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New Insight into the Antifibrotic Effects of Praziquantel on Mice in Infection with Schistosoma japonicum
BACKGROUND: Schistosomiasis is a parasitic disease infecting more than 200 million people in the world. Although chemotherapy targeting on killing schistosomes is one of the main strategies in the disease control, there are few effective ways of dealing with liver fibrosis caused by the parasite inf...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3101229/ https://www.ncbi.nlm.nih.gov/pubmed/21629648 http://dx.doi.org/10.1371/journal.pone.0020247 |
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author | Liang, Yue-Jin Luo, Jie Yuan, Quan Zheng, Dan Liu, Ya-Ping Shi, Lei Zhou, Ying Chen, Ai-Ling Ren, Yong-Ya Sun, Ke-Yi Sun, Yan Wang, Yong Zhang, Zhao-Song |
author_facet | Liang, Yue-Jin Luo, Jie Yuan, Quan Zheng, Dan Liu, Ya-Ping Shi, Lei Zhou, Ying Chen, Ai-Ling Ren, Yong-Ya Sun, Ke-Yi Sun, Yan Wang, Yong Zhang, Zhao-Song |
author_sort | Liang, Yue-Jin |
collection | PubMed |
description | BACKGROUND: Schistosomiasis is a parasitic disease infecting more than 200 million people in the world. Although chemotherapy targeting on killing schistosomes is one of the main strategies in the disease control, there are few effective ways of dealing with liver fibrosis caused by the parasite infection in the chronic and advanced stages of schistosomiasis. For this reason, new strategies and prospective drugs, which exert antifibrotic effects, are urgently required. METHODS AND FINDINGS: The antifibrotic effects of praziquantel were assessed in the murine models of schistosomiasis japonica. Murine fibrosis models were established by cutaneous infection with 14±2 Schistosoma japonicum cercariae. Then, the mice of both chronic (8 weeks post-infection) and advanced (15 weeks post-infection) schistosomiasis were treated by gavage of praziquantel (250 mg/kg, once daily for 3 days) to eliminate worms, and followed by praziquantel anti-fibrosis treatment (300 mg/kg, twice daily for 30 days). The fibrosis-related parameters assessed were areas of collagen deposition, content of hydroxyproline and mRNA expressions of Col1α1, Col3α1, α-SMA, TGF-β, MMP9, TIMP1, IL-4, IL-10, IL-13 and IFN-γ of liver. Spleen weight index, alanine aminotransferase activity and liver portal venous pressure were also measured. The results showed that anti-fibrosis treatment improved liver fibrosis, splenomegaly, hepatic function, as well as liver portal hypertension. In order to confirm the anti-fibrotic properties of praziquantel, we established a CCL(4)-induced model and revealed that CCL(4)-induced liver fibrosis was inhibited by PZQ treatment for 30 days. Furthermore, we analyzed the effects of praziquantel on mouse primary hepatic stellate cells (HSCs). It is indicated that mRNA expressions of Col1α1, Col3α1, α-SMA, TGF-β, MMP9 and TIMP1 of HSCs were all inhibited after praziquantel anti-parasite treatments. CONCLUSIONS: The significant amelioration of hepatic fibrosis by praziquantel treatment validates it as a promising drug of anti-fibrosis and offers potential of a new chemotherapy for hepatic fibrosis resulting from schistosomiasis. |
format | Text |
id | pubmed-3101229 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-31012292011-05-31 New Insight into the Antifibrotic Effects of Praziquantel on Mice in Infection with Schistosoma japonicum Liang, Yue-Jin Luo, Jie Yuan, Quan Zheng, Dan Liu, Ya-Ping Shi, Lei Zhou, Ying Chen, Ai-Ling Ren, Yong-Ya Sun, Ke-Yi Sun, Yan Wang, Yong Zhang, Zhao-Song PLoS One Research Article BACKGROUND: Schistosomiasis is a parasitic disease infecting more than 200 million people in the world. Although chemotherapy targeting on killing schistosomes is one of the main strategies in the disease control, there are few effective ways of dealing with liver fibrosis caused by the parasite infection in the chronic and advanced stages of schistosomiasis. For this reason, new strategies and prospective drugs, which exert antifibrotic effects, are urgently required. METHODS AND FINDINGS: The antifibrotic effects of praziquantel were assessed in the murine models of schistosomiasis japonica. Murine fibrosis models were established by cutaneous infection with 14±2 Schistosoma japonicum cercariae. Then, the mice of both chronic (8 weeks post-infection) and advanced (15 weeks post-infection) schistosomiasis were treated by gavage of praziquantel (250 mg/kg, once daily for 3 days) to eliminate worms, and followed by praziquantel anti-fibrosis treatment (300 mg/kg, twice daily for 30 days). The fibrosis-related parameters assessed were areas of collagen deposition, content of hydroxyproline and mRNA expressions of Col1α1, Col3α1, α-SMA, TGF-β, MMP9, TIMP1, IL-4, IL-10, IL-13 and IFN-γ of liver. Spleen weight index, alanine aminotransferase activity and liver portal venous pressure were also measured. The results showed that anti-fibrosis treatment improved liver fibrosis, splenomegaly, hepatic function, as well as liver portal hypertension. In order to confirm the anti-fibrotic properties of praziquantel, we established a CCL(4)-induced model and revealed that CCL(4)-induced liver fibrosis was inhibited by PZQ treatment for 30 days. Furthermore, we analyzed the effects of praziquantel on mouse primary hepatic stellate cells (HSCs). It is indicated that mRNA expressions of Col1α1, Col3α1, α-SMA, TGF-β, MMP9 and TIMP1 of HSCs were all inhibited after praziquantel anti-parasite treatments. CONCLUSIONS: The significant amelioration of hepatic fibrosis by praziquantel treatment validates it as a promising drug of anti-fibrosis and offers potential of a new chemotherapy for hepatic fibrosis resulting from schistosomiasis. Public Library of Science 2011-05-24 /pmc/articles/PMC3101229/ /pubmed/21629648 http://dx.doi.org/10.1371/journal.pone.0020247 Text en Liang et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Liang, Yue-Jin Luo, Jie Yuan, Quan Zheng, Dan Liu, Ya-Ping Shi, Lei Zhou, Ying Chen, Ai-Ling Ren, Yong-Ya Sun, Ke-Yi Sun, Yan Wang, Yong Zhang, Zhao-Song New Insight into the Antifibrotic Effects of Praziquantel on Mice in Infection with Schistosoma japonicum |
title | New Insight into the Antifibrotic Effects of Praziquantel on Mice in Infection with Schistosoma japonicum
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title_full | New Insight into the Antifibrotic Effects of Praziquantel on Mice in Infection with Schistosoma japonicum
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title_fullStr | New Insight into the Antifibrotic Effects of Praziquantel on Mice in Infection with Schistosoma japonicum
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title_full_unstemmed | New Insight into the Antifibrotic Effects of Praziquantel on Mice in Infection with Schistosoma japonicum
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title_short | New Insight into the Antifibrotic Effects of Praziquantel on Mice in Infection with Schistosoma japonicum
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title_sort | new insight into the antifibrotic effects of praziquantel on mice in infection with schistosoma japonicum |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3101229/ https://www.ncbi.nlm.nih.gov/pubmed/21629648 http://dx.doi.org/10.1371/journal.pone.0020247 |
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