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Vascular Ultrasound for In Vivo Assessment of Arterial Pathologies in a Murine Model of Atherosclerosis and Aortic Aneurysm
Vascular diseases like atherosclerosis and abdominal aortic aneurysm (AAA) are common pathologies in the western world, promoting various potentially fatal conditions. Here, we evaluate high-resolution (HR) ultrasound in mouse models of atherosclerosis and AAA as a useful tool for noninvasive monito...
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Published in: | International journal of molecular sciences 2023-10, Vol.24 (20), p.15261 |
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creator | Hof, Alexander Guthoff, Henning Ahdab, Maysam Landerer, Max Schäkel, Jasper Niehues, Jana Schorscher, Maximilian Zimmermann, Oscar Winkels, Holger von Stein, Philipp Geißen, Simon Baldus, Stephan Adam, Matti Mollenhauer, Martin Mehrkens, Dennis |
description | Vascular diseases like atherosclerosis and abdominal aortic aneurysm (AAA) are common pathologies in the western world, promoting various potentially fatal conditions. Here, we evaluate high-resolution (HR) ultrasound in mouse models of atherosclerosis and AAA as a useful tool for noninvasive monitoring of early vascular changes in vivo. We used Apolipoprotein E-deficient (
) mice as an atherosclerosis model and induced AAA development by the implementation of Angiotensin II-releasing osmotic minipumps. HR ultrasound of the carotid artery or the abdominal aorta was performed to monitor vascular remodeling in vivo. Images were analyzed by speckle tracking algorithms and correlated to histological analyses and subsequent automated collagen quantification. Consistent changes were observed via ultrasound in both models: Global radial strain (GRS) was notably reduced in the AAA model (23.8 ± 2.8% vs. 12.5 ± 2.5%,
= 0.01) and in the atherosclerotic mice (20.6 ± 1.3% vs. 15.8 ± 0.9%,
= 0.02). In mice with AAA, vessel distensibility was significantly reduced, whereas intima-media thickness was increased in atherosclerotic mice. The area and collagen content of the tunica media were increased in diseased arteries of both models as measured by automated image analysis of Picrosirius Red-stained aortic sections. Correlation analysis revealed a strong correlation of multiple parameters, predicting early vascular damage in HR ultrasound and histological examinations. In conclusion, our findings underscore the potential of HR ultrasound in effectively tracing early alterations in arterial wall properties in murine models of atherosclerosis and AAA. |
doi_str_mv | 10.3390/ijms242015261 |
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) mice as an atherosclerosis model and induced AAA development by the implementation of Angiotensin II-releasing osmotic minipumps. HR ultrasound of the carotid artery or the abdominal aorta was performed to monitor vascular remodeling in vivo. Images were analyzed by speckle tracking algorithms and correlated to histological analyses and subsequent automated collagen quantification. Consistent changes were observed via ultrasound in both models: Global radial strain (GRS) was notably reduced in the AAA model (23.8 ± 2.8% vs. 12.5 ± 2.5%,
= 0.01) and in the atherosclerotic mice (20.6 ± 1.3% vs. 15.8 ± 0.9%,
= 0.02). In mice with AAA, vessel distensibility was significantly reduced, whereas intima-media thickness was increased in atherosclerotic mice. The area and collagen content of the tunica media were increased in diseased arteries of both models as measured by automated image analysis of Picrosirius Red-stained aortic sections. Correlation analysis revealed a strong correlation of multiple parameters, predicting early vascular damage in HR ultrasound and histological examinations. In conclusion, our findings underscore the potential of HR ultrasound in effectively tracing early alterations in arterial wall properties in murine models of atherosclerosis and AAA.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms242015261</identifier><identifier>PMID: 37894941</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Abdomen ; Aneurysms ; Angiotensin II ; Animals ; Aorta, Abdominal - diagnostic imaging ; Aortic Aneurysm, Abdominal - diagnostic imaging ; Aortic Aneurysm, Abdominal - pathology ; Aortic aneurysms ; Atherosclerosis ; Atherosclerosis - diagnostic imaging ; Atherosclerosis - pathology ; Automation ; Carotid arteries ; Carotid Intima-Media Thickness ; Collagen ; Coronary vessels ; Correlation analysis ; Disease Models, Animal ; Mice ; Mice, Inbred C57BL ; Morphology ; Physiology ; Ultrasonic imaging ; Veins & arteries</subject><ispartof>International journal of molecular sciences, 2023-10, Vol.24 (20), p.15261</ispartof><rights>COPYRIGHT 2023 MDPI AG</rights><rights>2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2023 by the authors. 