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Effect of Sildenafil Citrate on Penile Weight and Physiology of Cavernous Smooth Muscle in a Post–radical Prostatectomy Model of Erectile Dysfunction in Rats
Objectives To evaluate the gross morphometric changes and in vitro responses of the corpus cavernosus of rats treated with sildenafil citrate after cavernous neurotomy. Methods The animals were divided into 3 groups. Group 1 consisted of sham-operated rats (n = 16); group 2 consisted of rats that un...
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Published in: | Urology (Ridgewood, N.J.) N.J.), 2011-03, Vol.77 (3), p.761.e1-761.e7 |
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description | Objectives To evaluate the gross morphometric changes and in vitro responses of the corpus cavernosus of rats treated with sildenafil citrate after cavernous neurotomy. Methods The animals were divided into 3 groups. Group 1 consisted of sham-operated rats (n = 16); group 2 consisted of rats that underwent bilateral cavernous neurotomy (BCN) (n = 16); and group 3 consisted of rats that underwent unilateral cavernous neurotomy (UCN) (n = 16). Each group of rats was further classified into 2 subgroups according to whether or not they received sildenafil treatment. The rats were killed on postoperative day 14, and penectomy was performed. Apoptosis was assessed by terminal deoxynucleotidyl transferase-mediated deoxyuridine triphosphate nick end labeling (TUNEL), and organ-bath studies were evaluated by Phenylephrine (Phe), acetylcholine (Ach), sodium nitroprusside (SNP), and electrical field stimulation (EFS) responses. Results Penile weight in the BCN group was significantly lower than that of sham-treated group. UCN allowed much more preservation of penile weight compared with that in the sham-treated group. Sildenafil citrate treatment had positive effects on penile weight of both BCN ( P = .003) and UCN ( P = .004) groups. BCN increased smooth muscle apoptosis when compared with the sham or UCN group. Sildenafil citrate had a positive effect on the apoptotic index. In the BCN group, responses to Phe, Ach, SNP, and EFS decreased significantly, and sildenafil treatment corrected the responses to Phe, Ach, and SNP. Conclusions Our experimental study results support that early and daily sildenafil citrate treatment has a protective affect on the adrenergic and cholinergic systems, which play a role in erectile function. |
doi_str_mv | 10.1016/j.urology.2010.10.009 |
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Methods The animals were divided into 3 groups. Group 1 consisted of sham-operated rats (n = 16); group 2 consisted of rats that underwent bilateral cavernous neurotomy (BCN) (n = 16); and group 3 consisted of rats that underwent unilateral cavernous neurotomy (UCN) (n = 16). Each group of rats was further classified into 2 subgroups according to whether or not they received sildenafil treatment. The rats were killed on postoperative day 14, and penectomy was performed. Apoptosis was assessed by terminal deoxynucleotidyl transferase-mediated deoxyuridine triphosphate nick end labeling (TUNEL), and organ-bath studies were evaluated by Phenylephrine (Phe), acetylcholine (Ach), sodium nitroprusside (SNP), and electrical field stimulation (EFS) responses. Results Penile weight in the BCN group was significantly lower than that of sham-treated group. UCN allowed much more preservation of penile weight compared with that in the sham-treated group. Sildenafil citrate treatment had positive effects on penile weight of both BCN ( P = .003) and UCN ( P = .004) groups. BCN increased smooth muscle apoptosis when compared with the sham or UCN group. Sildenafil citrate had a positive effect on the apoptotic index. In the BCN group, responses to Phe, Ach, SNP, and EFS decreased significantly, and sildenafil treatment corrected the responses to Phe, Ach, and SNP. Conclusions Our experimental study results support that early and daily sildenafil citrate treatment has a protective affect on the adrenergic and cholinergic systems, which play a role in erectile function.