects completed each phase in both studies without any complaints. There were significant ( P < 0.01 - 0.05) decreases in the serum levels of NO (30%, 26%), CRP (29%, 21%), γ-GT activity (14%, 17%), and blood pressure (systolic/diastolic, 3/6%, 3/3%) of Groups A and B, respectively, of free-living healthy seniors without affecting the total, HDL-, LDL-cholesterol or triglycerides compared to their respective baseline values. However, serum levels of NO (36%, 43%), CRP (31%, 48%), γ-GT (17%, 20%), total cholesterol (19%, 15%), LDL-cholesterol (28%, 20%), triglycerides (11%, 18%) of Groups C and D were significantly ( P < 0.01-0.05) decreased with NS-5 treatment of hypercholesterolemic subjects compared to baseline values, without affecting the serum HDL-cholesterol levels. The serum levels of total antioxidant status (TAS) were increased (10%, 14%; P < 0.05) in Groups A and B, increased (19%, 24%; P < 0.02), and blood pressure (systolic/diastolic, 5/6%, 3/5%) in Groups C and D with NS-5 treatment, compared to respective baseline values.

背景:年龄相关的氧化还原失衡改变和免疫功能失调,有助于各种年龄相关疾病的发展。炎症标志物和脂质谱是各种年龄相关疾病和心血管疾病的有用预后指标。我们之前已经在体外、体内、细胞系、动物模型和人类受试者中研究了几种蛋白酶体抑制剂对炎症和脂质谱的几种标志物的影响。目前的研究是这项工作的延伸。我们的主要假设是,结合多种天然存在的蛋白酶体抑制剂,抑制一氧化氮(NO)和c反应蛋白(CRP)介导的炎症,将在预防和治疗包括心血管疾病在内的年龄相关疾病方面有更好的疗效。方法:采用两项双盲、随机、安慰剂对照交叉试验,研究NS-5(白藜芦醇、紫菀芪、槲皮素、δ-生三烯醇、烟酸)混合物对血清NO、CRP、γ-谷氨酰基转移酶(γ-GT)活性、总抗氧化状态(TAS)、总胆固醇、低密度脂蛋白胆固醇、高密度脂蛋白胆固醇和甘油三酯水平的影响。健康老年人(第一组;n = 32)自由生活(A, B;16例/组)和高胆固醇血症(2组;n = 64)采用aha - step -1饮食的受试者分为两组(C, D;32 /组)。为上述参数建立了基线水平。A、C组给予NS-5 4粒/d, B、d组给予安慰剂(淀粉),疗程6周。各组被交叉,然后是2周的洗脱期。A、C组给予安慰剂4粒/d, B、d组给予NS-5 4粒/d,疗程6周。C、D组继续aa - step -1饮食。结果:所有受试者均完成了两项研究的每个阶段,无任何投诉。A组和B组自由生活健康老年人血清NO(30%, 26%)、CRP(29%, 21%)、γ-GT活性(14%,17%)和血压(收缩压/舒张压,3/6%,3/3%)水平均显著降低(P < 0.01 ~ 0.05),但总胆固醇、HDL-、ldl -胆固醇和甘油三酯水平均未受影响。然而,经NS-5治疗的高胆固醇血症患者血清NO(36%, 43%)、CRP(31%, 48%)、γ-GT(17%, 20%)、总胆固醇(19%,15%)、低密度脂蛋白胆固醇(28%,20%)、甘油三酯(11%,18%)水平与基线值相比显著(P < 0.01-0.05)降低,但血清hdl -胆固醇水平未受影响。血清总抗氧化状态(TAS)水平升高(10%,14%;P < 0.05),升高(19%,24%;P < 0.02),与各自的基线值相比,接受NS-5治疗的C组和D组的血压(收缩压/舒张压,5/6%,3/5%)。结论:服用NS-5混合物可显著降低血清NO、CRP和γ-GT水平,改善TAS和心血管危险的脂质谱,并有望延缓年龄相关疾病的发生。
{"title":"Nutritional Supplement-5 with a Combination of Proteasome Inhibitors (Resveratrol, Quercetin, <i>δ</i>-Tocotrienol) Modulate Age-Associated Biomarkers and Cardiovascular Lipid Parameters in Human Subjects.","authors":"Asaf A Qureshi,&nbsp;Dilshad A Khan,&nbsp;Wajiha Mahjabeen,&nbsp;Christopher J Papasian,&nbsp;Nilofer Qureshi","doi":"10.4172/2155-9880.1000238","DOIUrl":"https://doi.org/10.4172/2155-9880.1000238","url":null,"abstract":"<p><strong>Background: </strong>Age-associated altered redox imbalances and dysregulated immune function, contribute to the development of a variety of age associated diseases. Inflammatory markers and lipid profiles are useful prognostic indicators of a variety of age-associated and cardiovascular diseases. We have previously studied the impact of several proteasome inhibitors on several markers of inflammation and lipid profiles <i>in vitro, in vivo</i>, in cell lines, animal models, and in human subjects. The current study represents an extension of this work. Our main hypothesis is that a combination of various naturally-occurring proteasome inhibitors, which inhibits nitric oxide (NO), and C-reactive protein (CRP) mediated inflammation, will have better efficacy in the prevention and treatment of age-associated disorders including cardiovascular disease.</p><p><strong>Methods: </strong>Two double blind, randomized, placebo-controlled cross-over trials were conducted to determine the impact of a mixture of NS-5 (resveratrol, pterostilbene, quercetin, δ-tocotrienol, nicotinic acid) on serum NO, CRP, γ-glutamyl-transferase (γ-GT) activity, total antioxidant status (TAS), total cholesterol, LDL-cholesterol, HDL-cholesterol and triglycerides levels. Healthy seniors (Group-1; <i>n</i> = 32) free-living (A, B; 16/group), and hypercholesterolemic (Group-2; <i>n</i> = 64) subjects on AHA-Step-1-diet were divided into two groups (C, D; 32/group). Baseline levels were established for parameters as mentioned above. Groups A, C were administered 4-capsules/d of NS-5 and groups B, D, placebo (starch) for 6-weeks. Groups were crossed-over, followed by a 2-week wash-out period. Groups A, C were given 4-capsules/d of placebo and groups B, D, 4-capsules/d of NS-5 for 6-weeks. Groups C, D were continued on AHA-Step-1-diet.</p><p><strong>Results: </strong>All the subjects completed each phase in both studies without any complaints. There were significant ( <b><i>P</i></b> < 0.01 - 0.05) decreases in the serum levels of NO (30%, 26%), CRP (29%, 21%), γ-GT activity (14%, 17%), and blood pressure (systolic/diastolic, 3/6%, 3/3%) of Groups A and B, respectively, of free-living healthy seniors without affecting the total, HDL-, LDL-cholesterol or triglycerides compared to their respective baseline values. However, serum levels of NO (36%, 43%), CRP (31%, 48%), γ-GT (17%, 20%), total cholesterol (19%, 15%), LDL-cholesterol (28%, 20%), triglycerides (11%, 18%) of Groups C and D were significantly ( <b><i>P</i></b> < 0.01-0.05) decreased with NS-5 treatment of hypercholesterolemic subjects compared to baseline values, without affecting the serum HDL-cholesterol levels. The serum levels of total antioxidant status (TAS) were increased (10%, 14%; <b><i>P</i></b> < 0.05) in Groups A and B, increased (19%, 24%; <b><i>P</i></b> < 0.02), and blood pressure (systolic/diastolic, 5/6%, 3/5%) in Groups C and D with NS-5 treatment, compared to respective baseline values.</p><p><s","PeriodicalId":89581,"journal":{"name":"Journal of clinical & experimental cardiology","volume":"4 3","pages":""},"PeriodicalIF":0.0,"publicationDate":"2013-03-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4172/2155-9880.1000238","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31939230","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 15
Antipsychotics and the Risks of Sudden Cardiac Death and All-Cause Death: Cohort Studies in Medicaid and Dually-Eligible Medicaid-Medicare Beneficiaries of Five States. 抗精神病药物与心源性猝死和全因死亡的风险:对五个州的医疗补助受益人和符合医疗补助与医疗保险双重条件的受益人进行的队列研究。
Pub Date : 2013-01-01 DOI: 10.4172/2155-9880.S10-006
Charles E Leonard, Cristin P Freeman, Craig W Newcomb, Warren B Bilker, Stephen E Kimmel, Brian L Strom, Sean Hennessy

Context: Antipsychotic drugs have been linked to QT-interval prolongation, a presumed marker of cardiac risk, and torsade de pointes.

