Statins more than cholesterol lowering agents in Alzheimer disease: Their pleiotropic functions as potential therapeutic targets
Statins have been proposed to modulate several cellular pathways having neuroprotective or neurotoxic effects independent on their ability to lower cholesterol, but, rather, dependent on the kind of statin used. Atorvastatin treatment promoted a decrease of oxidative and nitrosative stress levels in...
Ausführliche Beschreibung
Autor*in: |
Barone, Eugenio [verfasserIn] |
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Sprache: |
Englisch |
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2014transfer abstract |
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Umfang: |
12 |
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Übergeordnetes Werk: |
Enthalten in: Mussel-inspired adhesive friction-controlled lubricating coating for titanium alloy used in artificial joint replacement - Chen, Zhuo ELSEVIER, 2023, Amsterdam [u.a.] |
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Übergeordnetes Werk: |
volume:88 ; year:2014 ; number:4 ; day:15 ; month:04 ; pages:605-616 ; extent:12 |
Links: |
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DOI / URN: |
10.1016/j.bcp.2013.10.030 |
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520 | |a Statins have been proposed to modulate several cellular pathways having neuroprotective or neurotoxic effects independent on their ability to lower cholesterol, but, rather, dependent on the kind of statin used. Atorvastatin treatment promoted a decrease of oxidative and nitrosative stress levels in the brain of a dog model of AD. These effects were mediated by an increased activity of the HO-1/BVR-A system having the anti-oxidant and anti-nitrosative bilirubin as end-product. In addition, increased BVR-A activation was negatively associated with BACE-1 protein levels. Thus, atorvastatin may have a neuroprotective role in the progression of AD by modulating the HO-1/BVR-A system. | ||
520 | |a Statins have been proposed to modulate several cellular pathways having neuroprotective or neurotoxic effects independent on their ability to lower cholesterol, but, rather, dependent on the kind of statin used. Atorvastatin treatment promoted a decrease of oxidative and nitrosative stress levels in the brain of a dog model of AD. These effects were mediated by an increased activity of the HO-1/BVR-A system having the anti-oxidant and anti-nitrosative bilirubin as end-product. In addition, increased BVR-A activation was negatively associated with BACE-1 protein levels. Thus, atorvastatin may have a neuroprotective role in the progression of AD by modulating the HO-1/BVR-A system. | ||
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10.1016/j.bcp.2013.10.030 doi GBVA2014019000001.pica (DE-627)ELV034169555 (ELSEVIER)S0006-2952(13)00714-4 DE-627 ger DE-627 rakwb eng 610 610 DE-600 670 530 660 VZ 33.68 bkl 35.18 bkl 52.78 bkl Barone, Eugenio verfasserin aut Statins more than cholesterol lowering agents in Alzheimer disease: Their pleiotropic functions as potential therapeutic targets 2014transfer abstract 12 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Statins have been proposed to modulate several cellular pathways having neuroprotective or neurotoxic effects independent on their ability to lower cholesterol, but, rather, dependent on the kind of statin used. Atorvastatin treatment promoted a decrease of oxidative and nitrosative stress levels in the brain of a dog model of AD. These effects were mediated by an increased activity of the HO-1/BVR-A system having the anti-oxidant and anti-nitrosative bilirubin as end-product. In addition, increased BVR-A activation was negatively associated with BACE-1 protein levels. Thus, atorvastatin may have a neuroprotective role in the progression of AD by modulating the HO-1/BVR-A system. Statins have been proposed to modulate several cellular pathways having neuroprotective