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1.
Chonnam Medical Journal ; : 187-195, 2017.
Article in English | WPRIM | ID: wpr-788390

ABSTRACT

Delayed arterial healing at culprit sites after drug-eluting stent (DES) placement for acute myocardial infarction (AMI) is associated with increased risk of late stent thrombosis. The Korea Acute Myocardial Infarction Registry was established in commemoration of the 50(th) anniversary of Korea Circulation Society. Between November 2005 and December 2016, more than 62,000 patients were registered from 50 primary percutaneous coronary intervention (PCI) centers in Korea. DES in AMI may be safe and effective, however, there is concern about increased stent thrombosis after DES implantation in AMI patients, requiring longer-term dual anti-platelet therapy to reduce the risk of late stent thrombosis. Device innovation is needed to overcome issues such as stent thrombosis and restenosis by using new coating materials with biocompatible polymers, different coating methods using non-polymer techniques, bioabsorbable stents and pro-healing stents. In this review article, we describe the current usage of DES in AMI in Korea and introduce novel DES uses in development for patients with AMI. We have developed many types of DES in our research laboratory. Abciximab-coated stents inhibited platelet thrombi and restenosis. Furthermore, anti-oxidants (carvedilol, probucol and alpha-lipoic acid) were used for stent coating. Currently we are developing novel DESs using polymer-free and natural binding techniques, peptide coating stents, gene-and-drug delivery, bioabsorbable stents using 3D printing, endothelial progenitor cell capturing stents to promote reendothelialization and reduce stent thrombosis. New DESs in development may be safe and effective in preventing late stent thrombosis and restenosis in patients with AMI.


Subject(s)
Humans , Anniversaries and Special Events , Blood Platelets , Drug-Eluting Stents , Endothelial Progenitor Cells , Korea , Myocardial Infarction , Percutaneous Coronary Intervention , Polymers , Printing, Three-Dimensional , Probucol , Stents , Thrombosis
2.
Chonnam Medical Journal ; : 187-195, 2017.
Article in English | WPRIM | ID: wpr-89702

ABSTRACT

Delayed arterial healing at culprit sites after drug-eluting stent (DES) placement for acute myocardial infarction (AMI) is associated with increased risk of late stent thrombosis. The Korea Acute Myocardial Infarction Registry was established in commemoration of the 50(th) anniversary of Korea Circulation Society. Between November 2005 and December 2016, more than 62,000 patients were registered from 50 primary percutaneous coronary intervention (PCI) centers in Korea. DES in AMI may be safe and effective, however, there is concern about increased stent thrombosis after DES implantation in AMI patients, requiring longer-term dual anti-platelet therapy to reduce the risk of late stent thrombosis. Device innovation is needed to overcome issues such as stent thrombosis and restenosis by using new coating materials with biocompatible polymers, different coating methods using non-polymer techniques, bioabsorbable stents and pro-healing stents. In this review article, we describe the current usage of DES in AMI in Korea and introduce novel DES uses in development for patients with AMI. We have developed many types of DES in our research laboratory. Abciximab-coated stents inhibited platelet thrombi and restenosis. Furthermore, anti-oxidants (carvedilol, probucol and alpha-lipoic acid) were used for stent coating. Currently we are developing novel DESs using polymer-free and natural binding techniques, peptide coating stents, gene-and-drug delivery, bioabsorbable stents using 3D printing, endothelial progenitor cell capturing stents to promote reendothelialization and reduce stent thrombosis. New DESs in development may be safe and effective in preventing late stent thrombosis and restenosis in patients with AMI.


Subject(s)
Humans , Anniversaries and Special Events , Blood Platelets , Drug-Eluting Stents , Endothelial Progenitor Cells , Korea , Myocardial Infarction , Percutaneous Coronary Intervention , Polymers , Printing, Three-Dimensional , Probucol , Stents , Thrombosis
3.
Rev. bras. enferm ; 67(5): 810-817, Sep-Oct/2014.
Article in Portuguese | LILACS, BDENF | ID: lil-731211

ABSTRACT

Estudo qualitativo e descritivo, cujo objetivo foi identificar e analisar as representações sociais de educação em saúde à pessoa vivendo com HIV entre profissionais de saúde. Os cenários foram três serviços de atenção à DST/HIV/AIDS, em Belém-PA, Brasil, e 37 profissionais de saúde participaram da pesquisa. A coleta de dados deu-se em 2012-2013 por meio de entrevista em profundidade; a análise utilizou o software Alceste 4.10. Com base no conjunto dos resultados foi possível vislumbrar que a educação em saúde pode ser compreendida a partir de categorias: a configuração do agir educativo; as condições sine qua non: educação no trabalho e estrutura da unidade; o processo pedagógico. Conclui-se que as representações sociais configuram-se como orientação-informação para precaução-prevenção e revelam-se no movimento do agir persistente ao emergente, o que suscita uma educação em saúde permanente para se chegar à integralidade nos serviços.


This is a qualitative and descriptive study, which aimed at identifying and analyzing social representations of health education to HIV patients among health professionals. The setting included three healthcare DST/HIV/AIDS services in Belém-PA, Brazil, and 37 health professionals participated in the study. Data collection was conducted in 2012-2013 on the basis of in-depth interviews and analysis was made on Alceste 4.0 software. Final results indicated that health education can be comprehended in light of categories: educational action; sine qua non: education and training at work, and unit structure; teaching-learning process. Conclusions show that social representations are set as guidance-information for precaution-prevention and that they come forth along continuous and emerging action flow, bringing about permanent health education to ensure healthcare services in full.


Estudio cualitativo y descriptivo, que objetivó identificar y analizar las representaciones sociales de educación en salud a la persona viviendo con HIV entre profesionales de salud. Los escenarios fueron tres servicios de atendimiento al DST/HIV/ SIDA, en Belém-PA, Brasil, y 37 profesionales de salud participaran del estudio. La colecta de datos se dio en 2012-2013, por medio de entrevista en profundidad y el análisis utilizo el software Alceste 4.10. Con base en el conjunto de los resultados fue posible vislumbrar que la educación en salud puede ser comprendida a partir de categorías: la configuración del acto educativo; las condiciones sine qua non: educación en el trabajo y estructura de la unidad; el proceso pedagógico. Se concluye que las representaciones sociales se configuran como orientación-información para precaución-prevención y se revelan en el movimiento del acto persistente al emergente, lo que suscita una educación en salud permanente para llegarse a la integralidad en los servicios.


Subject(s)
Humans , Animals , Male , Female , Rabbits , Antioxidants/administration & dosage , Arteriosclerosis/drug therapy , Probucol/administration & dosage , Ubiquinone/administration & dosage , Ubiquinone/analogs & derivatives , alpha-Tocopherol/administration & dosage , Antioxidants/pharmacokinetics , Aorta/metabolism , Aorta/pathology , Arteriosclerosis/metabolism , Arteriosclerosis/pathology , Coenzymes , Disease Models, Animal , Lipids/blood , Lipoproteins, LDL/metabolism , Probucol/pharmacokinetics , Ubiquinone/metabolism , Ubiquinone/pharmacokinetics , Vitamin E/metabolism , alpha-Tocopherol/pharmacokinetics
4.
Journal of Southern Medical University ; (12): 731-735, 2014.
Article in Chinese | WPRIM | ID: wpr-249370

ABSTRACT

<p><b>OBJECTIVE</b>To determine the effects of probucol on serum parameters and liver histopathology in rats with non-alcoholic steatohepatitis (NASH) and explore the mechanisms.</p><p><b>METHODS</b>Forty male Sprague-Dawley rats were randomly assigned into 4 equal groups, namely the normal control group (NC group) with a standard feeding, high-fat diet group (HD group) fed with a high-fat diet, probucol (500 mg/kg daily) control group (NP group) fed with standard diet, and probucol group fed with a high-fat diet (HP group). After 15 weeks of feeding, the rats were euthanized for histopathological inspection of the liver with HE staining and detection of farnesoid X receptor (FXR), SHP and SREBP-1C expressions using semi-quantitative RT-PCR and Western blotting.</p><p><b>RESULTS</b>After the 15-week feeding, the rats in HP group had significantly lower levels of serum ALT, AST, cholesterol, bile acid, and free fatty acid than those in HD group (P<0.01 or 0.05). Compared with the normal control group, high-fat diet feeding resulted in significantly decreased mRNA and protein levels of FXR and SHP (P<0.05) and significantly increased SREBP-1C level (P<0.05). These high-fat diet-induced gene expression changes were reversed by probucol intervention (P<0.05).</p><p><b>CONCLUSION</b>Probucol treatment has beneficial effects on serum parameters, hepatic steatosis, and lobular inflammation in high-fat diet-induced NASH possibly by up-regulating FXR expression.</p>


Subject(s)
Animals , Male , Rats , Anticholesteremic Agents , Pharmacology , Diet, High-Fat , Disease Models, Animal , Non-alcoholic Fatty Liver Disease , Blood , Drug Therapy , Probucol , Pharmacology , RNA, Messenger , Rats, Sprague-Dawley
5.
Chinese Journal of Cardiology ; (12): 1003-1008, 2012.
Article in Chinese | WPRIM | ID: wpr-292053

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the impact of adding folic acid, vitamin B(12) and probucol to standard antihypertensive medication on plasma homocysteine (Hcy) and asymmetric dimethylarginine (ADMA), serum NO and eNOS of essential hypertensive patients.</p><p><b>METHOD</b>A total of 120 patients with hypertension were randomly divided to three groups (n = 40 each): group 1 (standard medication), group 2 (adding folic acid 5 mg/day and vitamin B(12) 500 µg twice daily) and group 3 (adding folic acid 5 mg/day and vitamin B(12) 500 µg twice daily and probucol 500 mg twice daily). Plasma Hcy and ADMA, serum NO and eNOS levels were observed at baseline, 2 and 12 weeks after various therapy.</p><p><b>RESULTS</b>In group 1, concentrations of plasma Hcy [(23.06 ± 14.15) µmol/L, (23.67 ± 12.31) µmol/L, (23.25 ± 11.64) µmol/L], ADMA [(0.21 ± 0.12) µmol/L, (0.23 ± 0.13) µmol/L, (0.21 ± 0.09) µmol/L] and serum NO [(64.14 ± 15.07) µmol/L, (65.29 ± 15.04) µmol/L, (65.32 ± 13.58) µmol/L], eNOS [(20.02 ± 4.50) µg/L, (20.79 ± 4.03) µg/L, (19.82 ± 5.70) µg/L] remained unchanged during the 12 weeks therapy (all P > 0.05). In group 2, concentrations of plasma Hcy [(12.54 ± 6.49) µmol/L] and ADMA[(0.18 ± 0.07) µmol/L] were significantly decreased after the treatment of 12 weeks than the treatment baseline value [(21.51 ± 7.82) µmol/L, (0.20 ± 0.12) µmol/L] and 2 weeks value[(19.38 ± 8.14) µmol/L, (0.21 ± 0.12) µmol/L], however the concentrations of serum NO and eNOS showed contrary results of the Hcy and ADMA's. (all P < 0.05). In group 3, similar changes occurred at 2 weeks after therapy (P < 0.05 2 weeks vs. baseline and 12 weeks vs. 2 weeks). Plasma ADMA level was positively correlated with Hcy at baseline (r = 0.546, P < 0.05).</p><p><b>CONCLUSIONS</b>Supplementation of folic acid, VitB(12) and/or probucol helps to improve endothelial function and reduce plasma Hcy and ADMA levels in patients with hypertension.</p>


Subject(s)
Aged , Female , Humans , Male , Middle Aged , Antihypertensive Agents , Therapeutic Uses , Arginine , Blood , Folic Acid , Therapeutic Uses , Homocysteine , Blood , Hypertension , Blood , Drug Therapy , Nitric Oxide , Blood , Nitric Oxide Synthase Type III , Blood , Plasma , Metabolism , Probucol , Therapeutic Uses , Vitamin B 12 , Therapeutic Uses , Vitamin B Complex , Therapeutic Uses , Vitamins , Therapeutic Uses
6.
Chinese Medical Journal ; (24): 2472-2476, 2012.
Article in English | WPRIM | ID: wpr-283738

ABSTRACT

<p><b>BACKGROUND</b>The plasma cystatin C concentration (PcyC) has been demonstrated to have prognostic value in acute coronary syndrome, but the study of PcyC in patients with borderline coronary lesions is limited. Moreover, the effects of atorvastatin and probucol on PcyC and the severity of coronary lesions are unknown. This study was to evaluate the effects of the combination of atorvastatin and probucol on PcyC and severity of coronary lesion in patients with borderline coronary lesions.</p><p><b>METHODS</b>One hundred and thirty consecutive patients with borderline coronary lesions (40% to 60% isolated single stenosis assessed by quantitative coronary angiography) were enrolled into the borderline coronary lesion (BCL) group, and one hundred and thirty-six subjects without coronary lesions comprised the controls (CTR). The subjects in the BCL group were randomized into routine treatment (RTT, n = 60), and combined treatment with atorvastatin 20 mg plus probucol 1.0 g daily added to routine medication (CBT, n = 70), both groups were treated for 6 months continuously. The levels of PcyC, high-sensitive C-reactive protein (hs-CRP), total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C), and triglycerides (TG) were determined. One hundred and four subjects in the BCL group were rechecked by coronary angiography.</p><p><b>RESULTS</b>PcyC levels were significantly higher in the BCL group than in the CTR group; (2003.26 ± 825.73) ng/ml vs. (1897.83 ± 664.46) ng/ml (P < 0.01). Compared with patients in the RTT group, the levels of PcyC, TC, LDL-C, TG and hs-CRP were significantly lower in the CBT group (P < 0.05). Moreover, there was a trend towards a slight decrease in the RTT patients, (54.38 ± 10.67)% vs. (50.29 ± 9.89)% (P > 0.05), and a significant decrease in the CBT patients, (53.65 ± 9.48%) vs. (40.38 ± 12.93)% (P < 0.05), in the mean percent stenosis of borderline coronary lesions before and after six months of treatment.</p><p><b>CONCLUSIONS</b>Cystatin C played an important role in the development of coronary artery disease, and was associated with the severity of coronary lesions. The combination of atorvastatin and probucol decreased PcyC levels, and could be the treatment of choice.</p>


Subject(s)
Aged , Female , Humans , Male , Middle Aged , Anticholesteremic Agents , Therapeutic Uses , Atorvastatin , Coronary Disease , Blood , Drug Therapy , Pathology , Cystatin C , Blood , Heptanoic Acids , Therapeutic Uses , Probucol , Therapeutic Uses , Prospective Studies , Pyrroles , Therapeutic Uses
7.
Journal of Central South University(Medical Sciences) ; (12): 458-462, 2012.
Article in Chinese | WPRIM | ID: wpr-814651

ABSTRACT

OBJECTIVE@#To observe the therapeutic effect of probucol on serum malondialdehyde (MDA) and superoxide dismutase (SOD) in patients with primary hypertension.@*METHODS@#A randomized study was performed on 40 patients with hypertension. The patients were randomly assigned to the control (levamlodipine besylate 2.5 mg/d plus benazepril 10 mg/d, n=20) or probucol group (levamlodipine besylate 2.5 mg/d plus benazepril 10 mg/d plus probucol 500 mg/d, n=20). An additional twenty healthy people were enrolled in the study (normal group). All subjects were followed up for a period of four weeks. Lipids and hepatic/renal function were measured at baseline and after 4 weeks. The levels of serum MDA and SOD activity were assayed by chemical colorimetry, and other indices, including blood pressure, lipids and hepatic/renal function, were measured at baseline and after 4 weeks.@*RESULTS@#Compared to the normal group, the levels of MDA in all of the hypertension patient groups were higher, SOD was lower. The antihypertensive treatment decreased serum MDA levels but increased SOD content, and probucol treatment exaggerated these effects, with greater reduction of serum MDA levels and greater increase of SOD content.@*CONCLUSION@#The treatment with probucol can improve oxidative stress in hypertension patients, resulting in reduced serum MDA levels and improved SOD activity, thus contributing agreater antihypertensive effect.


Subject(s)
Adult , Female , Humans , Male , Middle Aged , Antioxidants , Therapeutic Uses , Hypertension , Drug Therapy , Malondialdehyde , Blood , Oxidative Stress , Probucol , Therapeutic Uses , Superoxide Dismutase , Blood
8.
Korean Journal of Pediatrics ; : 371-376, 2012.
Article in English | WPRIM | ID: wpr-213509

ABSTRACT

PURPOSE: Puromycin aminonucleoside (PAN) specifically injures podocytes, leading to foot process effacement, actin cytoskeleton disorganization, and abnormal distribution of slit diaphragm proteins. p130Cas is a docking protein connecting F-actin fibers to the glomerular basement membrane (GBM) and adapter proteins in glomerular epithelial cells (GEpCs; podocytes). We investigated the changes in the p130Cas expression level in the PAN-induced pathological changes of podocytes in vitro. METHODS: We observed changes in the p130Cas expression in cultured rat GEpCs and mouse podocytes treated with various concentrations of PAN and antioxidants, including probucol, epigallocatechin gallate (EGCG), and vitamin C. The changes in the p130Cas expression level were analyzed using confocal immunofluorescence imaging, Western blotting, and polymerase chain reaction. RESULTS: In the immunofluorescence study, p130Cas showed a diffuse cytoplasmic distribution with accumulation at distinct sites visible as short stripes and colocalized with P-cadherin. The fluorescences of the p130Cas protein were internalized and became granular by PAN administration in a dose-dependent manner, which had been restored by antioxidants, EGCG and vitamin C. PAN also decreased the protein and mRNA expression levels of p130Cas at high doses and in a longer exposed duration, which had been also reversed by antioxidants. CONCLUSION: These findings suggest that PAN modulates the quantitative and distributional changes of podocyte p130Cas through oxidative stress resulting in podocyte dysfunction.


Subject(s)
Animals , Mice , Rats , Actin Cytoskeleton , Actins , Antioxidants , Ascorbic Acid , Blotting, Western , Cadherins , Catechin , Crk-Associated Substrate Protein , Cytoplasm , Cytoskeleton , Diaphragm , Epithelial Cells , Fluorescent Antibody Technique , Foot , Glomerular Basement Membrane , Oxidative Stress , Podocytes , Probucol , Proteins , Puromycin , Puromycin Aminonucleoside , RNA, Messenger
9.
Chinese Journal of Integrated Traditional and Western Medicine ; (12): 1479-1482, 2011.
Article in Chinese | WPRIM | ID: wpr-326672

ABSTRACT

<p><b>OBJECTIVE</b>To observe the effects of combination of Lumbrukinase Capsule (LC) and Probucol Tablet (PT) in treating cerebral infarction (CI) patients' unstable atheromatous plaque of the carotid artery.</p><p><b>METHODS</b>150 patients were randomly assigned to the PT group and the LC group, 75 cases in each. Patients in the PT group took 0.5 g PT each time, twice daily. On the basis of PT, patients in the LC group also took 600 thousand U LC, thrice daily. The treatment course was 12 months for all. The serum levels of TC, TG, HDL-C, LDL-C, fibrinogen (FIB), and changes of the carotid atherosclerotic plaque were measured before treatment, 6 and 12 months after treatment. Meanwhile, adverse events were recorded.</p><p><b>RESULTS</b>The serum levels of TC, TG, and LDL-C were all lower 6 months after treatment than before treatment in the two groups, showing statistical significance (P < 0.05). The serum level of HDL-C was higher 6 months after treatment than before treatment in the two groups, showing no statistical significance (P > 0.05). When compared with before treatment in the same group, the serum level of FIB significantly decreased after treatment. Besides, there was statistical difference between the two groups (P < 0.05). There was no statistical difference in the serum levels of blood lipids or FIB between 12-month treatment and 6-month treatment in the same group (P > 0.05). The plaque effective rate in the LC group was superior to that of the PT group, showing statistical significance (P < 0.01). During the treatment period, the occurrence of cerebrovascular event was lower in the LC group than in the PT group (P < 0.05). Partial patients in the two groups had gastric discomfort.</p><p><b>CONCLUSIONS</b>The combination of LC and PT could prevent and treat arteriosclerosis, stabilize the plaque, effectively lower the occurrence of ischemic events. Its clinical application did not increase the risk of hemorrhage. It was safe and effective, worthy of spreading. It was necessary to further observe whether combination of LC and PT could increase side effects of the digestive tract.</p>


Subject(s)
Adult , Aged , Animals , Female , Humans , Male , Middle Aged , Biological Products , Therapeutic Uses , Carotid Artery Diseases , Drug Therapy , Cerebral Infarction , Drug Therapy , Pathology , Materia Medica , Therapeutic Uses , Oligochaeta , Plaque, Atherosclerotic , Drug Therapy , Probucol , Therapeutic Uses , Serine Endopeptidases , Therapeutic Uses , Treatment Outcome
10.
Chinese Medical Journal ; (24): 1840-1847, 2011.
Article in English | WPRIM | ID: wpr-338577

ABSTRACT

<p><b>BACKGROUND</b>Probucol is known to reduce the development of atherosclerotic lesions, but its impact on vascular remodeling associated with de novo atherosclerosis is incompletely understood. We therefore examined the effect of probucol on vascular remodeling in a rabbit model of established atherosclerosis.</p><p><b>METHODS</b>Aortic atherosclerosis was induced by a combination of endothelial injury and 10 weeks' atherogenic diet. Animals were then randomized to receive the foregoing diet without or with 1% (wt/wt) probucol for 16 weeks. At the end of week 26, in vivo intravascular ultrasound, pathological, immunohistochemical and gene expression studies were performed.</p><p><b>RESULTS</b>Probucol significantly decreased vessel cross-sectional area, plaque area and plaque burden without effect on lumen area. More negative remodeling and less positive remodeling occurred in the abdominal aortas of probucol group than the control group (56% vs. 21%, 18% vs. 54%, respectively, both P < 0.01). In addition, the probucol group showed a smaller mean remodeling index relative to the control group (0.93 ± 0.13 vs. 1.05 ± 0.16, P < 0.01). Furthermore, probucol treatment decreased macrophage infiltration, inhibited apoptosis of cells within plaques, and reduced the production of matrix metalloproteinases-2, -9, cathepsin K and cathepsin S (all P < 0.01).</p><p><b>CONCLUSIONS</b>These findings suggest that probucol may attenuate the enlargement of atherosclerotic vessel walls and be associated with a negative remodeling pattern without affecting the lumen size. This effect may involve inhibition of extracellular matrix degradation and prevention of apoptosis in atherosclerotic plaques.</p>


