Apixaban decreases brain thrombin activity in a male mouse model of acute ischemic stroke

2018 ◽  
Vol 96 (8) ◽  
pp. 1406-1411 ◽  
Author(s):  
Doron Bushi ◽  
Joab Chapman ◽  
Anton Wohl ◽  
Efrat Shavit Stein ◽  
Ekaterina Feingold ◽  
...  
Blood ◽  
2016 ◽  
Vol 127 (19) ◽  
pp. 2337-2345 ◽  
Author(s):  
Frederik Denorme ◽  
Friederike Langhauser ◽  
Linda Desender ◽  
Aline Vandenbulcke ◽  
Hanspeter Rottensteiner ◽  
...  

Key Points ADAMTS13 dissolves t-PA–resistant cerebral occlusions in a mouse model of stroke. The thrombolytic activity of ADAMTS13 could become useful for more efficient and safer thrombolytic treatment of acute ischemic stroke.


2021 ◽  
Vol 168 ◽  
pp. 156-164
Author(s):  
Zhandong Qiu ◽  
Jia Yang ◽  
Gang Deng ◽  
Dayong Li ◽  
Suming Zhang

Biomedicines ◽  
2021 ◽  
Vol 9 (11) ◽  
pp. 1719
Author(s):  
Cheng-Tien Wu ◽  
Man-Chih Chen ◽  
Shing-Hwa Liu ◽  
Ting-Hua Yang ◽  
Lin-Hwa Long ◽  
...  

Stroke, which is the second leading cause of mortality in the world, is urgently needed to explore the medical strategies for ischemic stroke treatment. Both icariin (ICA) and icaritin (ICT) are the major active flavonoids extracted from Herba epimedii that have been regarded as the neuroprotective agents in disease models. In this study, we aimed to investigate and compare the neuroprotective effects of ICA and ICT in a middle cerebral artery occlusion (MCAO) mouse model. Male ICR mice were pretreated with both ICA and ICT, which ameliorated body weight loss, neurological injury, infarct volume, and pathological change in acute ischemic stroke mice. Furthermore, administration of both ICA and ICT could also protect against neuronal cell apoptotic death, oxidative and nitrosative stress, lipid peroxidation, and extracellular matrix (ECM) accumulation in the brains. The neuroprotective effects of ICT are slightly better than that of ICA in acute cerebral ischemic stroke mice. These results suggest that pretreatment with both ICA and ICT improves the neuronal cell apoptosis and responses of oxidative/nitrosative stress and counteracts the ECM accumulation in the brains of acute cerebral ischemic stroke mice. Both ICA and ICT treatment may serve as a useful therapeutic strategy for acute ischemic stroke.


Stroke ◽  
2016 ◽  
Vol 47 (5) ◽  
pp. 1312-1318 ◽  
Author(s):  
Cyrille Orset ◽  
Benoit Haelewyn ◽  
Stuart M. Allan ◽  
Saema Ansar ◽  
Francesco Campos ◽  
...  

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Coral Torres-Querol ◽  
Pascual Torres ◽  
Noemí Vidal ◽  
Manel Portero-Otín ◽  
Gloria Arque ◽  
...  

AbstractSenescent cells are capable of expressing a myriad of inflammatory cytokines and this pro-inflammatory phenomenon is known as senescence-associated secretory phenotype (SASP). The contribution of this phenomenon in brain ischemia was scarce. A mouse model of transient focal cerebral ischemia by compressing the distal middle cerebral artery (tMCAo) for 60 min was used. SASP, pro-inflammatory cytokines and cell cycle mRNAs levels were quantified at 30-min and 72 h post-surgery. Immunohistochemistry in paraffin embedded human brain slides and mouse brain tissue was performed. Our results showed an increase of both p16 and p21 mRNA restricted to the infarct area in the tMCAo brain. Moreover, there was an induction of Il6, Tnfa, Cxc11, and its receptor Cxcr2 mRNA pro-inflammatory cytokines with a high positive correlation with p16/p21 mRNA levels. The p16 was mainly shown in cytoplasm of neurons and cytoplasm/membrane of microglial cells. The p21 was observed in membrane of neurons and also it showed a mixed cytoplasmic and membranous pattern in the microglial cells. In a human stroke patient, an increase of P16 in the perimeter of the MCA infarct area was observed. These suggest a role of SASP in tMCAo mouse model and in human brain tissue. SASP potentially has a physiological role in acute ischemic stroke and neurological function loss.


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