or neurotoxic effects independent on their ability to lower cholesterol, but, rather, dependent on the kind of statin used. Atorvastatin treatment promoted a decrease of oxidative and nitrosative stress levels in the brain of a dog model of AD. These effects were mediated by an increased activity of the HO-1/BVR-A system having the anti-oxidant and anti-nitrosative bilirubin as end-product. In addition, increased BVR-A activation was negatively associated with BACE-1 protein levels. Thus, atorvastatin may have a neuroprotective role in the progression of AD by modulating the HO-1/BVR-A system. Oxidative stress Elsevier Alzheimer disease Elsevier Heme oxygenase Elsevier Biliverdin reductase Elsevier Cognition Elsevier Statin Elsevier Di Domenico, Fabio oth Butterfield, D. Allan oth Enthalten in Elsevier Science Chen, Zhuo ELSEVIER Mussel-inspired adhesive friction-controlled lubricating coating for titanium alloy used in artificial joint replacement 2023 Amsterdam [u.a.] (DE-627)ELV010068619 volume:88 year:2014 number:4 day:15 month:04 pages:605-616 extent:12 https://doi.org/10.1016/j.bcp.2013.10.030 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA GBV_ILN_24 GBV_ILN_2002 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2018 GBV_ILN_2032 GBV_ILN_2037 GBV_ILN_2043 GBV_ILN_2091 GBV_ILN_2140 GBV_ILN_2165 GBV_ILN_2227 GBV_ILN_2285 GBV_ILN_2305 GBV_ILN_2421 GBV_ILN_2430 GBV_ILN_2520 GBV_ILN_2552 GBV_ILN_2568 33.68 Oberflächen Dünne Schichten Grenzflächen Physik VZ 35.18 Kolloidchemie Grenzflächenchemie VZ 52.78 Oberflächentechnik Wärmebehandlung VZ AR 88 2014 4 15 0415 605-616 12 045F 610 |
spelling |
10.1016/j.bcp.2013.10.030 doi GBVA2014019000001.pica (DE-627)ELV034169555 (ELSEVIER)S0006-2952(13)00714-4 DE-627 ger DE-627 rakwb eng 610 610 DE-600 670 530 660 VZ 33.68 bkl 35.18 bkl 52.78 bkl Barone, Eugenio verfasserin aut Statins more than cholesterol lowering agents in Alzheimer disease: Their pleiotropic functions as potential therapeutic targets 2014transfer abstract 12 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Statins have been proposed to modulate several cellular pathways having neuroprotective or neurotoxic effects independent on their ability to lower cholesterol, but, rather, dependent on the kind of statin used. Atorvastatin treatment promoted a decrease of oxidative and nitrosative stress levels in the brain of a dog model of AD. These effects were mediated by an increased activity of the HO-1/BVR-A system having the anti-oxidant and anti-nitrosative bilirubin as end-product. In addition, increased BVR-A activation was negatively associated with BACE-1 protein levels. Thus, atorvastatin may have a neuroprotective role in the progression of AD by modulating the HO-1/BVR-A system. Statins have been proposed to modulate several cellular pathways having neuroprotective or neurotoxic effects independent on their ability to lower cholesterol, but, rather, dependent on the kind of statin used. Atorvastatin treatment promoted a decrease of oxidative and nitrosative stress levels in the brain of a dog model of AD. These effects were mediated by an increased activity of the HO-1/BVR-A system having the anti-oxidant and anti-nitrosative bilirubin as end-product. In addition, increased BVR-A activation was negatively associated with BACE-1 protein levels. Thus, atorvastatin may have a neuroprotective role in the progression of AD by modulating the HO-1/BVR-A system. Oxidative stress Elsevier Alzheimer disease Elsevier Heme oxygenase Elsevier Biliverdin reductase Elsevier Cognition Elsevier Statin Elsevier Di Domenico, Fabio oth Butterfield, D. Allan oth Enthalten in Elsevier Science Chen, Zhuo ELSEVIER Mussel-inspired adhesive friction-controlled lubricating coating for titanium alloy used in artificial joint replacement 2023 Amsterdam [u.a.] (DE-627)ELV010068619 volume:88 year:2014 number:4 day:15 month:04 pages:605-616 extent:12 https://doi.org/10.1016/j.bcp.2013.10.030 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA GBV_ILN_24 GBV_ILN_2002 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2018 GBV_ILN_2032 GBV_ILN_2037 GBV_ILN_2043 GBV_ILN_2091 GBV_ILN_2140 GBV_ILN_2165 GBV_ILN_2227 GBV_ILN_2285 GBV_ILN_2305 GBV_ILN_2421 GBV_ILN_2430 GBV_ILN_2520 GBV_ILN_2552 GBV_ILN_2568 33.68 Oberflächen Dünne Schichten Grenzflächen Physik VZ 35.18 Kolloidchemie Grenzflächenchemie VZ 52.78 Oberflächentechnik Wärmebehandlung VZ AR 88 2014 4 15 0415 605-616 12 045F 610 |
