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Effect of Li-ESWT on Testicular Tissue and Function in Androgen-Deficient Rat Model
Low-intensity extracorporeal shockwave therapy (Li-ESWT), as a microenergy therapy, has the effects of inhibiting oxidative stress, antiapoptosis, and tissue repair, which is increasingly applied to a variety of diseases. Our research aims to explore the protective effects of Li-ESWT in the aging ra...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8938056/ https://www.ncbi.nlm.nih.gov/pubmed/35320975 http://dx.doi.org/10.1155/2022/5213573 |
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author | Tian, Wen Jie Jeon, Seung Hwan Cho, Hyuk Jin Ha, U-Syn Hong, Sung-Hoo Lee, Ji Youl Piao, Jun Jie Xin, Zhong Cheng Chen, Ye Gang Feng, Hong Yu Kim, Sae Woong Bae, Woong Jin Rajasekaran, Mahadevan Raj |
author_facet | Tian, Wen Jie Jeon, Seung Hwan Cho, Hyuk Jin Ha, U-Syn Hong, Sung-Hoo Lee, Ji Youl Piao, Jun Jie Xin, Zhong Cheng Chen, Ye Gang Feng, Hong Yu Kim, Sae Woong Bae, Woong Jin Rajasekaran, Mahadevan Raj |
author_sort | Tian, Wen Jie |
collection | PubMed |
description | Low-intensity extracorporeal shockwave therapy (Li-ESWT), as a microenergy therapy, has the effects of inhibiting oxidative stress, antiapoptosis, and tissue repair, which is increasingly applied to a variety of diseases. Our research aims to explore the protective effects of Li-ESWT in the aging rat model and its possible molecular mechanism through in vivo and in vitro experiments. In vitro, TM3 Leydig cells incubated with H(2)O(2) were treated with Li-ESWT at 4 energy levels (0.01, 0.05, 0.1, and 0.2 mJ/mm(2)). In vivo, we employed an androgen-deficient rat model to simulate male aging and treated it with Li-ESWT at three different energy levels (0.01, 0.05, and 0.2 mJ/mm(2)). Li-ESWT increased the expression of vascular endothelial growth factor (VEGF) in TM3 cells, improved antioxidant capacity, and reduced apoptosis, with the effect being most significant at 0.05 mJ/mm(2) energy level. In androgen-deficient rat model, LI-ESWT can improve sperm count, motility, and serum testosterone level, enhancing tissue antioxidant capacity and antiapoptotic ability, and the effect is most significant at 0.05 mJ/mm(2) energy level. Therefore, Li-ESWT at an appropriate energy level can improve sperm count, motility, and serum testosterone levels in androgen-deficient rat models, reduce oxidative stress in the testis, and increase antioxidant capacity and antiapoptotic abilities. The mechanism of this condition might be related to the increased VEGF expression in Leydig cells by Li-ESWT. |
format | Online Article Text |
id | pubmed-8938056 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-89380562022-03-22 Effect of Li-ESWT on Testicular Tissue and Function in Androgen-Deficient Rat Model Tian, Wen Jie Jeon, Seung Hwan Cho, Hyuk Jin Ha, U-Syn Hong, Sung-Hoo Lee, Ji Youl Piao, Jun Jie Xin, Zhong Cheng Chen, Ye Gang Feng, Hong Yu Kim, Sae Woong Bae, Woong Jin Rajasekaran, Mahadevan Raj Oxid Med Cell Longev Research Article Low-intensity extracorporeal shockwave therapy (Li-ESWT), as a microenergy therapy, has the effects of inhibiting oxidative stress, antiapoptosis, and tissue repair, which is increasingly applied to a variety of diseases. Our research aims to explore the protective effects of Li-ESWT in the aging rat model and its possible molecular mechanism through in vivo and in vitro experiments. In vitro, TM3 Leydig cells incubated with H(2)O(2) were treated with Li-ESWT at 4 energy levels (0.01, 0.05, 0.1, and 0.2 mJ/mm(2)). In vivo, we employed an androgen-deficient rat model to simulate male aging and treated it with Li-ESWT at three different energy levels (0.01, 0.05, and 0.2 mJ/mm(2)). Li-ESWT increased the expression of vascular endothelial growth factor (VEGF) in TM3 cells, improved antioxidant capacity, and reduced apoptosis, with the effect being most significant at 0.05 mJ/mm(2) energy level. In androgen-deficient rat model, LI-ESWT can improve sperm count, motility, and serum testosterone level, enhancing tissue antioxidant capacity and antiapoptotic ability, and the effect is most significant at 0.05 mJ/mm(2) energy level. Therefore, Li-ESWT at an appropriate energy level can improve sperm count, motility, and serum testosterone levels in androgen-deficient rat models, reduce oxidative stress in the testis, and increase antioxidant capacity and antiapoptotic abilities. The mechanism of this condition might be related to the increased VEGF expression in Leydig cells by Li-ESWT. Hindawi 2022-03-14 /pmc/articles/PMC8938056/ /pubmed/35320975 http://dx.doi.org/10.1155/2022/5213573 Text en Copyright © 2022 Wen Jie Tian et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Tian, Wen Jie Jeon, Seung Hwan Cho, Hyuk Jin Ha, U-Syn Hong, Sung-Hoo Lee, Ji Youl Piao, Jun Jie Xin, Zhong Cheng Chen, Ye Gang Feng, Hong Yu Kim, Sae Woong Bae, Woong Jin Rajasekaran, Mahadevan Raj Effect of Li-ESWT on Testicular Tissue and Function in Androgen-Deficient Rat Model |
title | Effect of Li-ESWT on Testicular Tissue and Function in Androgen-Deficient Rat Model |
title_full | Effect of Li-ESWT on Testicular Tissue and Function in Androgen-Deficient Rat Model |
title_fullStr | Effect of Li-ESWT on Testicular Tissue and Function in Androgen-Deficient Rat Model |
title_full_unstemmed | Effect of Li-ESWT on Testicular Tissue and Function in Androgen-Deficient Rat Model |
title_short | Effect of Li-ESWT on Testicular Tissue and Function in Androgen-Deficient Rat Model |
title_sort | effect of li-eswt on testicular tissue and function in androgen-deficient rat model |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8938056/ https://www.ncbi.nlm.nih.gov/pubmed/35320975 http://dx.doi.org/10.1155/2022/5213573 |
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