Shenfu Injection (参附注射液) suppresses inflammation by targeting haptoglobin and pentraxin 3 in rats with chronic ischemic heart failure

Objective To investigate the regulatory effects of Shenfu Injection (SFI, 参附注射液) on hemodynamic parameters and serum proteins in rats with post-infarction chronic heart failure (CHF). Methods Forty-five healthy Wistar rats were randomized into three groups: sham, heart failure (model) and SFI group....

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Veröffentlicht in:Chinese journal of integrative medicine 2015, Vol.21 (1), p.22-28
Hauptverfasser: Zheng, Si-dao, Wu, Hong-jin, Yu, Shao-ping, Ren, Jian-xun, Duo, Wei-wei, Ma, Zeng-chun, Gao, Yue, Wang, Sheng-qi, Liu, Yu-na
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container_title Chinese journal of integrative medicine
container_volume 21
creator Zheng, Si-dao
Wu, Hong-jin
Yu, Shao-ping
Ren, Jian-xun
Duo, Wei-wei
Ma, Zeng-chun
Gao, Yue
Wang, Sheng-qi
Liu, Yu-na
description Objective To investigate the regulatory effects of Shenfu Injection (SFI, 参附注射液) on hemodynamic parameters and serum proteins in rats with post-infarction chronic heart failure (CHF). Methods Forty-five healthy Wistar rats were randomized into three groups: sham, heart failure (model) and SFI group. The CHF was induced by left coronary artery ligation. Seven days after the surgical operation, animals in the sham group and the model group received saline (6.2 mL/kg/d), while animals in the SFI group received SFI (6.2 mL/kg d) intraperitoneally. Four weeks later, cardiac hemodynamic parameters were measured via the carotid route. The expression of serum proteins was analyzed by two-dimensional electrophoresis and matrix-assisted laser desorption/ionization time-of-flight mass spectrometer (MALDI-TOF MS). Results Recording of hemodynamic parameters showed that left ventricular systolic pressure (LVSP), maximum rate of left ventricular pressure (+dp/dt max ) rise, and maximum rate of left ventricular pressure (−dp/dt max ) decrease, while the left ventricular end diastolic pressure (LVEDP) rose in the model group compared to those in the sham group ( P
doi_str_mv 10.1007/s11655-013-1440-8
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Methods Forty-five healthy Wistar rats were randomized into three groups: sham, heart failure (model) and SFI group. The CHF was induced by left coronary artery ligation. Seven days after the surgical operation, animals in the sham group and the model group received saline (6.2 mL/kg/d), while animals in the SFI group received SFI (6.2 mL/kg d) intraperitoneally. Four weeks later, cardiac hemodynamic parameters were measured via the carotid route. The expression of serum proteins was analyzed by two-dimensional electrophoresis and matrix-assisted laser desorption/ionization time-of-flight mass spectrometer (MALDI-TOF MS). Results Recording of hemodynamic parameters showed that left ventricular systolic pressure (LVSP), maximum rate of left ventricular pressure (+dp/dt max ) rise, and maximum rate of left ventricular pressure (−dp/dt max ) decrease, while the left ventricular end diastolic pressure (LVEDP) rose in the model group compared to those in the sham group ( P &lt;0.05). The results of the MALDI-TOF MS indicated that haptoglobin (HP), pentraxin 3 (PTX3) and alpha-1-antitrypsin were up-regulated, while serum albumin and 40S ribosomal protein were down-regulated in the model group ( P &lt;0.05). Compared with the model group, LVSP, +dp/dt max and −dp/dt max were higher, while LVEDP was lower in the SFI group ( P &lt;0.05). Expression levels of HP and PTX3 were lower than in the model group ( P &lt;0.05). Conclusion SFI could improve hemodynamic function and decrease inflammatory reactions in the pathophysiology of CHF. The serum proteins HP and PTX3 could be potential biomarkers for chronic ischemic heart failure, and they could also be the serum protein targets of SFI.