allfields_unstemmed |
10.1016/j.bcp.2013.10.030 doi GBVA2014019000001.pica (DE-627)ELV034169555 (ELSEVIER)S0006-2952(13)00714-4 DE-627 ger DE-627 rakwb eng 610 610 DE-600 670 530 660 VZ 33.68 bkl 35.18 bkl 52.78 bkl Barone, Eugenio verfasserin aut Statins more than cholesterol lowering agents in Alzheimer disease: Their pleiotropic functions as potential therapeutic targets 2014transfer abstract 12 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Statins have been proposed to modulate several cellular pathways having neuroprotective or neurotoxic effects independent on their ability to lower cholesterol, but, rather, dependent on the kind of statin used. Atorvastatin treatment promoted a decrease of oxidative and nitrosative stress levels in the brain of a dog model of AD. These effects were mediated by an increased activity of the HO-1/BVR-A system having the anti-oxidant and anti-nitrosative bilirubin as end-product. In addition, increased BVR-A activation was negatively associated with BACE-1 protein levels. Thus, atorvastatin may have a neuroprotective role in the progression of AD by modulating the HO-1/BVR-A system. Statins have been proposed to modulate several cellular pathways having neuroprotective or neurotoxic effects independent on their ability to lower cholesterol, but, rather, dependent on the kind of statin used. Atorvastatin treatment promoted a decrease of oxidative and nitrosative stress levels in the brain of a dog model of AD. These effects were mediated by an increased activity of the HO-1/BVR-A system having the anti-oxidant and anti-nitrosative bilirubin as end-product. In addition, increased BVR-A activation was negatively associated with BACE-1 protein levels. Thus, atorvastatin may have a neuroprotective role in the progression of AD by modulating the HO-1/BVR-A system. Oxidative stress Elsevier Alzheimer disease Elsevier Heme oxygenase Elsevier Biliverdin reductase Elsevier Cognition Elsevier Statin Elsevier Di Domenico, Fabio oth Butterfield, D. Allan oth Enthalten in Elsevier Science Chen, Zhuo ELSEVIER Mussel-inspired adhesive friction-controlled lubricating coating for titanium alloy used in artificial joint replacement 2023 Amsterdam [u.a.] (DE-627)ELV010068619 volume:88 year:2014 number:4 day:15 month:04 pages:605-616 extent:12 https://doi.org/10.1016/j.bcp.2013.10.030 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA GBV_ILN_24 GBV_ILN_2002 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2018 GBV_ILN_2032 GBV_ILN_2037 GBV_ILN_2043 GBV_ILN_2091 GBV_ILN_2140 GBV_ILN_2165 GBV_ILN_2227 GBV_ILN_2285 GBV_ILN_2305 GBV_ILN_2421 GBV_ILN_2430 GBV_ILN_2520 GBV_ILN_2552 GBV_ILN_2568 33.68 Oberflächen Dünne Schichten Grenzflächen Physik VZ 35.18 Kolloidchemie Grenzflächenchemie VZ 52.78 Oberflächentechnik Wärmebehandlung VZ AR 88 2014 4 15 0415 605-616 12 045F 610 |
allfieldsGer |
10.1016/j.bcp.2013.10.030 doi GBVA2014019000001.pica (DE-627)ELV034169555 (ELSEVIER)S0006-2952(13)00714-4 DE-627 ger DE-627 rakwb eng 610 610 DE-600 670 530 660 VZ 33.68 bkl 35.18 bkl 52.78 bkl Barone, Eugenio verfasserin aut Statins more than cholesterol lowering agents in Alzheimer disease: Their pleiotropic functions as potential therapeutic targets 2014transfer abstract 12 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Statins have been proposed to modulate several cellular pathways having neuroprotective or neurotoxic effects independent on their ability to lower