The Therapeutic Effect of Ginsenoside Rb1 against Mechanical Trauma in a Rat Model of Postpartum Stress Urinary Incontinence
Aims. The aim of this study was to confirm the repairing effect of ginsenoside Rb1 (GS-Rb1) on mechanical trauma to periurethral tissues caused by childbirth and to explore its potential preventive mechanisms for mechanical trauma-induced stress urinary incontinence. Methods. 48 healthy adult female...
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description | Aims. The aim of this study was to confirm the repairing effect of ginsenoside Rb1 (GS-Rb1) on mechanical trauma to periurethral tissues caused by childbirth and to explore its potential preventive mechanisms for mechanical trauma-induced stress urinary incontinence. Methods. 48 healthy adult female Sprague–Dawley (SD) rats were randomly divided into four groups: normal control, SUI groups, L-GS-Rb1 groups, and H-GS-Rb1 groups, with 12 rats in each group. The histopathological examinations of the urethral were performed to detect the morphological changes after repair of periurethral traumatic tissue. The TGF-β1/Smad and NRF2/ARE signaling pathways related to periurethral tissue trauma repair were determined by RT-PCR and western blot. The bladder capacity and LPP were examined in rats. Results. GS-Rb1 significantly decreased the number of fragmented and disorganized elastic and muscle fibers in the urethra and anterior vaginal wall of SUI rats. GS-Rb1 also increased the collagen content and reduced damage to the structural integrity of the periurethral myofibers. Furthermore, GS-Rb1 promoted expressions of TGF-β1, Smad2, Smad3, Smad7, p-Smad3, p-Smad2, and collagens I and III. It also increased the protein levels of Nrf2, GPX1, and MnSOD. The bladder capacity and LPP of rats in the L-GS-Rb1 group were close to those of rats in the normal groups. Conclusions. Ginsenoside Rb1 promotes the repair of periurethral tissue trauma in the postpartum period and has a preventive effect on the occurrence of stress urinary incontinence. |
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The aim of this study was to confirm the repairing effect of ginsenoside Rb1 (GS-Rb1) on mechanical trauma to periurethral tissues caused by childbirth and to explore its potential preventive mechanisms for mechanical trauma-induced stress urinary incontinence. Methods. 48 healthy adult female Sprague–Dawley (SD) rats were randomly divided into four groups: normal control, SUI groups, L-GS-Rb1 groups, and H-GS-Rb1 groups, with 12 rats in each group. The histopathological examinations of the urethral were performed to detect the morphological changes after repair of periurethral traumatic tissue. The TGF-β1/Smad and NRF2/ARE signaling pathways related to periurethral tissue trauma repair were determined by RT-PCR and western blot. The bladder capacity and LPP were examined in rats. Results. GS-Rb1 significantly decreased the number of fragmented and disorganized elastic and muscle fibers in the urethra and anterior vaginal wall of SUI rats. GS-Rb1 also increased the collagen content and reduced damage to the structural integrity of the periurethral myofibers. Furthermore, GS-Rb1 promoted expressions of TGF-β1, Smad2, Smad3, Smad7, p-Smad3, p-Smad2, and collagens I and III. It also increased the protein levels of Nrf2, GPX1, and MnSOD. The bladder capacity and LPP of rats in the L-GS-Rb1 group were close to those of rats in the normal groups. Conclusions. Ginsenoside Rb1 promotes the repair of periurethral tissue trauma in the postpartum period and has a preventive effect on the occurrence of stress urinary incontinence.</description><identifier>ISSN: 0269-4727</identifier><identifier>EISSN: 1365-2710</identifier><identifier>DOI: 10.1155/2024/8495774</identifier><language>eng</language><publisher>Oxford: Hindawi</publisher><subject>Antioxidants ; Biotechnology ; Bladder ; Catheters ; Collagen ; Ginsenosides ; Laboratory animals ; Pelvis ; Polyethylene ; Postpartum ; Smad protein ; Smad2 protein ; Smad3 protein ; Smad7 protein ; Software ; Transforming growth factor-b1 ; Trauma ; Urethra ; Urinary incontinence ; Vagina ; Variance analysis</subject><ispartof>Journal of clinical pharmacy and therapeutics, 2024, Vol.2024 (1)</ispartof><rights>Copyright © 2024 Shaohui Chen et al.