4.7 Article

Effect of ulinastatin on the permeability of the blood-brain barrier on rats with global cerebral ischemia/reperfusion injury as assessed by MRI

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BIOMEDICINE & PHARMACOTHERAPY
卷 85, 期 -, 页码 412-417

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ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.biopha.2016.11.044

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Global cerebral ischemia/reperfusion injury; MRI; Ulinastatin

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The study was designed to evaluate the effect of ulinastatin on the permeability of the blood-brain barrier in rats with global cerebral ischemia/reperfusion injury using MRI. A total of 108 Wistar rats (240 g-280 g) were randomly divided into three groups (n = 36): sham group (S group), global cerebral ischemia/reperfusion model group (GCI/R group) and 10,000 U/kg ulinastatin intervention group (U group). Fiftyfour Wistar rats were used for MRI, and the rest were used for Evans Blue(EB) analysis. We used the Pulsinelli four-vessel occlusion (4-VO) model of global cerebral ischemia/reperfusion to investigate the integrity of the blood-brain barrier with Evans Blue (EB) staining at 15 min after ischemia and at 6 h (n = 6), 24 h (n = 6), and 48 h (n = 6) after reperfusion to assess blood-brain barrier permeability with MRI. In the ulinastatin treatment group, the area of EB staining was significantly smaller, the exudation of EB decreased significantly after cerebral ischemia/reperfusion at 6 h, 24 h, 48 h, compared to the model group at corresponding time points (P < 0.05) but increased compared to the sham group. The model group exhibited significantly highlighted regions of Gd-DTPA after post-contrast at the corresponding areas and time points compared with the sham group (P < 0.05). The highlighted regions of Gd-DTPA in the ulinastatin treatment group were significantly higher compared with those of the sham group but lower when compared with those of the model group (P < 0.05). The integrity of the blood-brain barrier after cerebral ischemia/reperfusion injury was damaged. Ulinastatin could significantly improve the permeability of the blood-brain barrier after cerebral ischemia/reperfusion injury in rats. (C) 2016 Elsevier Masson SAS. All rights reserved.

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