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10.1371/journal.pone.0131392 http://scihub22266oqcxt.onion/10.1371/journal.pone.0131392 C4489838!4489838 !26133377     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=26133377 &cmd=llinks): Failed to open stream: HTTP request failed! 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Antioxidant Properties of Whole Body Periodic Acceleration (pGz) |pdf=|usr=}}{{26133377 }} gab.com Text Antioxidant Properties of Whole Body Periodic Acceleration (pGz) JO: PLoS One http://www.kidney.de/pget.php?&tw=1&pmid=26133377 #FOAvip The recognition that oxidative stress is a major component of several chronic diseases has engendered numerous trials of antioxidant therapies with minimal or no direct benefits. Nanomolar quantities of nitric oxide released into the circulation by pharmacologic stimulation of eNOS have antioxidant properties but physiologic stimulation as through increased pulsatile shear stress of the endothelium has not been assessed. The present study utilized a non-invasive technology, periodic acceleration (pGz) that increases pulsatile shear stress such that upregulation of cardiac eNOS occurs, We assessed its efficacy in normal mice and mouse models with high levels of oxidative stress, e.g. Diabetes type 1 and mdx (Duchene Muscular Dystrophy). pGz increased protein expression and upregulated eNOS in hearts. Application of pGz was associated with significantly increased expression of endogenous antioxidants (Glutathioneperoxidase-1(GPX-1), Catalase (CAT), Superoxide, Superoxide Dismutase 1(SOD1). This led to an increase of total cardiac antioxidant capacity along with an increase in the antioxidant response element transcription factor Nrf2 translocation to the nucleus. pGz decreased reactive oxygen species in both mice models of oxidative stress. Thus, pGz is a novel non-pharmacologic method to harness endogenous antioxidant capacity. Twit Text FOAVip Antioxidant Properties of Whole Body Periodic Acceleration (pGz) ????PLoS One http://www.kidney.de/pget.php?&tw=1&pmid=26133377 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26133377 #FOAvip English Wikipedia <ref>{{Cite pmid|26133377 }}</ref> Antioxidant Properties of Whole Body Periodic Acceleration (pGz) #MMPMID26133377 Uryash A ; Bassuk J ; Kurlansky P ; Altamirano F ; Lopez JR ; Adams JA PLoS One 2015[]; 10 (7 ): e0131392 PMID26133377 show ga The recognition that oxidative stress is a major component of several chronic diseases has engendered numerous trials of antioxidant therapies with minimal or no direct benefits. Nanomolar quantities of nitric oxide released into the circulation by pharmacologic stimulation of eNOS have antioxidant properties but physiologic stimulation as through increased pulsatile shear stress of the endothelium has not been assessed. The present study utilized a non-invasive technology, periodic acceleration (pGz) that increases pulsatile shear stress such that upregulation of cardiac eNOS occurs, We assessed its efficacy in normal mice and mouse models with high levels of oxidative stress, e.g. Diabetes type 1 and mdx (Duchene Muscular Dystrophy). pGz increased protein expression and upregulated eNOS in hearts. Application of pGz was associated with significantly increased expression of endogenous antioxidants (Glutathioneperoxidase-1(GPX-1), Catalase (CAT), Superoxide, Superoxide Dismutase 1(SOD1). This led to an increase of total cardiac antioxidant capacity along with an increase in the antioxidant response element transcription factor Nrf2 translocation to the nucleus. pGz decreased reactive oxygen species in both mice models of oxidative stress. Thus, pGz is a novel non-pharmacologic method to harness endogenous antioxidant capacity. |*Acceleration [MESH] |*Oxidation-Reduction [MESH] |Animals [MESH] |Antioxidants/analysis/physiology [MESH] |Blood Pressure/physiology [MESH] |Blotting, Western [MESH] |Catalase/analysis [MESH] |Diabetes Mellitus, Experimental/metabolism/physiopathology [MESH] |Disease Models, Animal [MESH] |Enzyme-Linked Immunosorbent Assay [MESH] |Glutathione Peroxidase GPX1 [MESH] |Glutathione Peroxidase/analysis [MESH] |Heart Rate/physiology [MESH] |Male [MESH] |Mice [MESH] |Mice, Inbred C57BL [MESH] |Muscular Dystrophy, Duchenne/metabolism/physiopathology [MESH] |Myocardium/chemistry [MESH] |NF-E2-Related Factor 2/analysis [MESH] |Oxidative Stress/*physiology [MESH] |Reactive Oxygen Species/analysis [MESH] |Superoxide Dismutase-1 [MESH]Antioxidant Properties of Whole Body Periodic Acceleration (pGz) (epmc).pdf DeepDyve Pubget Overpricing