</description><identifier>ISSN: 1672-0415</identifier><identifier>EISSN: 1993-0402</identifier><identifier>DOI: 10.1007/s11655-013-1440-8</identifier><identifier>PMID: 23494325</identifier><language>eng</language><publisher>Heidelberg: Chinese Association of Traditional and Western Medicine</publisher><subject>Animals ; Blood Proteins - metabolism ; C-Reactive Protein - metabolism ; Chronic Disease ; Drugs, Chinese Herbal - therapeutic use ; Electrophoresis, Gel, Two-Dimensional ; Haptoglobins - metabolism ; Heart Failure - blood ; Heart Failure - complications ; Heart Failure - drug therapy ; Heart Failure - physiopathology ; Heart Function Tests ; Hemodynamics ; Hydrogen-Ion Concentration ; Imaging, Three-Dimensional ; Inflammation - complications ; Inflammation - drug therapy ; Male ; Medicine ; Medicine &amp; Public Health ; Myocardial Ischemia - blood ; Myocardial Ischemia - complications ; Myocardial Ischemia - drug therapy ; Myocardial Ischemia - physiopathology ; Original Article ; Phytotherapy ; Proteome - metabolism ; Rats, Wistar ; Serum Amyloid P-Component - metabolism ; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</subject><ispartof>Chinese journal of integrative medicine, 2015, Vol.21 (1), p.22-28</ispartof><rights>Chinese Association of the Integration of Traditional and Western Medicine and Springer-Verlag Berlin Heidelberg 2013</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2598-57238d381052974adf6280ef387f468585396eecca2354b4f3a64f47495f85e3</citedby><cites>FETCH-LOGICAL-c2598-57238d381052974adf6280ef387f468585396eecca2354b4f3a64f47495f85e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11655-013-1440-8$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11655-013-1440-8$$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/23494325$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zheng, Si-dao</creatorcontrib><creatorcontrib>Wu, Hong-jin</creatorcontrib><creatorcontrib>Yu, Shao-ping</creatorcontrib><creatorcontrib>Ren, Jian-xun</creatorcontrib><creatorcontrib>Duo, Wei-wei</creatorcontrib><creatorcontrib>Ma, Zeng-chun</creatorcontrib><creatorcontrib>Gao, Yue</creatorcontrib><creatorcontrib>Wang, Sheng-qi</creatorcontrib><creatorcontrib>Liu, Yu-na</creatorcontrib><title>Shenfu Injection (参附注射液) suppresses inflammation by targeting haptoglobin and pentraxin 3 in rats with chronic ischemic heart failure</title><title>Chinese journal of integrative medicine</title><addtitle>Chin. J. Integr. Med</addtitle><addtitle>Chin J Integr Med</addtitle><description>Objective To investigate the regulatory effects of Shenfu Injection (SFI, 参附注射液) on hemodynamic parameters and serum proteins in rats with post-infarction chronic heart failure (CHF). Methods Forty-five healthy Wistar rats were randomized into three groups: sham, heart failure (model) and SFI group. The CHF was induced by left coronary artery ligation. Seven days after the surgical operation, animals in the sham group and the model group received saline (6.2 mL/kg/d), while animals in the SFI group received SFI (6.2 mL/kg d) intraperitoneally. Four weeks later, cardiac hemodynamic parameters were measured via the carotid route. The expression of serum proteins was analyzed by two-dimensional electrophoresis and matrix-assisted laser desorption/ionization time-of-flight mass spectrometer (MALDI-TOF MS). Results Recording of hemodynamic parameters showed that left ventricular systolic pressure (LVSP), maximum rate of left ventricular pressure (+dp/dt max ) rise, and maximum rate of left ventricular pressure (−dp/dt max ) decrease, while the left ventricular end diastolic pressure (LVEDP) rose in the model group compared to those in the sham group ( P &lt;0.05). The results of the MALDI-TOF MS indicated that haptoglobin (HP), pentraxin 3 (PTX3) and alpha-1-antitrypsin were up-regulated, while serum albumin and 40S ribosomal protein were down-regulated in the model group ( P &lt;0.05). Compared with the model group, LVSP, +dp/dt max and −dp/dt max were higher, while LVEDP was lower in the SFI group ( P &lt;0.05). Expression levels of HP and PTX3 were lower than in the model group ( P &lt;0.05). Conclusion SFI could improve hemodynamic function and decrease inflammatory reactions in the pathophysiology of CHF. The serum proteins HP and PTX3 could be potential biomarkers for chronic ischemic heart failure, and they could also be the serum protein targets of SFI.