Gametocytocidal and sporontocidal activity of antimalarials against Plasmodium berghei ANKA in ICR Mice and Anopheles stephensi mosquitoes
- PMID: 1539752
- DOI: 10.4269/ajtmh.1992.46.169
Gametocytocidal and sporontocidal activity of antimalarials against Plasmodium berghei ANKA in ICR Mice and Anopheles stephensi mosquitoes
Abstract
The gametocytocidal and sporontocidal activity of three 8-aminoquinolines (primaquine, WR-238605, and WR-242511), three dihydroacridine-diones (floxacrine, WR-250547, and WR-250548), a 1,4-naphthoquinone (menoctone), a synthetic aminoalcohol (halofantrine), and a guanide (WR-182393) was determined against a cloned line of Plasmodium berghei ANKA. Gametocytocidal activity was assessed by treating mice with a single intraperitoneal inoculation of a given compound (25 mg base drug/kg mouse body weight) four days after the mice were infected with P. berghei. Thin blood smears were made every other day, and the percent parasitemia and macrogametocyte and microgametocyte rates were determined. Floxacrine, menoctone, WR-242511, WR-250547, and WR-250548 effectively cleared sexual and asexual parasites from the peripheral circulation within six days of drug administration. Halofantrine, primaquine, WR-182393, and WR-238605 were ineffective at clearing P. berghei ANKA from circulating erythrocytes at the doses tested; however, mice survival time increased markedly with these compounds when compared with the controls. Significant numbers of macrogametocytes and microgametocytes were present throughout the duration of the infection in mice treated with halofantrine, primaquine, WR-182393, and WR-238605. Sporontocidal activity was evaluated by allowing Anopheles stephensi mosquitoes to feed on P. berghei-infected mice 90 min after treatment with a particular drug. Halofantrine and WR-182393 exhibited no sporontocidal activity, while floxacrine, menoctone, primaquine, WR-238605, WR-242511, WR-250547, and WR-250548 exhibited significant activity. Minimum effective doses (mg base drug/kg of mouse body weight) that prevented mosquitoes from developing sporozoite-infected salivary glands were 0.1563 mg/kg for WR-250547, 0.625 mg/kg for menoctone, 1.25 mg/kg for primaquine, 10 mg/kg for floxacrine, 10 mg/kg for WR-242511, 10 mg/kg for WR-250548, and 25 mg/kg for WR-238605.
Similar articles
-
Sporontocidal activity of the antimalarial WR-238605 against Plasmodium berghei ANKA in Anopheles stephensi.Am J Trop Med Hyg. 1990 Mar;42(3):196-205. doi: 10.4269/ajtmh.1990.42.196. Am J Trop Med Hyg. 1990. PMID: 2180334
-
Prevention of sporogony of Plasmodium falciparum and P. berghei in Anopheles stephensi mosquitoes by transmission-blocking antimalarials.Am J Trop Med Hyg. 1994 May;50(5):646-53. doi: 10.4269/ajtmh.1994.50.646. Am J Trop Med Hyg. 1994. PMID: 8203716
-
Prevention of sporogony of Plasmodium vivax in Anopheles dirus mosquitoes by transmission-blocking antimalarials.Am J Trop Med Hyg. 2001 Sep;65(3):214-8. doi: 10.4269/ajtmh.2001.65.214. Am J Trop Med Hyg. 2001. PMID: 11561707
-
Transmission-blocking activity of tafenoquine (WR-238605) and artelinic acid against naturally circulating strains of Plasmodium vivax in Thailand.Am J Trop Med Hyg. 2003 Nov;69(5):542-7. Am J Trop Med Hyg. 2003. PMID: 14695093
-
Primaquine resistance in Plasmodium vivax.Am J Trop Med Hyg. 1996 Sep;55(3):243-9. doi: 10.4269/ajtmh.1996.55.243. Am J Trop Med Hyg. 1996. PMID: 8842108 Review.
Cited by
-
Tafenoquine and G6PD: a primer for clinicians.J Travel Med. 2019 Jun 1;26(4):taz023. doi: 10.1093/jtm/taz023. J Travel Med. 2019. PMID: 30941413 Free PMC article. Review.
-
Lead clinical and preclinical antimalarial drugs can significantly reduce sporozoite transmission to vertebrate populations.Antimicrob Agents Chemother. 2015 Jan;59(1):490-7. doi: 10.1128/AAC.03942-14. Epub 2014 Nov 10. Antimicrob Agents Chemother. 2015. PMID: 25385107 Free PMC article.
-
The evolution of tafenoquine--antimalarial for a new millennium?J R Soc Med. 1999 Jul;92(7):345-52. doi: 10.1177/014107689909200705. J R Soc Med. 1999. PMID: 10615272 Free PMC article. Review. No abstract available.
-
Assessment of the prophylactic activity and pharmacokinetic profile of oral tafenoquine compared to primaquine for inhibition of liver stage malaria infections.Malar J. 2014 Apr 14;13:141. doi: 10.1186/1475-2875-13-141. Malar J. 2014. PMID: 24731238 Free PMC article.
-
Epidemiology and infectivity of Plasmodium falciparum and Plasmodium vivax gametocytes in relation to malaria control and elimination.Clin Microbiol Rev. 2011 Apr;24(2):377-410. doi: 10.1128/CMR.00051-10. Clin Microbiol Rev. 2011. PMID: 21482730 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical