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1.
Biochem Cell Biol ; 97(6): 702-708, 2019 12.
Article in English | MEDLINE | ID: mdl-31770017

ABSTRACT

Hemorrhagic transformation (HT) is a devastating complication for patients with acute ischemic stroke (AIS) who are treated with tissue plasminogen activator (tPA). HT is associated with high morbidity and mortality, but no effective treatments are currently available to reduce the risk of HT. Therefore, methods to prevent HT are urgently needed. In this study, we used IM-12, an inhibitor of glycogen synthase kinase 3ß (GSK-3ß), to evaluate the role of the Wnt-ß-catenin signaling pathway in recombinant tPA (rtPA)-induced HT. Sprague-Dawley rats were subjected to a middle cerebral artery occlusion (MCAO) model of ischemic stroke, and then were either administered rtPA, rtPA combined with IM-12, or the vehicle at 4 h after stroke was induced. Our results indicate that rats subjected to HT had more severe neurological deficits, brain edema, and blood-brain barrier (BBB) breakdown, and had a greater infarction volume than the control group. Rats treated with IM-12 had improved outcomes compared with those of rats treated with rtPA alone. Moreover, IM-12 increased the protein expression of ß-catenin and downstream proteins while suppressing the expression of GSK-3ß. These results suggest that IM-12 reduces rtPA-induced HT and attenuates BBB disruption, possibly through activation of the Wnt-ß-catenin signaling pathway, and provides a potential therapeutic strategy for preventing tPA-induced HT after AIS.


Subject(s)
Hemorrhage/drug therapy , Indoles/pharmacology , Maleimides/pharmacology , Stroke/drug therapy , Tissue Plasminogen Activator/antagonists & inhibitors , Wnt Signaling Pathway/drug effects , Animals , Hemorrhage/metabolism , Male , Rats , Rats, Sprague-Dawley , Stroke/metabolism , Tissue Plasminogen Activator/pharmacology
2.
Nanoscale ; 7(19): 8811-8, 2015 May 21.
Article in English | MEDLINE | ID: mdl-25908551

ABSTRACT

Thanks to their outstanding properties and a wide range of promising applications, the development of a versatile and convenient preparation method for metallic copper nanocrystals with controllable shape is of primary significance. Different from the literature that utilized a capping agent bearing only one kind of Cu binding functionality, either an amino or a carboxylic unit, for their preparation and shape control, this contribution reports a convenient method to engage both amino and carboxylic binding units at the same time. In this method, natural amino acids have been chosen as capping agents and demonstrated their versatile capabilities for the preparation of both Cu nanoparticles and nanowires. Detailed X-ray photoelectron spectroscopy revealed that the binding mode between amino acids and the Cu surface is highly dependent on their chemical structures. Interestingly, the produced Cu nanocrystals, exhibited an extraordinarily excellent anti-oxidation power. Furthermore, it was found that the multiple functionalities of amino acids not only have a great impact on the properties of their capped nanocrystals, such as solvent dispersibility, but also provide a convenient route for their further modification and functionalization.


Subject(s)
Amino Acids/chemistry , Copper/chemistry , Metal Nanoparticles/chemistry , Metal Nanoparticles/ultrastructure , Microscopy, Electron, Scanning , Microscopy, Electron, Transmission , Oxidation-Reduction , Photoelectron Spectroscopy , Surface Properties
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