</description><identifier>ISSN: 0090-4295</identifier><identifier>EISSN: 1527-9995</identifier><identifier>DOI: 10.1016/j.urology.2010.10.009</identifier><identifier>PMID: 21256544</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Apoptosis - drug effects ; Erectile Dysfunction - etiology ; Erectile Dysfunction - pathology ; Erectile Dysfunction - physiopathology ; In Situ Nick-End Labeling ; In Vitro Techniques ; Male ; Muscle Contraction - drug effects ; Muscle, Smooth - innervation ; Muscle, Smooth - physiopathology ; Organ Size - drug effects ; Penis - drug effects ; Penis - innervation ; Penis - pathology ; Penis - physiopathology ; Phosphodiesterase 5 Inhibitors - pharmacology ; Piperazines - pharmacology ; Prostatectomy - adverse effects ; Purines - pharmacology ; Rats ; Rats, Wistar ; Sildenafil Citrate ; Sulfones - pharmacology ; Urology</subject><ispartof>Urology (Ridgewood, N.J.), 2011-03, Vol.77 (3), p.761.e1-761.e7</ispartof><rights>Elsevier Inc.</rights><rights>2011 Elsevier Inc.</rights><rights>Copyright © 2011 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c349t-3ede4977b8cec21468741ff63ec182db64300249b6d037d0d57bef84b4377a2d3</citedby><cites>FETCH-LOGICAL-c349t-3ede4977b8cec21468741ff63ec182db64300249b6d037d0d57bef84b4377a2d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21256544$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Özden, Ender</creatorcontrib><creatorcontrib>Öztürk, Bülent</creatorcontrib><creatorcontrib>Koşan, Murat</creatorcontrib><creatorcontrib>Tezel, Gaye Güler</creatorcontrib><creatorcontrib>Aki, Fazil Tuncay</creatorcontrib><creatorcontrib>Gür, Serap</creatorcontrib><creatorcontrib>Ergen, Ali</creatorcontrib><creatorcontrib>Özen, Haluk</creatorcontrib><title>Effect of Sildenafil Citrate on Penile Weight and Physiology of Cavernous Smooth Muscle in a Post–radical Prostatectomy Model of Erectile Dysfunction in Rats</title><title>Urology (Ridgewood, N.J.)</title><addtitle>Urology</addtitle><description>Objectives To evaluate the gross morphometric changes and in vitro responses of the corpus cavernosus of rats treated with sildenafil citrate after cavernous neurotomy. Methods The animals were divided into 3 groups. Group 1 consisted of sham-operated rats (n = 16); group 2 consisted of rats that underwent bilateral cavernous neurotomy (BCN) (n = 16); and group 3 consisted of rats that underwent unilateral cavernous neurotomy (UCN) (n = 16). Each group of rats was further classified into 2 subgroups according to whether or not they received sildenafil treatment. The rats were killed on postoperative day 14, and penectomy was performed. Apoptosis was assessed by terminal deoxynucleotidyl transferase-mediated deoxyuridine triphosphate nick end labeling (TUNEL), and organ-bath studies were evaluated by Phenylephrine (Phe), acetylcholine (Ach), sodium nitroprusside (SNP), and electrical field stimulation (EFS) responses. Results Penile weight in the BCN group was significantly lower than that of sham-treated group. UCN allowed much more preservation of penile weight compared with that in the sham-treated group. Sildenafil citrate treatment had positive effects on penile weight of both BCN ( P = .003) and UCN ( P = .004) groups. BCN increased smooth muscle apoptosis when compared with the sham or UCN group. Sildenafil citrate had a positive effect on the apoptotic index. In the BCN group, responses to Phe, Ach, SNP, and EFS decreased significantly, and sildenafil treatment corrected the responses to Phe, Ach, and SNP. Conclusions Our experimental study results support that early and daily sildenafil citrate treatment has a protective affect on the adrenergic and cholinergic systems, which play a role in erectile function.