Can Vitamin C Protect Against a Leishmaniasis Drug's Side Effects?
"New research explores how ascorbic acid could reduce the genetic damage caused by miltefosine, a key drug in treating Leishmaniasis."
Leishmaniasis is a parasitic disease found worldwide, caused by various species of Leishmania protozoa. Visceral leishmaniasis, the most severe form, can be fatal if left untreated, with a significant number of new cases and deaths occurring each year.
Miltefosine is a crucial oral medication used to combat leishmaniasis, particularly in cases resistant to traditional treatments. However, recent studies indicate that miltefosine can cause genomic lesions by DNA oxidation, raising concerns about its safety.
The use of antioxidants like Vitamin C (ascorbic acid) is being explored to mitigate the damaging effects of miltefosine. Researchers are investigating whether Vitamin C can reduce the genotoxic and mutagenic effects of miltefosine, and if it interferes with the drug's ability to fight the Leishmania parasite.
How Can Vitamin C Help?
A new study has explored the potential of Vitamin C to reduce the harmful side effects of miltefosine, a drug used to treat Leishmaniasis. The research focused on whether Vitamin C could protect against DNA damage caused by miltefosine without reducing the drug's effectiveness.
- Comet Assays: to assess DNA damage in cells.
- Micronucleus Tests: to evaluate genetic mutations.
- Superoxide Dismutase (SOD) Enzyme Dosages: to measure antioxidant enzyme activity.
- Parasitic Burden Assessments: to determine the effectiveness of the treatment in reducing the number of parasites.
The Future of Leishmaniasis Treatment
This study suggests that Vitamin C can help protect against the genotoxic effects of miltefosine, a key drug in treating Leishmaniasis, without reducing the drug's effectiveness. Further research is needed to optimize the method of Vitamin C delivery and fully understand its potential benefits for patients undergoing Leishmaniasis treatment. It also highlights the effectiveness of miltefosine in reducing parasitic burden, even at lower doses.