Cryptotanshinone from Salviae Miltiorrhizae Radix Inhibits Sodium-nitroprusside-induced Apoptosis in Neuro-2a Cells

The root of Salvia miltiorrhiza (Salviae miltiorrhizae radix), a herbal medicine has widely been used for the treatment of pain, miscarriage and oedema. In this study, we evaluated the neuroprotective effect of cryptotanshinone (CRT) from Salviae miltiorrhizae radix on sodium‐nitroprusside (SNP)‐ind...

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Veröffentlicht in:Phytotherapy research 2012-08, Vol.26 (8), p.1211-1219
Hauptverfasser: Mahesh, Ramalingam, Jung, Hyo Won, Kim, Gun Woo, Kim, Young Shik, Park, Yong-Ki
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container_issue 8
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container_title Phytotherapy research
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creator Mahesh, Ramalingam
Jung, Hyo Won
Kim, Gun Woo
Kim, Young Shik
Park, Yong-Ki
description The root of Salvia miltiorrhiza (Salviae miltiorrhizae radix), a herbal medicine has widely been used for the treatment of pain, miscarriage and oedema. In this study, we evaluated the neuroprotective effect of cryptotanshinone (CRT) from Salviae miltiorrhizae radix on sodium‐nitroprusside (SNP)‐induced apoptosis in neuro‐2a (N2a) cells, and further investigated its action mechanism in signalling pathways. The effects of CRT against SNP‐induced toxicity, mitochondrial membrane potential (MMP) changes, and oxidants/antioxidant defences and apoptotic signalling pathways were investigated in N2a cells. Cryptotanshinone significantly inhibited SNP‐induced cell toxicity and the generation of reactive oxygen and nitrogen species (RONS), and improved MMP in N2a cells. Cryptotanshinone significantly suppressed SNP‐induced peroxidation of lipid and protein, and the expression of Gclc mRNA. In the signalling pathway, CRT effectively blocked SNP‐induced activation of NF‐κB and ERK1/2 and JNK MAPK pathways through the elevation of Akt and cyclic AMP response element binding protein. Furthermore, CRT remarkably reduced the increase of mitochondrial Bax/Bcl‐2 ratio, the release of cytochrome c from mitochondria to cytosol, and the activations of cytosolic procaspase‐3 and nuclear inactive poly ADP (adenosine diphosphate)‐ribose polymerase by SNP‐induced apoptosis. These results indicate that CRT has neuroprotective effects against SNP‐induced apoptosis in neuronal cells via the regulation of mitochondrial apoptotic cascades and antiapoptotic cellular signalling pathways. Copyright © 2012 John Wiley & Sons, Ltd.
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In this study, we evaluated the neuroprotective effect of cryptotanshinone (CRT) from Salviae miltiorrhizae radix on sodium‐nitroprusside (SNP)‐induced apoptosis in neuro‐2a (N2a) cells, and further investigated its action mechanism in signalling pathways. The effects of CRT against SNP‐induced toxicity, mitochondrial membrane potential (MMP) changes, and oxidants/antioxidant defences and apoptotic signalling pathways were investigated in N2a cells. Cryptotanshinone significantly inhibited SNP‐induced cell toxicity and the generation of reactive oxygen and nitrogen species (RONS), and improved MMP in N2a cells. Cryptotanshinone significantly suppressed SNP‐induced peroxidation of lipid and protein, and the expression of Gclc mRNA. In the signalling pathway, CRT effectively blocked SNP‐induced activation of NF‐κB and ERK1/2 and JNK MAPK pathways through the elevation of Akt and cyclic AMP response element binding protein. Furthermore, CRT remarkably reduced the increase of mitochondrial Bax/Bcl‐2 ratio, the release of cytochrome c from mitochondria to cytosol, and the activations of cytosolic procaspase‐3 and nuclear inactive poly ADP (adenosine diphosphate)‐ribose polymerase by SNP‐induced apoptosis. These results indicate that CRT has neuroprotective effects against SNP‐induced apoptosis in neuronal cells via the regulation of mitochondrial apoptotic cascades and antiapoptotic cellular signalling pathways. 