Morphological and Functional Evidence for the Contribution of the Pudendal Artery in Aging-Induced Erectile Dysfunction
Aging increases the risk of both erectile dysfunction (ED) and cardiovascular disease. These conditions have similar etiologies and commonly coexist. One unifying concept is the role of arterial insufficiency which is a primary factor in the onset of age-related ED. Based on the novel finding that t...
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description | Aging increases the risk of both erectile dysfunction (ED) and cardiovascular disease. These conditions have similar etiologies and commonly coexist. One unifying concept is the role of arterial insufficiency which is a primary factor in the onset of age-related ED.
Based on the novel finding that the pudendal arteries contribute 70% of the total penile vascular resistance, our objective was to morphometrically and functionally characterize this vessel in young and old normotensive rats.
Erectile function was monitored in 15- and 77-week Sprague-Dawley rats using the apomorphine bioassay (80mg/kg, s.c.). Anesthetized animals were perfusion-fixed, aortic, renal, and internal pudendal arteries were excised, embedded, sectioned, stained, and morphometrically assessed using light microscopy. Hearts were excised, separated, and weighed prior to perfusion. Contractile and relaxation responses to acetylcholine (ACh) and phenylephrine (PE) were assessed by wire myograph.
Erectile function, morphological measurements, concentration response curves to ACh and PE.
With age, there were marked decreases in erectile responses compared to younger rats (2.8±0.87 vs. 0.3±0.58). The pudendal arteries had a relatively small lumen (303±13.8µm) and a thick medial layer (47±2.2µm). In aged pudendal arteries, the lumen diameter did not change, and yet the medial layer, cross sectional area, and extracellular matrix were markedly increased. In contrast, the lumen diameter and wall thickness of the aorta and renal arteries in aged rats increased proportionally. An increase in small, round, smooth muscle cells was seen in aged pudendal arteries. Functionally, there were no differences in contractile responses to PE; however, ACh-induced relaxation decreased with age.
In aged rats, erectile function was severely diminished when pudendal arteries had undergone marked phenotypic changes. Specifically, there was endothelial dysfunction and pathological remodeling of this vessel with age, characterized by medial thickening, impaired vasodilation and significantly reduced capacity for penile blood flow. Hannan JL, Blaser MC, Oldfield L, Pang JJ, Adams SM, Pang SC, and Adams MA. Morphological and functional evidence for the contribution of the pudendal artery in aging-induced erectile dysfunction. |
doi_str_mv | 10.1111/j.1743-6109.2010.01920.x |
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Based on the novel finding that the pudendal arteries contribute 70% of the total penile vascular resistance, our objective was to morphometrically and functionally characterize this vessel in young and old normotensive rats.
Erectile function was monitored in 15- and 77-week Sprague-Dawley rats using the apomorphine bioassay (80mg/kg, s.c.). Anesthetized animals were perfusion-fixed, aortic, renal, and internal pudendal arteries were excised, embedded, sectioned, stained, and morphometrically assessed using light microscopy. Hearts were excised, separated, and weighed prior to perfusion. Contractile and relaxation responses to acetylcholine (ACh) and phenylephrine (PE) were assessed by wire myograph.
Erectile function, morphological measurements, concentration response curves to ACh and PE.
With age, there were marked decreases in erectile responses compared to younger rats (2.8±0.87 vs. 0.3±0.58). The pudendal arteries had a relatively small lumen (303±13.8µm) and a thick medial layer (47±2.2µm). In aged pudendal arteries, the lumen diameter did not change, and yet the medial layer, cross sectional area, and extracellular matrix were markedly increased. In contrast, the lumen diameter and wall thickness of the aorta and renal arteries in aged rats increased proportionally. An increase in small, round, smooth muscle cells was seen in aged pudendal arteries. Functionally, there were no differences in contractile responses to PE; however, ACh-induced relaxation decreased with age.
In aged rats, erectile function was severely diminished when pudendal arteries had undergone marked phenotypic changes. Specifically, there was endothelial dysfunction and pathological remodeling of this vessel with age, characterized by medial thickening, impaired vasodilation and significantly reduced capacity for penile blood flow. Hannan JL, Blaser MC, Oldfield L, Pang JJ, Adams SM, Pang SC, and Adams MA. Morphological and functional evidence for the contribution of the pudendal artery in aging-induced erectile dysfunction.</description><identifier>ISSN: 1743-6095</identifier><identifier>EISSN: 1743-6109</identifier><identifier>DOI: 10.1111/j.1743-6109.2010.01920.x</identifier><identifier>PMID: 20584117</identifier><language>eng</language><publisher>Malden, USA: Elsevier Inc</publisher><subject>Acetylcholine - pharmacology ; Aging ; Aging - pathology ; Aging - physiology ; Animals ; Apomorphine ; Arteries - pathology ; Arteries - physiopathology ; Cardiovascular diseases ; Dose-Response Relationship, Drug ; Erectile Dysfunction ; Erectile Dysfunction - etiology ; Erectile Dysfunction - pathology ; Erectile Dysfunction - physiopathology ; Etiology ; Internal Pudendal Artery ; Male ; Penile Erection - drug effects ; Penile Erection - physiology ; Penis - blood supply ; Penis - drug effects ; Penis - pathology ; Penis - physiopathology ; Phenylephrine - pharmacology ; Rats ; Rats, Sprague-Dawley ; Sexual Health ; Vascular Health ; Vascular Remodelling</subject><ispartof>Journal of sexual medicine, 2010-10, Vol.7 (10), p.3373-3384</ispartof><rights>2010 International Society for Sexual Medicine</rights><rights>2010 International Society for Sexual Medicine.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5630-13abd0896fd0e4b7114d2fe59855524fcec8bf646fe3e72c2cc84db99f2751073</citedby><cites>FETCH-LOGICAL-c5630-13abd0896fd0e4b7114d2fe59855524fcec8bf646fe3e72c2cc84db99f2751073</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1743-6109.2010.01920.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1743-6109.2010.01920.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20584117$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hannan, Johanna L.</creatorcontrib><creatorcontrib>Blaser, Mark C.</creatorcontrib><creatorcontrib>Oldfield, Lauren</creatorcontrib><creatorcontrib>Pang, Judith J.</creatorcontrib><creatorcontrib>Adams, Stephen M.</creatorcontrib><creatorcontrib>Pang, Stephen C.</creatorcontrib><creatorcontrib>Adams, Michael A.</creatorcontrib><title>Morphological and Functional Evidence for the Contribution of the Pudendal Artery in Aging-Induced Erectile Dysfunction</title><title>Journal of sexual medicine</title><addtitle>J Sex Med</addtitle><description>Aging increases the risk of both erectile dysfunction (ED) and cardiovascular disease. These conditions have similar etiologies and commonly coexist. One unifying concept is the role of arterial insufficiency which is a primary factor in the onset of age-related ED.
Based on the novel finding that the pudendal arteries contribute 70% of the total penile vascular resistance, our objective was to morphometrically and functionally characterize this vessel in young and old normotensive rats.
Erectile function was monitored in 15- and 77-week Sprague-Dawley rats using the apomorphine bioassay (80mg/kg, s.c.). Anesthetized animals were perfusion-fixed, aortic, renal, and internal pudendal arteries were excised, embedded, sectioned, stained, and morphometrically assessed using light microscopy. Hearts were excised, separated, and weighed prior to perfusion. Contractile and relaxation responses to acetylcholine (ACh) and phenylephrine (PE) were assessed by wire myograph.
Erectile function, morphological measurements, concentration response curves to ACh and PE.
With age, there were marked decreases in erectile responses compared to younger rats (2.8±0.87 vs. 0.3±0.58). The pudendal arteries had a relatively small lumen (303±13.8µm) and a thick medial layer (47±2.2µm). In aged pudendal arteries, the lumen diameter did not change, and yet the medial layer, cross sectional area, and extracellular matrix were markedly increased. In contrast, the lumen diameter and wall thickness of the aorta and renal arteries in aged rats increased proportionally. An increase in small, round, smooth muscle cells was seen in aged pudendal arteries. Functionally, there were no differences in contractile responses to PE; however, ACh-induced relaxation decreased with age.
