1. Academic Validation
  2. Antischistosomal Properties of Hederacolchiside A1 Isolated from Pulsatilla chinensis

Antischistosomal Properties of Hederacolchiside A1 Isolated from Pulsatilla chinensis

  • Molecules. 2018 Jun 13;23(6):1431. doi: 10.3390/molecules23061431.
Naixin Kang 1 Wenhua Shen 2 Hongwei Gao 3 Yulin Feng 4 Weifeng Zhu 5 Shilin Yang 6 7 Yanli Liu 8 Qiongming Xu 9 Di Yu 10
Affiliations

Affiliations

  • 1 Department of Pharmacognosy, College of Pharmaceutical Science, Soochow University, Suzhou 215123, China. [email protected].
  • 2 College of Pharmaceutical Science, Jiangxi University of Traditional Chinese Medicine, Nanchang 330006, China. [email protected].
  • 3 College of Pharmacy, Guangxi University of Chinese Medicine, Nanning 530001, China. [email protected].
  • 4 College of Pharmaceutical Science, Jiangxi University of Traditional Chinese Medicine, Nanchang 330006, China. [email protected].
  • 5 College of Pharmaceutical Science, Jiangxi University of Traditional Chinese Medicine, Nanchang 330006, China. [email protected].
  • 6 Department of Pharmacognosy, College of Pharmaceutical Science, Soochow University, Suzhou 215123, China. [email protected].
  • 7 College of Pharmaceutical Science, Jiangxi University of Traditional Chinese Medicine, Nanchang 330006, China. [email protected].
  • 8 Department of Pharmacology, College of Pharmaceutical Science, Soochow University, Suzhou 215123, China. [email protected].
  • 9 Department of Pharmacognosy, College of Pharmaceutical Science, Soochow University, Suzhou 215123, China. [email protected].
  • 10 Department of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Uppsala 75105, Sweden. [email protected].
Abstract

Background: Schistosomiasis is a major neglected disease for which the current control strategy involves mass treatment with praziquantel, the only available drug. Hence, there is an urgent need to develop new antischistosomal compounds. Methods: The antischistosomal activity of hederacolchiside A1 (HSA) were determined by total or female worm burden reductions in mice harboring Schistosoma japonicum or S. mansoni. Pathology parameters were detected on HSA against 1-day-old S. japonicum-harboring mice. Moreover, we confirmed the antischistosomal effect of HSA on newly transformed schistosomula (NTS) of S. japonicum in vitro. Results: HSA, a natural product isolated from Pulsatilla chinensis (Bunge) Regel, was initially corroborated to possess promising antischistosomal properties. We demonstrated that HSA had high activity against S. japonicum and S. mansoni less in 11 days old parasites harbored in mice. The antischistosomal effect was even more than the currently used drugs, praziquantel, and artesunate. Furthermore, HSA could ameliorate the pathology parameters in mice harboring 1-day-old juvenile S. japonicum. We also confirmed that HSA-mediated antischistosomal activity is partly due to the morphological changes in the tegument system when NTS are exposed to HSA. Conclusions: HSA may have great potential to be an antischistosomal agent for further research.

Keywords

Schistosoma japonicum; Schistosoma mansoni; antischistosomal; hederacolchiside A1.

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