</description><subject>Animals</subject><subject>Apoptosis - drug effects</subject><subject>Erectile Dysfunction - etiology</subject><subject>Erectile Dysfunction - pathology</subject><subject>Erectile Dysfunction - physiopathology</subject><subject>In Situ Nick-End Labeling</subject><subject>In Vitro Techniques</subject><subject>Male</subject><subject>Muscle Contraction - drug effects</subject><subject>Muscle, Smooth - innervation</subject><subject>Muscle, Smooth - physiopathology</subject><subject>Organ Size - drug effects</subject><subject>Penis - drug effects</subject><subject>Penis - innervation</subject><subject>Penis - pathology</subject><subject>Penis - physiopathology</subject><subject>Phosphodiesterase 5 Inhibitors - pharmacology</subject><subject>Piperazines - pharmacology</subject><subject>Prostatectomy - adverse effects</subject><subject>Purines - pharmacology</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Sildenafil Citrate</subject><subject>Sulfones - pharmacology</subject><subject>Urology</subject><issn>0090-4295</issn><issn>1527-9995</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNqFUsuO0zAUtRCIKQOfAPKOVYrtOE68AaFSHtKMqCgIdpZj30xdUnuwk5Gy4x_4AP6NL8GZFhZsWNk-Og_de4zQY0qWlFDxbL8cY-jD1bRk5BZbEiLvoAWtWF1IKau7aJERUnAmqzP0IKU9IUQIUd9HZ4yySlScL9DPddeBGXDo8Nb1FrzuXI9Xboh6ABw83oB3PeDP4K52A9be4s1uSu42elat9A1EH8aEt4cQhh2-HJPJAuexxpuQhl_ff0RtndE93sT8zr5mCIcJXwYL_WyxjhmZQ15NqRt9vufcrP-gh_QQ3et0n-DR6TxHn16vP67eFhfv37xbvbwoTMnlUJRggcu6bhsDhlEumprTrhMlGNow2wpeEsK4bIUlZW2JreoWuoa3vKxrzWx5jp4efa9j-DZCGtTBJQN9rz3k4VRTVZKIUsjMrI5Mk6dJETp1Hd1Bx0lRouZq1F6dqlFzNTOci8i6J6eEsT2A_av600UmvDgSIM954yCqZBx4A9bNC1I2uP9GPP_HwfTOz6v_ChOkfRijz0tUVCWmiNrO_2P-HpQQ2nD2pfwNfQS68Q</recordid><startdate>20110301</startdate><enddate>20110301</enddate><creator>Özden, Ender</creator><creator>Öztürk, Bülent</creator><creator>Koşan, Murat</creator><creator>Tezel, Gaye Güler</creator><creator>Aki, Fazil Tuncay</creator><creator>Gür, Serap</creator><creator>Ergen, Ali</creator><creator>Özen, Haluk</creator><general>Elsevier Inc</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>20110301</creationdate><title>Effect of Sildenafil Citrate on Penile Weight and Physiology of Cavernous Smooth Muscle in a Post–radical Prostatectomy Model of Erectile Dysfunction in Rats</title><author>Özden, Ender ; Öztürk, Bülent ; Koşan, Murat ; Tezel, Gaye Güler ; Aki, Fazil Tuncay ; Gür, Serap ; Ergen, Ali ; Özen, Haluk</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c349t-3ede4977b8cec21468741ff63ec182db64300249b6d037d0d57bef84b4377a2d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Animals</topic><topic>Apoptosis - drug effects</topic><topic>Erectile Dysfunction - etiology</topic><topic>Erectile Dysfunction - pathology</topic><topic>Erectile Dysfunction - physiopathology</topic><topic>In Situ Nick-End Labeling</topic><topic>In Vitro Techniques</topic><topic>Male</topic><topic>Muscle Contraction - drug effects</topic><topic>Muscle, Smooth - innervation</topic><topic>Muscle, Smooth - physiopathology</topic><topic>Organ Size - drug effects</topic><topic>Penis - drug effects</topic><topic>Penis - innervation</topic><topic>Penis - pathology</topic><topic>Penis - physiopathology</topic><topic>Phosphodiesterase 5 Inhibitors - pharmacology</topic><topic>Piperazines - pharmacology</topic><topic>Prostatectomy - adverse effects</topic><topic>Purines - pharmacology</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Sildenafil Citrate</topic><topic>Sulfones - pharmacology</topic><topic>Urology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Özden, Ender</creatorcontrib><creatorcontrib>Öztürk, Bülent</creatorcontrib><creatorcontrib>Koşan, Murat</creatorcontrib><creatorcontrib>Tezel, Gaye Güler</creatorcontrib><creatorcontrib>Aki, Fazil Tuncay</creatorcontrib><creatorcontrib>Gür, Serap</creatorcontrib><creatorcontrib>Ergen, Ali</creatorcontrib><creatorcontrib>Özen, Haluk</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>Urology (Ridgewood, N.J.