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Effects of 5,8-dimethylthieno[2,3-b]quinoline-2-carboxylic acid on the antioxidative defense and lipid membranes in Plasmodium berghei-infected erythrocytes.
- Source :
-
Experimental parasitology [Exp Parasitol] 2015 Aug; Vol. 155, pp. 26-34. Date of Electronic Publication: 2015 May 05. - Publication Year :
- 2015
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Abstract
- Plasmodium parasites degrade hemoglobin producing reactive oxygen species as toxic byproducts which are detoxified by a series of antioxidant mechanisms. Quinoline compounds have demonstrated activity against hemoglobin degradation with 5,8-dimethylthieno[2,3-b]quinoline-2-carboxylic acid (TQCA) representing a recent compound inhibiting this process. Thus, this study was undertaken to determine the ability of TQCA to modify the oxidative status in Plasmodium berghei-infected erythrocytes. After hemolysis, activities of superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx), glutathione reductase (GR) and dehydrogenase enzymes as well as lipid peroxidation were investigated by spectrophotometry. Saturated and unsaturated fatty acids were determined by gas-liquid chromatography and the in vivo effects of TQCA were confirmed by a malaria murine model (Rane test). The activity of glucose-6-phosphate dehydrogenase (G6PDH) and 6-phosphogluconate dehydrogenase (6PGDH) in infected cells was diminished by this compound compared to control infection in 75.1 ± 3.5% and 26.5 ± 0.3%, respectively, while that of GPx and GR was also lowered (p <0.05). As an adaptive response we appreciated a 2.3-fold increase of SOD activity compared to control infection. Lipid peroxidation and the saturated/unsaturated fatty acids ratio were also decreased by this quinoline derivate in 49.2 ± 1.32% and 37 ± 0.06%, respectively, protecting the cells from hemolysis caused by the infection. The in vitro results were in concordance with the potential in vivo activity of this compound in an established malaria murine model in which TQCA showed significant decrease in the parasitemia levels and increased the mean survival days of infected mice. In conclusion, the antioxidant defense represents a biochemical target for TQCA actions as a potent antimalarial whose effects were also confirmed in vivo.<br /> (Copyright © 2015 Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Antimalarials chemical synthesis
Antioxidants metabolism
Catalase metabolism
Erythrocyte Membrane drug effects
Erythrocytes drug effects
Erythrocytes metabolism
Glucosephosphate Dehydrogenase metabolism
Glutathione Peroxidase metabolism
Glutathione Reductase metabolism
Lipid Peroxidation
Male
Membrane Lipids blood
Mice
Mice, Inbred BALB C
Phosphogluconate Dehydrogenase metabolism
Plasmodium berghei drug effects
Quinolines chemical synthesis
Superoxide Dismutase metabolism
Thiophenes chemical synthesis
Antimalarials pharmacology
Erythrocytes parasitology
Plasmodium berghei physiology
Quinolines pharmacology
Thiophenes pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1090-2449
- Volume :
- 155
- Database :
- MEDLINE
- Journal :
- Experimental parasitology
- Publication Type :
- Academic Journal
- Accession number :
- 25956945
- Full Text :
- https://doi.org/10.1016/j.exppara.2015.04.026