cholesterol, but, rather, dependent on the kind of statin used. Atorvastatin treatment promoted a decrease of oxidative and nitrosative stress levels in the brain of a dog model of AD. These effects were mediated by an increased activity of the HO-1/BVR-A system having the anti-oxidant and anti-nitrosative bilirubin as end-product. In addition, increased BVR-A activation was negatively associated with BACE-1 protein levels. Thus, atorvastatin may have a neuroprotective role in the progression of AD by modulating the HO-1/BVR-A system. Statins have been proposed to modulate several cellular pathways having neuroprotective or neurotoxic effects independent on their ability to lower cholesterol, but, rather, dependent on the kind of statin used. Atorvastatin treatment promoted a decrease of oxidative and nitrosative stress levels in the brain of a dog model of AD. These effects were mediated by an increased activity of the HO-1/BVR-A system having the anti-oxidant and anti-nitrosative bilirubin as end-product. In addition, increased BVR-A activation was negatively associated with BACE-1 protein levels. Thus, atorvastatin may have a neuroprotective role in the progression of AD by modulating the HO-1/BVR-A system. Oxidative stress Elsevier Alzheimer disease Elsevier Heme oxygenase Elsevier Biliverdin reductase Elsevier Cognition Elsevier Statin Elsevier Di Domenico, Fabio oth Butterfield, D. Allan oth Enthalten in Elsevier Science Chen, Zhuo ELSEVIER Mussel-inspired adhesive friction-controlled lubricating coating for titanium alloy used in artificial joint replacement 2023 Amsterdam [u.a.] (DE-627)ELV010068619 volume:88 year:2014 number:4 day:15 month:04 pages:605-616 extent:12 https://doi.org/10.1016/j.bcp.2013.10.030 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA GBV_ILN_24 GBV_ILN_2002 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2018 GBV_ILN_2032 GBV_ILN_2037 GBV_ILN_2043 GBV_ILN_2091 GBV_ILN_2140 GBV_ILN_2165 GBV_ILN_2227 GBV_ILN_2285 GBV_ILN_2305 GBV_ILN_2421 GBV_ILN_2430 GBV_ILN_2520 GBV_ILN_2552 GBV_ILN_2568 33.68 Oberflächen Dünne Schichten Grenzflächen Physik VZ 35.18 Kolloidchemie Grenzflächenchemie VZ 52.78 Oberflächentechnik Wärmebehandlung VZ AR 88 2014 4 15 0415 605-616 12 045F 610 |
allfieldsSound |
10.1016/j.bcp.2013.10.030 doi GBVA2014019000001.pica (DE-627)ELV034169555 (ELSEVIER)S0006-2952(13)00714-4 DE-627 ger DE-627 rakwb eng 610 610 DE-600 670 530 660 VZ 33.68 bkl 35.18 bkl 52.78 bkl Barone, Eugenio verfasserin aut Statins more than cholesterol lowering agents in Alzheimer disease: Their pleiotropic functions as potential therapeutic targets 2014transfer abstract 12 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Statins have been proposed to modulate several cellular pathways having neuroprotective or neurotoxic effects independent on their ability to lower cholesterol, but, rather, dependent on the kind of statin used. Atorvastatin treatment promoted a decrease of oxidative and nitrosative stress levels in the brain of a dog model of AD. These effects were mediated by an increased activity of the HO-1/BVR-A system having the anti-oxidant and anti-nitrosative bilirubin as end-product. In addition, increased BVR-A activation was negatively associated with BACE-1 protein levels. Thus, atorvastatin may have a neuroprotective role in the progression of AD by modulating the HO-1/BVR-A system. Statins have been proposed to modulate several cellular pathways having neuroprotective or neurotoxic effects independent on their ability to lower cholesterol, but, rather, dependent on the kind of statin used. Atorvastatin treatment promoted a decrease of oxidative and nitrosative stress levels in the brain of a dog model of AD. These effects were mediated by an increased activity of the HO-1/BVR-A system having the anti-oxidant and anti-nitrosative bilirubin as end-product. In addition, increased BVR-A activation was negatively associated with BACE-1 protein levels. Thus, atorvastatin