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How do Chinese medicines that tonify the kidney inhibit dopaminergic neuron apoptosis?

Wistar rats were intragastrically perfused with Chinese medicines used for tonifying the kidney. These included 0.180 g/mL of Herba Epimedii (Epimedium), Semen Cuscutae (Dodder Seed), or Herba Cistanches (Desertliving Cistanche), 0.04 mg/mL monoamine oxidase-B inhibitor selegiline, or distilled wate...

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Autores principales: Lin, Shaogang, Ye, Shuifen, Huang, Jinmu, Tian, Yun, Xu, Yihui, Wu, Mengqi, Wang, Jingxia, Wu, Songying, Cai, Jing
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/PMC4146012/
https://www.ncbi.nlm.nih.gov/pubmed/25206603
http://dx.doi.org/10.3969/j.issn.1673-5374.2013.30.004
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author Lin, Shaogang
Ye, Shuifen
Huang, Jinmu
Tian, Yun
Xu, Yihui
Wu, Mengqi
Wang, Jingxia
Wu, Songying
Cai, Jing
author_facet Lin, Shaogang
Ye, Shuifen
Huang, Jinmu
Tian, Yun
Xu, Yihui
Wu, Mengqi
Wang, Jingxia
Wu, Songying
Cai, Jing
author_sort Lin, Shaogang
collection PubMed
description Wistar rats were intragastrically perfused with Chinese medicines used for tonifying the kidney. These included 0.180 g/mL of Herba Epimedii (Epimedium), Semen Cuscutae (Dodder Seed), or Herba Cistanches (Desertliving Cistanche), 0.04 mg/mL monoamine oxidase-B inhibitor selegiline, or distilled water for 14 consecutive days to prepare drug-containing serum or blank serum. MES23.5 cells in the logarithmic phase were cultured in media supplemented with 15% drug-containing serum for 24 hours, followed by incubation in culture solution containing 100 μmol/L H(2)O(2) for 3 hours. 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) and flow tometry results showed that all drug-containing serums improved the survival rate of H(2)O(2)-injured MES23.5 cells, inhibited pro-apoptotic FasL and caspase-3 expression, promoted anti-apoptotic Bcl-2 expression. However, drug-containing serums had little influence on Fas expression in H(2)O(2)-injured MES23.5 cells. Enzyme-linked immunosorbent assay results showed that serum containing Herba Cistanches or Herba Epimedii increased the expression of nerve growth factor, brain-derived neurotrophic factor, and glial cell line-derived neurotrophic factor in injured MES23.5 cells; serum containing Semen Cuscutae only increased brain-derived neurotrophic factor expression; while expression of the above neurotrophic factors remained the same in cells treated with serum containing selegiline. These findings indicate that Chinese medicines used to tonify the kidney can protect nerve cells by regulating the expression of apoptosis-related factors and neuro-trophic factors in MES23.5 cells.
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spelling pubmed-41460122014-09-09 How do Chinese medicines that tonify the kidney inhibit dopaminergic neuron apoptosis? Lin, Shaogang Ye, Shuifen Huang, Jinmu Tian, Yun Xu, Yihui Wu, Mengqi Wang, Jingxia Wu, Songying Cai, Jing Neural Regen Res Research and Report Article: Neurodegenerative Disease and Neural Regeneration Wistar rats were intragastrically perfused with Chinese medicines used for tonifying the kidney. These included 0.180 g/mL of Herba Epimedii (Epimedium), Semen Cuscutae (Dodder Seed), or Herba Cistanches (Desertliving Cistanche), 0.04 mg/mL monoamine oxidase-B inhibitor selegiline, or distilled water for 14 consecutive days to prepare drug-containing serum or blank serum. MES23.5 cells in the logarithmic phase were cultured in media supplemented with 15% drug-containing serum for 24 hours, followed by incubation in culture solution containing 100 μmol/L H(2)O(2) for 3 hours. 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) and flow tometry results showed that all drug-containing serums improved the survival rate of H(2)O(2)-injured MES23.5 cells, inhibited pro-apoptotic FasL and caspase-3 expression, promoted anti-apoptotic Bcl-2 expression. However, drug-containing serums had little influence on Fas expression in H(2)O(2)-injured MES23.5 cells. Enzyme-linked immunosorbent assay results showed that serum containing Herba Cistanches or Herba Epimedii increased the expression of nerve growth factor, brain-derived neurotrophic factor, and glial cell line-derived neurotrophic factor in injured MES23.5 cells; serum containing Semen Cuscutae only increased brain-derived neurotrophic factor expression; while expression of the above neurotrophic factors remained the same in cells treated with serum containing selegiline. These findings indicate that Chinese medicines used to tonify the kidney can protect nerve cells by regulating the expression of apoptosis-related factors and neuro-trophic factors in MES23.5 cells. Medknow Publications & Media Pvt Ltd 2013-10-25 /pmc/articles/PMC4146012/ /pubmed/25206603 http://dx.doi.org/10.3969/j.issn.1673-5374.2013.30.004 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 Research and Report Article: Neurodegenerative Disease and Neural Regeneration
Lin, Shaogang
Ye, Shuifen
Huang, Jinmu
Tian, Yun
Xu, Yihui
Wu, Mengqi
Wang, Jingxia
Wu, Songying
Cai, Jing
How do Chinese medicines that tonify the kidney inhibit dopaminergic neuron apoptosis?
title How do Chinese medicines that tonify the kidney inhibit dopaminergic neuron apoptosis?
title_full How do Chinese medicines that tonify the kidney inhibit dopaminergic neuron apoptosis?
title_fullStr How do Chinese medicines that tonify the kidney inhibit dopaminergic neuron apoptosis?
title_full_unstemmed How do Chinese medicines that tonify the kidney inhibit dopaminergic neuron apoptosis?
title_short How do Chinese medicines that tonify the kidney inhibit dopaminergic neuron apoptosis?
title_sort how do chinese medicines that tonify the kidney inhibit dopaminergic neuron apoptosis?
topic Research and Report Article: Neurodegenerative Disease and Neural Regeneration
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4146012/
https://www.ncbi.nlm.nih.gov/pubmed/25206603
http://dx.doi.org/10.3969/j.issn.1673-5374.2013.30.004
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