Cardiovascular Protection and Antioxidant Activity of the Extracts from the Mycelia of Cordyceps Sinensis Act Partially Via Adenosine Receptors

Mycelia of cultured Cordyceps sinensis (CS) is one of the most common substitutes for natural CS and was approved for arrhythmia in China. However, the role of CS in ameliorating injury during ischemia‐reperfusion (I/R) is still unclear. We examined effects of extracts from CS on I/R and investigate...

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Veröffentlicht in:Phytotherapy research 2013-11, Vol.27 (11), p.1597-1604
Hauptverfasser: Yan, Xiao-Feng, Zhang, Zhong-Miao, Yao, Hong-Yi, Guan, Yan, Zhu, Jian-Ping, Zhang, Lin-Hui, Jia, Yong-Liang, Wang, Ru-Wei
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container_end_page 1604
container_issue 11
container_start_page 1597
container_title Phytotherapy research
container_volume 27
creator Yan, Xiao-Feng
Zhang, Zhong-Miao
Yao, Hong-Yi
Guan, Yan
Zhu, Jian-Ping
Zhang, Lin-Hui
Jia, Yong-Liang
Wang, Ru-Wei
description Mycelia of cultured Cordyceps sinensis (CS) is one of the most common substitutes for natural CS and was approved for arrhythmia in China. However, the role of CS in ameliorating injury during ischemia‐reperfusion (I/R) is still unclear. We examined effects of extracts from CS on I/R and investigated the possible mechanisms. Post‐ischemic coronary perfusion pressure, ventricular function, and coronary flow were measured using the Langendorff mouse heart model. Oxidative stress of cardiac homogenates was performed using an ELISA. Our results indicate that CS affords cardioprotection possibly through enhanced adenosine receptor activation. Cardioprotection was demonstrated by reduced post‐ischemic diastolic dysfunction and improved recovery of pressure development and coronary flow. Treatment with CS largely abrogates oxidative stress and damage in glucose‐ or pyruvate‐perfused hearts. Importantly, observed reductions in oxidative stress [glutathione disulfide (GSSG)]/[GSSG + glutathione] and [malondialdehyde (MDA)]/[superoxide dismutase + MDA] ratios as well as the resultant damage upon CS treatment correlate with functional markers of post‐ischemic myocardial outcome. These effects of CS were partially blocked by 8‐ρ‐sulfophenyltheophylline, an adenosine receptor antagonist. Our results demonstrate a suppressive role of CS in ischemic contracture. Meanwhile, the results also suggest pre‐ischemic adenosine receptor activation may be involved in reducing contracture in hearts pretreated with CS. Copyright © 2012 John Wiley & Sons, Ltd.
doi_str_mv 10.1002/ptr.4899
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However, the role of CS in ameliorating injury during ischemia‐reperfusion (I/R) is still unclear. We examined effects of extracts from CS on I/R and investigated the possible mechanisms. Post‐ischemic coronary perfusion pressure, ventricular function, and coronary flow were measured using the Langendorff mouse heart model. Oxidative stress of cardiac homogenates was performed using an ELISA. Our results indicate that CS affords cardioprotection possibly through enhanced adenosine receptor activation. Cardioprotection was demonstrated by reduced post‐ischemic diastolic dysfunction and improved recovery of pressure development and coronary flow. Treatment with CS largely abrogates oxidative stress and damage in glucose‐ or pyruvate‐perfused hearts. Importantly, observed reductions in oxidative stress [glutathione disulfide (GSSG)]/[GSSG + glutathione] and [malondialdehyde (MDA)]/[superoxide dismutase + MDA] ratios as well as the resultant damage upon CS treatment correlate with functional markers of post‐ischemic myocardial outcome. These effects of CS were partially blocked by 8‐ρ‐sulfophenyltheophylline, an adenosine receptor antagonist. Our results demonstrate a suppressive role of CS in ischemic contracture. Meanwhile, the results also suggest pre‐ischemic adenosine receptor activation may be involved in reducing contracture in hearts pretreated with CS. 