Paeoniflorin Improves Regional Cerebral Blood Flow and Suppresses Inflammatory Factors in the Hippocampus of Rats with Vascular Dementia
Objective: To explore the delayed neuroprotection induced by paeoniflorin(PF), the principal component of Paeoniae radix prescribed in Chinese medicine, and its underlying mechanisms in rats subjected to vascular dementia(VD). Methods: A rat model of VD was induced by bilateral common carotid arteri...
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description | Objective: To explore the delayed neuroprotection induced by paeoniflorin(PF), the principal component of Paeoniae radix prescribed in Chinese medicine, and its underlying mechanisms in rats subjected to vascular dementia(VD). Methods: A rat model of VD was induced by bilateral common carotid arteries occlusion(BCCAO). Low-dose or high-dose PF(20 or 40 mg/kg once per day) was administrated for 28 days after VD. The behavioral analysis of rat was measured by water morris. Regional cerebral blood volume(r CBV), regional cerebral blood flow(r CBF) and mean transit time(MTT) were measured in the bilateral hippocampus by perfusion-weighted imaging(PWI). The levels of interleukin-1β(IL-1β), interleukin-6(IL-6), and tumor necrosis factor alpha(TNF-α) were measured by commercially available enzyme-linked immunosorbent assay kits. Protein levels were evaluated by western blot analysis. m RNA levels were evaluated by real time-polymerase chain reaction. Western blotting was used to estimate p65 translocation. Results: The behavioral analysis showed that PF could decrease the escape latency time(P〈0.05), and increase the residence time of the original platform quadrant and the across platform frequency in water maze in VD rats(P〈0.05). Likewise, PF remarkably promoted the r CBV(P〈0.05), r CBF and decreased per minute MTT(P〈0.05) in hippocampus of VD rats. Furthermore, PF decreased the release of IL-1β, IL-6 and TNF-α as well as inhibited the m RNA expression of IL-1β, IL-6 and TNF-α in the hippocampus of VD rats(P〈0.05 or P〈0.01). PF also could decrease the protein expressions of inducible nitric oxide synthase and cyclooxygenase-2 in the hippocampus of VD rats(P〈0.05 or P〈0.01). In addition, PF significantly inhibited the nuclear factor κB(NF-κB) pathway in the hippocampus of VD rats. Conclusions: PF significantly attenuates cognitive impairment, improves hippocampus perfusion and inhibits inflammatory response in VD rats. In addition, the anti-inflammatory effects of PF might be due to inhibiting the NF-κB pathway. PF may be a potential clinical application in improving VD. |
doi_str_mv | 10.1007/s11655-015-2124-3 |
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Methods: A rat model of VD was induced by bilateral common carotid arteries occlusion(BCCAO). Low-dose or high-dose PF(20 or 40 mg/kg once per day) was administrated for 28 days after VD. The behavioral analysis of rat was measured by water morris. Regional cerebral blood volume(r CBV), regional cerebral blood flow(r CBF) and mean transit time(MTT) were measured in the bilateral hippocampus by perfusion-weighted imaging(PWI). The levels of interleukin-1β(IL-1β), interleukin-6(IL-6), and tumor necrosis factor alpha(TNF-α) were measured by commercially available enzyme-linked immunosorbent assay kits. Protein levels were evaluated by western blot analysis. m RNA levels were evaluated by real time-polymerase chain reaction. Western blotting was used to estimate p65 translocation. Results: The behavioral analysis showed that PF could decrease the escape latency time(P〈0.05), and increase the residence time of the original platform quadrant and the across platform frequency in water maze in VD rats(P〈0.05). Likewise, PF remarkably promoted the r CBV(P〈0.05), r CBF and decreased per minute MTT(P〈0.05) in