# Disruption of mitochondrial function in blood and sexual stages of Plasmodium falciparum by ferulenol

**Authors:** Gamolthip Niramolyanun, Chonnipa Praikongkatham, Wang Nguitragool, Jetsumon Sattabongkot, Niwat Kangwanrangsan

PMC · DOI: 10.1186/s13071-025-07103-4 · Parasites & Vectors · 2025-11-05

## TL;DR

Ferulenol shows strong antimalarial effects by disrupting mitochondrial function in both blood and sexual stages of Plasmodium falciparum.

## Contribution

This study is the first to demonstrate ferulenol's dual efficacy against asexual and sexual stages of P. falciparum.

## Key findings

- Ferulenol inhibited asexual blood-stage proliferation by 88% at the highest dose.
- Gametocyte development was inhibited by 82% in early stages and 90% in late stages.
- Male gamete formation was more affected than female, with 81% and 27% inhibition, respectively.

## Abstract

Malaria continues to be a significant global health challenge, necessitating the development of novel antimalarial compounds. This study explores the effects of ferulenol on multiple lifecycle stages of Plasmodium falciparum. Ferulenol has been identified as a promising antimalarial candidate, demonstrating high efficacy in inhibiting asexual blood-stage parasites at low micromolar concentrations. However, its effects on other parasite stages remain unexplored, despite its mitochondrial target being critical for sexual stage development. This study aims to investigate ferulenol’s potential as a dual-target antimalarial by assessing its effects on development of asexual blood-stage and transmission precursor-stage parasites.

Falciparum malaria parasites were cultured in vitro and incubated with or without ferulenol. Effects of the treatment on the development of the asexual blood-stage, early-stage gametocyte, late-stage gametocyte, and gamete formation were assessed using light microscopy. The impact of ferulenol on mitochondrial membrane potential was investigated using JC-1 staining and analyzed by fluorescence microscopy.

The highest dose of ferulenol inhibited asexual blood-stage proliferation by 88%, early-stage gametocyte development by 82%, and stage V gametocyte maturation at about 90%. Moreover, the effect of ferulenol was more pronounced on male gamete formation than on female gamete formation, with the development inhibited at 81% and 27%, respectively.

These findings position ferulenol as a promising dual antimalarial activity on asexual blood-stage and gametocyte stages, which could lead the compound to disrupt both severity and transmission of disease.

The online version contains supplementary material available at 10.1186/s13071-025-07103-4.

## Linked entities

- **Chemicals:** ferulenol (PubChem CID 54679300)
- **Diseases:** malaria (MONDO:0005136)
- **Species:** Plasmodium falciparum (taxon 5833)

## Full-text entities

- **Diseases:** Malaria (MESH:D008288)
- **Chemicals:** Ferulenol (MESH:C092340), JC-1 (MESH:C068624)
- **Species:** Plasmodium falciparum (malaria parasite P. falciparum, species) [taxon 5833]

## Full text

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## Figures

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Source: https://tomesphere.com/paper/PMC12590880