Chronic Estrogen Supplementation Following Ovariectomy Improves the Emotional Stress-Induced Cardiovascular Responses by Indirect Action on the Nervous System and by Direct Action on the Heart

Background Takotsubo cardiomyopathy is triggered by emotional or physical stress especially in post-menopausal women. A reduction in estrogen levels following menopause might underlie the high incidence of takotsubo cardiomyopathy. Methods and Results The left ventricular contraction between ovariec...

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Veröffentlicht in:Circulation Journal 2007, Vol.71(4), pp.565-573
Hauptverfasser: Ueyama, Takashi, Ishikura, Fuminobu, Matsuda, Akiko, Asanuma, Toshihiko, Ueda, Kazuki, Ichinose, Masao, Kasamatsu, Ken, Hano, Takuzo, Akasaka, Takashi, Tsuruo, Yoshihiro, Morimoto, Keiko, Beppu, Shintaro
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container_end_page 573
container_issue 4
container_start_page 565
container_title Circulation Journal
container_volume 71
creator Ueyama, Takashi
Ishikura, Fuminobu
Matsuda, Akiko
Asanuma, Toshihiko
Ueda, Kazuki
Ichinose, Masao
Kasamatsu, Ken
Hano, Takuzo
Akasaka, Takashi
Tsuruo, Yoshihiro
Morimoto, Keiko
Beppu, Shintaro
description Background Takotsubo cardiomyopathy is triggered by emotional or physical stress especially in post-menopausal women. A reduction in estrogen levels following menopause might underlie the high incidence of takotsubo cardiomyopathy. Methods and Results The left ventricular contraction between ovariectomized rats (OVX) and OVX with estrogen supplementation (OVX + E) while subjected to immobilization stress (IMO) was compared. The IMO in combination with general anesthesia impaired the left ventricular contraction in both OVX and OVX + E. Estrogen supplementation tended to improve the IMO-induced cardiac dysfunction and significantly attenuated the increase of blood pressure and heart rate. To understand the protective mechanism of estrogen, the expression of c-fos mRNA, a marker of cellular activation was compared. The mRNA expression of cardioprotective substances in the heart was also investigated. In the OVX + E, the levels of c-fos mRNA were significantly decreased in the paraventricular hypothalamic nucleus, adrenal gland and left ventricle, suggesting that an increase of estrogen attenuates the emotional stress-induced hypothalamo-sympatho-adrenal outflow from the central nervous system to the target organs. An expression of heat shock protein 70 and atrial natriuretic peptide was significantly augmented in the OVX + E. Conclusions These data suggest that estrogen supplementation partially prevents emotional stress-induced cardiovascular responses both by indirect action on the nervous system and by direct action on the heart. (Circ J 2007; 71: 565 - 573)
doi_str_mv 10.1253/circj.71.565
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A reduction in estrogen levels following menopause might underlie the high incidence of takotsubo cardiomyopathy. Methods and Results The left ventricular contraction between ovariectomized rats (OVX) and OVX with estrogen supplementation (OVX + E) while subjected to immobilization stress (IMO) was compared. The IMO in combination with general anesthesia impaired the left ventricular contraction in both OVX and OVX + E. Estrogen supplementation tended to improve the IMO-induced cardiac dysfunction and significantly attenuated the increase of blood pressure and heart rate. To understand the protective mechanism of estrogen, the expression of c-fos mRNA, a marker of cellular activation was compared. The mRNA expression of cardioprotective substances in the heart was also investigated. In the OVX + E, the levels of c-fos mRNA were significantly decreased in the paraventricular hypothalamic nucleus, adrenal gland and left ventricle, suggesting that an increase of estrogen attenuates the emotional stress-induced hypothalamo-sympatho-adrenal outflow from the central nervous system to the target organs. An expression of heat shock protein 70 and atrial natriuretic peptide was significantly augmented in the OVX + E. Conclusions These data suggest that estrogen supplementation partially prevents emotional stress-induced cardiovascular responses both by indirect action on the nervous system and by direct action on the heart. 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A reduction in estrogen levels following menopause might underlie the high incidence of takotsubo cardiomyopathy. Methods and Results The left ventricular contraction between ovariectomized rats (OVX) and OVX with estrogen supplementation (OVX + E) while subjected to immobilization stress (IMO) was compared. The IMO in combination with general anesthesia impaired the left ventricular contraction in both OVX and OVX + E. Estrogen supplementation tended to improve the IMO-induced cardiac dysfunction and significantly attenuated the increase of blood pressure and heart rate. To understand the protective mechanism of estrogen, the expression of c-fos mRNA, a marker of cellular activation was compared. The mRNA expression of cardioprotective substances in the heart was also investigated. In the OVX + E, the levels of c-fos mRNA were significantly decreased in the paraventricular hypothalamic nucleus, adrenal gland and left ventricle, suggesting that an increase of estrogen attenuates the emotional stress-induced hypothalamo-sympatho-adrenal outflow from the central nervous system to the target organs. An expression of heat shock protein 70 and atrial natriuretic peptide was significantly augmented in the OVX + E. Conclusions These data suggest that estrogen supplementation partially prevents emotional stress-induced cardiovascular responses both by indirect action on the nervous system and by direct action on the heart. 