Subject(s)
Animals , Male , Rabbits , Anticholesteremic Agents , Pharmacology , Aorta , Pathology , Apoptosis , Atherosclerosis , Drug Therapy , Metabolism , Pathology , Lipids , Blood , Macrophages , Physiology , Matrix Metalloproteinase 2 , Metabolism , Matrix Metalloproteinase 9 , Metabolism , Oxidative Stress , Probucol , Pharmacology , Ultrasonography, Interventional , Methods
11.
Chinese Journal of Cardiology ; (12): 900-903, 2009.
Article in Chinese | WPRIM | ID: wpr-323926

ABSTRACT

<p><b>OBJECTIVES</b>To evaluate the effects of combined atorvastatin and probucol use on endothelial function in patients with acute coronary syndrome (ACS).</p><p><b>METHODS</b>Thirty patients with ACS were randomized to receive atorvastatin (20 mg/d) and probucol (500 mg/d, combination group, n = 15) or atorvastatin (20 mg/d) alone (atorvastatin group) within 24 h after admission for 4 weeks. Endothelium-dependent flow-mediated dilatation (FMD) and endothelium-independent sublingual nitroglycerin-mediated dilatation (NMD) as well as the levels of lipids and C-reactive protein were assessed at baseline, 1 week and 4 weeks after therapy.</p><p><b>RESULTS</b>Compared to baseline, the levels of total cholesterol, LDL-C and C-reactive protein were significantly reduced after 1 week and 4 weeks in both groups, FMD equally increased after 1 week in both groups (atorvastatin group: 3.75% +/- 0.78% vs. 1.09% +/- 0.44%, combination group: 3.67% +/- 0.36% vs. 1.24% +/- 0.37%, P < 0.01). Post 4 weeks therapy, FMD increase was significantly higher in combination group (3.67% +/- 0.36% at 1 week vs. 6.85% +/- 0.64% at 4 weeks, P < 0.01) than that in atorvastatin group (3.75% +/- 0.78% vs. 3.80% +/- 0.31%, P = 0.954). NMD also equally and increased over 4 weeks in two groups (P < 0.01 vs. baseline). There was no correlation between the change in FMD/NMD and the changes in lipids or C-reactive protein levels.</p><p><b>CONCLUSIONS</b>The combined atorvastatin and probucol therapy early after ACS is superior to atorvastatin alone on improving endothelial function.</p>


Subject(s)
Adult , Aged , Female , Humans , Male , Middle Aged , Acute Coronary Syndrome , Drug Therapy , Metabolism , Anticholesteremic Agents , Therapeutic Uses , Atorvastatin , C-Reactive Protein , Metabolism , Cholesterol, LDL , Blood , Drug Therapy, Combination , Endothelium, Vascular , Metabolism , Heptanoic Acids , Therapeutic Uses , Probucol , Therapeutic Uses , Pyrroles , Therapeutic Uses
12.
Chinese Journal of Cardiology ; (12): 385-388, 2009.
Article in Chinese | WPRIM | ID: wpr-294732

ABSTRACT

<p><b>OBJECTIVE</b>Contrast induced acute kidney injury (CIAKI) is a significant clinical problem. We, therefore, performed a prospective, randomized trial to investigate the role of probucol in the prevention of CIAKI in patients with unstable angina pectoris (UAP) undergoing percutaneous coronary angiography (CAG) and interventions (PCI).</p><p><b>METHODS</b>We studied 205 patients with UAP, who underwent CAG or PCI prospectively. Patients were randomly assigned to probucol group (n = 102) and control group (n = 103). In the probucol group, the patients received probucol tablets 500 mg b.i.d for 3 days before and after intervention. All the patients, after intervention, underwent hydration with intravenous saline at a rate of 1 ml per kilogram of body weight per hour for 12 hours.</p><p><b>RESULTS</b>Patients were well-matched with no significant difference at baseline in majority measured parameters between two groups. CIAKI occurred in 23 of the 205 (11.22%) patients. Multivariate logistic regression was used to identify correlates of CIAKI and clinical data. CIAKI was most strongly associated with Scr > or = 132.6 micromol/L (OR = 21.11, 95%CI 1.95 - 56.06, P < 0.001), Ccr < 60 ml/min (OR = 4.19, 95%CI 1.94 - 9.05, P < 0.001), heart function > class II (OR = 6.23, 95%CI 2.73 - 14.21, P < 0.001), Diabetes (OR = 2.049, 95%CI 1.19 - 5.25, P < 0.001), age > or = 70 yrs (OR = 3.52, 95%CI 1.66 - 7.43, P < 0.001), coronary artery calcification shown by CAG (OR = 4.29, 95%CI 1.99 - 9.24, P < 0.001). The rate of CIAKI in probucol groups was slightly lower compared with control group (7.84% vs. 14.56%), without significant difference. The post-procedure mean peak of Scr [(101.62 +/- 42.98) micromol/L vs. (117.67 +/- 68.77) micromol/L, P = 0.047] and the post-procedure increasing Scr from baseline (DeltaScr) [(13.49 +/- 19.61) micromol/L vs. (22.50 +/- 18.31) micromol/L, P = 0.001] in the probucol group decreased significantly compared with that of control group.</p><p><b>CONCLUSION</b>Prophylactic treatment with probucol 500 mg b.i.d during periprocedural stage in patients with UAP has preventing role against CIAKI after cardiac catheterization.</p>


