Immunomodulatory imide drugs inhibit human detrusor smooth muscle contraction and growth of human detrusor smooth muscle cells, and exhibit vaso-regulatory functions
The immunomodulatory imide drugs (IMiDs) thalidomide, lenalidomide and pomalidomide may exhibit therapeutic efficacy in the prostate. In lower urinary tract symptoms (LUTS), voiding and storage disorders may arise from benign prostate hyperplasia, or overactive bladder. While current therapeutic opt...
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Veröffentlicht in: | Biomedicine & pharmacotherapy 2024-08, Vol.177, p.117066, Article 117066 |
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creator | Tamalunas, Alexander Wendt, Amin Springer, Florian Vigodski, Victor Trieb, Moritz Eitelberger, Nikolaus Poth, Henrik Ciotkowska, Anna Rutz, Beata Hu, Sheng Schulz, Heiko Ledderose, Stephan Rogenhofer, Nina Kolben, Thomas Nössner, Elfriede Stief, Christian G. Hennenberg, Martin |
description | The immunomodulatory imide drugs (IMiDs) thalidomide, lenalidomide and pomalidomide may exhibit therapeutic efficacy in the prostate. In lower urinary tract symptoms (LUTS), voiding and storage disorders may arise from benign prostate hyperplasia, or overactive bladder. While current therapeutic options target smooth muscle contraction or cell proliferation, side effects are mostly cardiovascular. Therefore, we investigated effects of IMiDs on human detrusor and porcine artery smooth muscle contraction, and growth-related functions in detrusor smooth muscle cells (HBdSMC).
Cell viability was assessed by CCK8, and apoptosis and cell death by flow cytometry in cultured HBdSMC. Contractions of human detrusor tissues and porcine interlobar and coronary arteries were induced by contractile agonists, or electric field stimulation (EFS) in the presence or absence of an IMID using an organ bath. Proliferation was assessed by EdU assay and colony formation, cytoskeletal organization by phalloidin staining,
Depending on tissue type, IMiDs inhibited cholinergic contractions with varying degree, up to 50 %, while non-cholinergic contractions were inhibited up to 80 % and 60 % for U46619 and endothelin-1, respectively, and EFS-induced contractions up to 75 %. IMiDs reduced viable HBdSM cells in a time-dependent manner. Correspondingly, proliferation was reduced, without showing pro-apoptotic effects. In parallel, IMiDs induced cytoskeletal disorganization.
IMiDs exhibit regulatory functions in various smooth muscle-rich tissues, and of cell proliferation in the lower urinary tract. This points to a novel drug class effect for IMiDs, in which the molecular mechanisms of action of IMiDs merit further consideration for the application in LUTS.
[Display omitted]
•Immunomodulatory imide drugs (IMiDs) inhibit bladder smooth muscle contraction.•IMiDs reduce bladder detrusor cell growth and actin formation.•IMiDs exhibit vasoregulatory functions in organ baths.•Novel drug class effect for IMiDs.•Molecular mechanisms of action of IMiDs merit further consideration for the application in LUTS. |
doi_str_mv | 10.1016/j.biopha.2024.117066 |
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Cell viability was assessed by CCK8, and apoptosis and cell death by flow cytometry in cultured HBdSMC. Contractions of human detrusor tissues and porcine interlobar and coronary arteries were induced by contractile agonists, or electric field stimulation (EFS) in the presence or absence of an IMID using an organ bath. Proliferation was assessed by EdU assay and colony formation, cytoskeletal organization by phalloidin staining,
Depending on tissue type, IMiDs inhibited cholinergic contractions with varying degree, up to 50 %, while non-cholinergic contractions were inhibited up to 80 % and 60 % for U46619 and endothelin-1, respectively, and EFS-induced contractions up to 75 %. IMiDs reduced viable HBdSM cells in a time-dependent manner. Correspondingly, proliferation was reduced, without showing pro-apoptotic effects. In parallel, IMiDs induced cytoskeletal disorganization.