</description><subject>Animals</subject><subject>Blood Proteins - metabolism</subject><subject>C-Reactive Protein - metabolism</subject><subject>Chronic Disease</subject><subject>Drugs, Chinese Herbal - therapeutic use</subject><subject>Electrophoresis, Gel, Two-Dimensional</subject><subject>Haptoglobins - metabolism</subject><subject>Heart Failure - blood</subject><subject>Heart Failure - complications</subject><subject>Heart Failure - drug therapy</subject><subject>Heart Failure - physiopathology</subject><subject>Heart Function Tests</subject><subject>Hemodynamics</subject><subject>Hydrogen-Ion Concentration</subject><subject>Imaging, Three-Dimensional</subject><subject>Inflammation - complications</subject><subject>Inflammation - drug therapy</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Myocardial Ischemia - blood</subject><subject>Myocardial Ischemia - complications</subject><subject>Myocardial Ischemia - drug therapy</subject><subject>Myocardial Ischemia - physiopathology</subject><subject>Original Article</subject><subject>Phytotherapy</subject><subject>Proteome - metabolism</subject><subject>Rats, Wistar</subject><subject>Serum Amyloid P-Component - metabolism</subject><subject>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</subject><issn>1672-0415</issn><issn>1993-0402</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kb1uFDEUha0IRH7gAdIgl6GY4P_xlFEEJFIkCtJb3tnrHa9mPIPtUUgbpU_NG1BGQeKNEilvgcMGSiof637nyL4HoX1KDikh9ftEqZKyIpRXVAhS6S20Q5uGV0QQ9qJoVbOiqdxGuymtCZG1IvIV2mZcNIIzuYNuvnQQ3IxPwxra7MeAD-5vrh6_Xz_8_HF_e_3w6-4dTvM0RUgJEvbB9XYY7B9ycYmzjSvIPqxwZ6c8rvpx4QO2YYknCDnab-XGiwtHmxO-8LnDbRfH4FvsU9vBUEQHNmbsrO_nCK_RS2f7BG-ezz10_vHD-fFJdfb50-nx0VnVMtnoStaM6yXXlEjW1MIunWKagOO6dkJpqSVvFEDbWsalWAjHrRJO1KKRTkvge-hgEzvF8esMKZuhvAf63gYY52SoEoSzmglVULpB2zimFMGZKfrBxktDiXmqwWxqMKUG81SD0cXz9jl-Xgyw_Of4u_cCsA2QyiisIJr1OMdQfvyf1N8GPJkN</recordid><startdate>2015</startdate><enddate>2015</enddate><creator>Zheng, Si-dao</creator><creator>Wu, Hong-jin</creator><creator>Yu, Shao-ping</creator><creator>Ren, Jian-xun</creator><creator>Duo, Wei-wei</creator><creator>Ma, Zeng-chun</creator><creator>Gao, Yue</creator><creator>Wang, Sheng-qi</creator><creator>Liu, Yu-na</creator><general>Chinese Association of Traditional and Western Medicine</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></search><sort><creationdate>2015</creationdate><title>Shenfu Injection (参附注射液) suppresses inflammation by targeting haptoglobin and pentraxin 3 in rats with chronic ischemic heart failure</title><author>Zheng, Si-dao ; Wu, Hong-jin ; Yu, Shao-ping ; Ren, Jian-xun ; Duo, Wei-wei ; Ma, Zeng-chun ; Gao, Yue ; Wang, Sheng-qi ; Liu, Yu-na</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2598-57238d381052974adf6280ef387f468585396eecca2354b4f3a64f47495f85e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Blood Proteins - metabolism</topic><topic>C-Reactive Protein - metabolism</topic><topic>Chronic Disease</topic><topic>Drugs, Chinese Herbal - therapeutic use</topic><topic>Electrophoresis, Gel, Two-Dimensional</topic><topic>Haptoglobins - metabolism</topic><topic>Heart Failure - blood</topic><topic>Heart Failure - complications</topic><topic>Heart Failure - drug therapy</topic><topic>Heart Failure - physiopathology</topic><topic>Heart Function Tests</topic><topic>Hemodynamics</topic><topic>Hydrogen-Ion Concentration</topic><topic>Imaging, Three-Dimensional</topic><topic>Inflammation - complications</topic><topic>Inflammation - drug therapy</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Myocardial Ischemia - blood</topic><topic>Myocardial Ischemia - complications</topic><topic>Myocardial Ischemia - drug therapy</topic><topic>Myocardial Ischemia - physiopathology</topic><topic>Original Article</topic><topic>Phytotherapy</topic><topic>Proteome - metabolism</topic><topic>Rats, Wistar</topic><topic>Serum Amyloid P-Component - metabolism</topic><topic>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zheng, Si-dao</creatorcontrib><creatorcontrib>Wu, Hong-jin</creatorcontrib><creatorcontrib>Yu, Shao-ping</creatorcontrib><creatorcontrib>Ren, Jian-xun</creatorcontrib><creatorcontrib>Duo, Wei-wei</creatorcontrib><creatorcontrib>Ma, Zeng-chun</creatorcontrib><creatorcontrib>Gao, Yue</creatorcontrib><creatorcontrib>Wang, Sheng-qi</creatorcontrib><creatorcontrib>Liu, Yu-na</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><jtitle>Chinese journal of integrative medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zheng, Si-dao</au><au>Wu, Hong-jin</au><au>Yu, Shao-ping</au><au>Ren, Jian-xun</au><au>Duo, Wei-wei</au><au>Ma, Zeng-chun</au><au>Gao, Yue</au><au>Wang, Sheng-qi</au><au>Liu, Yu-na</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Shenfu Injection (参附注射液) suppresses inflammation by targeting haptoglobin and pentraxin 3 in rats with chronic ischemic heart failure</atitle><jtitle>Chinese journal of integrative medicine</jtitle><stitle>Chin. J. Integr. Med</stitle><addtitle>Chin J Integr Med</addtitle><date>2015</date><risdate>2015</risdate><volume>21</volume><issue>1</issue><spage>22</spage><epage>28</epage><pages>22-28</pages><issn>1672-0415</issn><eissn>1993-0402</eissn><abstract>Objective To investigate the regulatory effects of Shenfu Injection (SFI, 参附注射液) on hemodynamic parameters and serum proteins in rats with post-infarction chronic heart failure (CHF). Methods Forty-five healthy Wistar rats were randomized into three groups: sham, heart failure (model) and SFI group. The CHF was induced by left coronary artery ligation. Seven days after the surgical operation, animals in the sham group and the model group received saline (6.2 mL/kg/d), while animals in the SFI group received SFI (6.2 mL/kg d) intraperitoneally. Four weeks later, cardiac hemodynamic parameters were measured via the carotid route. The expression of serum proteins was analyzed by two-dimensional electrophoresis and matrix-assisted laser desorption/ionization time-of-flight mass spectrometer (MALDI-TOF MS). Results Recording of hemodynamic parameters showed that left ventricular systolic pressure (LVSP), maximum rate of left ventricular pressure (+dp/dt max ) rise, and maximum rate of left ventricular pressure (−dp/dt max ) decrease, while the left ventricular end diastolic pressure (LVEDP) rose in the model group compared to those in the sham group ( P &lt;0.05). The results of the MALDI-TOF MS indicated that haptoglobin (HP), pentraxin 3 (PTX3) and alpha-1-antitrypsin were up-regulated, while serum albumin and 40S ribosomal protein were down-regulated in the model group ( P &lt;0.05). Compared with the model group, LVSP, +dp/dt max and −dp/dt max were higher, while LVEDP was lower in the SFI group ( P &lt;0.05). Expression levels of HP and PTX3 were lower than in the model group ( P &lt;0.05). Conclusion SFI could improve hemodynamic function and decrease inflammatory reactions in the pathophysiology of CHF. The serum proteins HP and PTX3 could be potential biomarkers for chronic ischemic heart failure, and they could also be the serum protein targets of SFI.</abstract><cop>Heidelberg</cop><pub>Chinese Association of Traditional and Western Medicine</pub><pmid>23494325</pmid><doi>10.1007/s11655-013-1440-8</doi><tpages>7</tpages></addata></record>
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subjects Animals
Blood Proteins - metabolism
C-Reactive Protein - metabolism
Chronic Disease
Drugs, Chinese Herbal - therapeutic use
Electrophoresis, Gel, Two-Dimensional
Haptoglobins - metabolism
Heart Failure - blood
Heart Failure - complications
Heart Failure - drug therapy
Heart Failure - physiopathology
Heart Function Tests
Hemodynamics
Hydrogen-Ion Concentration
Imaging, Three-Dimensional
Inflammation - complications
Inflammation - drug therapy
Male
Medicine
Medicine & Public Health
Myocardial Ischemia - blood
Myocardial Ischemia - complications
Myocardial Ischemia - drug therapy
Myocardial Ischemia - physiopathology
Original Article
Phytotherapy
Proteome - metabolism
Rats, Wistar
Serum Amyloid P-Component - metabolism
Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
title Shenfu Injection (参附注射液) suppresses inflammation by targeting haptoglobin and pentraxin 3 in rats with chronic ischemic heart failure
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