Artesunate-tinospora combination treatment decreases nuclear factor kappa-B and intercellular adhesion molecule-1 expression in mouse malarial models

Background Cerebral malaria is a severe form of malaria caused by brain ischemia. Artesunate, an artemisinin derivative, is the standard WHO therapy for severe malaria. Tinospora crispa (brotowali) is a traditional plant with antiinflammatory, antioxidant and antiparasitic properties. The aim of thi...

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Main Authors: Nur Izzati, Loeki Enggar Fitri, Mochammad Dalhar
Format: Article
Language:English
Published: Faculty of Medicine Trisakti University 2016-12-01
Series:Universa Medicina
Subjects:
Online Access:https://univmed.org/ejurnal/index.php/medicina/article/view/353
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spelling doaj-59f4eb6d58354fa78956d3cbb255f0232020-11-25T03:26:01ZengFaculty of Medicine Trisakti UniversityUniversa Medicina1907-30622407-22302016-12-0135322222810.18051/UnivMed.2016.v35.222-228280Artesunate-tinospora combination treatment decreases nuclear factor kappa-B and intercellular adhesion molecule-1 expression in mouse malarial modelsNur Izzati0Loeki Enggar Fitri1Mochammad Dalhar2Master of Biomedical Science Program, Study Program for Specialist in Neurology, Faculty of Medicine, Brawijaya University/ RSUD dr.Saiful Anwar MalangDepartment of Parasitology, Faculty of Medicine, Brawijaya University, MalanDepartment of Neurology, Faculty of Medicine, Brawijaya University/ RSUD dr.Saiful Anwar, MalangBackground Cerebral malaria is a severe form of malaria caused by brain ischemia. Artesunate, an artemisinin derivative, is the standard WHO therapy for severe malaria. Tinospora crispa (brotowali) is a traditional plant with antiinflammatory, antioxidant and antiparasitic properties. The aim of this study was to determine the effect of combinations of artesunate and T. crispa extract on nuclear factor kappa-B (NFêB) and intercellular adhesion molecule-1 (ICAM-1) expression in the brain of mouse malaria models. Methods This was an experimental post-test only control group study using C57BL/6J mice infected with Plasmodium berghei, divided into 7 groups: negative control, positive control, group receiving artesunate 32 mg/kgBW, group receiving tinospora extract 3.5 mg/kgBW, and three groups receiving combinations of artesunate 32 mg/kgBW and tinospora extract 2.5 mg/kgBW, 3 mg/kgBW and 3.5 mg/BW, respectively. The expression of NFêB and ICAM-1 was measured by immunohistochemistry. One-way ANOVA was used to analyze the data. Results NFkB and ICAM-1 expression increased significantly in the positive controls compared to all other groups (p=0.000). NFkB expression was significantly lower in the groups receiving artesunate and tinospora at 3 mg/kgBW and 3.5 mg/kgBW, as compared with the artesunate only group (p=0.003; p=0.005) and the tinospora extract only group (p=0.001; p=0.003). NFkB expression in all combination treatment groups was similar to that in the negative controls (p>0.05), whereas ICAM-1 expression did not differ between single and combination treatment groups (p>0.05). Conclusion The combination of artesunate and T. crispa extract is better in decreasing NFêB and ICAM-1 expression in the brain of mouse malaria models.https://univmed.org/ejurnal/index.php/medicina/article/view/353artesunatetinosporaicam-1malarianfkbmouse
collection DOAJ
language English
format Article
sources DOAJ
author Nur Izzati
Loeki Enggar Fitri
Mochammad Dalhar
spellingShingle Nur Izzati
Loeki Enggar Fitri
Mochammad Dalhar
Artesunate-tinospora combination treatment decreases nuclear factor kappa-B and intercellular adhesion molecule-1 expression in mouse malarial models
Universa Medicina
artesunate
tinospora
icam-1
malaria
nfkb
mouse
author_facet Nur Izzati
Loeki Enggar Fitri
Mochammad Dalhar
author_sort Nur Izzati
title Artesunate-tinospora combination treatment decreases nuclear factor kappa-B and intercellular adhesion molecule-1 expression in mouse malarial models
title_short Artesunate-tinospora combination treatment decreases nuclear factor kappa-B and intercellular adhesion molecule-1 expression in mouse malarial models
title_full Artesunate-tinospora combination treatment decreases nuclear factor kappa-B and intercellular adhesion molecule-1 expression in mouse malarial models
title_fullStr Artesunate-tinospora combination treatment decreases nuclear factor kappa-B and intercellular adhesion molecule-1 expression in mouse malarial models
title_full_unstemmed Artesunate-tinospora combination treatment decreases nuclear factor kappa-B and intercellular adhesion molecule-1 expression in mouse malarial models
title_sort artesunate-tinospora combination treatment decreases nuclear factor kappa-b and intercellular adhesion molecule-1 expression in mouse malarial models
publisher Faculty of Medicine Trisakti University
series Universa Medicina
issn 1907-3062
2407-2230
publishDate 2016-12-01
description Background Cerebral malaria is a severe form of malaria caused by brain ischemia. Artesunate, an artemisinin derivative, is the standard WHO therapy for severe malaria. Tinospora crispa (brotowali) is a traditional plant with antiinflammatory, antioxidant and antiparasitic properties. The aim of this study was to determine the effect of combinations of artesunate and T. crispa extract on nuclear factor kappa-B (NFêB) and intercellular adhesion molecule-1 (ICAM-1) expression in the brain of mouse malaria models. Methods This was an experimental post-test only control group study using C57BL/6J mice infected with Plasmodium berghei, divided into 7 groups: negative control, positive control, group receiving artesunate 32 mg/kgBW, group receiving tinospora extract 3.5 mg/kgBW, and three groups receiving combinations of artesunate 32 mg/kgBW and tinospora extract 2.5 mg/kgBW, 3 mg/kgBW and 3.5 mg/BW, respectively. The expression of NFêB and ICAM-1 was measured by immunohistochemistry. One-way ANOVA was used to analyze the data. Results NFkB and ICAM-1 expression increased significantly in the positive controls compared to all other groups (p=0.000). NFkB expression was significantly lower in the groups receiving artesunate and tinospora at 3 mg/kgBW and 3.5 mg/kgBW, as compared with the artesunate only group (p=0.003; p=0.005) and the tinospora extract only group (p=0.001; p=0.003). NFkB expression in all combination treatment groups was similar to that in the negative controls (p>0.05), whereas ICAM-1 expression did not differ between single and combination treatment groups (p>0.05). Conclusion The combination of artesunate and T. crispa extract is better in decreasing NFêB and ICAM-1 expression in the brain of mouse malaria models.
topic artesunate
tinospora
icam-1
malaria
nfkb
mouse
url https://univmed.org/ejurnal/index.php/medicina/article/view/353
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