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Paeonol attenuates inflammation-mediated neurotoxicity and microglial activation

Chronic activation of microglial cells endangers neuronal survival through the release of various proinflammatory and neurotoxic factors. The root of Paeonia lactiflora Pall has been considered useful for the treatment of various disorders in traditional oriental medicine. Paeonol, found in the root...

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Autores principales: Nam, Kyong Nyon, Woo, Byung-Cheol, Moon, Sang-Kwan, Park, Seong-Uk, Park, Joo-young, Hwang, Jae-Woong, Bae, Hyung-Sup, Ko, Chang-Nam, Lee, Eunjoo Hwang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4145915/
https://www.ncbi.nlm.nih.gov/pubmed/25206460
http://dx.doi.org/10.3969/j.issn.1673-5374.2013.18.001
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author Nam, Kyong Nyon
Woo, Byung-Cheol
Moon, Sang-Kwan
Park, Seong-Uk
Park, Joo-young
Hwang, Jae-Woong
Bae, Hyung-Sup
Ko, Chang-Nam
Lee, Eunjoo Hwang
author_facet Nam, Kyong Nyon
Woo, Byung-Cheol
Moon, Sang-Kwan
Park, Seong-Uk
Park, Joo-young
Hwang, Jae-Woong
Bae, Hyung-Sup
Ko, Chang-Nam
Lee, Eunjoo Hwang
author_sort Nam, Kyong Nyon
collection PubMed
description Chronic activation of microglial cells endangers neuronal survival through the release of various proinflammatory and neurotoxic factors. The root of Paeonia lactiflora Pall has been considered useful for the treatment of various disorders in traditional oriental medicine. Paeonol, found in the root of Paeonia lactiflora Pall, has a wide range of pharmacological functions, including anti-oxidative, anti-inflammatory and neuroprotective activities. The objective of this study was to examine the efficacy of paeonol in the repression of inflammation-induced neurotoxicity and microglial cell activation. Organotypic hippocampal slice cultures and primary microglial cells from rat brain were stimulated with bacterial lipopolysaccharide. Paeonol pretreatment was performed for 30 minutes prior to lipopolysaccharide addition. Cell viability and nitrite (the production of nitric oxide), tumor necrosis factor-alpha and interleukin-1beta products were measured after lipopolysaccharide treatment. In organotypic hippocampal slice cultures, paeonol blocked lipopolysaccharide-related hippocampal cell death and inhibited the release of nitrite and interleukin-1beta. Paeonol was effective in inhibiting nitric oxide release from primary microglial cells. It also reduced the lipopolysaccharide-stimulated release of tumor necrosis factor-alpha and interleukin-1β from microglial cells. Paeonol possesses neuroprotective activity in a model of inflammation-induced neurotoxicity and reduces the release of neurotoxic and proinflammatory factors in activated microglial cells.
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spelling pubmed-41459152014-09-09 Paeonol attenuates inflammation-mediated neurotoxicity and microglial activation Nam, Kyong Nyon Woo, Byung-Cheol Moon, Sang-Kwan Park, Seong-Uk Park, Joo-young Hwang, Jae-Woong Bae, Hyung-Sup Ko, Chang-Nam Lee, Eunjoo Hwang Neural Regen Res Traditional Chinese Medicine and Neural Regeneration Chronic activation of microglial cells endangers neuronal survival through the release of various proinflammatory and neurotoxic factors. The root of Paeonia lactiflora Pall has been considered useful for the treatment of various disorders in traditional oriental medicine. Paeonol, found in the root of Paeonia lactiflora Pall, has a wide range of pharmacological functions, including anti-oxidative, anti-inflammatory and neuroprotective activities. The objective of this study was to examine the efficacy of paeonol in the repression of inflammation-induced neurotoxicity and microglial cell activation. Organotypic hippocampal slice cultures and primary microglial cells from rat brain were stimulated with bacterial lipopolysaccharide. Paeonol pretreatment was performed for 30 minutes prior to lipopolysaccharide addition. Cell viability and nitrite (the production of nitric oxide), tumor necrosis factor-alpha and interleukin-1beta products were measured after lipopolysaccharide treatment. In organotypic hippocampal slice cultures, paeonol blocked lipopolysaccharide-related hippocampal cell death and inhibited the release of nitrite and interleukin-1beta. Paeonol was effective in inhibiting nitric oxide release from primary microglial cells. It also reduced the lipopolysaccharide-stimulated release of tumor necrosis factor-alpha and interleukin-1β from microglial cells. Paeonol possesses neuroprotective activity in a model of inflammation-induced neurotoxicity and reduces the release of neurotoxic and proinflammatory factors in activated microglial cells. Medknow Publications & Media Pvt Ltd 2013-06-25 /pmc/articles/PMC4145915/ /pubmed/25206460 http://dx.doi.org/10.3969/j.issn.1673-5374.2013.18.001 Text en Copyright: © Neural Regeneration Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Traditional Chinese Medicine and Neural Regeneration
Nam, Kyong Nyon
Woo, Byung-Cheol
Moon, Sang-Kwan
Park, Seong-Uk
Park, Joo-young
Hwang, Jae-Woong
Bae, Hyung-Sup
Ko, Chang-Nam
Lee, Eunjoo Hwang
Paeonol attenuates inflammation-mediated neurotoxicity and microglial activation
title Paeonol attenuates inflammation-mediated neurotoxicity and microglial activation
title_full Paeonol attenuates inflammation-mediated neurotoxicity and microglial activation
title_fullStr Paeonol attenuates inflammation-mediated neurotoxicity and microglial activation
title_full_unstemmed Paeonol attenuates inflammation-mediated neurotoxicity and microglial activation
title_short Paeonol attenuates inflammation-mediated neurotoxicity and microglial activation
title_sort paeonol attenuates inflammation-mediated neurotoxicity and microglial activation
topic Traditional Chinese Medicine and Neural Regeneration
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4145915/
https://www.ncbi.nlm.nih.gov/pubmed/25206460
http://dx.doi.org/10.3969/j.issn.1673-5374.2013.18.001
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