effect of aqueous garlic extract on interleukin-12 and 10 levels in Leishmania major [MRHO/IR/75/ER] infected macrophages

The aim of the present study was to investigate the immunomodulation effects of aqueous garlic extract [AGE] in the cultured macrophages infected by Leishmania major. After J774 macrophages proliferation in RPMI1640 and incubation with Leishmania for 72 hours, AGE was added in doses of 9.25, 18.5, 37, 74 and 148 mg/ml for 18, 24 and 48 hours and cell culture supernatants were harvested. The Leishmania infected J774 cells to assess the cell viability was examined using trypan blue and methylthiazol tetrazolium assay [MTT]. An enzyme-linked immunosorbent assay [ELISA] was performed on cell culture supernatants for measurement of interleukin IL-10 and IL-12. Dose of 37 mg/ml for 48 hours of garlic extract was the most potent dose for activation of amastigotes infected macrophages. In addition, AGE increased the level of IL-12 in Leishmania infected cell lines significantly. AGE treated cell is effective against parasitic pathogens, and AGE induced IL-12 differentially affected the immune response to invading Leishmania parasites

Induction of apoptosis by miltefosine in Iranian strain of Leishmania infantum promastigotes

Miltefosine is a new drug of choice for the treatment of visceral leishmaniasis. Numerous experimental studies have shown miltefosine is effective on Leishmania donovani, however, effectiveness of miltefosine in treatment of L infantum is not fully understood. The aims of the present study were to evaluate cytotoxic effects of miltefosine on Iranian strain of L infantum, and to determine its 50% inhibitory concentration [IC50] as well as lethal dose. Anti-L. infantum activity of miltefosine was studied by treatment of cultured promastigotes with various concentration of miltefosine. MTT assay was used to determine L infantum viability and the results were expressed as IC50. Annexin-V FLUOS staining was performed to study apoptotic properties of this drug by using FACS flow cytometry. Miltefosine led to dose-dependent death of L. infantum with features compatible with apoptosis including cell shrinkage, DNA laddering, and externalization of phosphatidylserine with preservation of integrity of plasma membrane. The 100% effect was achieved at 22 micro M and IC50 after 48 hours of incubation was 7 micro M. Miltefosine exerts cytotoxic effect on Iranian strain of L. infantum via an apoptosis-related mechanism