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Res</addtitle><description>Mycelia of cultured Cordyceps sinensis (CS) is one of the most common substitutes for natural CS and was approved for arrhythmia in China. However, the role of CS in ameliorating injury during ischemia‐reperfusion (I/R) is still unclear. We examined effects of extracts from CS on I/R and investigated the possible mechanisms. Post‐ischemic coronary perfusion pressure, ventricular function, and coronary flow were measured using the Langendorff mouse heart model. Oxidative stress of cardiac homogenates was performed using an ELISA. Our results indicate that CS affords cardioprotection possibly through enhanced adenosine receptor activation. Cardioprotection was demonstrated by reduced post‐ischemic diastolic dysfunction and improved recovery of pressure development and coronary flow. Treatment with CS largely abrogates oxidative stress and damage in glucose‐ or pyruvate‐perfused hearts. Importantly, observed reductions in oxidative stress [glutathione disulfide (GSSG)]/[GSSG + glutathione] and [malondialdehyde (MDA)]/[superoxide dismutase + MDA] ratios as well as the resultant damage upon CS treatment correlate with functional markers of post‐ischemic myocardial outcome. These effects of CS were partially blocked by 8‐ρ‐sulfophenyltheophylline, an adenosine receptor antagonist. Our results demonstrate a suppressive role of CS in ischemic contracture. Meanwhile, the results also suggest pre‐ischemic adenosine receptor activation may be involved in reducing contracture in hearts pretreated with CS. 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Res</addtitle><date>2013-11</date><risdate>2013</risdate><volume>27</volume><issue>11</issue><spage>1597</spage><epage>1604</epage><pages>1597-1604</pages><issn>0951-418X</issn><eissn>1099-1573</eissn><coden>PHYREH</coden><abstract>Mycelia of cultured Cordyceps sinensis (CS) is one of the most common substitutes for natural CS and was approved for arrhythmia in China. However, the role of CS in ameliorating injury during ischemia‐reperfusion (I/R) is still unclear. We examined effects of extracts from CS on I/R and investigated the possible mechanisms. Post‐ischemic coronary perfusion pressure, ventricular function, and coronary flow were measured using the Langendorff mouse heart model. Oxidative stress of cardiac homogenates was performed using an ELISA. Our results indicate that CS affords cardioprotection possibly through enhanced adenosine receptor activation. Cardioprotection was demonstrated by reduced post‐ischemic diastolic dysfunction and improved recovery of pressure development and coronary flow. Treatment with CS largely abrogates oxidative stress and damage in glucose‐ or pyruvate‐perfused hearts. Importantly, observed reductions in oxidative stress [glutathione disulfide (GSSG)]/[GSSG + glutathione] and [malondialdehyde (MDA)]/[superoxide dismutase + MDA] ratios as well as the resultant damage upon CS treatment correlate with functional markers of post‐ischemic myocardial outcome. These effects of CS were partially blocked by 8‐ρ‐sulfophenyltheophylline, an adenosine receptor antagonist. Our results demonstrate a suppressive role of CS in ischemic contracture. Meanwhile, the results also suggest pre‐ischemic adenosine receptor activation may be involved in reducing contracture in hearts pretreated with CS. Copyright © 2012 John Wiley &amp; Sons, Ltd.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>23192916</pmid><doi>10.1002/ptr.4899</doi><tpages>8</tpages></addata></record>
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subjects Adenosine
adenosine receptor
Animals
antioxidant stress
Antioxidants - pharmacology
Cardiology
Cardiotonic Agents - pharmacology
Cordyceps - chemistry
Cordyceps sinensis
Glutathione - metabolism
Glutathione Disulfide - metabolism
Heart
Heart - drug effects
Heart - physiopathology
In Vitro Techniques
ischemia-reperfusion
Male
Malondialdehyde - metabolism
Mice
Mice, Inbred C57BL
Mycelium - chemistry
Myocardium - metabolism
Oxidation-Reduction
Oxidative stress
Oxidative Stress - drug effects
Receptors, Purinergic P1 - metabolism
Reperfusion Injury - drug therapy
Rodents
Superoxide Dismutase - metabolism
Theophylline - analogs & derivatives
Theophylline - pharmacology
title Cardiovascular Protection and Antioxidant Activity of the Extracts from the Mycelia of Cordyceps Sinensis Act Partially Via Adenosine Receptors
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