Valeriana officinalis extract and its main component, valerenic acid, ameliorate d-galactose-induced reductions in memory, cell proliferation, and neuroblast differentiation by reducing corticosterone levels and lipid peroxidation

Valeriana officinalis is used in herbal medicine of many cultures as mild sedatives and tranquilizers. In this study, we investigated the effects of extract from valerian root extracts and its major component, valerenic acid on memory function, cell proliferation, neuroblast differentiation, serum c...

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Veröffentlicht in:Experimental gerontology 2013-11, Vol.48 (11), p.1369-1377
Hauptverfasser: Nam, Sung Min, Choi, Jung Hoon, Yoo, Dae Young, Kim, Woosuk, Jung, Hyo Young, Kim, Jong Whi, Kang, Soo-Yong, Park, Jaeil, Kim, Dong-Woo, Kim, Wan Jae, Yoon, Yeo Sung, Hwang, In Koo
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container_end_page 1377
container_issue 11
container_start_page 1369
container_title Experimental gerontology
container_volume 48
creator Nam, Sung Min
Choi, Jung Hoon
Yoo, Dae Young
Kim, Woosuk
Jung, Hyo Young
Kim, Jong Whi
Kang, Soo-Yong
Park, Jaeil
Kim, Dong-Woo
Kim, Wan Jae
Yoon, Yeo Sung
Hwang, In Koo
description Valeriana officinalis is used in herbal medicine of many cultures as mild sedatives and tranquilizers. In this study, we investigated the effects of extract from valerian root extracts and its major component, valerenic acid on memory function, cell proliferation, neuroblast differentiation, serum corticosterone, and lipid peroxidation in adult and aged mice. For the aging model, d-galactose (100mg/kg) was administered subcutaneously to 6-week-old male mice for 10weeks. At 13weeks of age, valerian root extracts (100mg/kg) or valerenic acid (340μg/kg) was administered orally to control and d-galactose-treated mice for 3weeks. The dosage of valerenic acid (340μg/kg), which is the active ingredient of valerian root extract, was determined by the content of valerenic acid in valerian root extract (3.401±0.066mg/g) measured by HPLC. The administration of valerian root extract and valerenic acid significantly improved the preferential exploration of new objects in novel object recognition test and the escape latency, swimming speeds, platform crossings, and spatial preference for the target quadrant in Morris water maze test compared to the d-galactose-treated mice. Cell proliferation and neuroblast differentiation were significantly decreased, while serum corticosterone level and lipid peroxidation in hippocampus were significantly increased in the d-galactose-treated group compared to that in the control group. The administration of valerian root extract significantly ameliorated these changes in the dentate gyrus of both control and d-galactose-treated groups. In addition, valerenic acid also mitigated the d-galactose-induced reduction of these changes. These results indicate that valerian root extract and valerenic acid enhance cognitive function, promote cell proliferation and neuroblast differentiation, and reduce serum corticosterone and lipid peroxidation in aged mice. •Valerian root extract (VE) has 3.401mg/g valerenic acid (VAL, an active ingredient).•VE and VAL improve the memory deficits induced by d-galactose.•VE and VAL ameliorated the reduction of neurogenesis induced by d-galactose.•VE and VAL decrease the serum corticosterone and lipid peroxidation in brain.
