author_facet Lei, Yen‐Ping
Liu, Cheng‐Tzu
Sheen, Lee‐Yan
Chen, Haw‐Wen
Lii, Chong‐Kuei
Lei, Yen‐Ping
Liu, Cheng‐Tzu
Sheen, Lee‐Yan
Chen, Haw‐Wen
Lii, Chong‐Kuei
author Lei, Yen‐Ping
Liu, Cheng‐Tzu
Sheen, Lee‐Yan
Chen, Haw‐Wen
Lii, Chong‐Kuei
spellingShingle Lei, Yen‐Ping
Liu, Cheng‐Tzu
Sheen, Lee‐Yan
Chen, Haw‐Wen
Lii, Chong‐Kuei
Molecular Nutrition & Food Research
Diallyl disulfide and diallyl trisulfide protect endothelial nitric oxide synthase against damage by oxidized low‐density lipoprotein
Food Science
Biotechnology
author_sort lei, yen‐ping
spelling Lei, Yen‐Ping Liu, Cheng‐Tzu Sheen, Lee‐Yan Chen, Haw‐Wen Lii, Chong‐Kuei 1613-4125 1613-4133 Wiley Food Science Biotechnology http://dx.doi.org/10.1002/mnfr.200900278 <jats:title>Abstract</jats:title><jats:p>Garlic is viewed as an effective health food against atherosclerosis. In this study, we examined whether diallyl disulfide (DADS) and diallyl trisulfide (DATS) protect endothelial nitric oxide synthase (eNOS) activation against oxidized LDL (ox‐LDL) insult and through what mechanism. We found that DADS and DATS reversed the suppression of eNOS Ser1177 phosphorylation by ox‐LDL, and wortmannin abolished the reversal by DADS and DATS. Similarly, the inhibition of cellular cGMP and nitric oxide production by ox‐LDL was reversed by DADS and DATS (<jats:italic>p</jats:italic>&lt;0.05). This increase in nitric oxide bioavailability by the allyl sulfides was attenuated by wortmannin. Immunoprecipitation assay revealed that DADS and DATS preserved the interaction of eNOS with caveolin‐1 in the membrane. In addition, DADS and DATS suppressed the reduction of the cellular eNOS protein content by ox‐LDL. When cycloheximide was added to block protein synthesis, DADS and DATS suppressed eNOS protein degradation similarly to that noted by MG132. Ox‐LDL increased chymotrypsin‐like proteasome activity, and this increase was inhibited by the allyl sulfides and MG132 (<jats:italic>p</jats:italic>&lt;0.05). These results suggest that DADS and DATS protect eNOS activity against ox‐LDL insult. This protection can be attributed partly to their mediation of phosphatidylinositol 3‐kinase/protein kinase B signaling and prevention of eNOS degradation.</jats:p> Diallyl disulfide and diallyl trisulfide protect endothelial nitric oxide synthase against damage by oxidized low‐density lipoprotein Molecular Nutrition & Food Research
doi_str_mv 10.1002/mnfr.200900278
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series Molecular Nutrition & Food Research
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title Diallyl disulfide and diallyl trisulfide protect endothelial nitric oxide synthase against damage by oxidized low‐density lipoprotein
title_unstemmed Diallyl disulfide and diallyl trisulfide protect endothelial nitric oxide synthase against damage by oxidized low‐density lipoprotein
title_full Diallyl disulfide and diallyl trisulfide protect endothelial nitric oxide synthase against damage by oxidized low‐density lipoprotein
title_fullStr Diallyl disulfide and diallyl trisulfide protect endothelial nitric oxide synthase against damage by oxidized low‐density lipoprotein
title_full_unstemmed Diallyl disulfide and diallyl trisulfide protect endothelial nitric oxide synthase against damage by oxidized low‐density lipoprotein
title_short Diallyl disulfide and diallyl trisulfide protect endothelial nitric oxide synthase against damage by oxidized low‐density lipoprotein
title_sort diallyl disulfide and diallyl trisulfide protect endothelial nitric oxide synthase against damage by oxidized low‐density lipoprotein
topic Food Science
Biotechnology
url http://dx.doi.org/10.1002/mnfr.200900278
publishDate 2010
physical
description <jats:title>Abstract</jats:title><jats:p>Garlic is viewed as an effective health food against atherosclerosis. In this study, we examined whether diallyl disulfide (DADS) and diallyl trisulfide (DATS) protect endothelial nitric oxide synthase (eNOS) activation against oxidized LDL (ox‐LDL) insult and through what mechanism. We found that DADS and DATS reversed the suppression of eNOS Ser1177 phosphorylation by ox‐LDL, and wortmannin abolished the reversal by DADS and DATS. Similarly, the inhibition of cellular cGMP and nitric oxide production by ox‐LDL was reversed by DADS and DATS (<jats:italic>p</jats:italic>&lt;0.05). This increase in nitric oxide bioavailability by the allyl sulfides was attenuated by wortmannin. Immunoprecipitation assay revealed that DADS and DATS preserved the interaction of eNOS with caveolin‐1 in the membrane. In addition, DADS and DATS suppressed the reduction of the cellular eNOS protein content by ox‐LDL. When cycloheximide was added to block protein synthesis, DADS and DATS suppressed eNOS protein degradation similarly to that noted by MG132. Ox‐LDL increased chymotrypsin‐like proteasome activity, and this increase was inhibited by the allyl sulfides and MG132 (<jats:italic>p</jats:italic>&lt;0.05). These results suggest that DADS and DATS protect eNOS activity against ox‐LDL insult. This protection can be attributed partly to their mediation of phosphatidylinositol 3‐kinase/protein kinase B signaling and prevention of eNOS degradation.</jats:p>