hippocampus of VD rats. Furthermore, PF decreased the release of IL-1β, IL-6 and TNF-α as well as inhibited the m RNA expression of IL-1β, IL-6 and TNF-α in the hippocampus of VD rats(P〈0.05 or P〈0.01). PF also could decrease the protein expressions of inducible nitric oxide synthase and cyclooxygenase-2 in the hippocampus of VD rats(P〈0.05 or P〈0.01). In addition, PF significantly inhibited the nuclear factor κB(NF-κB) pathway in the hippocampus of VD rats. Conclusions: PF significantly attenuates cognitive impairment, improves hippocampus perfusion and inhibits inflammatory response in VD rats. In addition, the anti-inflammatory effects of PF might be due to inhibiting the NF-κB pathway. PF may be a potential clinical application in improving VD.</description><identifier>ISSN: 1672-0415</identifier><identifier>EISSN: 1993-0402</identifier><identifier>DOI: 10.1007/s11655-015-2124-3</identifier><identifier>PMID: 26577108</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Animals ; Cerebrovascular Circulation - drug effects ; Cognitive Dysfunction - complications ; Cognitive Dysfunction - drug therapy ; Cognitive Dysfunction - physiopathology ; Cyclooxygenase 2 - metabolism ; Dementia, Vascular - drug therapy ; Dementia, Vascular - enzymology ; Dementia, Vascular - pathology ; Down-Regulation - drug effects ; Glucosides - chemistry ; Glucosides - pharmacology ; Glucosides - therapeutic use ; Hippocampus - blood supply ; Hippocampus - drug effects ; Hippocampus - pathology ; Inflammation Mediators - metabolism ; Male ; Maze Learning - drug effects ; Medicine ; Medicine & Public Health ; Memory Disorders - complications ; Memory Disorders - drug therapy ; Memory Disorders - physiopathology ; Monoterpenes - chemistry ; Monoterpenes - pharmacology ; Monoterpenes - therapeutic use ; Nitric Oxide Synthase Type II - metabolism ; Original Article ; Rats, Sprague-Dawley ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; Transcription Factor RelA - metabolism ; Western印迹法 ; 大鼠 ; 海马 ; 炎症因子 ; 芍药苷 ; 血流量 ; 血管性痴呆 ; 酶联免疫吸附测定</subject><ispartof>Chinese journal of integrative medicine, 2017-09, Vol.23 (9), p.696-702</ispartof><rights>Chinese Association of the Integration of Traditional and Western Medicine and Springer-Verlag Berlin Heidelberg 2017</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c371t-25757099014e75bce5357b08263228577eda046a8e15d8cc39d1d960f84ed90b3</citedby><cites>FETCH-LOGICAL-c371t-25757099014e75bce5357b08263228577eda046a8e15d8cc39d1d960f84ed90b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/86437A/86437A.jpg</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11655-015-2124-3$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11655-015-2124-3$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26577108$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Li-gong</creatorcontrib><creatorcontrib>Wang, Li-jun</creatorcontrib><creatorcontrib>Shen, Qing-qing</creatorcontrib><creatorcontrib>Wang, Hao-feng</creatorcontrib><creatorcontrib>Zhang, Ying</creatorcontrib><creatorcontrib>Shi, Cui-ge</creatorcontrib><creatorcontrib>Zhang, Shu-cheng</creatorcontrib><creatorcontrib>Zhang, Meng-yuan</creatorcontrib><title>Paeoniflorin Improves Regional Cerebral Blood Flow and Suppresses Inflammatory Factors in the Hippocampus of Rats with Vascular Dementia</title><title>Chinese journal of integrative medicine</title><addtitle>Chin. J. Integr. Med</addtitle><addtitle>Chinese Journal of Integrative Medicine</addtitle><description>Objective: To explore the delayed neuroprotection induced by paeoniflorin(PF), the principal component of Paeoniae radix prescribed in Chinese medicine, and its underlying mechanisms in rats subjected to vascular dementia(VD). Methods: A rat model of VD was induced by bilateral common carotid arteries occlusion(BCCAO). Low-dose