</rights><rights>Copyright © 2024 Shaohui Chen et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. https://creativecommons.org/licenses/by/4.0</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c294t-58d01a31902d1c9f2793908f31ee1677b7909279f24fabe2b6db2aab2928733d3</cites><orcidid>0000-0002-6378-8056</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2973763246/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2973763246?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,778,782,4012,21371,21372,27906,27907,27908,33513,33727,43642,43788,64366,64370,72220,73855,74053</link.rule.ids></links><search><contributor>Liu, Hongda</contributor><contributor>Hongda Liu</contributor><creatorcontrib>Chen, Shaohui</creatorcontrib><creatorcontrib>Wei, Bingyan</creatorcontrib><creatorcontrib>Zhang, Sanyuan</creatorcontrib><creatorcontrib>li, Hongmei</creatorcontrib><creatorcontrib>Huang, Rui</creatorcontrib><title>The Therapeutic Effect of Ginsenoside Rb1 against Mechanical Trauma in a Rat Model of Postpartum Stress Urinary Incontinence</title><title>Journal of clinical pharmacy and therapeutics</title><description>Aims. The aim of this study was to confirm the repairing effect of ginsenoside Rb1 (GS-Rb1) on mechanical trauma to periurethral tissues caused by childbirth and to explore its potential preventive mechanisms for mechanical trauma-induced stress urinary incontinence. Methods. 48 healthy adult female Sprague–Dawley (SD) rats were randomly divided into four groups: normal control, SUI groups, L-GS-Rb1 groups, and H-GS-Rb1 groups, with 12 rats in each group. The histopathological examinations of the urethral were performed to detect the morphological changes after repair of periurethral traumatic tissue. The TGF-β1/Smad and NRF2/ARE signaling pathways related to periurethral tissue trauma repair were determined by RT-PCR and western blot. The bladder capacity and LPP were examined in rats. Results. GS-Rb1 significantly decreased the number of fragmented and disorganized elastic and muscle fibers in the urethra and anterior vaginal wall of SUI rats. GS-Rb1 also increased the collagen content and reduced damage to the structural integrity of the periurethral myofibers. Furthermore, GS-Rb1 promoted expressions of TGF-β1, Smad2, Smad3, Smad7, p-Smad3, p-Smad2, and collagens I and III. It also increased the protein levels of Nrf2, GPX1, and MnSOD. The bladder capacity and LPP of rats in the L-GS-Rb1 group were close to those of rats in the normal groups. Conclusions. Ginsenoside Rb1 promotes the repair of periurethral tissue trauma in the postpartum period and has a preventive effect on the occurrence of stress urinary incontinence.</description><subject>Antioxidants</subject><subject>Biotechnology</subject><subject>Bladder</subject><subject>Catheters</subject><subject>Collagen</subject><subject>Ginsenosides</subject><subject>Laboratory animals</subject><subject>Pelvis</subject><subject>Polyethylene</subject><subject>Postpartum</subject><subject>Smad protein</subject><subject>Smad2 protein</subject><subject>Smad3 protein</subject><subject>Smad7 protein</subject><subject>Software</subject><subject>Transforming growth factor-b1</subject><subject>Trauma</subject><subject>Urethra</subject><subject>Urinary incontinence</subject><subject>Vagina</subject><subject>Variance analysis</subject><issn>0269-4727</issn><issn>1365-2710</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>RHX</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNp9kE9LAzEQxYMoWKs3P0DAo67Nn93N5iil1kJFqe15mc0mNqXN1iSLCH54U9qzh2HgzW_mDQ-hW0oeKS2KESMsH1W5LITIz9CA8rLImKDkHA0IK2WWCyYu0VUIG0JIKRgfoN_lWuNUHva6j1bhiTFaRdwZPLUuaNcF22q8aCiGT0hKxK9arcFZBVu89NDvAFuHAS8gjbpWbw-7712Ie_Cx3-GP6HUIeOWtA_-DZ051LlqnndLX6MLANuibUx-i1fNkOX7J5m_T2fhpnikm85gVVUsocCoJa6mShgnJJakMp1rTUohGSCKTaFhuoNGsKduGATRMskpw3vIhujve3fvuq9ch1puu9y5Z1kwKLkrO8jJRD0dK-S4Er02993aXfq4pqQ_51od861O-Cb8_4mvrWvi2_9N_rnh5-w</recordid><startdate>2024</startdate><enddate>2024</enddate><creator>Chen, Shaohui</creator><creator>Wei, Bingyan</creator><creator>Zhang, Sanyuan</creator><creator>li, Hongmei</creator><creator>Huang, Rui</creator><general>Hindawi</general><general>Hindawi Limited</general><scope>RHU</scope><scope>RHW</scope><scope>RHX</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7TM</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</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>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M7N</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><orcidid>https://orcid.org/0000-0002-6378-8056</orcidid></search><sort><creationdate>2024</creationdate><title>The