Objective: To examine the associations between antipsychotics and 1) outpatient-originated sudden cardiac death and ventricular arrhythmia (SD/VA) and 2) all-cause death.

Design: Two retrospective cohort studies.

Setting: Medicaid programs of California, Florida, New York, Ohio and Pennsylvania.

Patients: Incident antipsychotic users aged 30-75 years.

Main outcome measures: 1) Incident, first-listed emergency department or principal inpatient SD/VA diagnoses; and 2) death reported in the Social Security Administration Death Master File.

Results: Among 459,614 incident antipsychotic users, the incidences of SD/VA and death were 3.4 and 35.1 per 1,000 person-years, respectively. Compared to olanzapine as the referent, adjusted hazard ratios (HRs) for SD/VA were 2.06 (95% CI, 1.20-3.53) for chlorpromazine, 1.72 (1.28-2.31) for haloperidol, and 0.73 (0.57-0.93) for quetiapine. Adjusted HRs for perphenazine and risperidone were consistent with unity. In a subanalysis limited to first prescription exposures, HRs for chlorpromazine and haloperidol were further elevated (2.54 [1.07-5.99] and 2.68 [1.59-4.53], respectively), with the latter exhibiting a dose-response relationship. Results for death were similar.

Conclusions: Haloperidol and chlorpromazine had less favorable cardiac safety profiles than olanzapine. Among atypical agents, risperidone had a similar cardiac safety profile to olanzapine, whereas quetiapine was associated with 30% and 20% lower risks of SD/VA and death, respectively, compared to olanzapine. These measured risks do not correlate well with average QT prolongation, further supporting the notion that average QT prolongation may be a poor surrogate of antipsychotic arrhythmogenicity.

背景:抗精神病药物与QT间期延长(一种推测的心脏风险标志物)和心动过速有关:目的:研究抗精神病药物与 1)门诊病人引发的心脏性猝死和室性心律失常(SD/VA)以及 2)全因死亡之间的关系:设计:两项回顾性队列研究:背景:加利福尼亚州、佛罗里达州、纽约州、俄亥俄州和宾夕法尼亚州的医疗补助计划:患者:年龄在 30-75 岁之间的抗精神病药物使用者:主要结果测量指标:1)事件、首次列入急诊科或主要住院病人 SD/VA 诊断;2)社会保障局死亡主档案中报告的死亡:在 459,614 位抗精神病药物使用者中,SD/VA 和死亡的发生率分别为每千人年 3.4 例和 35.1 例。与作为参照物的奥氮平相比,氯丙嗪的SD/VA调整后危险比(HRs)为2.06(95% CI,1.20-3.53),氟哌啶醇为1.72(1.28-2.31),喹硫平为0.73(0.57-0.93)。培非那嗪和利培酮的调整HR值与统一值一致。在一项仅限于首次处方暴露的子分析中,氯丙嗪和氟哌啶醇的HRs进一步升高(分别为2.54[1.07-5.99]和2.68[1.59-4.53]),后者表现出剂量反应关系。死亡结果类似:结论:氟哌啶醇和氯丙嗪的心脏安全性不如奥氮平。在非典型药物中,利培酮的心脏安全性与奥氮平相似,而与奥氮平相比,喹硫平的SD/VA和死亡风险分别低30%和20%。这些测得的风险与平均QT延长没有很好的相关性,进一步支持了平均QT延长可能是抗精神病药物致心律失常性的不良替代物这一观点。
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引用次数: 0
The Sirtuin System: The Holy Grail of Resveratrol? Sirtuin系统:白藜芦醇的圣杯?
Pub Date : 2012-11-01 DOI: 10.4172/2155-9880.1000216
Dilbahar S Mohar, Shaista Malik

The oxidative stress theory has been associated with atherosclerosis and has prompted a multitude of studies to evaluate the effects of antioxidants on cardiovascular disease prevention. Resveratrol, a relatively new antioxidant has gained considerable curiosity. This polyphenol stilbene identified in grape skin, is believed to be the main component contributing to the anti-atherosclerotic benefits linked to red wine consumption. It has demonstrated the ability to protect endothelial cells from lipid damage, promote vasodilation via modulation of nitric oxide synthesis, and inhibit platelet aggregation and smooth muscle proliferation. Although the complete mechanism of Resveratrol has yet to be fully elucidated, the Sirtuin system, consisting of 7 highly conserved families of regulator genes, are thought to be instrumental in establishing the various health benefits. In this article we assess the current applications, mechanism, pharmacokinetics, bioavailability, and safety profile of the novel antioxidant Resveratrol and provide an in-depth review of the influence of the Sirtuin system on the Resveratrol mechanism of action. We resolve that while early data on Resveratrol are promising, the anti-oxidative and ultimately, anti-atherosclerotic potential depends on further clarification of the intricate and complex relationship between Resveratrol and the Sirtruin system.

