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The Effect of Tissue Stromal Vascular Fraction as Compared to Cellular Stromal Vascular Fraction to Treat Anal Sphincter Incontinence

Background: The long-term prognosis of current treatments for anal sphincter incontinence (ASI) is poor. Here, we explored the efficacy of tissue adipose stromal vascular fraction SVF (tSVF) on ASI and compared it to that of cellular SVF (cSVF). We then investigated possible mechanisms. Methods: Rat...

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Autores principales: Chen, Wenbin, He, Zijian, Li, Shuyu, Wu, Zixin, Tan, Jin, Yang, Weifeng, Li, Guanwei, Pan, Xiaoling, Liu, Yuying, Lyu, Feng-Juan, Li, Wanglin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9854502/
https://www.ncbi.nlm.nih.gov/pubmed/36671604
http://dx.doi.org/10.3390/bioengineering10010032
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author Chen, Wenbin
He, Zijian
Li, Shuyu
Wu, Zixin
Tan, Jin
Yang, Weifeng
Li, Guanwei
Pan, Xiaoling
Liu, Yuying
Lyu, Feng-Juan
Li, Wanglin
author_facet Chen, Wenbin
He, Zijian
Li, Shuyu
Wu, Zixin
Tan, Jin
Yang, Weifeng
Li, Guanwei
Pan, Xiaoling
Liu, Yuying
Lyu, Feng-Juan
Li, Wanglin
author_sort Chen, Wenbin
collection PubMed
description Background: The long-term prognosis of current treatments for anal sphincter incontinence (ASI) is poor. Here, we explored the efficacy of tissue adipose stromal vascular fraction SVF (tSVF) on ASI and compared it to that of cellular SVF (cSVF). We then investigated possible mechanisms. Methods: Rat cSVF and tSVF were isolated and labeled with DIL. One day after modeling, three groups received phosphate-buffered saline (PBS), cSVF, tSVF, respectively. The control group received nil modeling nor any treatments. The effect was assessed by function test for anal pressure and electromyography, and staining for fiber content, proliferation and differentiation at day 5 and day 10. Results: cSVF injection resulted in faster healing than tSVF. The cSVF group showed significant improvement on anal pressure on day 10. For the electromyography test, cSVF showed significant improvement for the frequencies on day 10, and for the peak values on both time points, while tSVF showed significant improvement for the peak values on day 10. The two SVF both alleviated fibrosis. Immunofluorescence tracing identified differentiation of some injected cells towards myosatellite cells and smooth muscle cells in both SVF groups. For all the tests, the tSVF group tends to have similar or lower effects than the cSVF group with no significant difference. Conclusion: cSVF and tSVF are both safe and effective in treating ASI, while the effect of cSVF is slighter higher than tSVF.
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spelling pubmed-98545022023-01-21 The Effect of Tissue Stromal Vascular Fraction as Compared to Cellular Stromal Vascular Fraction to Treat Anal Sphincter Incontinence Chen, Wenbin He, Zijian Li, Shuyu Wu, Zixin Tan, Jin Yang, Weifeng Li, Guanwei Pan, Xiaoling Liu, Yuying Lyu, Feng-Juan Li, Wanglin Bioengineering (Basel) Article Background: The long-term prognosis of current treatments for anal sphincter incontinence (ASI) is poor. Here, we explored the efficacy of tissue adipose stromal vascular fraction SVF (tSVF) on ASI and compared it to that of cellular SVF (cSVF). We then investigated possible mechanisms. Methods: Rat cSVF and tSVF were isolated and labeled with DIL. One day after modeling, three groups received phosphate-buffered saline (PBS), cSVF, tSVF, respectively. The control group received nil modeling nor any treatments. The effect was assessed by function test for anal pressure and electromyography, and staining for fiber content, proliferation and differentiation at day 5 and day 10. Results: cSVF injection resulted in faster healing than tSVF. The cSVF group showed significant improvement on anal pressure on day 10. For the electromyography test, cSVF showed significant improvement for the frequencies on day 10, and for the peak values on both time points, while tSVF showed significant improvement for the peak values on day 10. The two SVF both alleviated fibrosis. Immunofluorescence tracing identified differentiation of some injected cells towards myosatellite cells and smooth muscle cells in both SVF groups. For all the tests, the tSVF group tends to have similar or lower effects than the cSVF group with no significant difference. Conclusion: cSVF and tSVF are both safe and effective in treating ASI, while the effect of cSVF is slighter higher than tSVF. MDPI 2022-12-26 /pmc/articles/PMC9854502/ /pubmed/36671604 http://dx.doi.org/10.3390/bioengineering10010032 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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/).
spellingShingle Article
Chen, Wenbin
He, Zijian
Li, Shuyu
Wu, Zixin
Tan, Jin
Yang, Weifeng
Li, Guanwei
Pan, Xiaoling
Liu, Yuying
Lyu, Feng-Juan
Li, Wanglin
The Effect of Tissue Stromal Vascular Fraction as Compared to Cellular Stromal Vascular Fraction to Treat Anal Sphincter Incontinence
title The Effect of Tissue Stromal Vascular Fraction as Compared to Cellular Stromal Vascular Fraction to Treat Anal Sphincter Incontinence
title_full The Effect of Tissue Stromal Vascular Fraction as Compared to Cellular Stromal Vascular Fraction to Treat Anal Sphincter Incontinence
title_fullStr The Effect of Tissue Stromal Vascular Fraction as Compared to Cellular Stromal Vascular Fraction to Treat Anal Sphincter Incontinence
title_full_unstemmed The Effect of Tissue Stromal Vascular Fraction as Compared to Cellular Stromal Vascular Fraction to Treat Anal Sphincter Incontinence
title_short The Effect of Tissue Stromal Vascular Fraction as Compared to Cellular Stromal Vascular Fraction to Treat Anal Sphincter Incontinence
title_sort effect of tissue stromal vascular fraction as compared to cellular stromal vascular fraction to treat anal sphincter incontinence
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9854502/
https://www.ncbi.nlm.nih.gov/pubmed/36671604
http://dx.doi.org/10.3390/bioengineering10010032
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