Subject(s)
Aged , Female , Humans , Male , Middle Aged , Acute Kidney Injury , Angina, Unstable , Diagnostic Imaging , Contrast Media , Coronary Angiography , Probucol , Therapeutic Uses , Prospective Studies
13.
Chinese Medical Journal ; (24): 74-82, 2009.
Article in English | WPRIM | ID: wpr-265871

ABSTRACT

<p><b>BACKGROUND</b>We hypothesize that increased atrial oxidative stress and inflammation may play an important role in atrial nerve sprouting and heterogeneous sympathetic hyperinnervation during atrial fibrillation (AF). To test the hypothesis, we examined whether the antioxidant and anti-inflammatory treatment with probucol attenuates atrial autonomic remodeling in a canine model of AF produced by prolonged rapid right atrial pacing.</p><p><b>METHODS</b>Twenty-one dogs were divided into a sham-operated group, a control group and a probucol group. Dogs in the control group and probucol group underwent right atrial pacing at 400 beats per minute for 6 weeks, and those in the probucol group received probucol 1 week before rapid atrial pacing until pacing stopped. After 6-week rapid atrial pacing, general properties including left atrial structure and function, atrial hemodynamics and the inducibility and duration of AF were measured in all the groups. Atrial oxidative stress markers and serum C-reactive protein (CRP) concentration were estimated. The degree of nerve sprouting and sympathetic innervation at the right atrial anterior wall (RAAW) and the left atrial anterior wall (LAAW) were quantified by immunohistochemistry, atrial norepinephrine contents were also detected. Atrial beta-nerve growth factor (beta-NGF) mRNA and protein expression at the RAAW and LAAW were assessed by real-time quantitative RT-PCR and Western blotting respectively.</p><p><b>RESULTS</b>Atrial tachypacing induced significant nerve sprouting and heterogeneous sympathetic hyperinnervation, and the magnitude of nerve sprouting and hyperinnervation was higher in the RAAW than in the LAAW. Atrial beta-NGF mRNA and protein levels were significantly increased at the RAAW and LAAW, and the upregulation of beta-NGF expression was greater at the RAAW than at the LAAW in the control group. The beta-NGF protein level was positively correlated with the density of sympathetic nerves in all groups. Probucol decreased the increase of CRP concentration and attenuated atrial oxidative stress caused by atrial tachypacing. In addition, probucol could effectively inhibit atrial beta-NGF upregulation, significantly attenuate atrial nerve sprouting and heterogeneous sympathetic hyperinnervation, and dramatically reduce the inducibility and duration of AF.</p><p><b>CONCLUSIONS</b>The atrial over-expression of beta-NGF possibly caused by increased oxidative stress and inflammation may be the main mechanism underlying atrial autonomic remodeling during AF. Probucol attenuates atrial autonomic remodeling possibly by its antioxidant and anti-inflammatory actions.</p>


Subject(s)
Animals , Dogs , Female , Male , Antioxidants , Therapeutic Uses , Atrial Fibrillation , Drug Therapy , Blotting, Western , C-Reactive Protein , Metabolism , Cardiac Pacing, Artificial , Disease Models, Animal , Electrocardiography , Heart Atria , Immunohistochemistry , Nerve Growth Factor , Genetics , Metabolism , Norepinephrine , Metabolism , Probucol , Therapeutic Uses , Reverse Transcriptase Polymerase Chain Reaction
14.
Middle East Journal of Digestive Diseases. 2009; 1 (2): 89-99
in English | IMEMR | ID: emr-129158

ABSTRACT

No treatment has been proven to be effective in nonalcoholic fatty liver disease [NAFLD] and/or steatohepatitis [NASH]. Numerous studies have addressed this issue. However conclusive recommendations cannot be drawn solely from the currently available studies. Hence we performed this systematic review to determine which of the available therapeutic modalities are supported by adequate evidence in terms of decreasing the adverse clinical outcomes of interest. A specific strategy was utilized to perform a computerized literature search in MEDLINE; of which, a total of 375 studies were retrieved. According to current literature, modifying the potential risk factors such as obesity, hyperlipidemia, and poor diabetic control in all patients is considered the treatment of choice. Certain treatments can be recommended under special circumstances and some medications, although used clinically, are not supported by adequate evidence to be recommended for the treatment of NAFLD/NASH


Subject(s)
Humans , Risk Factors , Obesity , Hyperlipidemias , Diabetes Mellitus , Weight Loss , Vitamin E , Insulin Resistance , Probucol , Antioxidants , Betaine , Ursodeoxycholic Acid , Probiotics , Hydroxymethylglutaryl-CoA Reductase Inhibitors , Angiotensin Receptor Antagonists , Lactones
15.
The Korean Journal of Physiology and Pharmacology ; : 165-170, 2008.
Article in English | WPRIM | ID: wpr-728591

ABSTRACT

In the present study, we aimed to identify the synergistic effects of concurrent treatment of low concentrations of cilostazol and probucol to inhibit the oxidative stress with suppression of inflammatory markers in the cultured human coronary artery endothelial cells (HCAECs). Combination of cilostazol (0.3~3micrometer) with probucol (0.03~0.3micrometer) significantly suppressed TNF-alpha-stimulated NAD(P)H-dependent superoxide, lipopolysaccharide (LPS)-induced intracellular reactive oxygen species (ROS) production and TNF-alpha release in comparison with probucol or cilostazol alone. The combination of cilostazol (0.3~3micrometer) with probucol (0.1~0.3micrometer) inhibited the expression of vascular cell adhesion molecule-1 (VCAM-1) and monocyte chemoattractant protein-1 (MCP-1) more significantly than did the monotherapy with either probucol or cilostazol. In line with these results, combination therapy significantly suppressed monocyte adhesion to endothelial cells. Taken together, it is suggested that the synergistic effectiveness of the combination therapy with cilostazol and probucol may provide a beneficial therapeutic window in preventing atherosclerosis and protecting from cerebral ischemic injury.


