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  1. Article ; Online: Antioxidant enzyme gene transfer for ischemic diseases.

    Wu, Jian / Hecker, James G / Chiamvimonvat, Nipavan

    Advanced drug delivery reviews

    2009  Volume 61, Issue 4, Page(s) 351–363

    Abstract: ... the therapeutic benefits and potential risks, to develop disease-specific antioxidant gene transfer strategies ... free radical scavengers and their mimetics, as well as gene transfer approaches to overexpress antioxidant genes represent ... potential therapeutic options to correct the redox imbalance. Among them, antioxidant gene transfer ...

    Abstract The balance of redox is pivotal for normal function and integrity of tissues. Ischemic insults occur as results of a variety of conditions, leading to an accumulation of reactive oxygen species (ROS) and an imbalanced redox status in the tissues. The oxidant stress may activate signaling mechanisms provoking more toxic events, and eventually cause tissue damage. Therefore, treatments with antioxidants, free radical scavengers and their mimetics, as well as gene transfer approaches to overexpress antioxidant genes represent potential therapeutic options to correct the redox imbalance. Among them, antioxidant gene transfer may enhance the production of antioxidant scavengers, and has been employed to experimentally prevent or treat ischemic injury in cardiovascular, pulmonary, hepatic, intestinal, central nervous or other systems in animal models. With improvements in vector systems and delivery approaches, innovative antioxidant gene therapy has conferred better outcomes for myocardial infarction, reduced restenosis after coronary angioplasty, improved the quality and function of liver grafts, as well as outcome of intestinal and cerebral ischemic attacks. However, it is crucial to be mindful that like other therapeutic armentarium, the efficacy of antioxidant gene transfer requires extensive preclinical investigation before it can be used in patients, and that it may have unanticipated short- or long-term adverse effects. Thus, it is critical to balance between the therapeutic benefits and potential risks, to develop disease-specific antioxidant gene transfer strategies, to deliver the therapy with an optimal time window and in a safe manner. This review attempts to provide the rationale, the most effective approaches and the potential hurdles of available antioxidant gene transfer approaches for ischemic injury in various organs, as well as the possible directions of future preclinical and clinical investigations of this highly promising therapeutic modality.
    MeSH term(s) Animals ; Antioxidants/administration & dosage ; Gene Transfer Techniques/trends ; Genetic Therapy/methods ; Genetic Therapy/trends ; Humans ; Ischemia/enzymology ; Ischemia/genetics ; Ischemia/therapy ; Oxidative Stress/drug effects ; Oxidative Stress/genetics ; Reactive Oxygen Species/metabolism
    Chemical Substances Antioxidants ; Reactive Oxygen Species
    Language English
    Publishing date 2009-02-20
    Publishing country Netherlands
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, Non-P.H.S. ; Review
    ZDB-ID 639113-8
    ISSN 1872-8294 ; 0169-409X
    ISSN (online) 1872-8294
    ISSN 0169-409X
    DOI 10.1016/j.addr.2009.01.005
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Copper Transport Protein Antioxidant-1 Promotes Inflammatory Neovascularization via Chaperone and Transcription Factor Function.

    Chen, Gin-Fu / Sudhahar, Varadarajan / Youn, Seock-Won / Das, Archita / Cho, Jaehyung / Kamiya, Tetsuro / Urao, Norifumi / McKinney, Ronald D / Surenkhuu, Bayasgalan / Hamakubo, Takao / Iwanari, Hiroko / Li, Senlin / Christman, John W / Shantikumar, Saran / Angelini, Gianni D / Emanueli, Costanza / Ushio-Fukai, Masuko / Fukai, Tohru

    Scientific reports

    2015  Volume 5, Page(s) 14780

    Abstract: ... for treatment of ischemic disease. ... reconstitution, and Atox1 gene transfer in Atox1(-/-) mice show that Atox1 in endothelial cells (ECs) is ... transporter ATP7A is required for VEGF-induced angiogenesis via activation of Cu enzyme lysyl oxidase ...

