In vitro Multistage Malaria Transmission Blocking Activity of Selected Malaria Box Compounds

• Published in: Drug design, development and therapy development and therapy, 2020-01, Vol.14, p.1593-1607
• Main Authors: Malebo, Hamisi M, D'Alessandro, Sarah, Ebstie, Yehenew A, Sorè, Harouna, Tenoh Guedoung, Alain R, Katani, Shaaban J, Parapini, Silvia, Taramelli, Donatella, Habluetzel, Annette
• Format: Article
• Language: English
• Subjects: Animals; Antimalarials; Antimalarials - administration & dosage; Antimalarials - pharmacology; Artemisinin; Disease eradication; Disease transmission; Diseases; Dose-Response Relationship, Drug; Drugs; Enzyme inhibitors; Explosives; Injections, Intraperitoneal; Malaria; Malaria - drug therapy; Malaria - transmission; malaria elimination; Mice; Mice, Inbred BALB C; Molecular Structure; Mosquitoes; multi-stage antimalarials; Original Research; Parasitic Sensitivity Tests; Phenylhydrazines - administration & dosage; Phenylhydrazines - pharmacology; Physiological aspects; plasmodium; Plasmodium berghei - drug effects; Plasmodium falciparum; Plasmodium falciparum - drug effects; Polyamines; Structure-Activity Relationship; transmission blocking drugs
• ISSN: 1177-8881; 1177-8881
• DOI: 10.2147/DDDT.S242883

Continuous efforts into the discovery and development of new antimalarials are required to face the emerging resistance of the parasite to available treatments. Thus, new effective drugs, ideally able to inhibit the life-cycle stages that cause the disease as well as those responsible for its transmission, are needed. Eight compounds from the Medicines for Malaria Venture (MMV) Malaria Box, potentially interfering with the parasite polyamine biosynthesis were selected and assessed in vitro for activity against malaria transmissible stages, namely mature gametocytes and early sporogonic stages. Compound activity against asexual blood stages of chloroquine-sensitive 3D7 and chloroquine-resistant W2 strains of was tested measuring the parasite lactate dehydrogenase activity. The gametocytocidal effect was determined against the 3D7elo1-pfs16-CBG99 strain with a luminescent method. The murine CTRP.GFP strain was employed to assess compounds activities against early sporogonic stage development in an in vitro assay simulating mosquito midgut conditions. Among the eight tested molecules, MMV000642, MMV000662 and MMV006429, containing a 1,2,3,4-tetrahydroisoquinoline-4-carboxamide chemical skeleton substituted at N-2, C-3 and C-4, displayed multi-stage activity. Activity against asexual blood stages of both strains was confirmed with values of IC (50% inhibitory concentration) in the range of 0.07-0.13 µM. They were also active against mature stage V gametocytes with IC values below 5 µM (range: 3.43-4.42 µM). These molecules exhibited moderate effects on early sporogonic stage development, displaying IC values between 20 and 40 µM. Given the multi-stage, transmission-blocking profiles of MMV000642, MMV000662, MMV006429, and their chemical characteristics, these compounds can be considered worthy for further optimisation toward a TCP5 or TCP6 target product profile proposed by MMV for transmission-blocking antimalarials.