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author Lei, Yen‐Ping, Liu, Cheng‐Tzu, Sheen, Lee‐Yan, Chen, Haw‐Wen, Lii, Chong‐Kuei
author_facet Lei, Yen‐Ping, Liu, Cheng‐Tzu, Sheen, Lee‐Yan, Chen, Haw‐Wen, Lii, Chong‐Kuei, Lei, Yen‐Ping, Liu, Cheng‐Tzu, Sheen, Lee‐Yan, Chen, Haw‐Wen, Lii, Chong‐Kuei
author_sort lei, yen‐ping
container_issue S1
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container_title Molecular Nutrition & Food Research
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description <jats:title>Abstract</jats:title><jats:p>Garlic is viewed as an effective health food against atherosclerosis. In this study, we examined whether diallyl disulfide (DADS) and diallyl trisulfide (DATS) protect endothelial nitric oxide synthase (eNOS) activation against oxidized LDL (ox‐LDL) insult and through what mechanism. We found that DADS and DATS reversed the suppression of eNOS Ser1177 phosphorylation by ox‐LDL, and wortmannin abolished the reversal by DADS and DATS. Similarly, the inhibition of cellular cGMP and nitric oxide production by ox‐LDL was reversed by DADS and DATS (<jats:italic>p</jats:italic>&lt;0.05). This increase in nitric oxide bioavailability by the allyl sulfides was attenuated by wortmannin. Immunoprecipitation assay revealed that DADS and DATS preserved the interaction of eNOS with caveolin‐1 in the membrane. In addition, DADS and DATS suppressed the reduction of the cellular eNOS protein content by ox‐LDL. When cycloheximide was added to block protein synthesis, DADS and DATS suppressed eNOS protein degradation similarly to that noted by MG132. Ox‐LDL increased chymotrypsin‐like proteasome activity, and this increase was inhibited by the allyl sulfides and MG132 (<jats:italic>p</jats:italic>&lt;0.05). These results suggest that DADS and DATS protect eNOS activity against ox‐LDL insult. This protection can be attributed partly to their mediation of phosphatidylinositol 3‐kinase/protein kinase B signaling and prevention of eNOS degradation.</jats:p>
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spelling Lei, Yen‐Ping Liu, Cheng‐Tzu Sheen, Lee‐Yan Chen, Haw‐Wen Lii, Chong‐Kuei 1613-4125 1613-4133 Wiley Food Science Biotechnology http://dx.doi.org/10.1002/mnfr.200900278 <jats:title>Abstract</jats:title><jats:p>Garlic is viewed as an effective health food against atherosclerosis. In this study, we examined whether diallyl disulfide (DADS) and diallyl trisulfide (DATS) protect endothelial nitric oxide synthase (eNOS) activation against oxidized LDL (ox‐LDL) insult and through what mechanism. We found that DADS and DATS reversed the suppression of eNOS Ser1177 phosphorylation by ox‐LDL, and wortmannin abolished the reversal by DADS and DATS. Similarly, the inhibition of cellular cGMP and nitric oxide production by ox‐LDL was reversed by DADS and DATS (<jats:italic>p</jats:italic>&lt;0.05). This increase in nitric oxide bioavailability by the allyl sulfides was attenuated by wortmannin. Immunoprecipitation assay revealed that DADS and DATS preserved the interaction of eNOS with caveolin‐1 in the membrane. In addition, DADS and DATS suppressed the reduction of the cellular eNOS protein content by ox‐LDL. When cycloheximide was added to block protein synthesis, DADS and DATS suppressed eNOS protein degradation similarly to that noted by MG132. Ox‐LDL increased chymotrypsin‐like proteasome activity, and this increase was inhibited by the allyl sulfides and MG132 (<jats:italic>p</jats:italic>&lt;0.05). These results suggest that DADS and DATS protect eNOS activity against ox‐LDL insult. This protection can be attributed partly to their mediation of phosphatidylinositol 3‐kinase/protein kinase B signaling and prevention of eNOS degradation.</jats:p> Diallyl disulfide and diallyl trisulfide protect endothelial nitric oxide synthase against damage by oxidized low‐density lipoprotein Molecular Nutrition & Food Research
spellingShingle Lei, Yen‐Ping, Liu, Cheng‐Tzu, Sheen, Lee‐Yan, Chen, Haw‐Wen, Lii, Chong‐Kuei, Molecular Nutrition & Food Research, Diallyl disulfide and diallyl trisulfide protect endothelial nitric oxide synthase against damage by oxidized low‐density lipoprotein, Food Science, Biotechnology
title Diallyl disulfide and diallyl trisulfide protect endothelial nitric oxide synthase against damage by oxidized low‐density lipoprotein
title_full Diallyl disulfide and diallyl trisulfide protect endothelial nitric oxide synthase against damage by oxidized low‐density lipoprotein
title_fullStr Diallyl disulfide and diallyl trisulfide protect endothelial nitric oxide synthase against damage by oxidized low‐density lipoprotein
title_full_unstemmed Diallyl disulfide and diallyl trisulfide protect endothelial nitric oxide synthase against damage by oxidized low‐density lipoprotein
title_short Diallyl disulfide and diallyl trisulfide protect endothelial nitric oxide synthase against damage by oxidized low‐density lipoprotein
title_sort diallyl disulfide and diallyl trisulfide protect endothelial nitric oxide synthase against damage by oxidized low‐density lipoprotein
title_unstemmed Diallyl disulfide and diallyl trisulfide protect endothelial nitric oxide synthase against damage by oxidized low‐density lipoprotein
topic Food Science, Biotechnology
url http://dx.doi.org/10.1002/mnfr.200900278