doi_str_mv 10.1016/j.exger.2013.09.002
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In this study, we investigated the effects of extract from valerian root extracts and its major component, valerenic acid on memory function, cell proliferation, neuroblast differentiation, serum corticosterone, and lipid peroxidation in adult and aged mice. For the aging model, d-galactose (100mg/kg) was administered subcutaneously to 6-week-old male mice for 10weeks. At 13weeks of age, valerian root extracts (100mg/kg) or valerenic acid (340μg/kg) was administered orally to control and d-galactose-treated mice for 3weeks. The dosage of valerenic acid (340μg/kg), which is the active ingredient of valerian root extract, was determined by the content of valerenic acid in valerian root extract (3.401±0.066mg/g) measured by HPLC. The administration of valerian root extract and valerenic acid significantly improved the preferential exploration of new objects in novel object recognition test and the escape latency, swimming speeds, platform crossings, and spatial preference for the target quadrant in Morris water maze test compared to the d-galactose-treated mice. Cell proliferation and neuroblast differentiation were significantly decreased, while serum corticosterone level and lipid peroxidation in hippocampus were significantly increased in the d-galactose-treated group compared to that in the control group. The administration of valerian root extract significantly ameliorated these changes in the dentate gyrus of both control and d-galactose-treated groups. In addition, valerenic acid also mitigated the d-galactose-induced reduction of these changes. 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In this study, we investigated the effects of extract from valerian root extracts and its major component, valerenic acid on memory function, cell proliferation, neuroblast differentiation, serum corticosterone, and lipid peroxidation in adult and aged mice. For the aging model, d-galactose (100mg/kg) was administered subcutaneously to 6-week-old male mice for 10weeks. At 13weeks of age, valerian root extracts (100mg/kg) or valerenic acid (340μg/kg) was administered orally to control and d-galactose-treated mice for 3weeks. The dosage of valerenic acid (340μg/kg), which is the active ingredient of valerian root extract, was determined by the content of valerenic acid in valerian root extract (3.401±0.066mg/g) measured by HPLC. The administration of valerian root extract and valerenic acid significantly improved the preferential exploration of new objects in novel object recognition test and the escape latency, swimming speeds, platform crossings, and spatial preference for the target quadrant in Morris water maze test compared to the d-galactose-treated mice. Cell proliferation and neuroblast differentiation were significantly decreased, while serum corticosterone level and lipid peroxidation in hippocampus were significantly increased in the d-galactose-treated group compared to that in the control group. The administration of valerian root extract significantly ameliorated these changes in the dentate gyrus of both control and d-galactose-treated groups. In addition, valerenic acid also mitigated the d-galactose-induced reduction of these changes. These results indicate that valerian root extract and valerenic acid enhance cognitive function, promote cell proliferation and neuroblast differentiation, and reduce serum corticosterone and lipid peroxidation in aged mice. •Valerian root extract (VE) has 3.401mg/g valerenic acid (VAL, an active ingredient).•VE and VAL improve the memory deficits induced by d-galactose.•VE and VAL ameliorated the reduction of neurogenesis induced by d-galactose.•VE and VAL decrease the serum corticosterone and lipid peroxidation in brain.