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Özden, Ender</au><au>Öztürk, Bülent</au><au>Koşan, Murat</au><au>Tezel, Gaye Güler</au><au>Aki, Fazil Tuncay</au><au>Gür, Serap</au><au>Ergen, Ali</au><au>Özen, Haluk</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of Sildenafil Citrate on Penile Weight and Physiology of Cavernous Smooth Muscle in a Post–radical Prostatectomy Model of Erectile Dysfunction in Rats</atitle><jtitle>Urology (Ridgewood, N.J.)</jtitle><addtitle>Urology</addtitle><date>2011-03-01</date><risdate>2011</risdate><volume>77</volume><issue>3</issue><spage>761.e1</spage><epage>761.e7</epage><pages>761.e1-761.e7</pages><issn>0090-4295</issn><eissn>1527-9995</eissn><abstract>Objectives To evaluate the gross morphometric changes and in vitro responses of the corpus cavernosus of rats treated with sildenafil citrate after cavernous neurotomy. Methods The animals were divided into 3 groups. Group 1 consisted of sham-operated rats (n = 16); group 2 consisted of rats that underwent bilateral cavernous neurotomy (BCN) (n = 16); and group 3 consisted of rats that underwent unilateral cavernous neurotomy (UCN) (n = 16). Each group of rats was further classified into 2 subgroups according to whether or not they received sildenafil treatment. The rats were killed on postoperative day 14, and penectomy was performed. Apoptosis was assessed by terminal deoxynucleotidyl transferase-mediated deoxyuridine triphosphate nick end labeling (TUNEL), and organ-bath studies were evaluated by Phenylephrine (Phe), acetylcholine (Ach), sodium nitroprusside (SNP), and electrical field stimulation (EFS) responses. Results Penile weight in the BCN group was significantly lower than that of sham-treated group. UCN allowed much more preservation of penile weight compared with that in the sham-treated group. Sildenafil citrate treatment had positive effects on penile weight of both BCN ( P = .003) and UCN ( P = .004) groups. BCN increased smooth muscle apoptosis when compared with the sham or UCN group. Sildenafil citrate had a positive effect on the apoptotic index. In the BCN group, responses to Phe, Ach, SNP, and EFS decreased significantly, and sildenafil treatment corrected the responses to Phe, Ach, and SNP. Conclusions Our experimental study results support that early and daily sildenafil citrate treatment has a protective affect on the adrenergic and cholinergic systems, which play a role in erectile function.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>21256544</pmid><doi>10.1016/j.urology.2010.10.009</doi></addata></record> |
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subjects | Animals Apoptosis - drug effects Erectile Dysfunction - etiology Erectile Dysfunction - pathology Erectile Dysfunction - physiopathology In Situ Nick-End Labeling In Vitro Techniques Male Muscle Contraction - drug effects Muscle, Smooth - innervation Muscle, Smooth - physiopathology Organ Size - drug effects Penis - drug effects Penis - innervation Penis - pathology Penis - physiopathology Phosphodiesterase 5 Inhibitors - pharmacology Piperazines - pharmacology Prostatectomy - adverse effects Purines - pharmacology Rats Rats, Wistar Sildenafil Citrate Sulfones - pharmacology Urology |
title | Effect of Sildenafil Citrate on Penile Weight and Physiology of Cavernous Smooth Muscle in a Post–radical Prostatectomy Model of Erectile Dysfunction in Rats |
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