or high-dose PF(20 or 40 mg/kg once per day) was administrated for 28 days after VD. The behavioral analysis of rat was measured by water morris. Regional cerebral blood volume(r CBV), regional cerebral blood flow(r CBF) and mean transit time(MTT) were measured in the bilateral hippocampus by perfusion-weighted imaging(PWI). The levels of interleukin-1β(IL-1β), interleukin-6(IL-6), and tumor necrosis factor alpha(TNF-α) were measured by commercially available enzyme-linked immunosorbent assay kits. Protein levels were evaluated by western blot analysis. m RNA levels were evaluated by real time-polymerase chain reaction. Western blotting was used to estimate p65 translocation. Results: The behavioral analysis showed that PF could decrease the escape latency time(P〈0.05), and increase the residence time of the original platform quadrant and the across platform frequency in water maze in VD rats(P〈0.05). Likewise, PF remarkably promoted the r CBV(P〈0.05), r CBF and decreased per minute MTT(P〈0.05) in hippocampus of VD rats. Furthermore, PF decreased the release of IL-1β, IL-6 and TNF-α as well as inhibited the m RNA expression of IL-1β, IL-6 and TNF-α in the hippocampus of VD rats(P〈0.05 or P〈0.01). PF also could decrease the protein expressions of inducible nitric oxide synthase and cyclooxygenase-2 in the hippocampus of VD rats(P〈0.05 or P〈0.01). In addition, PF significantly inhibited the nuclear factor κB(NF-κB) pathway in the hippocampus of VD rats. Conclusions: PF significantly attenuates cognitive impairment, improves hippocampus perfusion and inhibits inflammatory response in VD rats. In addition, the anti-inflammatory effects of PF might be due to inhibiting the NF-κB pathway. PF may be a potential clinical application in improving VD.</description><subject>Animals</subject><subject>Cerebrovascular Circulation - drug effects</subject><subject>Cognitive Dysfunction - complications</subject><subject>Cognitive Dysfunction - drug therapy</subject><subject>Cognitive Dysfunction - physiopathology</subject><subject>Cyclooxygenase 2 - metabolism</subject><subject>Dementia, Vascular - drug therapy</subject><subject>Dementia, Vascular - enzymology</subject><subject>Dementia, Vascular - pathology</subject><subject>Down-Regulation - drug effects</subject><subject>Glucosides - chemistry</subject><subject>Glucosides - pharmacology</subject><subject>Glucosides - therapeutic use</subject><subject>Hippocampus - blood supply</subject><subject>Hippocampus - drug effects</subject><subject>Hippocampus - pathology</subject><subject>Inflammation Mediators - metabolism</subject><subject>Male</subject><subject>Maze Learning - drug effects</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Memory Disorders - complications</subject><subject>Memory Disorders - drug therapy</subject><subject>Memory Disorders - physiopathology</subject><subject>Monoterpenes - chemistry</subject><subject>Monoterpenes - pharmacology</subject><subject>Monoterpenes - therapeutic use</subject><subject>Nitric Oxide Synthase Type II - metabolism</subject><subject>Original Article</subject><subject>Rats, Sprague-Dawley</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>Transcription Factor RelA - metabolism</subject><subject>Western印迹法</subject><subject>大鼠</subject><subject>海马</subject><subject>炎症因子</subject><subject>芍药苷</subject><subject>血流量</subject><subject>血管性痴呆</subject><subject>酶联免疫吸附测定</subject><issn>1672-0415</issn><issn>1993-0402</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc1u1DAUhSNERX_gAdggixWbwLUd28kSpkw7UqVW5WdrOc7NTCrHTu2Eqm_AY9fVDF2yukfyOZ987ymK9xQ-UwD1JVEqhSiBipJRVpX8VXFCm4aXUAF7nbVULGsqjovTlO4AhJIg3hTHTAqlKNQnxd8bg8EPvQtx8GQzTjH8wURucTsEbxxZYcQ2ZvHNhdCRtQsPxPiO_FimKWJK2bvxvTPjaOYQH8na2DwTybB5h-RymKZgzTgtiYSe3Jo5kYdh3pHfJtnFmUjOcUQ_D-ZtcdQbl_DdYZ4Vv9bff64uy6vri83q61VpuaJzyYQSCpoGaIVKtBYFF6qFmknOWJ23ws5AJU2NVHS1tbzpaNdI6OsKuwZaflZ82nPzpvcLplmPQ7LonPEYlqRpRkkOombZSvdWG0NKEXs9xWE08VFT0M8F6H0BOhegnwvQPGc-HPBLO2L3kvh38Wxge0PKT36LUd-FJeZTp_9SPx5-sgt-e59zL2CpOEhBOedP7cmdDg</recordid><startdate>20170901</startdate><enddate>20170901</enddate><creator>Zhang, Li-gong</creator><creator>Wang, Li-jun</creator><creator>Shen, Qing-qing</creator><creator>Wang, Hao-feng</creator><creator>Zhang, Ying</creator><creator>Shi, Cui-ge</creator><creator>Zhang, Shu-cheng</creator><creator>Zhang, Meng-yuan</creator><general>Springer