Inhibition of Giardia duodenalis by isocryptolepine -triazole adducts and derivatives
Issued Date
2024-12-01
Resource Type
eISSN
22113207
Scopus ID
2-s2.0-85201071695
Journal Title
International Journal for Parasitology: Drugs and Drug Resistance
Volume
26
Rights Holder(s)
SCOPUS
Bibliographic Citation
International Journal for Parasitology: Drugs and Drug Resistance Vol.26 (2024)
Suggested Citation
Popruk S., Tummatorn J., Sreesai S., Ampawong S., Thiangtrongjit T., Tipthara P., Tarning J., Thongsornkleeb C., Ruchirawat S., Reamtong O. Inhibition of Giardia duodenalis by isocryptolepine -triazole adducts and derivatives. International Journal for Parasitology: Drugs and Drug Resistance Vol.26 (2024). doi:10.1016/j.ijpddr.2024.100561 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/100558
Title
Inhibition of Giardia duodenalis by isocryptolepine -triazole adducts and derivatives
Corresponding Author(s)
Other Contributor(s)
Abstract
Giardia duodenalis, a widespread parasitic flagellate protozoan causing giardiasis, affects millions annually, particularly impacting children and travellers. With no effective vaccine available, treatment primarily relies on the oral administration of drugs targeting trophozoites in the small intestine. However, existing medications pose challenges due to side effects and drug resistance, necessitating the exploration of novel therapeutic options. Isocryptolepine, derived from Cryptolepis sanguinolenta, has demonstrated promising antimicrobial and anticancer properties. This study evaluated eighteen isocryptolepine-triazole adducts for their antigiardial activities and cytotoxicity, with ISO2 demonstrating potent antigiardial activity and minimal cytotoxicity on human intestinal cells. Metabolomics analysis revealed significant alterations in G. duodenalis metabolism upon ISO2 treatment, particularly affecting phospholipid metabolism. Notably, the upregulation of phytosphingosine and triglycerides, and downregulation of certain fatty acids, suggest a profound impact on membrane composition and integrity, potentially contributing to the parasite's demise. Pathway analysis highlighted glycerophospholipid metabolism, cytochrome b5 family heme/steroid binding domain, and P-type ATPase mechanisms as critical pathways affected by ISO2 treatment, underscoring its importance as a potential target for antigiardial therapy. These findings shed light on the mode of action of ISO2 against G. duodenalis and provide valuable insights for further drug development. Moreover, the study also offers a promising avenue for the exploration of isocryptolepine derivatives as novel therapeutic agents for giardiasis, addressing the urgent need for more effective and safer treatment options.