4.6 Article

Inhibitory effect of naphthoquine phosphate on Babesia gibsoni in vitro and Babesia rodhaini in vivo

Journal

PARASITES & VECTORS
Volume 15, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s13071-021-05127-0

Keywords

Naphthoquine phosphate; Babesia gibsoni; Babesia rodhaini; In vitro; In vivo

Funding

  1. Ministry of Education, Culture, Sports, Science, and Technology of Japan [18H02336, 18KK0188]
  2. Japan Society for the Promotion of Science Core-toCore Program from the Ministry of Education, Culture, Sports, Science, and Technology of Japan
  3. Strategic International Collaborative Research Project by the Ministry of Agriculture, Forestry and Fisheries of Japan [JPJ008837]
  4. Grants-in-Aid for Scientific Research [18H02336, 18KK0188] Funding Source: KAKEN

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This study evaluated the in vitro and in vivo anti-Babesia activity of naphthoquine phosphate (NQP) and found that NQP showed promising therapeutic efficacy against Babesia infections.
Background: Drug resistance and toxic side effects are major challenges in the treatment of babesiosis. As such, new drugs are needed to combat the emergence of drug resistance in Babesia parasites and to develop alternative treatment strategies. A combination of naphthoquine (NQ) and artemisinin is an antimalarial therapy in pharmaceutical markets. The present study repurposed NQ as a drug for the treatment of babesiosis by evaluating the anti-Babesia activity of naphthoquine phosphate (NQP) alone. Methods: An in vitro growth inhibition assay of NQP was tested on Babesia gibsoni cultures using a SYBR Green I-based fluorescence assay. In addition, the in vivo growth inhibitory effect of NQP was evaluated using BALB/c mice infected with Babesia rodhaini. The parasitemia level and hematocrit values were monitored to determine the therapeutic efficacy of NQP and the clinical improvements in NQP-treated mice. Results: The half maximal inhibitory concentration of NQP against B. gibsoni in vitro was 3.3 +/- 0.5 mu M. Oral administration of NQP for 5 consecutive days at a dose of 40 mg/kg of body weight resulted in significant inhibition of B. rodhaini growth in mice as compared with that of the control group. All NQP-treated mice survived, whereas the mice in the control group died between days 6 and 9 post-infection. Conclusion: This is the first study to evaluate the anti-Babesia activity of NQP in vitro and in vivo. Our findings suggest that NQP is a promising drug for treating Babesia infections, and drug repurposing may provide new treatment strategies for babesiosis.

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