IMiDs exhibit regulatory functions in various smooth muscle-rich tissues, and of cell proliferation in the lower urinary tract. This points to a novel drug class effect for IMiDs, in which the molecular mechanisms of action of IMiDs merit further consideration for the application in LUTS.
[Display omitted]
•Immunomodulatory imide drugs (IMiDs) inhibit bladder smooth muscle contraction.•IMiDs reduce bladder detrusor cell growth and actin formation.•IMiDs exhibit vasoregulatory functions in organ baths.•Novel drug class effect for IMiDs.•Molecular mechanisms of action of IMiDs merit further consideration for the application in LUTS.</description><identifier>ISSN: 0753-3322</identifier><identifier>ISSN: 1950-6007</identifier><identifier>EISSN: 1950-6007</identifier><identifier>DOI: 10.1016/j.biopha.2024.117066</identifier><identifier>PMID: 38981242</identifier><language>eng</language><publisher>France: Elsevier Masson SAS</publisher><subject>Animals ; Apoptosis - drug effects ; bladder smooth muscle cell proliferation ; bladder smooth muscle contraction ; Cell Proliferation - drug effects ; Cell Survival - drug effects ; Cells, Cultured ; Humans ; Immunomodulating Agents - pharmacology ; lenalidomide ; Lenalidomide - pharmacology ; Lower urinary tract symptoms (LUTS) ; Male ; Muscle Contraction - drug effects ; Muscle, Smooth - drug effects ; Myocytes, Smooth Muscle - drug effects ; overactive bladder (OAB) ; pomalidomide ; Swine ; thalidomide ; Thalidomide - analogs & derivatives ; Thalidomide - pharmacology ; Urinary Bladder - drug effects</subject><ispartof>Biomedicine & pharmacotherapy, 2024-08, Vol.177, p.117066, Article 117066</ispartof><rights>2024 The Authors</rights><rights>Copyright © 2024 The Authors. Published by Elsevier Masson SAS.. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c357t-88fc5b083fbb67a3959b8e1c1a0deff0200b1404b9cd77d5b321d1622750c42c3</cites><orcidid>0000-0002-4659-2262 ; 0000-0001-7313-2088</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0753332224009508$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38981242$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tamalunas, Alexander</creatorcontrib><creatorcontrib>Wendt, Amin</creatorcontrib><creatorcontrib>Springer, Florian</creatorcontrib><creatorcontrib>Vigodski, Victor</creatorcontrib><creatorcontrib>Trieb, Moritz</creatorcontrib><creatorcontrib>Eitelberger, Nikolaus</creatorcontrib><creatorcontrib>Poth, Henrik</creatorcontrib><creatorcontrib>Ciotkowska, Anna</creatorcontrib><creatorcontrib>Rutz, Beata</creatorcontrib><creatorcontrib>Hu, Sheng</creatorcontrib><creatorcontrib>Schulz, Heiko</creatorcontrib><creatorcontrib>Ledderose, Stephan</creatorcontrib><creatorcontrib>Rogenhofer, Nina</creatorcontrib><creatorcontrib>Kolben, Thomas</creatorcontrib><creatorcontrib>Nössner, Elfriede</creatorcontrib><creatorcontrib>Stief, Christian G.</creatorcontrib><creatorcontrib>Hennenberg, Martin</creatorcontrib><title>Immunomodulatory imide drugs inhibit human detrusor smooth muscle contraction and growth of human detrusor smooth muscle cells, and exhibit vaso-regulatory functions</title><title>Biomedicine & pharmacotherapy</title><addtitle>Biomed Pharmacother</addtitle><description>The immunomodulatory imide drugs (IMiDs) thalidomide, lenalidomide and pomalidomide may exhibit therapeutic efficacy in the prostate. In lower urinary tract symptoms (LUTS), voiding and storage disorders may arise from benign prostate hyperplasia, or overactive bladder. While current therapeutic options target smooth muscle contraction or cell proliferation, side effects are mostly cardiovascular. Therefore, we investigated effects of IMiDs on human detrusor and porcine artery smooth muscle contraction, and growth-related functions in detrusor smooth muscle cells (HBdSMC).