Subject(s)
Humans , Atherosclerosis , Chemokine CCL2 , Coronary Vessels , Endothelial Cells , Monocytes , Oxidative Stress , Probucol , Reactive Oxygen Species , Superoxides , Tetrazoles , Tumor Necrosis Factor-alpha , Vascular Cell Adhesion Molecule-1
16.
Acta Pharmaceutica Sinica ; (12): 553-558, 2008.
Article in Chinese | WPRIM | ID: wpr-277797

ABSTRACT

Heme oxygenase-1 (HO-1) is a cellular stress protein, and its expression plays an important regulatory role in a lot of physiological and pathological processes. Although the expression of HO-1 in most tissues of body is low, a number of clinical and pharmacological experiments have proved that many compounds can induce HO-1 expression. The increase of HO-1 expression is the result of regulating different signaling pathways and transcription factors, and this induction of HO-1 is suggested to be partially therapeutic efficacy of these compounds. This article summarizes some kinds of compounds in this field of research at home and abroad over the last 10 years, and provides a brief analysis of the mechanism.


Subject(s)
Animals , Humans , Antineoplastic Agents , Pharmacology , Antioxidants , Pharmacology , Coumarins , Pharmacology , Drugs, Chinese Herbal , Pharmacology , Enzyme Induction , Gene Expression Regulation, Enzymologic , Heme Oxygenase-1 , Genetics , Metabolism , Lovastatin , Pharmacology , Nitric Oxide , Pharmacology , Peptide Hormones , Pharmacology , Probucol , Pharmacology , Signal Transduction , Transcription Factors , Metabolism
17.
Minoufia Medical Journal. 2008; 21 (1): 91-108
in English | IMEMR | ID: emr-89144

ABSTRACT

Doxorubicin is one of the first anthracyclines in clinical use and has a broad anti-tumor spectrum. With the increasing use of anthracycline antibiotic, acute and cumulative dose-related cardiotoxicity have been recognized. This work was undertaken with the aim of studying the histological, Ultrastructural and immunohistochemical changes in the myocardium of albino rats following doxorubicin administration and the possible protective role of an antioxidant [probucol]. Sixty adult albino rats of both sexes weighing 200 - 250 gms, were used in this study. They were divided into four groups: a control group [group I] composed of 30 rats and three treated groups [10 rats for each]. Probucol treated group [group II], were injected intraperitoneally [IP] with probucol in a dose of 10 mg / kg b. w every other day for four weeks. Doxorubicin treated group [group III], were injected [IP] with doxorubicin in a dose of 2.5 mg / kg b. w. every other day for two weeks. Probucol and doxorubicin treated group [group IV], were injected [IP] with probucol for two weeks followed by probucl plus doxorubicin for another two weeks with the same doses and ways mentioned before. The control animals were divided into three subgroups [10 rats for each], [group la], were injected [IP] with 1ml corn oil [solvent for probucol]. [group Ib] were injected [IP] with 1ml physiological saline [solvent for doxorubicin]. [group Ic] were injected [IP] with 1ml physiological saline and 1 ml corn oil by the same ways and durations mentioned before with treated animals. Heart specimens were taken two and four weeks after the last injection and processed for histological, Ultrastructural and immunohistochemical studies. Light microscopic studies revealed many degenerative changes that were time-dependent varying from vacuolation to myocytolysis and loss of myofibrils. Evidences of apoptosis were detected in the form of cytoplasmic eosinophilia and the nuclei varying from peripheral margination of chromatin up to pyknosis, confirmed immunohistochemically with positive reaction for caspase-3 activity that was increased in a time-dependent manner to reach up to four times of the control level four weeks after doxorubicin treatment, as detected by image analysis. Ultrastructural examination showed extensive degeneration of the muscle fibers with marked loss and even complete disappearance of myofibrils, there was dilatation of smooth endoplasmic reticulum, increased amount of glycogen granules and mitochondriosis, with degeneration and moth-eaten appearance of many mitochondria. The nucleus appeared hyperchromatic with peripherally clumped chromatin. The above mentioned toxic effects of doxorubicin on the myocardium were markedly attenuated by probucol administration before and in combination with doxorubicin injections. From this study, it was concluded that, probucol markedly attenuated doxorubicin induced cardiomyopathic changes which is time- dependent


Subject(s)
Animals, Laboratory , Heart/drug effects , Microscopy, Electron , Protective Agents , Probucol , Antioxidants , Immunohistochemistry , Treatment Outcome , Rats , Models, Animal , Doxorubicin/toxicity
18.
Rev. AMRIGS ; 51(4): 275-279, out.-dez. 2007. ilus, tab
Article in Portuguese | LILACS | ID: biblio-859916