氧化应激理论与动脉粥样硬化有关,并促使大量研究评估抗氧化剂对心血管疾病预防的影响。白藜芦醇是一种相对较新的抗氧化剂,引起了人们的极大兴趣。葡萄皮中发现的这种多酚二苯乙烯被认为是红酒抗动脉粥样硬化的主要成分。它已被证明能够保护内皮细胞免受脂质损伤,通过调节一氧化氮合成促进血管舒张,抑制血小板聚集和平滑肌增殖。尽管白藜芦醇的完整机制尚未完全阐明,但Sirtuin系统由7个高度保守的调节基因家族组成,被认为在建立各种健康益处方面发挥了重要作用。本文综述了新型抗氧化剂白藜芦醇的应用现状、作用机制、药代动力学、生物利用度和安全性,并对Sirtuin系统对白藜芦醇作用机制的影响进行了深入的综述。我们认为,虽然白藜芦醇的早期数据是有希望的,但抗氧化和最终抗动脉粥样硬化的潜力取决于进一步澄清白藜芦醇和Sirtruin系统之间错综复杂的关系。
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引用次数: 61
Isolation, Characterization, and Spatial Distribution of Cardiac Progenitor Cells in the Sheep Heart. 绵羊心脏祖细胞的分离、表征和空间分布。
Xuwei Hou, Nancy Appleby, Tania Fuentes, Lawrence D Longo, Leonard L Bailey, Nahidh Hasaniya, Mary Kearns-Jonker

Background: Laboratory large animal models are important for establishing the efficacy of stem cell therapies that may be translated into clinical use. The similarity of ovine and human cardiovascular systems provides an opportunity to use the sheep as a large animal model in which to optimize cell-based treatments for the heart. Recent clinical trials in humans using endogenous cardiovascular progenitor cells report significant improvement in cardiac function following stem cell-based therapy. To date, however, endogenous cardiovascular progenitor cells have not been isolated from the sheep heart.

Methods: Cardiovascular cells expressing SSEA-4, CD105 and c-kit were isolated by flow cytometry and cloned from the right atrium of neonatal sheep. The expression of GATA-4, c-kit, and Isl1 was identified by PCR in the cloned cells. Immunohistochemical staining was used to compare the number of SSEA-4 positive cells in the right auricle, right atrium, left ventricle and the apex of the heart of fetal, neonatal and adult sheep. The number of SSEA4+cells was also compared in fetal, pregnant and non-pregnant adult sheep.

Results: Four distinct cardiac progenitor cell sub-populations were identified in sheep, including CD105+SSEA-4+c-kit+Isl1+GATA-4+cells, CD105+SSEA-4+c-kit+Isl1+GATA-4-cells, CD105+SSEA-4-c-kit-Isl1+GATA-4-cells, and CD105+SSEA-4-c-kit+Isl1+GATA-4-cells. Immunohistochemical staining for SSEA-4 showed that labeled cells were most abundant in the right atrium of fetal hearts where niches of progenitor cells could be identified.

Conclusion: We determined the phenotype and distribution of cardiac progenitor cells in the sheep heart. The availability of cloned endogenous cardiac progenitor cells from sheep will provide a valuable resource for optimizing the conditions for cardiac repair in the ovine model.

