Apoorv Thittayil Suresh, Karthik Chintanuri, Babu Phanithi Prakash
Department of Biotechnology and Bioinformatics, School of Life Sciences, University of Hyderabad, Hyderabad, 500 046, Telangana State, India.
Department of Biotechnology and Bioinformatics, School of Life Sciences, University of Hyderabad, Hyderabad, 500 046, Telangana State, India.
Neurosci Lett. 2018 Jan 1;662:290-294. doi: 10.1016/j.neulet.2017.10.054. Epub 2017 Oct 28.
Cerebral malaria (CM) is a severe form of malaria caused by Plasmodium falciparum and P.vivax. CM affects the brain leading to coma and is the leading cause of death in malaria patients. The enzyme, adenosine 5'-monophosphate-activated protein kinase (AMPK), is an important metabolic sensor that helps in maintaining energy homeostasis during normal physiological as well as pathological conditions. In the present study, we studied the status of AMPK in the mouse model of CM. The C57BL/6 mice infected by rodent-specific P.berghei ANKA were used for the study. We found a statistically significant reduction in the gene expressions of Prkaa1 (α1 subunit) and Prkaa2 (α2 subunit) in the brains of CM mice compared to uninfected control. Also, there was a statistically significant reduction in the ratio of phospho-AMPK/AMPK protein levels in CM compared to uninfected control. There was no statistically significant decrease in phospho-ACC/ACC ratio in the brain compared to control. As AMPK is downregulated in CM, there is a possible involvement in neuronal cell death during CM pathogenesis, and therefore we feel that novel AMPK activating drugs might be helpful as an adjunctive therapy for conferring neuroprotection.
脑型疟疾(CM)是由恶性疟原虫和间日疟原虫引起的一种严重疟疾形式。CM会影响大脑导致昏迷,是疟疾患者死亡的主要原因。腺苷5'-单磷酸激活蛋白激酶(AMPK)是一种重要的代谢传感器,在正常生理和病理状态下有助于维持能量稳态。在本研究中,我们研究了CM小鼠模型中AMPK的状态。使用感染啮齿动物特异性伯氏疟原虫ANKA的C57BL/6小鼠进行研究。我们发现,与未感染的对照相比,CM小鼠大脑中Prkaa1(α1亚基)和Prkaa2(α2亚基)的基因表达有统计学意义的降低。此外,与未感染的对照相比,CM中磷酸化AMPK/AMPK蛋白水平的比率有统计学意义的降低。与对照相比,大脑中磷酸化ACC/ACC比率没有统计学意义的下降。由于CM中AMPK被下调,在CM发病机制中可能参与神经元细胞死亡,因此我们认为新型AMPK激活药物可能有助于作为一种辅助治疗来提供神经保护。