Cell viability was assessed by CCK8, and apoptosis and cell death by flow cytometry in cultured HBdSMC. Contractions of human detrusor tissues and porcine interlobar and coronary arteries were induced by contractile agonists, or electric field stimulation (EFS) in the presence or absence of an IMID using an organ bath. Proliferation was assessed by EdU assay and colony formation, cytoskeletal organization by phalloidin staining,
Depending on tissue type, IMiDs inhibited cholinergic contractions with varying degree, up to 50 %, while non-cholinergic contractions were inhibited up to 80 % and 60 % for U46619 and endothelin-1, respectively, and EFS-induced contractions up to 75 %. IMiDs reduced viable HBdSM cells in a time-dependent manner. Correspondingly, proliferation was reduced, without showing pro-apoptotic effects. In parallel, IMiDs induced cytoskeletal disorganization.
IMiDs exhibit regulatory functions in various smooth muscle-rich tissues, and of cell proliferation in the lower urinary tract. This points to a novel drug class effect for IMiDs, in which the molecular mechanisms of action of IMiDs merit further consideration for the application in LUTS.
[Display omitted]
•Immunomodulatory imide drugs (IMiDs) inhibit bladder smooth muscle contraction.•IMiDs reduce bladder detrusor cell growth and actin formation.•IMiDs exhibit vasoregulatory functions in organ baths.•Novel drug class effect for IMiDs.•Molecular mechanisms of action of IMiDs merit further consideration for the application in LUTS.</description><subject>Animals</subject><subject>Apoptosis - drug effects</subject><subject>bladder smooth muscle cell proliferation</subject><subject>bladder smooth muscle contraction</subject><subject>Cell Proliferation - drug effects</subject><subject>Cell Survival - drug effects</subject><subject>Cells, Cultured</subject><subject>Humans</subject><subject>Immunomodulating Agents - pharmacology</subject><subject>lenalidomide</subject><subject>Lenalidomide - pharmacology</subject><subject>Lower urinary tract symptoms (LUTS)</subject><subject>Male</subject><subject>Muscle Contraction - drug effects</subject><subject>Muscle, Smooth - drug effects</subject><subject>Myocytes, Smooth Muscle - drug effects</subject><subject>overactive bladder (OAB)</subject><subject>pomalidomide</subject><subject>Swine</subject><subject>thalidomide</subject><subject>Thalidomide - analogs & derivatives</subject><subject>Thalidomide - pharmacology</subject><subject>Urinary Bladder - drug effects</subject><issn>0753-3322</issn><issn>1950-6007</issn><issn>1950-6007</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1u1DAQxy0EokvhDRDykQNZxnZiJxckVNFSqRIXOFv-yq5Xsb3YcUsfiPck27Qc4TSH-X_M6IfQWwJbAoR_PGy1T8e92lKg7ZYQAZw_QxsydNBwAPEcbUB0rGGM0jP0qpQDAHSc9S_RGeuHntCWbtDv6xBqTCHZOqk55Xvsg7cO21x3Bfu499rPeF-Diti6OdeSMi4hpXmPQy1mctikOGdlZp8iVtHiXU53yzaN_7G5aSofHhzu11pzq0pqsts9nTLW-BBbXqMXo5qKe_M4z9GPyy_fL742N9-uri8-3zSGdWJu-n40nYaejVpzodjQDbp3xBAF1o0jUABNWmj1YKwQttOMEks4paID01LDztH7NfeY08_qyiyDL6dDVXSpFslAiGEA3vNF2q5Sk1Mp2Y3ymH1Q-V4SkCdA8iBXQPIESK6AFtu7x4aqg7N_TU9EFsGnVeCWP2-9y7IY76Jx1mdnZmmT_3fDHwZ4qJQ</recordid><startdate>202408</startdate><enddate>202408</enddate><creator>Tamalunas, Alexander</creator><creator>Wendt, Amin</creator><creator>Springer, Florian</creator><creator>Vigodski, Victor</creator><creator>Trieb, Moritz</creator><creator>Eitelberger, Nikolaus</creator><creator>Poth, Henrik</creator><creator>Ciotkowska, Anna</creator><creator>Rutz, Beata</creator><creator>Hu, Sheng</creator><creator>Schulz, Heiko</creator><creator>Ledderose, Stephan</creator><creator>Rogenhofer, Nina</creator><creator>Kolben, Thomas</creator><creator>Nössner, Elfriede</creator><creator>Stief, Christian G.