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c439t-1c3c5bfde971a5872a35134b35207f0e68ea75c816db98e693e82a91684dc7693</cites><orcidid>0000-0001-5996-8292 ; 0000-0001-6554-8892 ; 0000-0002-0979-1190 ; 0000-0002-3220-9269 ; 0000-0002-8578-0290 ; 0000-0003-4548-3897 ; 0000-0003-1333-2031</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2882595417/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2882595417?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25752,27923,27924,37011,37012,44589,53790,53792,74897</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37894941$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hof, Alexander</creatorcontrib><creatorcontrib>Guthoff, Henning</creatorcontrib><creatorcontrib>Ahdab, Maysam</creatorcontrib><creatorcontrib>Landerer, Max</creatorcontrib><creatorcontrib>Schäkel, Jasper</creatorcontrib><creatorcontrib>Niehues, Jana</creatorcontrib><creatorcontrib>Schorscher, Maximilian</creatorcontrib><creatorcontrib>Zimmermann, Oscar</creatorcontrib><creatorcontrib>Winkels, Holger</creatorcontrib><creatorcontrib>von Stein, Philipp</creatorcontrib><creatorcontrib>Geißen, Simon</creatorcontrib><creatorcontrib>Baldus, Stephan</creatorcontrib><creatorcontrib>Adam, Matti</creatorcontrib><creatorcontrib>Mollenhauer, Martin</creatorcontrib><creatorcontrib>Mehrkens, Dennis</creatorcontrib><title>Vascular Ultrasound for In Vivo Assessment of Arterial Pathologies in a Murine Model of Atherosclerosis and Aortic Aneurysm</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>Vascular diseases like atherosclerosis and abdominal aortic aneurysm (AAA) are common pathologies in the western world, promoting various potentially fatal conditions. Here, we evaluate high-resolution (HR) ultrasound in mouse models of atherosclerosis and AAA as a useful tool for noninvasive monitoring of early vascular changes in vivo. We used Apolipoprotein E-deficient (
) mice as an atherosclerosis model and induced AAA development by the implementation of Angiotensin II-releasing osmotic minipumps. HR ultrasound of the carotid artery or the abdominal aorta was performed to monitor vascular remodeling in vivo. Images were analyzed by speckle tracking algorithms and correlated to histological analyses and subsequent automated collagen quantification. Consistent changes were observed via ultrasound in both models: Global radial strain (GRS) was notably reduced in the AAA model (23.8 ± 2.8% vs. 12.5 ± 2.5%,
= 0.01) and in the atherosclerotic mice (20.6 ± 1.3% vs. 15.8 ± 0.9%,
= 0.02). In mice with AAA, vessel distensibility was significantly reduced, whereas intima-media thickness was increased in atherosclerotic mice. The area and collagen content of the tunica media were increased in diseased arteries of both models as measured by automated image analysis of Picrosirius Red-stained aortic sections. Correlation analysis revealed a strong correlation of multiple parameters, predicting early vascular damage in HR ultrasound and histological examinations. In conclusion, our findings underscore the potential of HR ultrasound in effectively tracing early alterations in arterial wall properties in murine models of atherosclerosis and AAA.</description><subject>Abdomen</subject><subject>Aneurysms</subject><subject>Angiotensin II</subject><subject>Animals</subject><subject>Aorta, Abdominal - diagnostic imaging</subject><subject>Aortic Aneurysm, Abdominal - diagnostic imaging</subject><subject>Aortic Aneurysm, Abdominal - pathology</subject><subject>Aortic aneurysms</subject><subject>Atherosclerosis</subject><subject>Atherosclerosis - diagnostic imaging</subject><subject>Atherosclerosis - pathology</subject><subject>Automation</subject><subject>Carotid arteries</subject><subject>Carotid Intima-Media Thickness</subject><subject>Collagen</subject><subject>Coronary vessels</subject><subject>Correlation analysis</subject><subject>Disease Models, Animal</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Morphology</subject><subject>Physiology</subject><subject>Ultrasonic imaging</subject><subject>Veins & arteries</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNptkstrFTEUxoMotlaXbiXgxs3UPCaTZCVDUVto0YXtNuRmztybSyapyUyh-M-bax_2igTy_J0vfB8HobeUHHOuyUe_nQprGaGCdfQZOqQtYw0hnXz-ZH-AXpWyJYRxJvRLdMCl0q1u6SH6dWWLW4LN-DLM2Za0xAGPKeOziK_8TcJ9KVDKBHHGacR9niF7G_B3O29SSGsPBfuILb5Yso-AL9IA4Q85byCn4sJu9gXbqtunPHuH-whLvi3Ta_RitKHAm_v1CF1--fzj5LQ5__b17KQ_b1zL9dxQx51YjQNoSa1QklkuKG9XXDAiRwKdAiuFU7QbVlpBpzkoZjXtVDs4WY9H6NOd7vWymmBw1Uu2wVxnP9l8a5L1Zv8l-o1ZpxtDSUek6GRV-HCvkNPPBcpsJl8chGAjpKUYphQXknLWVvT9P-g2LTlWfzuqxi9aKv9SaxvA-Dim-rHbiZpeSqopEZpW6vg_VB0DTN6lCKOv93sFzV2Bq6GXDOOjSUrMrl3MXrtU_t3TZB7ph_7gvwGsErsb</recordid><startdate>20231017</startdate><enddate>20231017</enddate><creator>Hof, Alexander</creator><creator>Guthoff, Henning</creator><creator>Ahdab, Maysam</creator><creator>Landerer, Max</creator><creator>Schäkel, Jasper</creator><creator>Niehues, Jana</creator><creator>Schorscher, Maximilian</creator><creator>Zimmermann, Oscar</creator><creator>Winkels, Holger</creator><creator>von Stein, Philipp</creator><creator>Geißen, Simon</creator><creator>Baldus, Stephan</creator><creator>Adam, Matti</creator><creator>Mollenhauer, Martin</creator><creator>Mehrkens, Dennis</creator><general>MDPI AG</general><general>MDPI</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-5996-8292</orcidid><orcidid>https://orcid.org/0000-0001-6554-8892</orcidid><orcidid>https://orcid.org/0000-0002-0979-1190</orcidid><orcidid>https://orcid.org/0000-0002-3220-9269</orcidid><orcidid>https://orcid.org/0000-0002-8578-0290</orcidid><orcidid>https://orcid.org/0000-0003-4548-3897</orcidid><orcidid>https://orcid.org/0000-0003-1333-2031</orcidid></search><sort><creationdate>20231017</creationdate><title>Vascular Ultrasound for In Vivo Assessment of Arterial Pathologies in a Murine Model of Atherosclerosis and Aortic Aneurysm</title><author>Hof, Alexander ; Guthoff, Henning ; Ahdab, Maysam ; Landerer, Max ; Schäkel, Jasper ; Niehues, Jana ; Schorscher, Maximilian ; Zimmermann, Oscar ; Winkels, Holger ; von Stein, Philipp ; Geißen, Simon ; Baldus, Stephan ; Adam, Matti ; Mollenhauer, Martin ; Mehrkens, Dennis</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c439t-1c3c5bfde971a5872a35134b35207f0e68ea75c816db98e693e82a91684dc7693</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Abdomen</topic><topic>Aneurysms</topic><topic>Angiotensin II</topic><topic>Animals</topic><topic>Aorta, Abdominal - 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Here, we evaluate high-resolution (HR) ultrasound in mouse models of atherosclerosis and AAA as a useful tool for noninvasive monitoring of early vascular changes in vivo. We used Apolipoprotein E-deficient (
) mice as an atherosclerosis model and induced AAA development by the implementation of Angiotensin II-releasing osmotic minipumps. HR ultrasound of the carotid artery or the abdominal aorta was performed to monitor vascular remodeling in vivo. Images were analyzed by speckle tracking algorithms and correlated to histological analyses and subsequent automated collagen quantification. Consistent changes were observed via ultrasound in both models: Global radial strain (GRS) was notably reduced in the AAA model (23.8 ± 2.8% vs. 12.5 ± 2.5%,
= 0.01) and in the atherosclerotic mice (20.6 ± 1.3% vs. 15.8 ± 0.9%,
= 0.02). In mice with AAA, vessel distensibility was significantly reduced, whereas intima-media thickness was increased in atherosclerotic mice. The area and collagen content of the tunica media were increased in diseased arteries of both models as measured by automated image analysis of Picrosirius Red-stained aortic sections. Correlation analysis revealed a strong correlation of multiple parameters, predicting early vascular damage in HR ultrasound and histological examinations. In conclusion, our findings underscore the potential of HR ultrasound in effectively tracing early alterations in arterial wall properties in murine models of atherosclerosis and AAA.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>37894941</pmid><doi>10.3390/ijms242015261</doi><orcidid>https://orcid.org/0000-0001-5996-8292</orcidid><orcidid>https://orcid.org/0000-0001-6554-8892</orcidid><orcidid>https://orcid.org/0000-0002-0979-1190</orcidid><orcidid>https://orcid.org/0000-0002-3220-9269</orcidid><orcidid>https://orcid.org/0000-0002-8578-0290</orcidid><orcidid>https://orcid.org/0000-0003-4548-3897</orcidid><orcidid>https://orcid.org/0000-0003-1333-2031</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Abdomen Aneurysms Angiotensin II Animals Aorta, Abdominal - diagnostic imaging Aortic Aneurysm, Abdominal - diagnostic imaging Aortic Aneurysm, Abdominal - pathology Aortic aneurysms Atherosclerosis Atherosclerosis - diagnostic imaging Atherosclerosis - pathology Automation Carotid arteries Carotid Intima-Media Thickness Collagen Coronary vessels Correlation analysis Disease Models, Animal Mice Mice, Inbred C57BL Morphology Physiology Ultrasonic imaging Veins & arteries |
title | Vascular Ultrasound for In Vivo Assessment of Arterial Pathologies in a Murine Model of Atherosclerosis and Aortic Aneurysm |
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