背景:实验室大型动物模型对于建立可能转化为临床应用的干细胞疗法的有效性是重要的。绵羊和人类心血管系统的相似性为利用羊作为大型动物模型来优化基于细胞的心脏治疗提供了机会。最近在人类中使用内源性心血管祖细胞的临床试验报告了干细胞治疗后心功能的显著改善。然而,到目前为止,内源性心血管祖细胞尚未从羊心脏中分离出来。方法:采用流式细胞术分离表达SSEA-4、CD105和c-kit的新生羊右心房心血管细胞,并进行克隆。通过PCR检测克隆细胞中GATA-4、c-kit和Isl1的表达。采用免疫组化染色法比较胎羊、新生羊和成年羊的右耳、右心房、左心室和心尖组织中SSEA-4阳性细胞的数量。并比较了胎羊、妊娠羊和非妊娠羊中SSEA4+细胞的数量。结果:在绵羊中鉴定出4个不同的心脏祖细胞亚群,包括CD105+SSEA-4+c-kit+Isl1+GATA-4+细胞、CD105+SSEA-4+c-kit+Isl1+GATA-4细胞、CD105+SSEA-4-c-kit-Isl1+GATA-4细胞和CD105+SSEA-4-c-kit+Isl1+GATA-4细胞。SSEA-4的免疫组化染色显示,标记细胞在胎心右心房最丰富,在右心房可以发现祖细胞的龛位。结论:我们确定了绵羊心脏祖细胞的表型和分布。绵羊内源性心脏祖细胞克隆的可行性将为优化绵羊心脏修复模型的条件提供宝贵的资源。
{"title":"Isolation, Characterization, and Spatial Distribution of Cardiac Progenitor Cells in the Sheep Heart.","authors":"Xuwei Hou,&nbsp;Nancy Appleby,&nbsp;Tania Fuentes,&nbsp;Lawrence D Longo,&nbsp;Leonard L Bailey,&nbsp;Nahidh Hasaniya,&nbsp;Mary Kearns-Jonker","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Background: </strong>Laboratory large animal models are important for establishing the efficacy of stem cell therapies that may be translated into clinical use. The similarity of ovine and human cardiovascular systems provides an opportunity to use the sheep as a large animal model in which to optimize cell-based treatments for the heart. Recent clinical trials in humans using endogenous cardiovascular progenitor cells report significant improvement in cardiac function following stem cell-based therapy. To date, however, endogenous cardiovascular progenitor cells have not been isolated from the sheep heart.</p><p><strong>Methods: </strong>Cardiovascular cells expressing SSEA-4, CD105 and c-kit were isolated by flow cytometry and cloned from the right atrium of neonatal sheep. The expression of GATA-4, c-kit, and Isl1 was identified by PCR in the cloned cells. Immunohistochemical staining was used to compare the number of SSEA-4 positive cells in the right auricle, right atrium, left ventricle and the apex of the heart of fetal, neonatal and adult sheep. The number of SSEA4+cells was also compared in fetal, pregnant and non-pregnant adult sheep.</p><p><strong>Results: </strong>Four distinct cardiac progenitor cell sub-populations were identified in sheep, including CD105+SSEA-4+c-kit+Isl1+GATA-4+cells, CD105+SSEA-4+c-kit+Isl1+GATA-4-cells, CD105+SSEA-4-c-kit-Isl1+GATA-4-cells, and CD105+SSEA-4-c-kit+Isl1+GATA-4-cells. Immunohistochemical staining for SSEA-4 showed that labeled cells were most abundant in the right atrium of fetal hearts where niches of progenitor cells could be identified.</p><p><strong>Conclusion: </strong>We determined the phenotype and distribution of cardiac progenitor cells in the sheep heart. The availability of cloned endogenous cardiac progenitor cells from sheep will provide a valuable resource for optimizing the conditions for cardiac repair in the ovine model.</p>","PeriodicalId":89581,"journal":{"name":"Journal of clinical & experimental cardiology","volume":"S6 ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2012-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3607208/pdf/nihms-428771.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40234407","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Regulatory T cells and Atherosclerosis. 调节性T细胞与动脉粥样硬化。
Pub Date : 2012-10-08 DOI: 10.4172/2155-9880.S12-002
Jahaira Lopez Pastrana, Xiaojin Sha, Anthony Virtue, Jietang Mai, Ramon Cueto, In Ae Lee, Hong Wang, Xiao-Feng Yang

Atherosclerosis is a chronic autoimmune inflammatory disease. The involvement of both innate and adaptive immune responses in the pathogenesis of the disease has been well recognized. Tregs are an essential part of the immune system and have indispensable functions in maintaining immune system homeostasis, mediating peripheral tolerance, preventing autoimmune diseases, and suppressing inflammatory and proatherogenic immune response. Tregs carry out their immunosuppressive functions via several mechansims. One of the well-documented suppressive mechanisms of Tregs is the secretion of anti-inflammatory cytokines including IL-10, TGF-β, and IL-35. Studies have found that IL-10 and TGF-β have atheroprotective properties. In addition, Tregs can suppress the activity of proatherogenic effector T cells, suggesting an atheroprotective role. In fact, fewer Tregs are found in atherogenic ApoE-/- mice comparing to wild-type mice, suggesting an uncontrolled balance between weakened Tregs and effector T cells in atherogenesis. Some clinical studies of autoimmune diseases also suggest that decreased Tregs numbers are associated with increased disease activity. The importance of Tregs in many autoimmune diseases and experimental atherosclerosis has been established in in vivo and in vitro studies. However, the roles of Tregs in atherosclerosis in the clinical setting remains to be further characterized.

