sincalide and Encephalitis

Inflammatory reaction plays a crucial role in cerebral ischemia reperfusion (IR) injury. It has been shown that activated microglia long-term existed in cerebral ischemia and induced second injury. Therefore, we hypothesize that prepared phosphatidylserine (PS)-modified microbubbles (PS-MBs) combined with ultrasound-targeted microbubble destruction (UTMD) can safely open the blood-brain barrier (BBB) and target activated microglia for inflammatory area in the later stage of ischemia reperfusion.. To verify our hypothesis, rat model of IR was established, then the change of activated microglia/macrophage (M/M) and permeability of BBB at 1, 7, 14, and 21 days could be clearly observed post IR. And the activated M/M still can be observed during the whole experiment.. The Evans blue extravasation of BBB gradually declined from day 1 to day 21. Compared to the control group, microbubbles containing PS were taken up more by activated M/M (approximately twofold) both in vitro and in vivo.. PS-MBs combined with ultrasound (US) exposure could safely open BBB, and the resulting PS nanoparticles (PS-NPs) could further target activated M/M in the neuroinflammation.

Topics: Animals; Blood-Brain Barrier; Cerebral Infarction; Disease Models, Animal; Dose-Response Relationship, Drug; Encephalitis; Hypoxia-Ischemia, Brain; Macrophages; Magnetic Resonance Imaging; Male; Microbubbles; Microglia; Permeability; Phosphatidylserines; Rats; Rats, Sprague-Dawley; Sincalide; Time Factors; Ultrasonography