Annona muricata modulate brain-CXCL10 expression during cerebral malaria phase

2nd International Conference on Tropical and Coastal Region Eco Development 2016

地球科学;生态环境科学

Djamiatun, Kis^1,2 ; Matug, Sumia M. A.^2 ; Prasetyo, Awal^2,3 ; Wijayahadi, Noor^4 ; Nugroho, Djoko^5

Parasitology Department, Medical Faculty, Diponegoro University, Indonesia^1

Biomedical Science Post Graduate Program, Medical Faculty, Diponegoro University, Indonesia^2

Pathology Anatomy Department, Medical Faculty, Diponegoro University, Indonesia^3

Farmacology Department, Medical Faculty, Diponegoro University, Indonesia^4

Biostatistic Department, Public Health Faculty, Diponegoro University, Indonesia^5

关键词: Angiopoietin-2;    Annona muricata;    Control groups;    CXCL10;    Immune response;    Kruskal-Wallis tests;    Leaf extracts;    malaria;   

Others  :  https://iopscience.iop.org/article/10.1088/1755-1315/55/1/012034/pdf
DOI  :  10.1088/1755-1315/55/1/012034

学科分类：环境科学（综合）

来源: IOP

【 摘 要 】

Cerebral malaria (CM) contributes in malaria mortality. People in endemic region get benefices by using A. muricata-leaf extract (AME) before qualified for receiving standard anti-malaria, because AME restrains malaria infection and modulate immune responses. CXCL10 expressed by astrocytes limit brain inflammation. Vascular leakage was found in the brain of experimental CM. Additionally, biomarker related with vascular leakage, angiopoietin-2 (Ang-2) levels increase in CM-patients. Objectives of this study were to determine the efficacy of ethanolic-AME in regulating brain-CXCL10-expression and Ang-2 levels during CM-phase. The study was post-test-only-control-group design. Thirty Swiss-mice were randomly divided in 6 groups. C+ and C- groups were PbA-inoculated and healthy-mice, respectively. X1 and X2 groups were healthy-mice treated with AME 100 and 150 mg/Kg BW/day, respectively. X3 and X4 groups were PbA-inoculated and received either dose mentioned above. CXCL10 was stained by IHC, and determined by Allred score. Plasma-Ang-2 was measured by elisa-method. Kruskal-Wallis-test showed the difference of CXCL10-expression among the studied groups (p=0.003). CXCL10-expression of C+ group was lower than healthy-mice which were C-, X1 and X2 groups (p=0.008, p=0.045, and p=0.012). CXCL10-expression of X3 was comparable to healthy mice (C-, X1 and X2), and was higher than C+ and X4 groups (p=0.012 and p=0.028). CXCL10-expression of X4 group was lower than C- and X2 groups (p=0.011 and p=0.016). Kruskal-Wallis-test showed no difference of Ang-2-levels among 6 groups (p = 0.175). The conclusion is A. muricata influences brain-CXCL10 expression during CM phase, but has no association with Ang-2 levels during CM phase.