Berlin Heidelberg</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W91</scope><scope>~WA</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20170901</creationdate><title>Paeoniflorin Improves Regional Cerebral Blood Flow and Suppresses Inflammatory Factors in the Hippocampus of Rats with Vascular Dementia</title><author>Zhang, Li-gong ; Wang, Li-jun ; Shen, Qing-qing ; Wang, Hao-feng ; Zhang, Ying ; Shi, Cui-ge ; Zhang, Shu-cheng ; Zhang, Meng-yuan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c371t-25757099014e75bce5357b08263228577eda046a8e15d8cc39d1d960f84ed90b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Animals</topic><topic>Cerebrovascular Circulation - drug effects</topic><topic>Cognitive Dysfunction - complications</topic><topic>Cognitive Dysfunction - drug therapy</topic><topic>Cognitive Dysfunction - physiopathology</topic><topic>Cyclooxygenase 2 - metabolism</topic><topic>Dementia, Vascular - drug therapy</topic><topic>Dementia, Vascular - enzymology</topic><topic>Dementia, Vascular - pathology</topic><topic>Down-Regulation - drug effects</topic><topic>Glucosides - chemistry</topic><topic>Glucosides - pharmacology</topic><topic>Glucosides - therapeutic use</topic><topic>Hippocampus - blood supply</topic><topic>Hippocampus - drug effects</topic><topic>Hippocampus - pathology</topic><topic>Inflammation Mediators - metabolism</topic><topic>Male</topic><topic>Maze Learning - drug effects</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Memory Disorders - complications</topic><topic>Memory Disorders - drug therapy</topic><topic>Memory Disorders - physiopathology</topic><topic>Monoterpenes - chemistry</topic><topic>Monoterpenes - pharmacology</topic><topic>Monoterpenes - therapeutic use</topic><topic>Nitric Oxide Synthase Type II - metabolism</topic><topic>Original Article</topic><topic>Rats, Sprague-Dawley</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Messenger - metabolism</topic><topic>Transcription Factor RelA - metabolism</topic><topic>Western印迹法</topic><topic>大鼠</topic><topic>海马</topic><topic>炎症因子</topic><topic>芍药苷</topic><topic>血流量</topic><topic>血管性痴呆</topic><topic>酶联免疫吸附测定</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Li-gong</creatorcontrib><creatorcontrib>Wang, Li-jun</creatorcontrib><creatorcontrib>Shen, Qing-qing</creatorcontrib><creatorcontrib>Wang, Hao-feng</creatorcontrib><creatorcontrib>Zhang, Ying</creatorcontrib><creatorcontrib>Shi, Cui-ge</creatorcontrib><creatorcontrib>Zhang, Shu-cheng</creatorcontrib><creatorcontrib>Zhang, Meng-yuan</creatorcontrib><collection>中文科技期刊数据库</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>中文科技期刊数据库-7.0平台</collection><collection>中文科技期刊数据库-医药卫生</collection><collection>中文科技期刊数据库- 镜像站点</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Chinese journal of integrative medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Li-gong</au><au>Wang, Li-jun</au><au>Shen, Qing-qing</au><au>Wang, Hao-feng</au><au>Zhang, Ying</au><au>Shi, Cui-ge</au><au>Zhang, Shu-cheng</au><au>Zhang, Meng-yuan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Paeoniflorin Improves Regional Cerebral Blood Flow and Suppresses Inflammatory Factors in the Hippocampus of Rats with Vascular Dementia</atitle><jtitle>Chinese journal