In aged rats, erectile function was severely diminished when pudendal arteries had undergone marked phenotypic changes. Specifically, there was endothelial dysfunction and pathological remodeling of this vessel with age, characterized by medial thickening, impaired vasodilation and significantly reduced capacity for penile blood flow. Hannan JL, Blaser MC, Oldfield L, Pang JJ, Adams SM, Pang SC, and Adams MA. Morphological and functional evidence for the contribution of the pudendal artery in aging-induced erectile dysfunction.</description><subject>Acetylcholine - pharmacology</subject><subject>Aging</subject><subject>Aging - pathology</subject><subject>Aging - physiology</subject><subject>Animals</subject><subject>Apomorphine</subject><subject>Arteries - pathology</subject><subject>Arteries - physiopathology</subject><subject>Cardiovascular diseases</subject><subject>Dose-Response Relationship, Drug</subject><subject>Erectile Dysfunction</subject><subject>Erectile Dysfunction - etiology</subject><subject>Erectile Dysfunction - pathology</subject><subject>Erectile Dysfunction - physiopathology</subject><subject>Etiology</subject><subject>Internal Pudendal Artery</subject><subject>Male</subject><subject>Penile Erection - drug effects</subject><subject>Penile Erection - physiology</subject><subject>Penis - blood supply</subject><subject>Penis - drug effects</subject><subject>Penis - pathology</subject><subject>Penis - physiopathology</subject><subject>Phenylephrine - pharmacology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Sexual Health</subject><subject>Vascular Health</subject><subject>Vascular Remodelling</subject><issn>1743-6095</issn><issn>1743-6109</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU1z2yAQhjWdZpo06V_ocOtJDiAhpEMPtuN8jZM2_ZgeGQkWB1cWDkiJ_e-LLMfXdC8su8-7DPtGESJ4REKcL0eEp0mcEVyMKA5VTAqKR5t30cmh8f41xwU7jj56v8Q4CUE_RMcUszwlhJ9EL3fWrR9tbRdGljUqG4Uuu0a2xjbhOns2ChoJSFuH2kdAU9u0zlRd30dW72rfu8CoQI9dC26LTIPGC9Ms4ptGdRIUmjkIA2tAF1uv98PPoiNd1h4-7c_T6Pfl7Nf0Op5_u7qZjuexZFmCY5KUlcJ5kWmFIa04IamiGliRM8ZoqiXIvNJZmmlIgFNJpcxTVRWFppwRzJPT6Mswd-3sUwe-FSvjJdR12YDtvChYyvLdYt4ieUbTnIatBTIfSOms9w60WDuzKt1WECx6f8RS9KsXvQ2i90fs_BGbIP28f6SrVqAOwldDAvB1AF7Cwrb_PVjc_rzrs6CPB73xLWwO-tL9FRlPOBN_7q_E5Ho6uX_4kYh54CcDD8GEZwNOeGl6y5XpXRPKmrd_9Q80JMOd</recordid><startdate>201010</startdate><enddate>201010</enddate><creator>Hannan, Johanna L.</creator><creator>Blaser, Mark C.</creator><creator>Oldfield, Lauren</creator><creator>Pang, Judith J.</creator><creator>Adams, Stephen M.</creator><creator>Pang, Stephen C.</creator><creator>Adams, Michael A.</creator><general>Elsevier Inc</general><general>Blackwell Publishing Inc</general><scope>BSCLL</scope><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><scope>7U1</scope><scope>7U2</scope><scope>C1K</scope></search><sort><creationdate>201010</creationdate><title>Morphological and Functional Evidence for the Contribution of the Pudendal Artery in Aging-Induced Erectile Dysfunction</title><author>Hannan, Johanna L. ; Blaser, Mark C. ; Oldfield, Lauren ; Pang, Judith J. ; Adams, Stephen M. ; Pang, Stephen C. ; Adams, Michael A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5630-13abd0896fd0e4b7114d2fe59855524fcec8bf646fe3e72c2cc84db99f2751073</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Acetylcholine - pharmacology</topic><topic>Aging</topic><topic>Aging - pathology</topic><topic>Aging - physiology</topic><topic>Animals</topic><topic>Apomorphine</topic><topic>Arteries - pathology</topic><topic>Arteries - physiopathology</topic><topic>Cardiovascular diseases</topic><topic>Dose-Response Relationship, Drug</topic><topic>Erectile Dysfunction</topic><topic>Erectile Dysfunction - etiology</topic><topic>Erectile Dysfunction - pathology</topic><topic>Erectile Dysfunction - physiopathology</topic><topic>Etiology</topic><topic>Internal Pudendal Artery</topic><topic>Male</topic><topic>Penile Erection - drug effects</topic><topic>Penile Erection - physiology</topic><topic>Penis - blood supply</topic><topic>Penis - drug effects</topic><topic>Penis - pathology</topic><topic>Penis - physiopathology</topic><topic>Phenylephrine - pharmacology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Sexual Health</topic><topic>Vascular Health</topic><topic>Vascular Remodelling</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hannan, Johanna L.</creatorcontrib><creatorcontrib>Blaser, Mark C.