</creator><creator>Hennenberg, Martin</creator><general>Elsevier Masson SAS</general><scope>6I.</scope><scope>AAFTH</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><orcidid>https://orcid.org/0000-0002-4659-2262</orcidid><orcidid>https://orcid.org/0000-0001-7313-2088</orcidid></search><sort><creationdate>202408</creationdate><title>Immunomodulatory imide drugs inhibit human detrusor smooth muscle contraction and growth of human detrusor smooth muscle cells, and exhibit vaso-regulatory functions</title><author>Tamalunas, Alexander ; Wendt, Amin ; Springer, Florian ; Vigodski, Victor ; Trieb, Moritz ; Eitelberger, Nikolaus ; Poth, Henrik ; Ciotkowska, Anna ; Rutz, Beata ; Hu, Sheng ; Schulz, Heiko ; Ledderose, Stephan ; Rogenhofer, Nina ; Kolben, Thomas ; Nössner, Elfriede ; Stief, Christian G. ; Hennenberg, Martin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c357t-88fc5b083fbb67a3959b8e1c1a0deff0200b1404b9cd77d5b321d1622750c42c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Animals</topic><topic>Apoptosis - drug effects</topic><topic>bladder smooth muscle cell proliferation</topic><topic>bladder smooth muscle contraction</topic><topic>Cell Proliferation - drug effects</topic><topic>Cell Survival - drug effects</topic><topic>Cells, Cultured</topic><topic>Humans</topic><topic>Immunomodulating Agents - pharmacology</topic><topic>lenalidomide</topic><topic>Lenalidomide - pharmacology</topic><topic>Lower urinary tract symptoms (LUTS)</topic><topic>Male</topic><topic>Muscle Contraction - drug effects</topic><topic>Muscle, Smooth - drug effects</topic><topic>Myocytes, Smooth Muscle - drug effects</topic><topic>overactive bladder (OAB)</topic><topic>pomalidomide</topic><topic>Swine</topic><topic>thalidomide</topic><topic>Thalidomide - analogs & derivatives</topic><topic>Thalidomide - pharmacology</topic><topic>Urinary Bladder - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tamalunas, Alexander</creatorcontrib><creatorcontrib>Wendt, Amin</creatorcontrib><creatorcontrib>Springer, Florian</creatorcontrib><creatorcontrib>Vigodski, Victor</creatorcontrib><creatorcontrib>Trieb, Moritz</creatorcontrib><creatorcontrib>Eitelberger, Nikolaus</creatorcontrib><creatorcontrib>Poth, Henrik</creatorcontrib><creatorcontrib>Ciotkowska, Anna</creatorcontrib><creatorcontrib>Rutz, Beata</creatorcontrib><creatorcontrib>Hu, Sheng</creatorcontrib><creatorcontrib>Schulz, Heiko</creatorcontrib><creatorcontrib>Ledderose, Stephan</creatorcontrib><creatorcontrib>Rogenhofer, Nina</creatorcontrib><creatorcontrib>Kolben, Thomas</creatorcontrib><creatorcontrib>Nössner, Elfriede</creatorcontrib><creatorcontrib>Stief, Christian G.</creatorcontrib><creatorcontrib>Hennenberg, Martin</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</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><jtitle>Biomedicine & pharmacotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tamalunas, Alexander</au><au>Wendt, Amin</au><au>Springer, Florian</au><au>Vigodski, Victor</au><au>Trieb, Moritz</au><au>Eitelberger, Nikolaus</au><au>Poth, Henrik</au><au>Ciotkowska, Anna</au><au>Rutz, Beata</au><au>Hu, Sheng</au><au>Schulz, Heiko</au><au>Ledderose, Stephan</au><au>Rogenhofer, Nina</au><au>Kolben, Thomas</au><au>Nössner, Elfriede</au><au>Stief, Christian G.