    Abstract Copper (Cu), an essential micronutrient, plays a fundamental role in inflammation and angiogenesis; however, its precise mechanism remains undefined. Here we uncover a novel role of Cu transport protein Antioxidant-1 (Atox1), which is originally appreciated as a Cu chaperone and recently discovered as a Cu-dependent transcription factor, in inflammatory neovascularization. Atox1 expression is upregulated in patients and mice with critical limb ischemia. Atox1-deficient mice show impaired limb perfusion recovery with reduced arteriogenesis, angiogenesis, and recruitment of inflammatory cells. In vivo intravital microscopy, bone marrow reconstitution, and Atox1 gene transfer in Atox1(-/-) mice show that Atox1 in endothelial cells (ECs) is essential for neovascularization and recruitment of inflammatory cells which release VEGF and TNFα. Mechanistically, Atox1-depleted ECs demonstrate that Cu chaperone function of Atox1 mediated through Cu transporter ATP7A is required for VEGF-induced angiogenesis via activation of Cu enzyme lysyl oxidase. Moreover, Atox1 functions as a Cu-dependent transcription factor for NADPH oxidase organizer p47phox, thereby increasing ROS-NFκB-VCAM-1/ICAM-1 expression and monocyte adhesion in ECs inflamed with TNFα in an ATP7A-independent manner. These findings demonstrate a novel linkage between Atox1 and NADPH oxidase involved in inflammatory neovascularization and suggest Atox1 as a potential therapeutic target for treatment of ischemic disease.
    MeSH term(s) Adenosine Triphosphatases/genetics ; Adenosine Triphosphatases/metabolism ; Animals ; Cation Transport Proteins/genetics ; Cation Transport Proteins/metabolism ; Cell Adhesion Molecules/genetics ; Cell Adhesion Molecules/metabolism ; Cell Line ; Copper Transport Proteins ; Copper-Transporting ATPases ; Gene Expression Regulation ; Hindlimb ; Human Umbilical Vein Endothelial Cells/cytology ; Human Umbilical Vein Endothelial Cells/metabolism ; Humans ; Ischemia/genetics ; Ischemia/metabolism ; Ischemia/pathology ; Leg/blood supply ; Leg/pathology ; Metallochaperones/genetics ; Metallochaperones/metabolism ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Molecular Chaperones ; Monocytes/metabolism ; Monocytes/pathology ; NADPH Oxidases/genetics ; NADPH Oxidases/metabolism ; Neovascularization, Pathologic/genetics ; Neovascularization, Pathologic/metabolism ; Neovascularization, Pathologic/pathology ; Protein-Lysine 6-Oxidase/genetics ; Protein-Lysine 6-Oxidase/metabolism ; Reactive Oxygen Species/metabolism ; Signal Transduction ; Tumor Necrosis Factor-alpha/genetics ; Tumor Necrosis Factor-alpha/metabolism ; Vascular Endothelial Growth Factor A/genetics ; Vascular Endothelial Growth Factor A/metabolism
    Chemical Substances ATOX1 protein, human ; Cation Transport Proteins ; Cell Adhesion Molecules ; Copper Transport Proteins ; Metallochaperones ; Molecular Chaperones ; Reactive Oxygen Species ; Tumor Necrosis Factor-alpha ; VEGFA protein, human ; Vascular Endothelial Growth Factor A ; Protein-Lysine 6-Oxidase (EC 1.4.3.13) ; NADPH Oxidases (EC 1.6.3.-) ; neutrophil cytosolic factor 1 (EC 1.6.3.1) ; Adenosine Triphosphatases (EC 3.6.1.-) ; ATP7A protein, human (EC 7.2.2.8) ; Copper-Transporting ATPases (EC 7.2.2.8)
    Language English
    Publishing date 2015-10-06
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2615211-3
    ISSN 2045-2322 ; 2045-2322
    ISSN (online) 2045-2322
    ISSN 2045-2322
    DOI 10.1038/srep14780
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Effects of antioxidant gene therapy on retinal neurons and oxidative stress in a model of retinal ischemia/reperfusion.

    Liu, Yu / Tang, Luosheng / Chen, Baihua

    Free radical biology & medicine

    2012  Volume 52, Issue 5, Page(s) 909–915

    Abstract: ... nitrotyrosine level were measured by fluorescence staining, immunohistochemistry, and enzyme-linked ... nitrotyrosine and prevented the damage to RGCs and IPL. Delivery of the antioxidant gene inhibited I/R-induced ... relevant for the neuroprotection of the inner retina from I/R-related diseases. ...