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Ishikura, Fuminobu ; Matsuda, Akiko ; Asanuma, Toshihiko ; Ueda, Kazuki ; Ichinose, Masao ; Kasamatsu, Ken ; Hano, Takuzo ; Akasaka, Takashi ; Tsuruo, Yoshihiro ; Morimoto, Keiko ; Beppu, Shintaro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c576t-bde03b5cc2091848dd7411acab7f9696fc0c14bbf1fece9e67e3dd6c1b2dd3b93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Animals</topic><topic>Disease Models, Animal</topic><topic>Drug Implants</topic><topic>Echocardiography</topic><topic>Emotional stress</topic><topic>Estrogen</topic><topic>Estrogens - administration &amp; dosage</topic><topic>Estrogens - blood</topic><topic>Estrogens - pharmacology</topic><topic>Female</topic><topic>Gene Expression Regulation - drug effects</topic><topic>Heart - drug effects</topic><topic>Myocardium - metabolism</topic><topic>Nervous System - drug effects</topic><topic>Ovariectomy</topic><topic>Paraventricular hypothalamic nucleus</topic><topic>Postmenopause</topic><topic>Proto-Oncogene Proteins c-fos - genetics</topic><topic>Proto-Oncogene Proteins c-fos - metabolism</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Restraint, Physical</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Messenger - metabolism</topic><topic>Stress, Psychological - complications</topic><topic>Sympathetic nervous system</topic><topic>Ventricular Dysfunction, Left - etiology</topic><topic>Ventricular Dysfunction, Left - prevention &amp; control</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ueyama, Takashi</creatorcontrib><creatorcontrib>Ishikura, Fuminobu</creatorcontrib><creatorcontrib>Matsuda, Akiko</creatorcontrib><creatorcontrib>Asanuma, Toshihiko</creatorcontrib><creatorcontrib>Ueda, Kazuki</creatorcontrib><creatorcontrib>Ichinose, Masao</creatorcontrib><creatorcontrib>Kasamatsu, Ken</creatorcontrib><creatorcontrib>Hano, Takuzo</creatorcontrib><creatorcontrib>Akasaka, Takashi</creatorcontrib><creatorcontrib>Tsuruo, Yoshihiro</creatorcontrib><creatorcontrib>Morimoto, Keiko</creatorcontrib><creatorcontrib>Beppu, Shintaro</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>Circulation Journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ueyama, Takashi</au><au>Ishikura, Fuminobu</au><au>Matsuda, Akiko</au><au>Asanuma, Toshihiko</au><au>Ueda, Kazuki</au><au>Ichinose, Masao</au><au>Kasamatsu, Ken</au><au>Hano, Takuzo</au><au>Akasaka, Takashi</au><au>Tsuruo, Yoshihiro</au><au>Morimoto, Keiko</au><au>Beppu, Shintaro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chronic Estrogen Supplementation Following Ovariectomy Improves the Emotional Stress-Induced Cardiovascular Responses by Indirect Action on the Nervous System and by Direct Action on the Heart</atitle><jtitle>Circulation Journal</jtitle><addtitle>Circ J</addtitle><date>2007</date><risdate>2007</risdate><volume>71</volume><issue>4</issue><spage>565</spage><epage>573</epage><pages>565-573</pages><issn>1346-9843</issn><eissn>1347-4820</eissn><abstract>Background Takotsubo cardiomyopathy is triggered by emotional or physical stress especially in post-menopausal women. A reduction in estrogen levels following menopause might underlie the high incidence of takotsubo cardiomyopathy. Methods and Results The left ventricular contraction between ovariectomized rats (OVX) and OVX with estrogen supplementation (OVX + E) while subjected to immobilization stress (IMO) was compared. The IMO in combination with general anesthesia impaired the left ventricular contraction in both OVX and OVX + E. Estrogen supplementation tended to improve the IMO-induced cardiac dysfunction and significantly attenuated the increase of blood pressure and heart rate. To understand the protective mechanism of estrogen, the expression of c-fos mRNA, a marker of cellular activation was compared. The mRNA expression of cardioprotective substances in the heart was also investigated. In the OVX + E, the levels of c-fos mRNA were significantly decreased in the paraventricular hypothalamic nucleus, adrenal gland and left ventricle, suggesting that an increase of estrogen attenuates the emotional stress-induced hypothalamo-sympatho-adrenal outflow from the central nervous system to the target organs. An expression of heat shock protein 70 and atrial natriuretic peptide was significantly augmented in the OVX + E. Conclusions These data suggest that estrogen supplementation partially prevents emotional stress-induced cardiovascular responses both by indirect action on the nervous system and by direct action on the heart. (Circ J 2007; 71: 565 - 573)</abstract><cop>Japan</cop><pub>The Japanese Circulation Society</pub><pmid>17384461</pmid><doi>10.1253/circj.71.565</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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subjects Animals
Disease Models, Animal
Drug Implants
Echocardiography
Emotional stress
Estrogen
Estrogens - administration & dosage
Estrogens - blood
Estrogens - pharmacology
Female
Gene Expression Regulation - drug effects
Heart - drug effects
Myocardium - metabolism
Nervous System - drug effects
Ovariectomy
Paraventricular hypothalamic nucleus
Postmenopause
Proto-Oncogene Proteins c-fos - genetics
Proto-Oncogene Proteins c-fos - metabolism
Rats
Rats, Sprague-Dawley
Restraint, Physical
RNA, Messenger - genetics
RNA, Messenger - metabolism
Stress, Psychological - complications
Sympathetic nervous system
Ventricular Dysfunction, Left - etiology
Ventricular Dysfunction, Left - prevention & control
title Chronic Estrogen Supplementation Following Ovariectomy Improves the Emotional Stress-Induced Cardiovascular Responses by Indirect Action on the Nervous System and by Direct Action on the Heart
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