</creatorcontrib><creatorcontrib>Oldfield, Lauren</creatorcontrib><creatorcontrib>Pang, Judith J.</creatorcontrib><creatorcontrib>Adams, Stephen M.</creatorcontrib><creatorcontrib>Pang, Stephen C.</creatorcontrib><creatorcontrib>Adams, Michael A.</creatorcontrib><collection>Istex</collection><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><collection>Risk Abstracts</collection><collection>Safety Science and Risk</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Journal of sexual medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hannan, Johanna L.</au><au>Blaser, Mark C.</au><au>Oldfield, Lauren</au><au>Pang, Judith J.</au><au>Adams, Stephen M.</au><au>Pang, Stephen C.</au><au>Adams, Michael A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Morphological and Functional Evidence for the Contribution of the Pudendal Artery in Aging-Induced Erectile Dysfunction</atitle><jtitle>Journal of sexual medicine</jtitle><addtitle>J Sex Med</addtitle><date>2010-10</date><risdate>2010</risdate><volume>7</volume><issue>10</issue><spage>3373</spage><epage>3384</epage><pages>3373-3384</pages><issn>1743-6095</issn><eissn>1743-6109</eissn><abstract>Aging increases the risk of both erectile dysfunction (ED) and cardiovascular disease. These conditions have similar etiologies and commonly coexist. One unifying concept is the role of arterial insufficiency which is a primary factor in the onset of age-related ED.
Based on the novel finding that the pudendal arteries contribute 70% of the total penile vascular resistance, our objective was to morphometrically and functionally characterize this vessel in young and old normotensive rats.
Erectile function was monitored in 15- and 77-week Sprague-Dawley rats using the apomorphine bioassay (80mg/kg, s.c.). Anesthetized animals were perfusion-fixed, aortic, renal, and internal pudendal arteries were excised, embedded, sectioned, stained, and morphometrically assessed using light microscopy. Hearts were excised, separated, and weighed prior to perfusion. Contractile and relaxation responses to acetylcholine (ACh) and phenylephrine (PE) were assessed by wire myograph.
Erectile function, morphological measurements, concentration response curves to ACh and PE.
With age, there were marked decreases in erectile responses compared to younger rats (2.8±0.87 vs. 0.3±0.58). The pudendal arteries had a relatively small lumen (303±13.8µm) and a thick medial layer (47±2.2µm). In aged pudendal arteries, the lumen diameter did not change, and yet the medial layer, cross sectional area, and extracellular matrix were markedly increased. In contrast, the lumen diameter and wall thickness of the aorta and renal arteries in aged rats increased proportionally. An increase in small, round, smooth muscle cells was seen in aged pudendal arteries. Functionally, there were no differences in contractile responses to PE; however, ACh-induced relaxation decreased with age.
In aged rats, erectile function was severely diminished when pudendal arteries had undergone marked phenotypic changes. Specifically, there was endothelial dysfunction and pathological remodeling of this vessel with age, characterized by medial thickening, impaired vasodilation and significantly reduced capacity for penile blood flow. Hannan JL, Blaser MC, Oldfield L, Pang JJ, Adams SM, Pang SC, and Adams MA. Morphological and functional evidence for the contribution of the pudendal artery in aging-induced erectile dysfunction.</abstract><cop>Malden, USA</cop><pub>Elsevier Inc</pub><pmid>20584117</pmid><doi>10.1111/j.1743-6109.2010.01920.x</doi><tpages>12</tpages></addata></record> |
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subjects | Acetylcholine - pharmacology Aging Aging - pathology Aging - physiology Animals Apomorphine Arteries - pathology Arteries - physiopathology Cardiovascular diseases Dose-Response Relationship, Drug Erectile Dysfunction Erectile Dysfunction - etiology Erectile Dysfunction - pathology Erectile Dysfunction - physiopathology Etiology Internal Pudendal Artery Male Penile Erection - drug effects Penile Erection - physiology Penis - blood supply Penis - drug effects Penis - pathology Penis - physiopathology Phenylephrine - pharmacology Rats Rats, Sprague-Dawley Sexual Health Vascular Health Vascular Remodelling |
title | Morphological and Functional Evidence for the Contribution of the Pudendal Artery in Aging-Induced Erectile Dysfunction |
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