ABSTRACT

Objetivo: Estudar o papel do probucol na lesão pulmonar obtida pela administração de doxorrubicina em ratos. Método: foi realizado um estudo piloto experimental, onde o probucol foi testado como protetor da injúria pulmonar obtida pela administração de doxorrubicina em ratos. Resultados: Na análise comparativa dos grupos, estudados por microscopia óptica, não houve diferença significativa de critérios previamente definidos, exceto pelo edema pleural (p < 0,05). Já na microscopia eletrônica, a agressão da doxorrubicina foi identificada através da desorganização estrutural. No grupo que recebeu probucol e doxorrubicina, não foi observada a mesma desorganização (p < 0,05). Conclusões: os resultados deste estudo piloto sugerem que o probucol exerceu um efeito protetor no tecido pulmonar agredido pela doxorrubicina e que a microscopia eletrônica é mais sensível na identificação de critérios de injúria pulmonar decorrente da exposição à doxorrubicina (AU)


Objective: To study the role of probucol in the pulmonary injury caused by doxorubicin in rats. Methods: An experimental study was carried out to verify where the probucol was protective of the pulmonary injury caused by the administration of doxorubicin in rats. Results: In the comparative analysis of the groups studied by optic microscopy, it did not have significant difference in pre-definite criterions, except for pleural edema (p < 0,05). In eletronic microscopy, the aggression of the doxorubicin was indicated through the structural disorganization. In the group that received probucol and doxorubicin was not observed the same disorganization (p < 0,05). Conclusion: The results suggest that the probucol was effective in the protection of pulmonary injury caused by doxorubicin and that the eletronic microscopy is more sensitive for pre-definite criterions of pulmonary injury (AU)


Subject(s)
Animals , Male , Probucol/therapeutic use , Doxorubicin/toxicity , Lung Injury/chemically induced , Lung Injury/pathology , Sarcoma/secondary , Lipid Peroxidation/drug effects , Doxorubicin/antagonists & inhibitors , Lung/drug effects , Lung Neoplasms/secondary
19.
Journal of Central South University(Medical Sciences) ; (12): 254-257, 2006.
Article in Chinese | WPRIM | ID: wpr-813722

ABSTRACT

OBJECTIVE@#To investigate the effect of probucol and losartan on the prevention of restenosis after balloon angioplasty in hypercholesterolaemic rabbits, and to examine the expression of growth factors.@*METHODS@#Forty male New Zealand white rabbits were randomly divided into high cholesterol diet group, probucol group, losartan group and combined drugs group. After one week of diet, all rabbits were injured on iliac arteries with balloon. Four weeks after the injury, the morphology of the iliac arteries of the rabbits were observed, and the insulin-like growth factor-I receptor (IGF-IR) and vascular endothelial growth factor (VEGF) were examined by immunohistochemical methods.@*RESULTS@#Compared with the high cholesterol diet group, the lumen areas of the probucol group, losartan group and combined drugs group were larger (P < 0.01), the intimal areas were smaller (P < 0.05), and the expression of IGF-IR and VEGF significantly decreased (P < 0.05). There was no statistically significant difference among the three groups.@*CONCLUSION@#Probucol and losartan can prevent the restenosis of rabbits' iliac artery from balloon injury, and inhibit the expression of IGF-IR and VEGF. There is no statistical difference between combined drugs and single drug administration.


Subject(s)
Animals , Male , Rabbits , Angioplasty, Balloon , Anticholesteremic Agents , Pharmacology , Therapeutic Uses , Coronary Restenosis , Drug Therapy, Combination , Hypercholesterolemia , Therapeutics , Losartan , Pharmacology , Therapeutic Uses , Probucol , Pharmacology , Therapeutic Uses , Random Allocation , Receptor, IGF Type 1 , Genetics , Vascular Endothelial Growth Factor A , Genetics
20.
Korean Journal of Medicine ; : 158-165, 2006.
Article in Korean | WPRIM | ID: wpr-91913

ABSTRACT

BACKGROUND: Oxidative stress might be a role in atherosclerosis and increased intake of antioxidant appear to be protective and modify neointimal formation. An antioxidant and probucol prevents endothelial dysfunction and low density lipoprotein oxidation and also inhibits the secretion of cytokine by macrophages. We aimed 1) to study the effects of antioxidant (Vitamin C, E and probucol) supplementation on serum level of antioxidant status (TAS), P-selectin, MCP-1, IL-6 and IL-10 and 2) to investigate the effects of antioxidant intake on in-stent restenosis. METHODS: Total 90 patients were assigned to control or antioxidant group (probucol; 500 mg, vitamin C; 1,000 mg, vitamin E; 400 mg). We performed follow up coronary angiography in 35 patients of antioxidant group and 36 patients of control group after 6 months of coronary bare metal stent implantation. We counted the stenotic lesions more than 50% of implanted stent lumen as a restenosis by quantitative coronary angiography. The serum levels of total antioxidant status, P-selectin, MCP-1, IL-6 and IL-10 were measured. RESULTS: The serum levels of total antioxidant status was not elevated in antioxidant group. Antioxidant supplementation did not change the serum levels of P-selectin, MCP-1, IL-6 and IL-10. The 6-month angiographic in-stent restenosis rate was 27% versus 30% (p=NS) with an associated late loss of 0.76+/-1.01 mm versus 0.91+/-1.00 mm (p=NS) for antioxidant group and control group. The serum levels of total antioxidant status did not correlate with the restenosis or late loss after stent implantation. CONCLUSIONS: Vitamin C, E and probucol did not elevate the serum level of antioxidant status and could not prevent in-stent restenosis after bare metal stent implantation.


Subject(s)
Humans , Antioxidants , Ascorbic Acid , Atherosclerosis , Coronary Angiography , Coronary Restenosis , Cytokines , Follow-Up Studies , Interleukin-10 , Interleukin-6 , Lipoproteins , Macrophages , Oxidative Stress , P-Selectin , Probucol , Stents , Vitamin E , Vitamins
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