And the beat goes on: maintained cardiovascular function during aging in the longest-lived rodent, the naked mole-rat
The naked mole-rat (NMR) is the longest-lived rodent known, with a maximum lifespan potential (MLSP) of >31 years. Despite such extreme longevity, these animals display attenuation of many age-associated diseases and functional changes until the last quartile of their MLSP. We questioned if such...
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Veröffentlicht in: | American journal of physiology. Heart and circulatory physiology 2014-08, Vol.307 (3), p.H284-H291 |
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description | The naked mole-rat (NMR) is the longest-lived rodent known, with a maximum lifespan potential (MLSP) of >31 years. Despite such extreme longevity, these animals display attenuation of many age-associated diseases and functional changes until the last quartile of their MLSP. We questioned if such abilities would extend to cardiovascular function and structure in this species. To test this, we assessed cardiac functional reserve, ventricular morphology, and arterial stiffening in NMRs ranging from 2 to 24 years of age. Dobutamine echocardiography (3 μg/g ip) revealed no age-associated changes in left ventricular (LV) function either at baseline or with exercise-like stress. Baseline and dobutamine-induced LV pressure parameters also did not change. Thus the NMR, unlike other mammals, maintains cardiac reserve with age. NMRs showed no cardiac hypertrophy, evidenced by no increase in cardiomyocyte cross-sectional area or LV dimensions with age. Age-associated arterial stiffening does not occur since there are no changes in aortic blood pressures or pulse-wave velocity. Only LV interstitial collagen deposition increased 2.5-fold from young to old NMRs (P < 0.01). However, its effect on LV diastolic function is likely minor since NMRs experience attenuated age-related increases in diastolic dysfunction in comparison with other species. Overall, these findings conform to the negligible senescence phenotype, as NMRs largely stave off cardiovascular changes for at least 75% of their MLSP. This suggests that using a comparative strategy to find factors that change with age in other mammals but not NMRs could provide novel targets to slow or prevent cardiovascular aging in humans. |
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Despite such extreme longevity, these animals display attenuation of many age-associated diseases and functional changes until the last quartile of their MLSP. We questioned if such abilities would extend to cardiovascular function and structure in this species. To test this, we assessed cardiac functional reserve, ventricular morphology, and arterial stiffening in NMRs ranging from 2 to 24 years of age. Dobutamine echocardiography (3 μg/g ip) revealed no age-associated changes in left ventricular (LV) function either at baseline or with exercise-like stress. Baseline and dobutamine-induced LV pressure parameters also did not change. Thus the NMR, unlike other mammals, maintains cardiac reserve with age. NMRs showed no cardiac hypertrophy, evidenced by no increase in cardiomyocyte cross-sectional area or LV dimensions with age. Age-associated arterial stiffening does not occur since there are no changes in aortic blood pressures or pulse-wave velocity. Only LV interstitial collagen deposition increased 2.5-fold from young to old NMRs (P < 0.01). However, its effect on LV diastolic function is likely minor since NMRs experience attenuated age-related increases in diastolic dysfunction in comparison with other species. Overall, these findings conform to the negligible senescence phenotype, as NMRs largely stave off cardiovascular changes for at least 75% of their MLSP. This suggests that using a comparative strategy to find factors that change with age in other mammals but not NMRs could provide novel targets to slow or prevent cardiovascular aging in humans.</description><identifier>ISSN: 0363-6135</identifier><identifier>ISSN: 1522-1539</identifier><identifier>EISSN: 1522-1539</identifier><identifier>DOI: 10.1152/ajpheart.00305.2014</identifier><identifier>PMID: 24906918</identifier><identifier>CODEN: AJPPDI</identifier><language>eng</language><publisher>United States: American Physiological Society</publisher><subject>Age Factors ; Aging ; Aging - metabolism ; Aging - physiology ; Animals ; Aorta - physiology ; Arterial Pressure ; Call for Papers ; Cardiovascular system ; Collagen ; Collagen - metabolism ; Compliance ; Echocardiography, Stress ; Female ; Heart - physiology ; Heart Rate ; Longevity ; Male ; Mole Rats - metabolism ; Mole Rats - physiology ; Morphology ; Myocardium - metabolism ; NMR ; Nuclear magnetic resonance ; Pulse Wave Analysis ; Rodents ; Time Factors ; Vascular Stiffness ; Ventricular Function, Left</subject><ispartof>American journal of physiology. Heart and circulatory physiology, 2014-08, Vol.307 (3), p.H284-H291</ispartof><rights>Copyright American Physiological Society Aug 1, 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c499t-c9cbe7c847f2ebc4cd552d667b81b443cd5af8f720e4ef52c6afa1b3faf534e43</citedby><cites>FETCH-LOGICAL-c499t-c9cbe7c847f2ebc4cd552d667b81b443cd5af8f720e4ef52c6afa1b3faf534e43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,3026,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24906918$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Grimes, Kelly M</creatorcontrib><creatorcontrib>Reddy, Anilkumar K</creatorcontrib><creatorcontrib>Lindsey, Merry L</creatorcontrib><creatorcontrib>Buffenstein, Rochelle</creatorcontrib><title>And the beat goes on: maintained cardiovascular function during aging in the longest-lived rodent, the naked mole-rat</title><title>American journal of physiology. Heart and circulatory physiology</title><addtitle>Am J Physiol Heart Circ Physiol</addtitle><description>The naked mole-rat (NMR) is the longest-lived rodent known, with a maximum lifespan potential (MLSP) of >31 years. Despite such extreme longevity, these animals display attenuation of many age-associated diseases and functional changes until the last quartile of their MLSP. We questioned if such abilities would extend to cardiovascular function and structure in this species. To test this, we assessed cardiac functional reserve, ventricular morphology, and arterial stiffening in NMRs ranging from 2 to 24 years of age. Dobutamine echocardiography (3 μg/g ip) revealed no age-associated changes in left ventricular (LV) function either at baseline or with exercise-like stress. Baseline and dobutamine-induced LV pressure parameters also did not change. Thus the NMR, unlike other mammals, maintains cardiac reserve with age. NMRs showed no cardiac hypertrophy, evidenced by no increase in cardiomyocyte cross-sectional area or LV dimensions with age. Age-associated arterial stiffening does not occur since there are no changes in aortic blood pressures or pulse-wave velocity. Only LV interstitial collagen deposition increased 2.5-fold from young to old NMRs (P < 0.01). However, its effect on LV diastolic function is likely minor since NMRs experience attenuated age-related increases in diastolic dysfunction in comparison with other species. Overall, these findings conform to the negligible senescence phenotype, as NMRs largely stave off cardiovascular changes for at least 75% of their MLSP. This suggests that using a comparative strategy to find factors that change with age in other mammals but not NMRs could provide novel targets to slow or prevent cardiovascular aging in humans.</description><subject>Age Factors</subject><subject>Aging</subject><subject>Aging - metabolism</subject><subject>Aging - physiology</subject><subject>Animals</subject><subject>Aorta - physiology</subject><subject>Arterial Pressure</subject><subject>Call for Papers</subject><subject>Cardiovascular system</subject><subject>Collagen</subject><subject>Collagen - metabolism</subject><subject>Compliance</subject><subject>Echocardiography, Stress</subject><subject>Female</subject><subject>Heart - physiology</subject><subject>Heart Rate</subject><subject>Longevity</subject><subject>Male</subject><subject>Mole Rats - metabolism</subject><subject>Mole Rats - physiology</subject><subject>Morphology</subject><subject>Myocardium - metabolism</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Pulse Wave Analysis</subject><subject>Rodents</subject><subject>Time Factors</subject><subject>Vascular Stiffness</subject><subject>Ventricular Function, Left</subject><issn>0363-6135</issn><issn>1522-1539</issn><issn>1522-1539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdUUmLFDEYDaI47egvECTgZQ5WT9ZaPAjD4AYDXsZz-CqVVKetStok1eC_n1TPgnpIQvKWfI-H0FtKtpRKdgn7w85AzFtCOJFbRqh4hjYFYRWVvHuONoTXvKopl2foVUp7Qohsav4SnTHRkbqj7QYtV37AeWdwbyDjMZiEg_-IZ3A-l2UGrCEOLhwh6WWCiO3idXbB42GJzo8YxnV3_mQyBT-alKvJHYsyhsH4_OGEePhVXuYwmSpCfo1eWJiSefNwnqOfXz7fXn-rbn58_X59dVNp0XW50p3uTaNb0Vhmei30ICUb6rrpW9oLwcsdbGsbRowwVjJdgwXacwtWcmEEP0ef7n0PSz-bQZdxIkzqEN0M8Y8K4NS_iHc7NYajEpTRWvJicPFgEMPvpURTs0vaTBN4E5akqJSUMEab9a_3_1H3YYm-xFtZTHDaipXF71k6hpSisU_DUKLWWtVjrepUq1prLap3f-d40jz2yO8A7CGjJw</recordid><startdate>20140801</startdate><enddate>20140801</enddate><creator>Grimes, Kelly M</creator><creator>Reddy, Anilkumar K</creator><creator>Lindsey, Merry L</creator><creator>Buffenstein, Rochelle</creator><general>American Physiological Society</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>7QP</scope><scope>7QR</scope><scope>7TS</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20140801</creationdate><title>And the beat goes on: maintained cardiovascular function during aging in