Increased circulating levels of High Mobility Group Box 1 (HMGB1) in acute-phase Chikungunya virus infection: potential disease biomarker

2021 ◽  
pp. 105054
Author(s):  
Daniele C.P. Rocha ◽  
Thiara Manuelle Alves Souza ◽  
Priscila Conrado Guerra Nunes ◽  
Ronaldo Mohana-Borges ◽  
Marciano V. Paes ◽  
...  
2019 ◽  
Vol 24 (3) ◽  
pp. 363-370 ◽  
Author(s):  
Lidvine Godaert ◽  
Seendy Bartholet ◽  
Fatiha Najioullah ◽  
Hanitra Andrianasolo ◽  
Lukshe Kanagaratnam ◽  
...  

2017 ◽  
Vol 65 (11) ◽  
pp. 2510-2515 ◽  
Author(s):  
Lidvine Godaert ◽  
Fatiha Najioullah ◽  
Seendy Bartholet ◽  
Sébastien Colas ◽  
Sergio Yactayo ◽  
...  

2014 ◽  
Vol 58 (01) ◽  
pp. 69-75 ◽  
Author(s):  
X. Q. HOU ◽  
J. L. QIN ◽  
X. X. ZHENG ◽  
L. WANG ◽  
S. T. YANG ◽  
...  

2010 ◽  
Vol 204 (1) ◽  
pp. 115-123 ◽  
Author(s):  
Nadia Wauquier ◽  
Pierre Becquart ◽  
Dieudonné Nkoghe ◽  
Cindy Padilla ◽  
Angélique Ndjoyi-Mbiguino ◽  
...  

2004 ◽  
Vol 100 (2) ◽  
pp. 331-337 ◽  
Author(s):  
Hui-Bih Yuan ◽  
Yueming Huang ◽  
Shuqiu Zheng ◽  
Zhiyi Zuo

Background A period of hypothermia before ischemia (hypothermic preconditioning) induces a delayed phase of ischemic tolerance in rat brain. However, whether hypothermic preconditioning induces an acute phase (within a few hours after the hypothermia) of ischemic tolerance remains unknown. This study was designed to determine the time window of the hypothermic preconditioning-induced acute phase of neuroprotection, which is useful information for situations during surgery with anticipated ischemic episodes, and its involved mechanisms. Methods Survival of Purkinje cells in rat cerebellar slices was evaluated after a 20-min oxygen-glucose deprivation (OGD, in vitro simulated ischemia) followed by a 4-h recovery. Mild hypothermia (33 degrees C) for 20 min was applied at various times before the OGD. Results The hypothermia applied immediately to 3 h before the OGD equally effectively reduced OGD-induced Purkinje cell death/injury. Glibenclamide, a selective KATP channel blocker; 8-cyclopentyl-1,3-dipropylxanthine, a selective adenosine A1 receptor antagonist; and farnesyl protein transferase inhibitor III, a selective inhibitor to reduce Ras farnesylation, abolished hypothermic preconditioning-induced neuroprotection when applied during the hypothermia. OGD increased the expression of high-mobility group I(Y) proteins, which are nuclear transcription factors to enhance the expression of putatively damaging proteins such as cyclooxygenase-2, in cerebellar slices. This increase was attenuated by hypothermic preconditioning. Conclusions Hypothermic preconditioning induces an acute phase of neuroprotection. This neuroprotection depends on activation of the signaling molecules, adenosine A1 receptors, KATP channels, and Ras. Inhibition of putatively damaging proteins via the effects of hypothermic preconditioning on high-mobility group I(Y) expression may also be involved in hypothermic preconditioning-induced neuroprotection.


2008 ◽  
Vol 56 (2) ◽  
pp. 143-150 ◽  
Author(s):  
Lien-Cheng Chen ◽  
Trai-Ming Yeh ◽  
Huey-Nan Wu ◽  
Yi-Ying Lin ◽  
Huey-Wen Shyu

2020 ◽  
Vol 34 (7) ◽  
Author(s):  
Luciana C. Faria ◽  
Antônio Márcio F. Andrade ◽  
Cyntia G. M. C. Trant ◽  
Agnaldo S. Lima ◽  
Pedro A. B. Machado ◽  
...  

2014 ◽  
Vol 46 (7) ◽  
pp. 1127-1133 ◽  
Author(s):  
Ujjwal Kumar De ◽  
Reena Mukherjee ◽  
Sukdeb Nandi ◽  
Bhimnere Hanumatnagouda Manjunatha Patel ◽  
Umesh Dimri ◽  
...  

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