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Serum containing Gengnianchun formula suppresses amyloid β-induced inflammatory cytokines in BV-2 microglial cells by inhibiting the NF-κB and JNK signaling pathways
As the resident macrophages of the brain's innate immune system, microglial cells are key modulators in the neurodegenerative disease Alzheimer's disease (AD). In particular, the activation and accumulation of microglial cells around amyloid plaques is considered to result in chronic neuro...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5865966/ https://www.ncbi.nlm.nih.gov/pubmed/29393440 http://dx.doi.org/10.3892/mmr.2018.8524 |
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author | Chen, Pin-Li Wang, Wen-Jun Rao, Yan-Qiu Li, Jun Cheng, Ming-Jun |
author_facet | Chen, Pin-Li Wang, Wen-Jun Rao, Yan-Qiu Li, Jun Cheng, Ming-Jun |
author_sort | Chen, Pin-Li |
collection | PubMed |
description | As the resident macrophages of the brain's innate immune system, microglial cells are key modulators in the neurodegenerative disease Alzheimer's disease (AD). In particular, the activation and accumulation of microglial cells around amyloid plaques is considered to result in chronic neuroinflammation. Although the pathologic mechanism remains to be fully elucidated, inflammation has been shown to be critical in the pathogenesis of AD. The Gengnianchun (GNC) formula has long been used to treat perimenopausal syndrome clinically, and is particularly effective in improving learning ability and memory. Our previous study demonstrated that GNC formula had an anti-inflammatory effect and offered neuroprotection in animal experiments. In the present study, the anti-inflammatory properties of GNC and its underlying mechanism of action were examined in BV-2 microglial cells. Amyloid-β peptide (Aβ)-stimulated microglial cells were examined for the production of proinflammatory cytokines and the underlying signaling pathways. Compared with the normal control group, the protein expression levels of IL-1β and TNF-α were significantly increased following treatment with Aβ (P<0.01), but medicated rat serum containing GNC formula (MRS) could significantly attenuated the Aβ-induced secretion of these pro-inflammatory cytokines. It was identified by CCK-8 assay that the viability of the BV-2 cells was not reduced following treatment with various concentrations of MRS. The phosphorylation of factor-κB (NF-κB) and c-Jun N-terminal kinase (JNK) was markedly increased following treatment with Aβ, compared with the normal control group (P<0.01). However, treatment with MRS resulted in a significant reduction in the phosphorylation of NF-κB (P<0.05). These results suggested that MRS suppressed the Aβ-induced inflammatory response of microglial cells by inhibiting the NF-κB and JNK signaling pathways. These novel findings provide insights into the development of GNC formula as a therapeutic agent for the treatment of neurodegenerative disorders. |
format | Online Article Text |
id | pubmed-5865966 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-58659662018-03-28 Serum containing Gengnianchun formula suppresses amyloid β-induced inflammatory cytokines in BV-2 microglial cells by inhibiting the NF-κB and JNK signaling pathways Chen, Pin-Li Wang, Wen-Jun Rao, Yan-Qiu Li, Jun Cheng, Ming-Jun Mol Med Rep Articles As the resident macrophages of the brain's innate immune system, microglial cells are key modulators in the neurodegenerative disease Alzheimer's disease (AD). In particular, the activation and accumulation of microglial cells around amyloid plaques is considered to result in chronic neuroinflammation. Although the pathologic mechanism remains to be fully elucidated, inflammation has been shown to be critical in the pathogenesis of AD. The Gengnianchun (GNC) formula has long been used to treat perimenopausal syndrome clinically, and is particularly effective in improving learning ability and memory. Our previous study demonstrated that GNC formula had an anti-inflammatory effect and offered neuroprotection in animal experiments. In the present study, the anti-inflammatory properties of GNC and its underlying mechanism of action were examined in BV-2 microglial cells. Amyloid-β peptide (Aβ)-stimulated microglial cells were examined for the production of proinflammatory cytokines and the underlying signaling pathways. Compared with the normal control group, the protein expression levels of IL-1β and TNF-α were significantly increased following treatment with Aβ (P<0.01), but medicated rat serum containing GNC formula (MRS) could significantly attenuated the Aβ-induced secretion of these pro-inflammatory cytokines. It was identified by CCK-8 assay that the viability of the BV-2 cells was not reduced following treatment with various concentrations of MRS. The phosphorylation of factor-κB (NF-κB) and c-Jun N-terminal kinase (JNK) was markedly increased following treatment with Aβ, compared with the normal control group (P<0.01). However, treatment with MRS resulted in a significant reduction in the phosphorylation of NF-κB (P<0.05). These results suggested that MRS suppressed the Aβ-induced inflammatory response of microglial cells by inhibiting the NF-κB and JNK signaling pathways. These novel findings provide insights into the development of GNC formula as a therapeutic agent for the treatment of neurodegenerative disorders. D.A. Spandidos 2018-04 2018-01-31 /pmc/articles/PMC5865966/ /pubmed/29393440 http://dx.doi.org/10.3892/mmr.2018.8524 Text en Copyright: © Chen et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Chen, Pin-Li Wang, Wen-Jun Rao, Yan-Qiu Li, Jun Cheng, Ming-Jun Serum containing Gengnianchun formula suppresses amyloid β-induced inflammatory cytokines in BV-2 microglial cells by inhibiting the NF-κB and JNK signaling pathways |
title | Serum containing Gengnianchun formula suppresses amyloid β-induced inflammatory cytokines in BV-2 microglial cells by inhibiting the NF-κB and JNK signaling pathways |
title_full | Serum containing Gengnianchun formula suppresses amyloid β-induced inflammatory cytokines in BV-2 microglial cells by inhibiting the NF-κB and JNK signaling pathways |
title_fullStr | Serum containing Gengnianchun formula suppresses amyloid β-induced inflammatory cytokines in BV-2 microglial cells by inhibiting the NF-κB and JNK signaling pathways |
title_full_unstemmed | Serum containing Gengnianchun formula suppresses amyloid β-induced inflammatory cytokines in BV-2 microglial cells by inhibiting the NF-κB and JNK signaling pathways |
title_short | Serum containing Gengnianchun formula suppresses amyloid β-induced inflammatory cytokines in BV-2 microglial cells by inhibiting the NF-κB and JNK signaling pathways |
title_sort | serum containing gengnianchun formula suppresses amyloid β-induced inflammatory cytokines in bv-2 microglial cells by inhibiting the nf-κb and jnk signaling pathways |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5865966/ https://www.ncbi.nlm.nih.gov/pubmed/29393440 http://dx.doi.org/10.3892/mmr.2018.8524 |
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