the longest-lived rodent, the naked mole-rat</title><author>Grimes, Kelly M ; Reddy, Anilkumar K ; Lindsey, Merry L ; Buffenstein, Rochelle</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c499t-c9cbe7c847f2ebc4cd552d667b81b443cd5af8f720e4ef52c6afa1b3faf534e43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Age Factors</topic><topic>Aging</topic><topic>Aging - metabolism</topic><topic>Aging - physiology</topic><topic>Animals</topic><topic>Aorta - physiology</topic><topic>Arterial Pressure</topic><topic>Call for Papers</topic><topic>Cardiovascular system</topic><topic>Collagen</topic><topic>Collagen - metabolism</topic><topic>Compliance</topic><topic>Echocardiography, Stress</topic><topic>Female</topic><topic>Heart - physiology</topic><topic>Heart Rate</topic><topic>Longevity</topic><topic>Male</topic><topic>Mole Rats - metabolism</topic><topic>Mole Rats - physiology</topic><topic>Morphology</topic><topic>Myocardium - metabolism</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Pulse Wave Analysis</topic><topic>Rodents</topic><topic>Time Factors</topic><topic>Vascular Stiffness</topic><topic>Ventricular Function, Left</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Grimes, Kelly M</creatorcontrib><creatorcontrib>Reddy, Anilkumar K</creatorcontrib><creatorcontrib>Lindsey, Merry L</creatorcontrib><creatorcontrib>Buffenstein, Rochelle</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Physical Education Index</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>American journal of physiology. Heart and circulatory physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Grimes, Kelly M</au><au>Reddy, Anilkumar K</au><au>Lindsey, Merry L</au><au>Buffenstein, Rochelle</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>And the beat goes on: maintained cardiovascular function during aging in the longest-lived rodent, the naked mole-rat</atitle><jtitle>American journal of physiology. Heart and circulatory physiology</jtitle><addtitle>Am J Physiol Heart Circ Physiol</addtitle><date>2014-08-01</date><risdate>2014</risdate><volume>307</volume><issue>3</issue><spage>H284</spage><epage>H291</epage><pages>H284-H291</pages><issn>0363-6135</issn><issn>1522-1539</issn><eissn>1522-1539</eissn><coden>AJPPDI</coden><abstract>The naked mole-rat (NMR) is the longest-lived rodent known, with a maximum lifespan potential (MLSP) of >31 years. Despite such extreme longevity, these animals display attenuation of many age-associated diseases and functional changes until the last quartile of their MLSP. We questioned if such abilities would extend to cardiovascular function and structure in this species. To test this, we assessed cardiac functional reserve, ventricular morphology, and arterial stiffening in NMRs ranging from 2 to 24 years of age. Dobutamine echocardiography (3 μg/g ip) revealed no age-associated changes in left ventricular (LV) function either at baseline or with exercise-like stress. Baseline and dobutamine-induced LV pressure parameters also did not change. Thus the NMR, unlike other mammals, maintains cardiac reserve with age. NMRs showed no cardiac hypertrophy, evidenced by no increase in cardiomyocyte cross-sectional area or LV dimensions with age. Age-associated arterial stiffening does not occur since there are no changes in aortic blood pressures or pulse-wave velocity. Only LV interstitial collagen deposition increased 2.5-fold from young to old NMRs (P < 0.01). However, its effect on LV diastolic function is likely minor since NMRs experience attenuated age-related increases in diastolic dysfunction in comparison with other species. Overall, these findings conform to the negligible senescence phenotype, as NMRs largely stave off cardiovascular changes for at least 75% of their MLSP. This suggests that using a comparative strategy to find factors that change with age in other mammals but not NMRs could provide novel targets to slow or prevent cardiovascular aging in humans.</abstract><cop>United States</cop><pub>American Physiological Society</pub><pmid>24906918</pmid><doi>10.1152/ajpheart.00305.2014</doi><oa>free_for_read</oa></addata></record> |
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subjects | Age Factors Aging Aging - metabolism Aging - physiology Animals Aorta - physiology Arterial Pressure Call for Papers Cardiovascular system Collagen Collagen - metabolism Compliance Echocardiography, Stress Female Heart - physiology Heart Rate Longevity Male Mole Rats - metabolism Mole Rats - physiology Morphology Myocardium - metabolism NMR Nuclear magnetic resonance Pulse Wave Analysis Rodents Time Factors Vascular Stiffness Ventricular Function, Left |
title | And the beat goes on: maintained cardiovascular function during aging in the longest-lived rodent, the naked mole-rat |
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