    Abstract Retinal ischemia/reperfusion (I/R) results in neuronal death and generation of reactive oxygen species. The aim of this study was to investigate the neuroprotective effect of manganese superoxide dismutase (SOD2) on retinal ganglion cells (RGCs) in an I/R-induced retinal injury model. One eye of each Wistar rat was pretreated with recombinant adeno-associated virus containing the SOD2 gene (AAV-SOD2) or recombinant AAV containing the GFP gene (AAV-GFP) by intravitreal injection 21 days before initiation of I/R injury. Retinal I/R injury was induced by elevating intraocular pressure for 1h, and reperfusion was established immediately afterward. The number of RGCs and the inner plexiform layer (IPL) thickness were measured by Fluorogold retrograde labeling and hematoxylin and eosin staining at 6 h, 24 h, 72 h, and 5 days after injury. Superoxide anion, the number of RGCs, IPL thickness, malondialdehyde (MDA) level, 8-hydroxy-2-deoxyguanosine (8-OHdG) level, MnSOD (manganese superoxide dismutase) activity, and nitrotyrosine level were measured by fluorescence staining, immunohistochemistry, and enzyme-linked immunosorbent analysis at 5 days after I/R injury. Severe RGC loss, reduced IPL thickness, reduced MnSOD activity, and increased superoxide ion, MDA, 8-OHdG, and nitrotyrosine production were observed after I/R injury. Administration of AAV-SOD2 significantly reduced the levels of superoxide ion, MDA, 8-OHdG, and nitrotyrosine and prevented the damage to RGCs and IPL. Delivery of the antioxidant gene inhibited I/R-induced RGC and IPL damage by reducing oxidative stress and nitrative stress, suggesting that MnSOD may be relevant for the neuroprotection of the inner retina from I/R-related diseases.
    MeSH term(s) Animals ; DNA Adducts/metabolism ; Deoxyadenosines/metabolism ; Dependovirus/genetics ; Female ; Gene Transfer Techniques ; Genetic Therapy ; Ischemia/pathology ; Ischemia/therapy ; Malondialdehyde/metabolism ; Oxidation-Reduction ; Oxidative Stress ; Rats ; Rats, Wistar ; Recombinant Proteins/genetics ; Recombinant Proteins/metabolism ; Reperfusion Injury/genetics ; Reperfusion Injury/prevention & control ; Retina/metabolism ; Retina/pathology ; Retinal Ganglion Cells/metabolism ; Retinal Ganglion Cells/pathology ; Retinal Neurons/metabolism ; Retinal Neurons/pathology ; Retinal Vessels/pathology ; Superoxide Dismutase/genetics ; Superoxide Dismutase/metabolism ; Superoxides/metabolism ; Tyrosine/analogs & derivatives ; Tyrosine/metabolism
    Chemical Substances 8-hydroxy-2'-deoxyadenosine ; DNA Adducts ; Deoxyadenosines ; Recombinant Proteins ; Superoxides (11062-77-4) ; 3-nitrotyrosine (3604-79-3) ; Tyrosine (42HK56048U) ; Malondialdehyde (4Y8F71G49Q) ; Superoxide Dismutase (EC 1.15.1.1) ; superoxide dismutase 2 (EC 1.15.1.1)
    Language English
    Publishing date 2012-03-01
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 807032-5
    ISSN 1873-4596 ; 0891-5849
    ISSN (online) 1873-4596
    ISSN 0891-5849
    DOI 10.1016/j.freeradbiomed.2011.12.013
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: Targeting vascular redox biology through antioxidant gene delivery: a historical view and current perspectives.

    Van Assche, Tim / Huygelen, Véronique / Crabtree, Mark J

    Recent patents on cardiovascular drug discovery

    2011  Volume 6, Issue 2, Page(s) 89–102

    Abstract: ... perspectives for the treatment of vascular diseases in the future. The patents relevant to gene delivery are ... antioxidant treatment trials, promising findings have been reported using gene delivery of enzymes to improve ... demonstrated that gene delivery of antioxidative vascular wall-specific enzymes, such as heme oxygenase-1 ...

