Cargando…

Algae Undaria pinnatifida Protects Hypothalamic Neurons against Endoplasmic Reticulum Stress through Akt/mTOR Signaling

Increased endoplasmic reticulum (ER) stress is known to be one of the causes of hypothalamic neuronal damage, as well as a cause of metabolic disorders such as obesity and diabetes. Recent evidence has suggested that Undaria pinnatifida (UP), an edible brown algae, has antioxidant activity. However,...

Descripción completa

Detalles Bibliográficos
Autores principales: Kim, Jongwan, Moon, Il Soo, Goo, Tae-Won, Moon, Seong-Su, Seo, Minchul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6332416/
https://www.ncbi.nlm.nih.gov/pubmed/26610463
http://dx.doi.org/10.3390/molecules201219744
_version_ 1783387345674829824
author Kim, Jongwan
Moon, Il Soo
Goo, Tae-Won
Moon, Seong-Su
Seo, Minchul
author_facet Kim, Jongwan
Moon, Il Soo
Goo, Tae-Won
Moon, Seong-Su
Seo, Minchul
author_sort Kim, Jongwan
collection PubMed
description Increased endoplasmic reticulum (ER) stress is known to be one of the causes of hypothalamic neuronal damage, as well as a cause of metabolic disorders such as obesity and diabetes. Recent evidence has suggested that Undaria pinnatifida (UP), an edible brown algae, has antioxidant activity. However, the neuroprotective effect of UP has yet to be examined. In this study, to investigate the neuroprotective effect of UP on ER stress-induced neuronal damage in mouse hypothalamic neurons, mice immortal hypothalamic neurons (GT1-7) were incubated with extract of UP. ER stress was induced by treating with tunicamycin. Tunicamycin induced apoptotic cell death was compared with the vehicle treatment through excessive ER stress. However UP protected GT1-7 cells from cell death, occurring after treatment with tunicamycin by reducing ER stress. Treatment with UP resulted in reduced increment of ATF6 and CHOP, and recovered the decrease of phosphorylation of Akt/mTOR by tunicamycin and the increment of autophagy. These results show that UP protects GT1-7 cells from ER stress induced cell death through the Akt/mTOR pathway. The current study suggests that UP may have a beneficial effect on cerebral neuronal degeneration in metabolic diseases with elevated ER stress.
format Online
Article
Text
id pubmed-6332416
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-63324162019-01-24 Algae Undaria pinnatifida Protects Hypothalamic Neurons against Endoplasmic Reticulum Stress through Akt/mTOR Signaling Kim, Jongwan Moon, Il Soo Goo, Tae-Won Moon, Seong-Su Seo, Minchul Molecules Article Increased endoplasmic reticulum (ER) stress is known to be one of the causes of hypothalamic neuronal damage, as well as a cause of metabolic disorders such as obesity and diabetes. Recent evidence has suggested that Undaria pinnatifida (UP), an edible brown algae, has antioxidant activity. However, the neuroprotective effect of UP has yet to be examined. In this study, to investigate the neuroprotective effect of UP on ER stress-induced neuronal damage in mouse hypothalamic neurons, mice immortal hypothalamic neurons (GT1-7) were incubated with extract of UP. ER stress was induced by treating with tunicamycin. Tunicamycin induced apoptotic cell death was compared with the vehicle treatment through excessive ER stress. However UP protected GT1-7 cells from cell death, occurring after treatment with tunicamycin by reducing ER stress. Treatment with UP resulted in reduced increment of ATF6 and CHOP, and recovered the decrease of phosphorylation of Akt/mTOR by tunicamycin and the increment of autophagy. These results show that UP protects GT1-7 cells from ER stress induced cell death through the Akt/mTOR pathway. The current study suggests that UP may have a beneficial effect on cerebral neuronal degeneration in metabolic diseases with elevated ER stress. MDPI 2015-11-25 /pmc/articles/PMC6332416/ /pubmed/26610463 http://dx.doi.org/10.3390/molecules201219744 Text en © 2015 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons by Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kim, Jongwan
Moon, Il Soo
Goo, Tae-Won
Moon, Seong-Su
Seo, Minchul
Algae Undaria pinnatifida Protects Hypothalamic Neurons against Endoplasmic Reticulum Stress through Akt/mTOR Signaling
title Algae Undaria pinnatifida Protects Hypothalamic Neurons against Endoplasmic Reticulum Stress through Akt/mTOR Signaling
title_full Algae Undaria pinnatifida Protects Hypothalamic Neurons against Endoplasmic Reticulum Stress through Akt/mTOR Signaling
title_fullStr Algae Undaria pinnatifida Protects Hypothalamic Neurons against Endoplasmic Reticulum Stress through Akt/mTOR Signaling
title_full_unstemmed Algae Undaria pinnatifida Protects Hypothalamic Neurons against Endoplasmic Reticulum Stress through Akt/mTOR Signaling
title_short Algae Undaria pinnatifida Protects Hypothalamic Neurons against Endoplasmic Reticulum Stress through Akt/mTOR Signaling
title_sort algae undaria pinnatifida protects hypothalamic neurons against endoplasmic reticulum stress through akt/mtor signaling
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6332416/
https://www.ncbi.nlm.nih.gov/pubmed/26610463
http://dx.doi.org/10.3390/molecules201219744
work_keys_str_mv AT kimjongwan algaeundariapinnatifidaprotectshypothalamicneuronsagainstendoplasmicreticulumstressthroughaktmtorsignaling
AT moonilsoo algaeundariapinnatifidaprotectshypothalamicneuronsagainstendoplasmicreticulumstressthroughaktmtorsignaling
AT gootaewon algaeundariapinnatifidaprotectshypothalamicneuronsagainstendoplasmicreticulumstressthroughaktmtorsignaling
AT moonseongsu algaeundariapinnatifidaprotectshypothalamicneuronsagainstendoplasmicreticulumstressthroughaktmtorsignaling
AT seominchul algaeundariapinnatifidaprotectshypothalamicneuronsagainstendoplasmicreticulumstressthroughaktmtorsignaling