Combination Artesunate and Tinospora crispa Decreases Ubiquitin, HIF-1α, VEGF and iNOS Expression in Brain of Cerebral Malaria Mice Model

被引:0
作者
Fitri, L. E. [1 ]
Maharani, D. [2 ]
Margareta, A. [2 ]
Purnomo, H. [3 ]
Rahayu, M. [3 ]
Budiarti, N. [4 ]
机构
[1] Univ Brawijaya, Dept Parasitol, Malang, Indonesia
[2] Univ Brawijaya, Master Program Biomed Sci, Malang, Indonesia
[3] Univ Brawijaya, Dept Neurol, Malang, Indonesia
[4] Univ Brawijaya, Dept Internal Med, Malang, Indonesia
关键词
Cerebral malaria; Tinospora crispa; Ubiquitin; HIF-1; alpha; VEGF; iNOS; ENDOTHELIAL GROWTH-FACTOR; NITRIC-OXIDE; HYPOXIA; PATHWAY;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Introduction: Cerebral malaria is the most severe complication of Plasmodium falciparum infection. The pathophysiology of cerebral malaria is still unclear, but it is expected caused by cytoadherence, rosetting, auto-agglutinations and abundant pro-inflammatory response that will induce the release of secondary molecules like ubiquitin, HIF-1 alpha, VEGF, and iNOS. Aim: To determine the effect of Artesunate and brotowali extract (Tinospora crispa) against the expression of ubiquitin, HIF-1 alpha, VEGF and iNOS in the brain of cerebral malaria mice model. Methods: An experimental study of post-test only control group using CB57BL/6J mice model malaria had been done. Samples were divided into 7 groups: negative control (K-), positive control (K+), Artesunate 32 mg/BWkg/day (P1), Tinospora crispa 70 mg/BWkg/day (P2), combination Artesunate and Tinospora crispa dose 50 mg/kgBW (P3), combination Artesunate and Tinospora crispa dose 60 mg/kgBW (P4) and combination Artesunate and Tinospora crispa dose 70 mg/kgBW (P5). Mice model were decapitated at 7th day after infection. Expression of ubiquitin, HIF-1a, VEGF, and iNOS was measured by immunohistochemistry. Result: One Way ANOVA showed different expression of ubiquitin, HIF-1 alpha, VEGF and iNOS among groups. Tukey test showed, there was no significant difference in expression of ubiquitin, VEGF and iNOS among single therapy (Artesunate or Tinospora crispa) with combination therapy (p > 0.05). Expression of HIF-1 alpha were significantly different between single therapy (Artesunate or Tinospora crispa) with combination therapy of Artesunate and Tinospora crispa 60 mg/kgBW (p=0.019, p=0.013) and combination therapy of Artesunate and Tinospora crispa 70 mg/kgBW (p=0.034; p=0.023). Pearson correlation showed negative correlation between Tinospora crispa dose and expression of HIF-1 alpha (p=0.001; r=-0.832) and iNOS (p=0.001, r=-0.874). Conclusion: The combination of Artesunate and brotowali (Tinospora crispa) extract generally decreases Ubiquitin, HIF-1 alpha, VEGF and iNOS expression of cerebral malaria model although only brain HIF-1 alpha expression gives significant value.
引用
收藏
页码:98 / 109
页数:12
相关论文
共 37 条
[1]   Tinospora crispa (L.) Hook. f. & Thomson: A Review of Its Ethnobotanical, Phytochemical, and Pharmacological Aspects [J].
Ahmad, Waqas ;
Jantan, Ibrahim ;
Bukhari, Syed N. A. .
FRONTIERS IN PHARMACOLOGY, 2016, 7
[2]   Susceptibility to experimental cerebral malaria induced by Plasmodium berghei ANKA in inbred mouse strains recently derived from wild stock [J].
Bagot, S ;
Boubou, MI ;
Campino, S ;
Behrschmidt, C ;
Gorgette, O ;
Guénet, JL ;
Penha-Gonçalves, C ;
Mazier, D ;
Pied, S ;
Cazenave, PA .
INFECTION AND IMMUNITY, 2002, 70 (04) :2049-2056
[3]   Accumulation of Plasmodium berghei-Infected Red Blood Cells in the Brain Is Crucial for the Development of Cerebral Malaria in Mice [J].
Baptista, Fernanda G. ;
Pamplona, Ana ;
Pena, Ana C. ;
Mota, Maria M. ;
Pied, Sylviane ;
Vigario, Ana M. .
INFECTION AND IMMUNITY, 2010, 78 (09) :4033-4039
[4]   Protective or pathogenic effects of vascular endothelial growth factor (VEGF) as potential biomarker in cerebral malaria [J].
Canavese, Miriam ;
Spaccapelo, Roberta .
PATHOGENS AND GLOBAL HEALTH, 2014, 108 (02) :67-75
[5]   Vascular dysfunction as a target for adjuvant therapy in cerebral malaria [J].
de Moura Carvalho, Leonardo Jose ;
Moreira, Aline da Silva ;
Daniel-Ribeiro, Claudio Tadeu ;
Martins, Yuri Chaves .
MEMORIAS DO INSTITUTO OSWALDO CRUZ, 2014, 109 (05) :577-588
[6]  
Engwerda C, 2005, CURR TOP MICROBIOL, V297, P103
[7]   Fatal cerebral malaria: a venous efflux problem [J].
Frevert, Ute ;
Nacer, Adela .
FRONTIERS IN CELLULAR AND INFECTION MICROBIOLOGY, 2014, 4
[8]  
Fu Lingyi, 2013, PLOS ONE, V8, P1
[9]   CNS Hypoxia Is More Pronounced in Murine Cerebral than Noncerebral Malaria and Is Reversed by Erythropoietin [J].
Hempel, Casper ;
Combes, Valery ;
Hunt, Nicholas Henry ;
Kurtzhals, Jorgen Anders Lindholm ;
Grau, Georges Emile Raymond .
AMERICAN JOURNAL OF PATHOLOGY, 2011, 179 (04) :1939-1950
[10]   Pathogenesis, clinical features, and neurological outcome of cerebral malaria [J].
Idro, R ;
Jenkins, NE ;
Newton, CRJC .
LANCET NEUROLOGY, 2005, 4 (12) :827-840