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Res</addtitle><description>The root of Salvia miltiorrhiza (Salviae miltiorrhizae radix), a herbal medicine has widely been used for the treatment of pain, miscarriage and oedema. In this study, we evaluated the neuroprotective effect of cryptotanshinone (CRT) from Salviae miltiorrhizae radix on sodium‐nitroprusside (SNP)‐induced apoptosis in neuro‐2a (N2a) cells, and further investigated its action mechanism in signalling pathways. The effects of CRT against SNP‐induced toxicity, mitochondrial membrane potential (MMP) changes, and oxidants/antioxidant defences and apoptotic signalling pathways were investigated in N2a cells. Cryptotanshinone significantly inhibited SNP‐induced cell toxicity and the generation of reactive oxygen and nitrogen species (RONS), and improved MMP in N2a cells. Cryptotanshinone significantly suppressed SNP‐induced peroxidation of lipid and protein, and the expression of Gclc mRNA. In the signalling pathway, CRT effectively blocked SNP‐induced activation of NF‐κB and ERK1/2 and JNK MAPK pathways through the elevation of Akt and cyclic AMP response element binding protein. Furthermore, CRT remarkably reduced the increase of mitochondrial Bax/Bcl‐2 ratio, the release of cytochrome c from mitochondria to cytosol, and the activations of cytosolic procaspase‐3 and nuclear inactive poly ADP (adenosine diphosphate)‐ribose polymerase by SNP‐induced apoptosis. These results indicate that CRT has neuroprotective effects against SNP‐induced apoptosis in neuronal cells via the regulation of mitochondrial apoptotic cascades and antiapoptotic cellular signalling pathways. Copyright © 2012 John Wiley &amp; Sons, Ltd.</description><subject>Animals</subject><subject>Antineoplastic Agents, Phytogenic - pharmacology</subject><subject>apoptosis</subject><subject>Apoptosis - drug effects</subject><subject>Biological and medical sciences</subject><subject>Caspase 3 - metabolism</subject><subject>Cell Line, Tumor</subject><subject>Cell Survival</subject><subject>cryptotanshinone</subject><subject>Cytosol - metabolism</subject><subject>Drug Evaluation, Preclinical</subject><subject>General pharmacology</subject><subject>Glutamate-Cysteine Ligase - genetics</subject><subject>Glutamate-Cysteine Ligase - metabolism</subject><subject>Lipid Peroxidation</subject><subject>MAP Kinase Signaling System</subject><subject>Medical sciences</subject><subject>Membrane Potential, Mitochondrial - drug effects</subject><subject>Mice</subject><subject>mitochondria</subject><subject>Mitochondria - drug effects</subject><subject>Mitochondria - metabolism</subject><subject>Neuroblastoma - genetics</subject><subject>Neuroblastoma - metabolism</subject><subject>Neuroblastoma - pathology</subject><subject>Neuroprotective Agents - pharmacology</subject><subject>NF-kappa B - antagonists &amp; inhibitors</subject><subject>NF-kappa B - metabolism</subject><subject>Nitroprusside - adverse effects</subject><subject>Pharmacognosy. Homeopathy. Health food</subject><subject>Pharmacology. Drug treatments</subject><subject>Phenanthrenes - pharmacology</subject><subject>Reactive Nitrogen Species - metabolism</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>RNA, Messenger - genetics</subject><subject>Salvia miltiorrhiza</subject><subject>Salvia miltiorrhiza - chemistry</subject><subject>Salviae miltiorrhizae radix</subject><subject>sodium nitroprusside</subject><issn>0951-418X</issn><issn>1099-1573</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10E1PGzEQBmALFUFIK_UXVL5U4uLgj_U6PqK0hK_SioDCzXLWXmXazXpl7wLh17MoIZw6l9FIj96RXoS-MjpilPKTpo0joajcQwNGtSZMKvEJDaiWjGRs_HCIjlL6SynVnGYH6JD3M5Y6H6A0ieumDa2t0xLqUHtcxrDCM1s9gvX4F1QthBiX8NJft9bBM76ol7CANuFZcNCtSA1tDE3sUgLnCdSuK7zDp03ocxMkDDW-8V0MhFs88VWVPqP90lbJf9nuIbo_-3k3OSfXv6cXk9NrUvBxLonwWroFK2lROM0E81YwJlRWWs1VyRSTVgmtrM00z7SgIl8wIbTOM1dSzqUYouNNbhFDStGXpomwsnFtGDVvvZm-N_PWW0-_bWjTLVbe7eB7UT34vgU2FbYqo60LSB8u53kmNO0d2bgnqPz6vw_Nn7vb7eOth9T655238Z_JlVDSzG-mhk8vx2x2NTc_xCuN1ZQx</recordid><startdate>201208</startdate><enddate>201208</enddate><creator>Mahesh, Ramalingam</creator><creator>Jung, Hyo Won</creator><creator>Kim, Gun Woo</creator><creator>Kim, Young Shik</creator><creator>Park, Yong-Ki</creator><general>John Wiley &amp; Sons, Ltd</general><general>Wiley</general><scope>BSCLL</scope><scope>IQODW</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></search><sort><creationdate>201208</creationdate><title>Cryptotanshinone from Salviae Miltiorrhizae Radix Inhibits Sodium-nitroprusside-induced Apoptosis in Neuro-2a Cells</title><author>Mahesh, Ramalingam ; Jung, Hyo Won ; Kim, Gun Woo ; Kim, Young Shik ; Park, Yong-Ki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2865-3e95db1f0ccd9131ea311374fa927f1715a7397aa492493036b1339964df02253</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Animals</topic><topic>Antineoplastic Agents, Phytogenic - pharmacology</topic><topic>apoptosis</topic><topic>Apoptosis - drug effects</topic><topic>Biological and medical sciences</topic><topic>Caspase 3 - metabolism</topic><topic>Cell Line, Tumor</topic><topic>Cell Survival</topic><topic>cryptotanshinone</topic><topic>Cytosol - metabolism</topic><topic>Drug Evaluation, Preclinical</topic><topic>General pharmacology</topic><topic>Glutamate-Cysteine Ligase - genetics</topic><topic>Glutamate-Cysteine Ligase - metabolism</topic><topic>Lipid Peroxidation</topic><topic>MAP Kinase Signaling System</topic><topic>Medical sciences</topic><topic>Membrane Potential, Mitochondrial - drug effects</topic><topic>Mice</topic><topic>mitochondria</topic><topic>Mitochondria - drug effects</topic><topic>Mitochondria - metabolism</topic><topic>Neuroblastoma - genetics</topic><topic>Neuroblastoma - metabolism</topic><topic>Neuroblastoma - pathology</topic><topic>Neuroprotective Agents - pharmacology</topic><topic>NF-kappa B - antagonists &amp; inhibitors</topic><topic>NF-kappa B - metabolism</topic><topic>Nitroprusside - adverse effects</topic><topic>Pharmacognosy. Homeopathy. Health food</topic><topic>Pharmacology. Drug treatments</topic><topic>Phenanthrenes - pharmacology</topic><topic>Reactive Nitrogen Species - metabolism</topic><topic>Reactive Oxygen Species - metabolism</topic><topic>RNA, Messenger - genetics</topic><topic>Salvia miltiorrhiza</topic><topic>Salvia miltiorrhiza - chemistry</topic><topic>Salviae miltiorrhizae radix</topic><topic>sodium nitroprusside</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mahesh, Ramalingam</creatorcontrib><creatorcontrib>Jung, Hyo Won</creatorcontrib><creatorcontrib>Kim, Gun Woo</creatorcontrib><creatorcontrib>Kim, Young Shik</creatorcontrib><creatorcontrib>Park, Yong-Ki</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Phytotherapy research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mahesh, Ramalingam</au><au>Jung, Hyo