    Abstract Oxidative stress, resulting from a deregulated equilibrium between superoxide and nitric oxide (NO) production, contributes to the progression of different vascular diseases such as atherosclerosis, hypertension, ischemia/reperfusion injury and restenosis. Despite disappointing results of various oral antioxidant treatment trials, promising findings have been reported using gene delivery of enzymes to improve NO bioavailability and decrease oxidative stress in animal models for vascular diseases. NO production can be increased by overexpression of endothelial NO synthase (eNOS) in the vascular wall. However, the complex regulation of NOS needs to be carefully considered in the context of gene therapy along with the availability of its cofactor tetrahydrobiopterin and eNOS uncoupling. Furthermore, preclinical studies demonstrated that gene delivery of antioxidative vascular wall-specific enzymes, such as heme oxygenase-1, superoxide dismutase, catalase and glutathione peroxidase, has the potential to attenuate oxidative stress and inhibit atherosclerosis. Another option is to transfect vascular disease patients with secreted antioxidants such as high density lipoprotein-associated enzymes or soluble scavenger receptors. The advantage of the latter is that gene delivery of these enzymes and receptors does not need to be endothelium specific. Nonetheless, techniques to deliver genes specifically to the vascular wall are under development and hold interesting perspectives for the treatment of vascular diseases in the future. The patents relevant to gene delivery are also discussed in this review article.
    MeSH term(s) Animals ; Antioxidants/administration & dosage ; Gene Transfer Techniques ; Genetic Therapy/methods ; Humans ; Nitric Oxide/metabolism ; Oxidation-Reduction/drug effects ; Oxidative Stress/drug effects ; Patents as Topic ; Superoxides/metabolism ; Vascular Diseases/physiopathology ; Vascular Diseases/therapy
    Chemical Substances Antioxidants ; Superoxides (11062-77-4) ; Nitric Oxide (31C4KY9ESH)
    Language English
    Publishing date 2011-03-29
    Publishing country United Arab Emirates
    Document type Journal Article ; Review
    DOI 10.2174/157489011795933873
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Delivery of antioxidant enzyme genes to protect against ischemia/reperfusion-induced injury to retinal microvasculature.

    Chen, Baihua / Caballero, Sergio / Seo, Soojung / Grant, Maria B / Lewin, Alfred S

    Investigative ophthalmology & visual science

    2009  Volume 50, Issue 12, Page(s) 5587–5595

    Abstract: ... capillary degeneration, apoptosis of vascular cells, and ROS production, suggesting that antioxidant gene ... of the manganese superoxide dismutase gene (SOD2) or the catalase gene (CAT) could rescue the retinal vascular damage induced by I/R ... Purpose: Retinal ischemia/reperfusion (I/R) injury results in the generation ...