</description><subject>Aging</subject><subject>Aging - metabolism</subject><subject>Aging - pathology</subject><subject>Aging - psychology</subject><subject>Animals</subject><subject>Cell Differentiation - drug effects</subject><subject>Cell Proliferation - drug effects</subject><subject>Corticosterone - blood</subject><subject>Dentate Gyrus - cytology</subject><subject>Dentate Gyrus - drug effects</subject><subject>Dentate Gyrus - metabolism</subject><subject>Galactose - pharmacology</subject><subject>Hippocampus</subject><subject>Indenes - pharmacology</subject><subject>Lipid peroxidation</subject><subject>Lipid Peroxidation - drug effects</subject><subject>Male</subject><subject>Memory - drug effects</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Neural Stem Cells - cytology</subject><subject>Neural Stem Cells - drug effects</subject><subject>Neurogenesis</subject><subject>Neurogenesis - drug effects</subject><subject>Neurogenesis - physiology</subject><subject>Nootropic Agents - pharmacology</subject><subject>Plant Extracts - pharmacology</subject><subject>Plants, Medicinal - chemistry</subject><subject>Serum corticosterone</subject><subject>Sesquiterpenes - pharmacology</subject><subject>Valerian - chemistry</subject><subject>Valerian root extract</subject><subject>Valeriana officinalis</subject><issn>0531-5565</issn><issn>1873-6815</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUr2OEzEQXiEQFwJPgIRcUmSDvV7vT0GBTsAhnUQDtJbXHkcTee1gO1HywjzHOclBeVQjeb6fGc9XVW8ZXTPKug_bNRw3ENcNZXxNxzWlzbNqwYae193AxPNqQQVntRCduKlepbSllHYNZy-rm6alQgjGFtWfX8pBROUVCdaiRq8cJgLHHJXORHlDMCcyK_REh3kXPPi8IoczCzxqojSaFVEzOAxRZSCm3ihXuCFBjd7sNRgSodSMwSdSdGaYQzytiAbnyC4GhxYKtbRXF0MP-xgmp1ImBq09G2W89Ml0umqh35RxYkYdUoZYpiIODuDSRcDhDg3ZlfcjmgvxdfXCKpfgzWNdVj-_fP5xe1fff__67fbTfa352OTa6n4EGBrWT0KMzTBNjaHKTq0ZbGMGMdq-b8XUasa4bfiopq4bgY-MDYYz0_Jl9f6qW9b6vYeU5YzpvKfyEPZJMsHboekF6_8PbVveUsqK1bLiV6iOIaUIVu4iziqeJKPynAW5lZcsyHMWJB1lyUJhvXs02E8zmH-cv8cvgI9XQPk3OGChJ43gy8Ewgs7SBHzS4AGLn80p</recordid><startdate>201311</startdate><enddate>201311</enddate><creator>Nam, Sung Min</creator><creator>Choi, Jung Hoon</creator><creator>Yoo, Dae Young</creator><creator>Kim, Woosuk</creator><creator>Jung, Hyo Young</creator><creator>Kim, Jong Whi</creator><creator>Kang, Soo-Yong</creator><creator>Park, Jaeil</creator><creator>Kim, Dong-Woo</creator><creator>Kim, Wan Jae</creator><creator>Yoon, Yeo Sung</creator><creator>Hwang, In Koo</creator><general>Elsevier Inc</general><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><scope>7TK</scope></search><sort><creationdate>201311</creationdate><title>Valeriana officinalis extract and its main component, valerenic acid, ameliorate d-galactose-induced reductions in memory, cell proliferation, and neuroblast differentiation by reducing corticosterone levels and lipid peroxidation</title><author>Nam, Sung Min ; Choi, Jung Hoon ; Yoo, Dae Young ; Kim, Woosuk ; Jung, Hyo Young ; Kim, Jong Whi ; Kang, Soo-Yong ; Park, Jaeil ; Kim, Dong-Woo ; Kim, Wan Jae ; Yoon, Yeo Sung ; Hwang, In Koo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c392t-fc79ee8217b55928bb2d0afb4d8f2d859f7745b4c113f239ab669e39118d31d43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Aging</topic><topic>Aging - metabolism</topic><topic>Aging - pathology</topic><topic>Aging - psychology</topic><topic>Animals</topic><topic>Cell Differentiation - drug effects</topic><topic>Cell Proliferation - drug effects</topic><topic>Corticosterone - blood</topic><topic>Dentate Gyrus - cytology</topic><topic>Dentate Gyrus - drug effects</topic><topic>Dentate Gyrus - metabolism</topic><topic>Galactose - pharmacology</topic><topic>Hippocampus</topic><topic>Indenes - pharmacology</topic><topic>Lipid peroxidation</topic><topic>Lipid Peroxidation - drug effects</topic><topic>Male</topic><topic>Memory - drug effects</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Neural Stem Cells - cytology</topic><topic>Neural Stem Cells - drug effects</topic><topic>Neurogenesis</topic><topic>Neurogenesis - drug effects</topic><topic>Neurogenesis - physiology</topic><topic>Nootropic Agents - pharmacology</topic><topic>Plant Extracts - pharmacology</topic><topic>Plants, Medicinal - chemistry</topic><topic>Serum corticosterone</topic><topic>Sesquiterpenes - pharmacology</topic><topic>Valerian - chemistry</topic><topic>Valerian root extract</topic><topic>Valeriana officinalis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nam, Sung Min</creatorcontrib><creatorcontrib>Choi, Jung Hoon</creatorcontrib><creatorcontrib>Yoo, Dae Young</creatorcontrib><creatorcontrib>Kim, Woosuk</creatorcontrib><creatorcontrib>Jung, Hyo Young</creatorcontrib><creatorcontrib>Kim, Jong Whi</creatorcontrib><creatorcontrib>Kang, Soo-Yong</creatorcontrib><creatorcontrib>Park, Jaeil</creatorcontrib><creatorcontrib>Kim, Dong-Woo</creatorcontrib><creatorcontrib>Kim, Wan Jae</creatorcontrib><creatorcontrib>Yoon, Yeo Sung</creatorcontrib><creatorcontrib>Hwang, In Koo</creatorcontrib><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><collection>Neurosciences