Cargando…

Sanhua Decoction, a Classic Herbal Prescription, Exerts Neuroprotection Through Regulating Phosphorylated Tau Level and Promoting Adult Endogenous Neurogenesis After Cerebral Ischemia/Reperfusion Injury

Background: Ischemia stroke is the leading cause of death and long-term disability. Sanhua Decoction (SHD), a classic Chinese herbal prescription, has been used for ischemic stroke for about thousands of years. Here, we aim to investigate the neuroprotective effects of SHD on cerebral ischemia/reper...

Descripción completa

Detalles Bibliográficos
Autores principales: Fu, Deng-Lei, Li, Ji-Huang, Shi, Yi-Hua, Zhang, Xi-Le, Lin, Yan, Zheng, Guo-Qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7026024/
https://www.ncbi.nlm.nih.gov/pubmed/32116767
http://dx.doi.org/10.3389/fphys.2020.00057
_version_ 1783498602217209856
author Fu, Deng-Lei
Li, Ji-Huang
Shi, Yi-Hua
Zhang, Xi-Le
Lin, Yan
Zheng, Guo-Qing
author_facet Fu, Deng-Lei
Li, Ji-Huang
Shi, Yi-Hua
Zhang, Xi-Le
Lin, Yan
Zheng, Guo-Qing
author_sort Fu, Deng-Lei
collection PubMed
description Background: Ischemia stroke is the leading cause of death and long-term disability. Sanhua Decoction (SHD), a classic Chinese herbal prescription, has been used for ischemic stroke for about thousands of years. Here, we aim to investigate the neuroprotective effects of SHD on cerebral ischemia/reperfusion (CIR) injury rat models. Methods: The male Sprague-Dawley rats (body weight, 250–280 g; age, 7–8 weeks) were randomly divided into sham group, CIR group, and SHD group and were further divided into subgroups according to different time points at 6 h, 1, 3, 7, 14, 21, and 28 d, respectively. The SHD group received intragastric administration of SHD at 10 g kg(−1) d(−1). The focal CIR models were induced by middle cerebral artery occlusion according to Longa’s method, while sham group had the same operation without suture insertion. Neurological deficit score (NDS) was evaluated using the Longa’s scale. BrdU, doublecortin (DCX), and glial fibrillary acidic protein (GFAP) were used to label proliferation, migration, and differentiation of nerve cells before being observed by immunofluorescence. The expression of reelin, total tau (t-tau), and phosphorylated tau (p-tau) were evaluated by western blot and RT-qPCR. Results: SHD can significantly improve NDS at 1, 3, 7, and 14 d (p < 0.05), increase the number of BrdU positive and BrdU/DCX positive cells in subventricular zone at 3, 7, and 14 d (p < 0.05), upregulate BrdU/GFAP positive cells in the ischemic penumbra at 28 d after CIR (p < 0.05), and reduce p-tau level at 1, 3, 7, and 14 d (p < 0.05). There was no significant difference on reelin and t-tau level between three groups at each time points after CIR. Conclusions: SHD exerts neuroprotection probably by regulating p-tau level and promoting the proliferation, migration, and differentiation of endogenous neural stem cells, accompanying with neurobehavioral recovery.
format Online
Article
Text
id pubmed-7026024
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-70260242020-02-28 Sanhua Decoction, a Classic Herbal Prescription, Exerts Neuroprotection Through Regulating Phosphorylated Tau Level and Promoting Adult Endogenous Neurogenesis After Cerebral Ischemia/Reperfusion Injury Fu, Deng-Lei Li, Ji-Huang Shi, Yi-Hua Zhang, Xi-Le Lin, Yan Zheng, Guo-Qing Front Physiol Physiology Background: Ischemia stroke is the leading cause of death and long-term disability. Sanhua Decoction (SHD), a classic Chinese herbal prescription, has been used for ischemic stroke for about thousands of years. Here, we aim to investigate the neuroprotective effects of SHD on cerebral ischemia/reperfusion (CIR) injury rat models. Methods: The male Sprague-Dawley rats (body weight, 250–280 g; age, 7–8 weeks) were randomly divided into sham group, CIR group, and SHD group and were further divided into subgroups according to different time points at 6 h, 1, 3, 7, 14, 21, and 28 d, respectively. The SHD group received intragastric administration of SHD at 10 g kg(−1) d(−1). The focal CIR models were induced by middle cerebral artery occlusion according to Longa’s method, while sham group had the same operation without suture insertion. Neurological deficit score (NDS) was evaluated using the Longa’s scale. BrdU, doublecortin (DCX), and glial fibrillary acidic protein (GFAP) were used to label proliferation, migration, and differentiation of nerve cells before being observed by immunofluorescence. The expression of reelin, total tau (t-tau), and phosphorylated tau (p-tau) were evaluated by western blot and RT-qPCR. Results: SHD can significantly improve NDS at 1, 3, 7, and 14 d (p < 0.05), increase the number of BrdU positive and BrdU/DCX positive cells in subventricular zone at 3, 7, and 14 d (p < 0.05), upregulate BrdU/GFAP positive cells in the ischemic penumbra at 28 d after CIR (p < 0.05), and reduce p-tau level at 1, 3, 7, and 14 d (p < 0.05). There was no significant difference on reelin and t-tau level between three groups at each time points after CIR. Conclusions: SHD exerts neuroprotection probably by regulating p-tau level and promoting the proliferation, migration, and differentiation of endogenous neural stem cells, accompanying with neurobehavioral recovery. Frontiers Media S.A. 2020-02-11 /pmc/articles/PMC7026024/ /pubmed/32116767 http://dx.doi.org/10.3389/fphys.2020.00057 Text en Copyright © 2020 Fu, Li, Shi, Zhang, Lin and Zheng. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Fu, Deng-Lei
Li, Ji-Huang
Shi, Yi-Hua
Zhang, Xi-Le
Lin, Yan
Zheng, Guo-Qing
Sanhua Decoction, a Classic Herbal Prescription, Exerts Neuroprotection Through Regulating Phosphorylated Tau Level and Promoting Adult Endogenous Neurogenesis After Cerebral Ischemia/Reperfusion Injury
title Sanhua Decoction, a Classic Herbal Prescription, Exerts Neuroprotection Through Regulating Phosphorylated Tau Level and Promoting Adult Endogenous Neurogenesis After Cerebral Ischemia/Reperfusion Injury
title_full Sanhua Decoction, a Classic Herbal Prescription, Exerts Neuroprotection Through Regulating Phosphorylated Tau Level and Promoting Adult Endogenous Neurogenesis After Cerebral Ischemia/Reperfusion Injury
title_fullStr Sanhua Decoction, a Classic Herbal Prescription, Exerts Neuroprotection Through Regulating Phosphorylated Tau Level and Promoting Adult Endogenous Neurogenesis After Cerebral Ischemia/Reperfusion Injury
title_full_unstemmed Sanhua Decoction, a Classic Herbal Prescription, Exerts Neuroprotection Through Regulating Phosphorylated Tau Level and Promoting Adult Endogenous Neurogenesis After Cerebral Ischemia/Reperfusion Injury
title_short Sanhua Decoction, a Classic Herbal Prescription, Exerts Neuroprotection Through Regulating Phosphorylated Tau Level and Promoting Adult Endogenous Neurogenesis After Cerebral Ischemia/Reperfusion Injury
title_sort sanhua decoction, a classic herbal prescription, exerts neuroprotection through regulating phosphorylated tau level and promoting adult endogenous neurogenesis after cerebral ischemia/reperfusion injury
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7026024/
https://www.ncbi.nlm.nih.gov/pubmed/32116767
http://dx.doi.org/10.3389/fphys.2020.00057
work_keys_str_mv AT fudenglei sanhuadecoctionaclassicherbalprescriptionexertsneuroprotectionthroughregulatingphosphorylatedtaulevelandpromotingadultendogenousneurogenesisaftercerebralischemiareperfusioninjury
AT lijihuang sanhuadecoctionaclassicherbalprescriptionexertsneuroprotectionthroughregulatingphosphorylatedtaulevelandpromotingadultendogenousneurogenesisaftercerebralischemiareperfusioninjury
AT shiyihua sanhuadecoctionaclassicherbalprescriptionexertsneuroprotectionthroughregulatingphosphorylatedtaulevelandpromotingadultendogenousneurogenesisaftercerebralischemiareperfusioninjury
AT zhangxile sanhuadecoctionaclassicherbalprescriptionexertsneuroprotectionthroughregulatingphosphorylatedtaulevelandpromotingadultendogenousneurogenesisaftercerebralischemiareperfusioninjury
AT linyan sanhuadecoctionaclassicherbalprescriptionexertsneuroprotectionthroughregulatingphosphorylatedtaulevelandpromotingadultendogenousneurogenesisaftercerebralischemiareperfusioninjury
AT zhengguoqing sanhuadecoctionaclassicherbalprescriptionexertsneuroprotectionthroughregulatingphosphorylatedtaulevelandpromotingadultendogenousneurogenesisaftercerebralischemiareperfusioninjury