Therapeutic Effect of Ginsenoside Rb1 against Mechanical Trauma in a Rat Model of Postpartum Stress Urinary Incontinence</title><author>Chen, Shaohui ; Wei, Bingyan ; Zhang, Sanyuan ; li, Hongmei ; Huang, Rui</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c294t-58d01a31902d1c9f2793908f31ee1677b7909279f24fabe2b6db2aab2928733d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Antioxidants</topic><topic>Biotechnology</topic><topic>Bladder</topic><topic>Catheters</topic><topic>Collagen</topic><topic>Ginsenosides</topic><topic>Laboratory animals</topic><topic>Pelvis</topic><topic>Polyethylene</topic><topic>Postpartum</topic><topic>Smad protein</topic><topic>Smad2 protein</topic><topic>Smad3 protein</topic><topic>Smad7 protein</topic><topic>Software</topic><topic>Transforming growth factor-b1</topic><topic>Trauma</topic><topic>Urethra</topic><topic>Urinary incontinence</topic><topic>Vagina</topic><topic>Variance analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Shaohui</creatorcontrib><creatorcontrib>Wei, Bingyan</creatorcontrib><creatorcontrib>Zhang, Sanyuan</creatorcontrib><creatorcontrib>li, Hongmei</creatorcontrib><creatorcontrib>Huang, Rui</creatorcontrib><collection>Hindawi Publishing Complete</collection><collection>Hindawi Publishing Subscription Journals</collection><collection>Hindawi Publishing Open Access</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><jtitle>Journal of clinical pharmacy and therapeutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Shaohui</au><au>Wei, Bingyan</au><au>Zhang, Sanyuan</au><au>li, Hongmei</au><au>Huang, Rui</au><au>Liu, Hongda</au><au>Hongda Liu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Therapeutic Effect of Ginsenoside Rb1 against Mechanical Trauma in a Rat Model of Postpartum Stress Urinary Incontinence</atitle><jtitle>Journal of clinical pharmacy and therapeutics</jtitle><date>2024</date><risdate>2024</risdate><volume>2024</volume><issue>1</issue><issn>0269-4727</issn><eissn>1365-2710</eissn><abstract>Aims. The aim of this study was to confirm the repairing effect of ginsenoside Rb1 (GS-Rb1) on mechanical trauma to periurethral tissues caused by childbirth and to explore its potential preventive mechanisms for mechanical trauma-induced stress urinary incontinence. Methods. 48 healthy adult female Sprague–Dawley (SD) rats were randomly divided into four groups: normal control, SUI groups, L-GS-Rb1 groups, and H-GS-Rb1 groups, with 12 rats in each group. The histopathological examinations of the urethral were performed to detect the morphological changes after repair of periurethral traumatic tissue. The TGF-β1/Smad and NRF2/ARE signaling pathways related to periurethral tissue trauma repair were determined by RT-PCR and western blot. The bladder capacity and LPP were examined in rats. Results. GS-Rb1 significantly decreased the number of fragmented and disorganized elastic and muscle fibers in the urethra and anterior vaginal wall of SUI rats. GS-Rb1 also increased the collagen content and reduced damage to the structural integrity of the periurethral myofibers. Furthermore, GS-Rb1 promoted expressions of TGF-β1, Smad2, Smad3, Smad7, p-Smad3, p-Smad2, and collagens I and III. It also increased the protein levels of Nrf2, GPX1, and MnSOD. The bladder capacity and LPP of rats in the L-GS-Rb1 group were close to those of rats in the normal groups. Conclusions. Ginsenoside Rb1 promotes the repair of periurethral tissue trauma in the postpartum period and has a preventive effect on the occurrence of stress urinary incontinence.</abstract><cop>Oxford</cop><pub>Hindawi</pub><doi>10.1155/2024/8495774</doi><orcidid>https://orcid.org/0000-0002-6378-8056</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Antioxidants Biotechnology Bladder Catheters Collagen Ginsenosides Laboratory animals Pelvis Polyethylene Postpartum Smad protein Smad2 protein Smad3 protein Smad7 protein Software Transforming growth factor-b1 Trauma Urethra Urinary incontinence Vagina Variance analysis |
title | The Therapeutic Effect of Ginsenoside Rb1 against Mechanical Trauma in a Rat Model of Postpartum Stress Urinary Incontinence |
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