Won</au><au>Kim, Gun Woo</au><au>Kim, Young Shik</au><au>Park, Yong-Ki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cryptotanshinone from Salviae Miltiorrhizae Radix Inhibits Sodium-nitroprusside-induced Apoptosis in Neuro-2a Cells</atitle><jtitle>Phytotherapy research</jtitle><addtitle>Phytother. Res</addtitle><date>2012-08</date><risdate>2012</risdate><volume>26</volume><issue>8</issue><spage>1211</spage><epage>1219</epage><pages>1211-1219</pages><issn>0951-418X</issn><eissn>1099-1573</eissn><abstract>The root of Salvia miltiorrhiza (Salviae miltiorrhizae radix), a herbal medicine has widely been used for the treatment of pain, miscarriage and oedema. In this study, we evaluated the neuroprotective effect of cryptotanshinone (CRT) from Salviae miltiorrhizae radix on sodium‐nitroprusside (SNP)‐induced apoptosis in neuro‐2a (N2a) cells, and further investigated its action mechanism in signalling pathways. The effects of CRT against SNP‐induced toxicity, mitochondrial membrane potential (MMP) changes, and oxidants/antioxidant defences and apoptotic signalling pathways were investigated in N2a cells. Cryptotanshinone significantly inhibited SNP‐induced cell toxicity and the generation of reactive oxygen and nitrogen species (RONS), and improved MMP in N2a cells. Cryptotanshinone significantly suppressed SNP‐induced peroxidation of lipid and protein, and the expression of Gclc mRNA. In the signalling pathway, CRT effectively blocked SNP‐induced activation of NF‐κB and ERK1/2 and JNK MAPK pathways through the elevation of Akt and cyclic AMP response element binding protein. Furthermore, CRT remarkably reduced the increase of mitochondrial Bax/Bcl‐2 ratio, the release of cytochrome c from mitochondria to cytosol, and the activations of cytosolic procaspase‐3 and nuclear inactive poly ADP (adenosine diphosphate)‐ribose polymerase by SNP‐induced apoptosis. These results indicate that CRT has neuroprotective effects against SNP‐induced apoptosis in neuronal cells via the regulation of mitochondrial apoptotic cascades and antiapoptotic cellular signalling pathways. Copyright © 2012 John Wiley &amp; Sons, Ltd.</abstract><cop>Chichester, UK</cop><pub>John Wiley &amp; Sons, Ltd</pub><pmid>22228596</pmid><doi>10.1002/ptr.3705</doi><tpages>9</tpages></addata></record>
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subjects Animals
Antineoplastic Agents, Phytogenic - pharmacology
apoptosis
Apoptosis - drug effects
Biological and medical sciences
Caspase 3 - metabolism
Cell Line, Tumor
Cell Survival
cryptotanshinone
Cytosol - metabolism
Drug Evaluation, Preclinical
General pharmacology
Glutamate-Cysteine Ligase - genetics
Glutamate-Cysteine Ligase - metabolism
Lipid Peroxidation
MAP Kinase Signaling System
Medical sciences
Membrane Potential, Mitochondrial - drug effects
Mice
mitochondria
Mitochondria - drug effects
Mitochondria - metabolism
Neuroblastoma - genetics
Neuroblastoma - metabolism
Neuroblastoma - pathology
Neuroprotective Agents - pharmacology
NF-kappa B - antagonists & inhibitors
NF-kappa B - metabolism
Nitroprusside - adverse effects
Pharmacognosy. Homeopathy. Health food
Pharmacology. Drug treatments
Phenanthrenes - pharmacology
Reactive Nitrogen Species - metabolism
Reactive Oxygen Species - metabolism
RNA, Messenger - genetics
Salvia miltiorrhiza
Salvia miltiorrhiza - chemistry
Salviae miltiorrhizae radix
sodium nitroprusside
title Cryptotanshinone from Salviae Miltiorrhizae Radix Inhibits Sodium-nitroprusside-induced Apoptosis in Neuro-2a Cells
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