TY - JOUR
T1 - Use of wogonin as a cooperative drug with praziquantel to better combat schistosomiasis
AU - Pekkle Lam, Ho Yin
AU - Hung, Meng Yun
AU - Cheng, Po Ching
AU - Peng, Shih Yi
N1 - Funding Information:
This work was supported in part by grants from the Ministry of Science and Technology of Taiwan (Grant number: MOST-110-2320-B-320-004) and Tzu Chi Foundation , Taiwan (Grant number: TCU-B01). The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
Publisher Copyright:
© 2022
PY - 2022/8
Y1 - 2022/8
N2 - Background: Schistosomiasis is one of the most devastating tropical diseases in the world. Currently, praziquantel (PZQ) represents the best pharmacological option for the treatment of schistosomiasis as it effectively kills the worm. However, the inability to reverse established liver damages often makes treatment futile. In the current study, we investigate whether combining the use of wogonin, a compound that was found to be liver-protective, with PZQ can attribute to the greatest beneficial effect in Schistosoma mansoni-infected mice. Methods: To determine the protective effect of PZQ-wogonin treatment on S. manosni-infected mice, histopathological analysis was done to evaluate the granuloma size and fibrotic areas in the liver. Western blotting was performed to analyze several injuries-related markers including fibrotic markers, inflammasomes, and apoptotic markers. Scanning electron microscopy was done to evaluate the effect of wogonin on the worms, and the worm and egg burden was calculated. Results: Our results showed that PZQ-wogonin treatment significantly improved liver histopathology of S. mansoni-infected mice. Further analysis showed that PZQ-wogonin combinations are more effective in reducing fibrosis, inflammation, and apoptosis in the liver than that of individual drug use. Furthermore, our results revealed that wogonin is anthelmintic; and it works better with PZQ in reducing hepatic egg burden, further lessen the disease progression. Conclusion: In general, this combinatorial strategy may represent a new and effective approach to schistosomiasis treatment.
AB - Background: Schistosomiasis is one of the most devastating tropical diseases in the world. Currently, praziquantel (PZQ) represents the best pharmacological option for the treatment of schistosomiasis as it effectively kills the worm. However, the inability to reverse established liver damages often makes treatment futile. In the current study, we investigate whether combining the use of wogonin, a compound that was found to be liver-protective, with PZQ can attribute to the greatest beneficial effect in Schistosoma mansoni-infected mice. Methods: To determine the protective effect of PZQ-wogonin treatment on S. manosni-infected mice, histopathological analysis was done to evaluate the granuloma size and fibrotic areas in the liver. Western blotting was performed to analyze several injuries-related markers including fibrotic markers, inflammasomes, and apoptotic markers. Scanning electron microscopy was done to evaluate the effect of wogonin on the worms, and the worm and egg burden was calculated. Results: Our results showed that PZQ-wogonin treatment significantly improved liver histopathology of S. mansoni-infected mice. Further analysis showed that PZQ-wogonin combinations are more effective in reducing fibrosis, inflammation, and apoptosis in the liver than that of individual drug use. Furthermore, our results revealed that wogonin is anthelmintic; and it works better with PZQ in reducing hepatic egg burden, further lessen the disease progression. Conclusion: In general, this combinatorial strategy may represent a new and effective approach to schistosomiasis treatment.
KW - Liver fibrosis
KW - Praziquantel
KW - Schistosomiasis
KW - Wogonin
UR - http://www.scopus.com/inward/record.url?scp=85131450136&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85131450136&partnerID=8YFLogxK
U2 - 10.1016/j.jmii.2022.04.013
DO - 10.1016/j.jmii.2022.04.013
M3 - Article
C2 - 35654701
AN - SCOPUS:85131450136
SN - 1684-1182
VL - 55
SP - 757
EP - 765
JO - Journal of Microbiology, Immunology and Infection
JF - Journal of Microbiology, Immunology and Infection
IS - 4
ER -