    Abstract Purpose: Retinal ischemia/reperfusion (I/R) injury results in the generation of reactive oxygen species (ROS). The aim of this study was to investigate whether delivery of the manganese superoxide dismutase gene (SOD2) or the catalase gene (CAT) could rescue the retinal vascular damage induced by I/R in mice.
    Methods: I/R injury to the retina was induced in mice by elevating intraocular pressure for 2 hours, and reperfusion was established immediately afterward. One eye of each mouse was pretreated with plasmids encoding manganese superoxide dismutase or catalase complexed with cationic liposomes and delivered by intravitreous injection 48 hours before initiation of the procedure. Superoxide ion, hydrogen peroxide, and 4-hydroxynonenal (4-HNE) protein modifications were measured by fluorescence staining, immunohistochemistry, and Western blot analysis 1 day after the I/R injury. At 7 days after injury, retinal vascular cell apoptosis and acellular capillaries were quantitated.
    Results: Superoxide ion, hydrogen peroxide, and 4-HNE protein modifications increased at 24 hours after I/R injury. Administration of plasmids encoding SOD2 or CAT significantly reduced levels of superoxide ion, hydrogen peroxide, and 4-HNE. Retinal vascular cell apoptosis and acellular capillary numbers increased greatly by 7 days after the injury. Delivery of SOD2 or CAT inhibited the I/R-induced apoptosis of retinal vascular cell and retinal capillary degeneration.
    Conclusions: Delivery of antioxidant genes inhibited I/R-induced retinal capillary degeneration, apoptosis of vascular cells, and ROS production, suggesting that antioxidant gene therapy might be a treatment for I/R-related disease.
    MeSH term(s) Aldehydes/metabolism ; Animals ; Blotting, Western ; Capillaries/metabolism ; Catalase/genetics ; Female ; Gene Expression Regulation, Enzymologic/physiology ; Gene Transfer Techniques ; Hydrogen Peroxide/metabolism ; Immunohistochemistry ; In Situ Nick-End Labeling ; Liposomes ; Mice ; Mice, Inbred C57BL ; Plasmids ; Reactive Oxygen Species/metabolism ; Reperfusion Injury/metabolism ; Reperfusion Injury/prevention & control ; Retinal Degeneration/metabolism ; Retinal Degeneration/prevention & control ; Retinal Vessels/metabolism ; Spectrometry, Fluorescence ; Superoxide Dismutase/genetics ; Superoxides/metabolism
    Chemical Substances Aldehydes ; Liposomes ; Reactive Oxygen Species ; Superoxides (11062-77-4) ; Hydrogen Peroxide (BBX060AN9V) ; Catalase (EC 1.11.1.6) ; Superoxide Dismutase (EC 1.15.1.1) ; 4-hydroxy-2-nonenal (K1CVM13F96)
    Language English
    Publishing date 2009-07-23
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 391794-0
    ISSN 1552-5783 ; 0146-0404
    ISSN (online) 1552-5783
    ISSN 0146-0404
    DOI 10.1167/iovs.09-3633
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: New strategies for cardiovascular gene therapy: regulatable pre-emptive expression of pro-angiogenic and antioxidant genes.

    Dulak, Jozef / Zagorska, Anna / Wegiel, Barbara / Loboda, Agnieszka / Jozkowicz, Alicja

    Cell biochemistry and biophysics

    2006  Volume 44, Issue 1, Page(s) 31–42

    Abstract: Cardiovascular diseases are among the major targets for gene therapy. Initially, clinical ... experiments of gene transfer of vascular endothelial growth factor (VEGF) improved vascularization and ... Moreover, experimental approaches in animal models displayed the promise of gene transfer modulating ...

    Abstract Cardiovascular diseases are among the major targets for gene therapy. Initially, clinical experiments of gene transfer of vascular endothelial growth factor (VEGF) improved vascularization and prevented the amputation in patients with critical leg ischemia. However, the majority of trials did not provide conclusive results and therefore further preclinical studies are required. Importantly, data indicate the necessity of regulated expression of angiogenic factors, particularly VEGF, to obtain the therapeutic effect. It is also suggested that the combined delivery of two or more genes may improve the formation of mature vasculature and therefore may be more effective in the amelioration of ischemia. Moreover, experimental approaches in animal models displayed the promise of gene transfer modulating the inflammatory processes and oxidant status of the cells. Particularly, the concept of preemptive gene therapy has been tested, and recent studies have demonstrated that overexpression of heme oxygenase-1 or extracellular superoxide dismutase can prevent heart injury by myocardial infarction induced several weeks after gene instillation. The combination of a preemptive strategy with regulated gene expression, using the vectors in which the therapeutic transgene is driven by exogenously or endogenously controllable promoter, offers another modality. However, we hypothesize that regulatable gene therapy, dependent on the activity of endogenous factors, might be prone to limitations owing to the potential disturbance in the expression of endogenous genes. Here, we demonstrated some indications of these drawbacks. Therefore, the final acceptance of these promising strategies for clinical trials requires careful validation in animal experiments.
    MeSH term(s) Angiogenic Proteins/genetics ; Animals ; Antioxidants/metabolism ; Cardiovascular Diseases/prevention & control ; Cardiovascular Diseases/therapy ; Clinical Trials as Topic ; E2F Transcription Factors/genetics ; Genetic Therapy/adverse effects ; Genetic Therapy/methods ; Humans ; Hypoxia-Inducible Factor 1/genetics ; Superoxide Dismutase/genetics ; Treatment Outcome ; Vascular Endothelial Growth Factor A/genetics
    Chemical Substances Angiogenic Proteins ; Antioxidants ; E2F Transcription Factors ; Hypoxia-Inducible Factor 1 ; VEGFA protein, human ; Vascular Endothelial Growth Factor A ; Superoxide Dismutase (EC 1.15.1.1)
    Language English
    Publishing date 2006
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 1357904-6
    ISSN 1085-9195
    ISSN 1085-9195
    DOI 10.1385/CBB:44:1:031
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: Disturbance effects of PM10 on iNOS and eNOS mRNA expression levels and antioxidant activity induced by ischemia–reperfusion injury in isolated rat heart: protective role of vanillic acid

