1. Effects of cardanol-based phospholipid analogs on Trichomonas vaginalis.
- Author
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de Souza TG, de Lucena Costa B, Holanda CA, Soares Romeiro LA, de Souza W, and Benchimol M
- Subjects
- Humans, Female, Inhibitory Concentration 50, Apoptosis drug effects, Cell Membrane drug effects, Animals, Epithelial Cells drug effects, Epithelial Cells parasitology, Antiprotozoal Agents pharmacology, Antiprotozoal Agents toxicity, Antiprotozoal Agents therapeutic use, Antiprotozoal Agents chemistry, Metronidazole pharmacology, Trichomonas vaginalis drug effects, Trichomonas vaginalis ultrastructure, Microscopy, Electron, Scanning, Phospholipids chemistry, Microscopy, Electron, Transmission
- Abstract
Trichomonas vaginalis is a protist parasite of the urogenital tract, responsible for human trichomoniasis, an infection sexually transmitted that affects approximately 156 million people worldwide. This pathology is more evident in females and can cause miscarriages, premature births, and infertility. The disease can also lead to a greater predisposition to HIV infection and cervical and prostate cancer. Metronidazole (MTZ) is a drug that treats human trichomoniasis. The data from studies involving human subjects are limited regarding MTZ use during pregnancy. In addition to the toxicity of the treatment, some isolates have become resistant to MTZ. Therefore, searching for new compounds active for treating trichomoniasis becomes necessary. In the present study, we report results obtained using new phospholipid analogs. Two cardanol-based compounds designated LDT117 and LDT134 were active against T. vaginalis with an IC
50 of 4.58 and 10.24 μM, respectively. These compounds were not toxic to epithelial cells in culture. Scanning electron microscopy observations revealed a rounding of the cells, a shortening of the flagella, and protrusions on the surface of drug-treated cells. Transmission electron microscopy of treated cells revealed alterations in the plasma membrane with formations of blebs, protrusions, depressions, and vacuoles with myelin figures and vacuolization in the cytoplasm after incubation. Furthermore, after treatments with the compounds LDT117 and LDT134, the parasites presented a positive reaction for TUNEL, indicating death by a mechanism like apoptosis. Given the results obtained, further in vivo studies using animal experimental models are necessary to validate that these compounds are effective for treating human trichomoniasis., Competing Interests: Declaration of competing interest We do not have any interest., (Copyright © 2024 Elsevier Inc. All rights reserved.)- Published
- 2024
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