Synthetic Analogues of Gibbilimbol B Induce Bioenergetic Damage and Calcium Imbalance in Trypanosoma cruzi .
Maiara AmaralMarina T VarelaRavi KantMyron ChristodoulidesJoão Paulo Dos Santos FernandesAndre Gustavo TemponePublished in: Life (Basel, Switzerland) (2023)
Chagas disease is an endemic tropical disease caused by the protozoan Trypanosoma cruzi , which affects around 7 million people worldwide, mostly in development countries. The treatment relies on only two available drugs, with severe adverse effects and a limited efficacy. Therefore, the search for new therapies is a legitimate need. Within this context, our group reported the anti- Trypanosoma cruzi activity of gibbilimbol B, a natural alkylphenol isolated from the plant Piper malacophyllum . Two synthetic derivatives, LINS03018 (1) and LINS03024 (2), demonstrated a higher antiparasitic potency and were selected for mechanism of action investigations. Our studies revealed no alterations in the plasma membrane potential, but a rapid alkalinization of the acidocalcisomes. Nevertheless, compound 1 exhibit a pronounced effect in the bioenergetics metabolism, with a mitochondrial impairment and consequent decrease in ATP and reactive oxygen species (ROS) levels. Compound 2 only depolarized the mitochondrial membrane potential, with no interferences in the respiratory chain. Additionally, no macrophages response of nitric oxide (NO) was observed in both compounds. Noteworthy, simple structure modifications in these derivatives induced significant differences in their lethal effects. Thus, this work reinforces the importance of the mechanism of action investigations at the early phases of drug discovery and support further developments of the series.
Keyphrases
- trypanosoma cruzi
- reactive oxygen species
- drug discovery
- oxidative stress
- nitric oxide
- diabetic rats
- structure activity relationship
- drug induced
- human health
- dna damage
- climate change
- cell death
- high glucose
- molecular docking
- nitric oxide synthase
- single cell
- combination therapy
- risk assessment
- hydrogen peroxide
- endothelial cells
- early onset
- respiratory tract
- sensitive detection