动脉粥样硬化是一种慢性自身免疫性炎症性疾病。先天免疫和适应性免疫反应都参与了该病的发病机制,这一点已经得到了很好的认识。Tregs是免疫系统的重要组成部分,在维持免疫系统稳态、介导外周耐受、预防自身免疫性疾病、抑制炎症和致动脉粥样硬化性免疫反应等方面具有不可缺少的功能。treg通过多种机制实现其免疫抑制功能。Tregs的抑制机制之一是分泌抗炎细胞因子,包括IL-10、TGF-β和IL-35。研究发现IL-10和TGF-β具有动脉粥样硬化保护作用。此外,Tregs可以抑制促动脉粥样硬化效应T细胞的活性,提示其具有动脉粥样硬化保护作用。事实上,与野生型小鼠相比,在致动脉粥样硬化的ApoE-/-小鼠中发现的treg较少,这表明在动脉粥样硬化中,弱化的treg和效应T细胞之间存在不受控制的平衡。一些自身免疫性疾病的临床研究也表明Tregs数量的减少与疾病活动性的增加有关。Tregs在许多自身免疫性疾病和实验性动脉粥样硬化中的重要性已经在体内和体外研究中得到证实。然而,Tregs在动脉粥样硬化中的临床作用仍有待进一步研究。
{"title":"Regulatory T cells and Atherosclerosis.","authors":"Jahaira Lopez Pastrana,&nbsp;Xiaojin Sha,&nbsp;Anthony Virtue,&nbsp;Jietang Mai,&nbsp;Ramon Cueto,&nbsp;In Ae Lee,&nbsp;Hong Wang,&nbsp;Xiao-Feng Yang","doi":"10.4172/2155-9880.S12-002","DOIUrl":"https://doi.org/10.4172/2155-9880.S12-002","url":null,"abstract":"<p><p>Atherosclerosis is a chronic autoimmune inflammatory disease. The involvement of both innate and adaptive immune responses in the pathogenesis of the disease has been well recognized. Tregs are an essential part of the immune system and have indispensable functions in maintaining immune system homeostasis, mediating peripheral tolerance, preventing autoimmune diseases, and suppressing inflammatory and proatherogenic immune response. Tregs carry out their immunosuppressive functions via several mechansims. One of the well-documented suppressive mechanisms of Tregs is the secretion of anti-inflammatory cytokines including IL-10, TGF-β, and IL-35. Studies have found that IL-10 and TGF-β have atheroprotective properties. In addition, Tregs can suppress the activity of proatherogenic effector T cells, suggesting an atheroprotective role. In fact, fewer Tregs are found in atherogenic <i>ApoE</i>-/- mice comparing to wild-type mice, suggesting an uncontrolled balance between weakened Tregs and effector T cells in atherogenesis. Some clinical studies of autoimmune diseases also suggest that decreased Tregs numbers are associated with increased disease activity. The importance of Tregs in many autoimmune diseases and experimental atherosclerosis has been established in <i>in vivo</i> and <i>in vitro</i> studies. However, the roles of Tregs in atherosclerosis in the clinical setting remains to be further characterized.</p>","PeriodicalId":89581,"journal":{"name":"Journal of clinical & experimental cardiology","volume":"2012 Suppl 12","pages":"2"},"PeriodicalIF":0.0,"publicationDate":"2012-10-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4172/2155-9880.S12-002","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31700780","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 85
Cell-Based Therapies as an Adjunct to Revascularization in Experimental Atherosclerotic Reno Vascular Disease. 细胞疗法作为实验性动脉粥样硬化性肾血管疾病血运重建的辅助手段。
Pub Date : 2012-07-03 DOI: 10.4172/2155-9880.1000e108
Alfonso Eirin, Behzad Ebrahimi, Lilach O Lerman
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引用次数: 0
期刊
Journal of clinical & experimental cardiology
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