    Dianat, Mahin / Radmanesh, Esmat / Badavi, Mohammad / Mard, Seyed Ali / Goudarzi, Gholamraza

    Environmental science and pollution research international

    Volume v. 23,, Issue no. 6

    Abstract: ... of death from cardiovascular diseases (CVDs). The aim of this study was to investigate the effects of particulate matter (PM ... eNOS) messenger RNA (mRNA) level induced by ischemia–reperfusion injury, and the protective effects ... to a Langendorff apparatus. The hearts were subjected to 30 min of global ischemia followed by 60 min ...

    Abstract Myocardial infarction is the acute condition of myocardial necrosis that occurs as a result of imbalance between coronary blood supply and myocardial demand. Air pollution increases the risk of death from cardiovascular diseases (CVDs). The aim of this study was to investigate the effects of particulate matter (PM) on oxidative stress, the expression of inducible nitric oxide synthase (iNOS) and endothelial nitric oxide synthase (eNOS) messenger RNA (mRNA) level induced by ischemia–reperfusion injury, and the protective effects of vanillic acid (VA) in the isolated rat heart. Male Wistar rats were randomly divided into eight groups (n = 10), namely control, VAc, sham, VA, PMa (0.5 mg/kg), PMb (2.5 mg/kg), PMc (5 mg/kg), and PMc + VA groups. Particles with an aerodynamic diameter <10 μm (PM₁₀) was instilled into the trachea through a fine intubation tube. Two days following the PM₁₀ instillation, the animal’s hearts were isolated and transferred to a Langendorff apparatus. The hearts were subjected to 30 min of global ischemia followed by 60 min of reperfusion. The activities of superoxide dismutase (SOD), glutathione peroxidase (GPx), catalase (CAT), xanthine oxidase (XOX), and lactate dehydrogenase (LDH) were measured using special kits. Reverse transcription polymerase chain reaction (RT-PCR) was used to determine levels of iNOS and eNOS mRNA. An increase in left ventricular end-diastolic pressure (LVEDP), S–T elevation, and oxidative stress in PM₁₀ groups was observed. Ischemia–reperfusion (I/R) induction showed a significant augment in the expression of iNOS mRNA level and a significant decrease in the expression eNOS mRNA level. This effect was more pronounced in the PM groups than in the control and sham groups. Vanillic acid caused a significant decrease in LVEDP, S–T elevation, and also a significant difference in eNOS mRNA expression level, antioxidant enzymes, iNOS mRNA expression level, and oxidative stress occurred on myocardial dysfunction after I/R in isolated rat hearts. This study showed that PM₁₀ exposure had devastating effects on the myocardial heart, oxidative stress, and eNOS and iNOS mRNA expression levels. Vanillic acid was able to improve these parameters. Vanillic acid as a potent antioxidant could also provide protection against particulate matter-induced toxicity.
    Keywords myocardial infarction ; heart ; messenger RNA ; inducible nitric oxide synthase ; death ; males ; lactate dehydrogenase ; endothelial nitric oxide synthase ; blood ; catalase ; protective effect ; oxidative stress ; glutathione peroxidase ; reverse transcriptase polymerase chain reaction ; particulates ; air pollution ; risk ; antioxidant activity ; antioxidants ; toxicity ; vanillic acid ; necrosis ; gene expression ; xanthine oxidase ; superoxide dismutase ; rats
    Language English
    Document type Article
    ISSN 0944-1344
    Database AGRIS - International Information System for the Agricultural Sciences and Technology

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