Ethnopharmacological exploration and isolation of HIV-1 latency-reversing agents from Sudanese medicinal plants
- Front Pharmacol. 2025 Aug 6:16:1587128. doi: 10.3389/fphar.2025.1587128.
- 1. Global Center for Natural Products Research, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
- 2. Department of Environmental and Molecular Health Sciences, Faculty of Medical and Pharmaceutical Sciences, Kumamoto University, Kumamoto, Japan.
- 3. Department of Natural Medicines, Graduate School of Pharmaceutical Sciences, Kumamoto University, Kumamoto, Japan.
- 4. Department of Botany, Faculty of Science, University of Khartoum, Khartoum, Sudan.
- 5. Department of Pharmacognosy, Faculty of Pharmacy, Prince Sattam Bin Abdulaziz University, Al-kharj, Saudi Arabia.
- 6. Department of Pharmacognosy, Faculty of Pharmacy, University of Khartoum, Khartoum, Sudan.
- 7. Department of Biochemistry, Faculty of Medicine, University of Khartoum, Khartoum, Sudan.
- # Contributed equally.
HIV-1 Infection remains a major health challenge, especially in resource-limited settings such as Sudan, where traditional medicine is widely practiced for managing infectious diseases, including HIV/AIDS. In this study, we selected ten Sudanese medicinal Plants traditionally used to treat immune-related and infectious diseases. The selection was based on ethnobotanical reports and local knowledge of HIV/AIDS-related treatments. Crude extracts were prepared using either absolute methanol or 50% ethanol via maceration, resulting in a total of 20 extracts. The extracts were then screened for HIV-1 latency reversal using a luciferase reporter assay in TZM-bl cells. The 50% ethanolic extract of G. kraussiana showed the highest LTR activation (EC50 = 3.75 μg/mL) with no significant cytotoxicity observed. Bioactivity-guided fractionation of the Gnidia kraussiana extract led to the isolation of gnidilatidin, a daphnane-type diterpenoid, using ultrahigh-performance liquid chromatography coupled with high-resolution mass spectrometry (UHPLC-HRMS). Gnidilatidin demonstrated potent latency-reversing activity (EC50 = 5.49 nM in J-Lat 10.6 cells) and downregulated CD4 and CXCR4, suggesting enhanced inhibition of HIV-1 entry. This study supports the ethnopharmacological relevance of G. kraussiana and validates its traditional use. It also identifies gnidilatidin as a promising lead compound for HIV-1 latency-reversal-based strategies. Further studies are needed to optimize its pharmacological profile and further elucidate its therapeutic potential, particularly as part of an optimized combination regimen with combination antiretroviral therapy (cART).
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Cat. No.Product NameDescriptionTargetResearch Area
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target: DNA/RNA SynthesisResearch Areas: Cancer