Abstracts</collection><jtitle>Experimental gerontology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nam, Sung Min</au><au>Choi, Jung Hoon</au><au>Yoo, Dae Young</au><au>Kim, Woosuk</au><au>Jung, Hyo Young</au><au>Kim, Jong Whi</au><au>Kang, Soo-Yong</au><au>Park, Jaeil</au><au>Kim, Dong-Woo</au><au>Kim, Wan Jae</au><au>Yoon, Yeo Sung</au><au>Hwang, In Koo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Valeriana officinalis extract and its main component, valerenic acid, ameliorate d-galactose-induced reductions in memory, cell proliferation, and neuroblast differentiation by reducing corticosterone levels and lipid peroxidation</atitle><jtitle>Experimental gerontology</jtitle><addtitle>Exp Gerontol</addtitle><date>2013-11</date><risdate>2013</risdate><volume>48</volume><issue>11</issue><spage>1369</spage><epage>1377</epage><pages>1369-1377</pages><issn>0531-5565</issn><eissn>1873-6815</eissn><abstract>Valeriana officinalis is used in herbal medicine of many cultures as mild sedatives and tranquilizers. In this study, we investigated the effects of extract from valerian root extracts and its major component, valerenic acid on memory function, cell proliferation, neuroblast differentiation, serum corticosterone, and lipid peroxidation in adult and aged mice. For the aging model, d-galactose (100mg/kg) was administered subcutaneously to 6-week-old male mice for 10weeks. At 13weeks of age, valerian root extracts (100mg/kg) or valerenic acid (340μg/kg) was administered orally to control and d-galactose-treated mice for 3weeks. The dosage of valerenic acid (340μg/kg), which is the active ingredient of valerian root extract, was determined by the content of valerenic acid in valerian root extract (3.401±0.066mg/g) measured by HPLC. The administration of valerian root extract and valerenic acid significantly improved the preferential exploration of new objects in novel object recognition test and the escape latency, swimming speeds, platform crossings, and spatial preference for the target quadrant in Morris water maze test compared to the d-galactose-treated mice. Cell proliferation and neuroblast differentiation were significantly decreased, while serum corticosterone level and lipid peroxidation in hippocampus were significantly increased in the d-galactose-treated group compared to that in the control group. The administration of valerian root extract significantly ameliorated these changes in the dentate gyrus of both control and d-galactose-treated groups. In addition, valerenic acid also mitigated the d-galactose-induced reduction of these changes. These results indicate that valerian root extract and valerenic acid enhance cognitive function, promote cell proliferation and neuroblast differentiation, and reduce serum corticosterone and lipid peroxidation in aged mice. •Valerian root extract (VE) has 3.401mg/g valerenic acid (VAL, an active ingredient).•VE and VAL improve the memory deficits induced by d-galactose.•VE and VAL ameliorated the reduction of neurogenesis induced by d-galactose.•VE and VAL decrease the serum corticosterone and lipid peroxidation in brain.</abstract><cop>England</cop><pub>Elsevier Inc</pub><pmid>24055511</pmid><doi>10.1016/j.exger.2013.09.002</doi><tpages>9</tpages></addata></record>
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subjects Aging
Aging - metabolism
Aging - pathology
Aging - psychology
Animals
Cell Differentiation - drug effects
Cell Proliferation - drug effects
Corticosterone - blood
Dentate Gyrus - cytology
Dentate Gyrus - drug effects
Dentate Gyrus - metabolism
Galactose - pharmacology
Hippocampus
Indenes - pharmacology
Lipid peroxidation
Lipid Peroxidation - drug effects
Male
Memory - drug effects
Mice
Mice, Inbred C57BL
Neural Stem Cells - cytology
Neural Stem Cells - drug effects
Neurogenesis
Neurogenesis - drug effects
Neurogenesis - physiology
Nootropic Agents - pharmacology
Plant Extracts - pharmacology
Plants, Medicinal - chemistry
Serum corticosterone
Sesquiterpenes - pharmacology
Valerian - chemistry
Valerian root extract
Valeriana officinalis
title Valeriana officinalis extract and its main component, valerenic acid, ameliorate d-galactose-induced reductions in memory, cell proliferation, and neuroblast differentiation by reducing corticosterone levels and lipid peroxidation
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