may have a neuroprotective role in the progression of AD by modulating the HO-1/BVR-A system. Oxidative stress Elsevier Alzheimer disease Elsevier Heme oxygenase Elsevier Biliverdin reductase Elsevier Cognition Elsevier Statin Elsevier Di Domenico, Fabio oth Butterfield, D. Allan oth Enthalten in Elsevier Science Chen, Zhuo ELSEVIER Mussel-inspired adhesive friction-controlled lubricating coating for titanium alloy used in artificial joint replacement 2023 Amsterdam [u.a.] (DE-627)ELV010068619 volume:88 year:2014 number:4 day:15 month:04 pages:605-616 extent:12 https://doi.org/10.1016/j.bcp.2013.10.030 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA GBV_ILN_24 GBV_ILN_2002 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2018 GBV_ILN_2032 GBV_ILN_2037 GBV_ILN_2043 GBV_ILN_2091 GBV_ILN_2140 GBV_ILN_2165 GBV_ILN_2227 GBV_ILN_2285 GBV_ILN_2305 GBV_ILN_2421 GBV_ILN_2430 GBV_ILN_2520 GBV_ILN_2552 GBV_ILN_2568 33.68 Oberflächen Dünne Schichten Grenzflächen Physik VZ 35.18 Kolloidchemie Grenzflächenchemie VZ 52.78 Oberflächentechnik Wärmebehandlung VZ AR 88 2014 4 15 0415 605-616 12 045F 610 |
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Enthalten in Mussel-inspired adhesive friction-controlled lubricating coating for titanium alloy used in artificial joint replacement Amsterdam [u.a.] volume:88 year:2014 number:4 day:15 month:04 pages:605-616 extent:12 |
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Mussel-inspired adhesive friction-controlled lubricating coating for titanium alloy used in artificial joint replacement |
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Statins more than cholesterol lowering agents in Alzheimer disease: Their pleiotropic functions as potential therapeutic targets |
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Statins have been proposed to modulate several cellular pathways having neuroprotective or neurotoxic effects independent on their ability to lower cholesterol, but, rather, dependent on the kind of statin used. Atorvastatin treatment promoted a decrease of oxidative and nitrosative stress levels in the brain of a dog model of AD. These effects were mediated by an increased activity of the HO-1/BVR-A system having the anti-oxidant and anti-nitrosative bilirubin as end-product. In addition, increased BVR-A activation was negatively associated with BACE-1 protein levels. Thus, atorvastatin may have a neuroprotective role in the progression of AD by modulating the HO-1/BVR-A system. |
abstractGer |
Statins have been proposed to modulate several cellular pathways having neuroprotective or neurotoxic effects independent on their ability to lower cholesterol, but, rather, dependent on the kind of statin used. Atorvastatin treatment promoted a decrease of oxidative and nitrosative stress levels in the brain of a dog model of AD. These effects were mediated by an increased activity of the HO-1/BVR-A system having the anti-oxidant and anti-nitrosative bilirubin as end-product. In addition, increased BVR-A activation was negatively associated with BACE-1 protein levels. Thus, atorvastatin may have a neuroprotective role in the progression of AD by modulating the HO-1/BVR-A system. |
abstract_unstemmed |
Statins have been proposed to modulate several cellular pathways having neuroprotective or neurotoxic effects independent on their ability to lower cholesterol, but, rather, dependent on the kind of statin used. Atorvastatin treatment promoted a decrease of oxidative and nitrosative stress levels in the brain of a dog model of AD. These effects were mediated by an increased activity of the HO-1/BVR-A system having the anti-oxidant and anti-nitrosative bilirubin as end-product. In addition, increased BVR-A activation was negatively associated with BACE-1 protein levels. Thus, atorvastatin may have a neuroprotective role in the progression of AD by modulating the HO-1/BVR-A system. |
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