of integrative medicine</jtitle><stitle>Chin. J. Integr. Med</stitle><addtitle>Chinese Journal of Integrative Medicine</addtitle><date>2017-09-01</date><risdate>2017</risdate><volume>23</volume><issue>9</issue><spage>696</spage><epage>702</epage><pages>696-702</pages><issn>1672-0415</issn><eissn>1993-0402</eissn><abstract>Objective: To explore the delayed neuroprotection induced by paeoniflorin(PF), the principal component of Paeoniae radix prescribed in Chinese medicine, and its underlying mechanisms in rats subjected to vascular dementia(VD). Methods: A rat model of VD was induced by bilateral common carotid arteries occlusion(BCCAO). Low-dose or high-dose PF(20 or 40 mg/kg once per day) was administrated for 28 days after VD. The behavioral analysis of rat was measured by water morris. Regional cerebral blood volume(r CBV), regional cerebral blood flow(r CBF) and mean transit time(MTT) were measured in the bilateral hippocampus by perfusion-weighted imaging(PWI). The levels of interleukin-1β(IL-1β), interleukin-6(IL-6), and tumor necrosis factor alpha(TNF-α) were measured by commercially available enzyme-linked immunosorbent assay kits. Protein levels were evaluated by western blot analysis. m RNA levels were evaluated by real time-polymerase chain reaction. Western blotting was used to estimate p65 translocation. Results: The behavioral analysis showed that PF could decrease the escape latency time(P〈0.05), and increase the residence time of the original platform quadrant and the across platform frequency in water maze in VD rats(P〈0.05). Likewise, PF remarkably promoted the r CBV(P〈0.05), r CBF and decreased per minute MTT(P〈0.05) in hippocampus of VD rats. Furthermore, PF decreased the release of IL-1β, IL-6 and TNF-α as well as inhibited the m RNA expression of IL-1β, IL-6 and TNF-α in the hippocampus of VD rats(P〈0.05 or P〈0.01). PF also could decrease the protein expressions of inducible nitric oxide synthase and cyclooxygenase-2 in the hippocampus of VD rats(P〈0.05 or P〈0.01). In addition, PF significantly inhibited the nuclear factor κB(NF-κB) pathway in the hippocampus of VD rats. Conclusions: PF significantly attenuates cognitive impairment, improves hippocampus perfusion and inhibits inflammatory response in VD rats. In addition, the anti-inflammatory effects of PF might be due to inhibiting the NF-κB pathway. PF may be a potential clinical application in improving VD.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>26577108</pmid><doi>10.1007/s11655-015-2124-3</doi><tpages>7</tpages></addata></record> |
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subjects | Animals Cerebrovascular Circulation - drug effects Cognitive Dysfunction - complications Cognitive Dysfunction - drug therapy Cognitive Dysfunction - physiopathology Cyclooxygenase 2 - metabolism Dementia, Vascular - drug therapy Dementia, Vascular - enzymology Dementia, Vascular - pathology Down-Regulation - drug effects Glucosides - chemistry Glucosides - pharmacology Glucosides - therapeutic use Hippocampus - blood supply Hippocampus - drug effects Hippocampus - pathology Inflammation Mediators - metabolism Male Maze Learning - drug effects Medicine Medicine & Public Health Memory Disorders - complications Memory Disorders - drug therapy Memory Disorders - physiopathology Monoterpenes - chemistry Monoterpenes - pharmacology Monoterpenes - therapeutic use Nitric Oxide Synthase Type II - metabolism Original Article Rats, Sprague-Dawley RNA, Messenger - genetics RNA, Messenger - metabolism Transcription Factor RelA - metabolism Western印迹法 大鼠 海马 炎症因子 芍药苷 血流量 血管性痴呆 酶联免疫吸附测定 |
title | Paeoniflorin Improves Regional Cerebral Blood Flow and Suppresses Inflammatory Factors in the Hippocampus of Rats with Vascular Dementia |
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