Effects of cerebral ischemic reperfusion on the expression of NF-κBp65 and MMP-9 in diabetic rats
Jia Zhan
Abstract
Jia Zhan
Abstract
Objective To investigate the expression of cerebral nuclear transcription factor (NF)-KBp65, matrix metalloproteinase-9 (MMP-9), and their clinical significance in diabetic rats with cerebral is-chemic reperfusion. Methods Eighty-nine healthy Wistar rats were randomly divided into four groups: normal control group, sham operated group, normoglycemic cerebral ischemic reperfusion group (nIR) and diabetic cerebral ischemic reperfusion group (dIR), reperfusion for 0 h, 6 h, 12 h and 24 h. Diabetic model was made by injection of streptozotocin (STZ) through abdomen. The model of cerebral ischemia reperfusion was developed by thread embolism method. The expression of NF-KBp65 and MMP-9 were detected by immuno-histochemistry. Results The expression of NF-KBp65 and MMP-9 in both dIR group and nIR group after reperfusion was mainly around ischemic district. The percentage of positive cell indicated by NF-κBp65 increased in dIR group, which were (24.68±4.19)%, (53.37±7.86)%, (72.38±7.24)%, (60.66±5.02)% in reperfusion for 0h, 6h, 12h, 24h respectively, compared with the same time in nIR group (P0.01). The number of positive blood capillary indicated by MMP-9 increased in dIR group, which were (0.83±0.81), (2.44±1.61), (5.08±2.11), (3.63±1.60) in reperfusion for 0h, 6h, 12h, 24 h respectively, compared with the same time in nIR group (P0.01), except the subset Oh and 24 h (P0.05), and the expression of MMP-9 positive in subset 24 h was lower than that in subset 12 h (P0.05). There was a correlation of time with the expression of NF-κBp65 and MMP-9 around cerebral ischemia district. Conclusion In diabetic cerebral ischemic reperfusion rats the expression of NF-κBp65 and MMP-9 increased and advanced, which may be a mechanism of the cerebral ischemic reperfusion injury aggravated by diabetes.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objective To investigate the expression of cerebral nuclear transcription factor (NF)-KBp65, matrix metalloproteinase-9 (MMP-9), and their clinical significance in diabetic rats with cerebral is-chemic reperfusion. Methods Eighty-nine healthy Wistar rats were randomly divided into four groups: normal control group, sham operated group, normoglycemic cerebral ischemic reperfusion group (nIR) and diabetic cerebral ischemic reperfusion group (dIR), reperfusion for 0 h, 6 h, 12 h and 24 h. Diabetic model was made by injection of streptozotocin (STZ) through abdomen. The model of cerebral ischemia reperfusion was developed by thread embolism method. The expression of NF-KBp65 and MMP-9 were detected by immuno-histochemistry. Results The expression of NF-KBp65 and MMP-9 in both dIR group and nIR group after reperfusion was mainly around ischemic district. The percentage of positive cell indicated by NF-κBp65 increased in dIR group, which were (24.68±4.19)%, (53.37±7.86)%, (72.38±7.24)%, (60.66±5.02)% in reperfusion for 0h, 6h, 12h, 24h respectively, compared with the same time in nIR group (P0.01). The number of positive blood capillary indicated by MMP-9 increased in dIR group, which were (0.83±0.81), (2.44±1.61), (5.08±2.11), (3.63±1.60) in reperfusion for 0h, 6h, 12h, 24 h respectively, compared with the same time in nIR group (P0.01), except the subset Oh and 24 h (P0.05), and the expression of MMP-9 positive in subset 24 h was lower than that in subset 12 h (P0.05). There was a correlation of time with the expression of NF-κBp65 and MMP-9 around cerebral ischemia district. Conclusion In diabetic cerebral ischemic reperfusion rats the expression of NF-κBp65 and MMP-9 increased and advanced, which may be a mechanism of the cerebral ischemic reperfusion injury aggravated by diabetes.
Key concepts: Medicine, Ischemia, Streptozotocin, Reperfusion injury, Matrix metalloproteinase, Internal medicine, Diabetes mellitus, Anesthesia