</au><au>Hennenberg, Martin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immunomodulatory imide drugs inhibit human detrusor smooth muscle contraction and growth of human detrusor smooth muscle cells, and exhibit vaso-regulatory functions</atitle><jtitle>Biomedicine & pharmacotherapy</jtitle><addtitle>Biomed Pharmacother</addtitle><date>2024-08</date><risdate>2024</risdate><volume>177</volume><spage>117066</spage><pages>117066-</pages><artnum>117066</artnum><issn>0753-3322</issn><issn>1950-6007</issn><eissn>1950-6007</eissn><abstract>The immunomodulatory imide drugs (IMiDs) thalidomide, lenalidomide and pomalidomide may exhibit therapeutic efficacy in the prostate. In lower urinary tract symptoms (LUTS), voiding and storage disorders may arise from benign prostate hyperplasia, or overactive bladder. While current therapeutic options target smooth muscle contraction or cell proliferation, side effects are mostly cardiovascular. Therefore, we investigated effects of IMiDs on human detrusor and porcine artery smooth muscle contraction, and growth-related functions in detrusor smooth muscle cells (HBdSMC).
Cell viability was assessed by CCK8, and apoptosis and cell death by flow cytometry in cultured HBdSMC. Contractions of human detrusor tissues and porcine interlobar and coronary arteries were induced by contractile agonists, or electric field stimulation (EFS) in the presence or absence of an IMID using an organ bath. Proliferation was assessed by EdU assay and colony formation, cytoskeletal organization by phalloidin staining,
Depending on tissue type, IMiDs inhibited cholinergic contractions with varying degree, up to 50 %, while non-cholinergic contractions were inhibited up to 80 % and 60 % for U46619 and endothelin-1, respectively, and EFS-induced contractions up to 75 %. IMiDs reduced viable HBdSM cells in a time-dependent manner. Correspondingly, proliferation was reduced, without showing pro-apoptotic effects. In parallel, IMiDs induced cytoskeletal disorganization.
IMiDs exhibit regulatory functions in various smooth muscle-rich tissues, and of cell proliferation in the lower urinary tract. This points to a novel drug class effect for IMiDs, in which the molecular mechanisms of action of IMiDs merit further consideration for the application in LUTS.
[Display omitted]
•Immunomodulatory imide drugs (IMiDs) inhibit bladder smooth muscle contraction.•IMiDs reduce bladder detrusor cell growth and actin formation.•IMiDs exhibit vasoregulatory functions in organ baths.•Novel drug class effect for IMiDs.•Molecular mechanisms of action of IMiDs merit further consideration for the application in LUTS.</abstract><cop>France</cop><pub>Elsevier Masson SAS</pub><pmid>38981242</pmid><doi>10.1016/j.biopha.2024.117066</doi><orcidid>https://orcid.org/0000-0002-4659-2262</orcidid><orcidid>https://orcid.org/0000-0001-7313-2088</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animals Apoptosis - drug effects bladder smooth muscle cell proliferation bladder smooth muscle contraction Cell Proliferation - drug effects Cell Survival - drug effects Cells, Cultured Humans Immunomodulating Agents - pharmacology lenalidomide Lenalidomide - pharmacology Lower urinary tract symptoms (LUTS) Male Muscle Contraction - drug effects Muscle, Smooth - drug effects Myocytes, Smooth Muscle - drug effects overactive bladder (OAB) pomalidomide Swine thalidomide Thalidomide - analogs & derivatives Thalidomide - pharmacology Urinary Bladder - drug effects |
title | Immunomodulatory imide drugs inhibit human detrusor smooth muscle contraction and growth of human detrusor smooth muscle cells, and exhibit vaso-regulatory functions |
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