Objective: To study the correlation between aquaporin-4 ( AQP4) expression and diffusion-weighted imaging ( DWI) in the process of ischemic brain edema for the molecular biologic mechanism of DWI. Methods: A total of ...Objective: To study the correlation between aquaporin-4 ( AQP4) expression and diffusion-weighted imaging ( DWI) in the process of ischemic brain edema for the molecular biologic mechanism of DWI. Methods: A total of 34 Wistar rats were divided into 8 groups randomly: Non-operated group (n = 4) , sham-operated group (n = 6) , and operated group, receiving right middle cerebral artery occlusion ( MCAO) for 15 and 30 min, and 1,3,6 and 24 h respectively (6 subgroups, n =4). All groups were imaged with DWI and T2WI. The apparent diffusion coefficient (ADC) , relevant density (rd) and relevant area (rs) of hyperintensity of the lesions on DWI and T2WI were measured. Relevant ADC (rADC) , relevant area of immunohistochemical staining for AQP4 (rS) , optical density of AQP4 hybridization (a) were calculated. After that the animals were sacrificed and perfused at different time intervals, correlations between DWI, ADC, and AQP4 expression (rS, a) in ischemic tissue was made. Results: There was a significant correlation between rS and a ( r = 0. 949 ). The abnormal high intensity was found in DWI of the ipsilateral MAC territory at 15 min after MCAO. The ADC value decreased quickly within 1 h after MCAO, the rd and rs of DWI increased rapidly and the expression of AQP4 increased quickly, too. However, there was no change on the T2WI. In the period of time (15 min - 1 h) , the AQP4 expression( a) had a strong relation to the rd and rs( r = 0. 914, 0. 895). With the progress of the time, the ADC value of MCAO decreased further to (2.1±0.6)×10-4 mm2/s at 3 h, and then followed an increased slowly till 24 h, but the rd and the rs as well as the expression of AQP4 continuously increased during the stage. The T2WI detected the lesion at the average time (1.4 h) after MCAO, and the rs of T2WI was less than that of DWI at the same time in the same layer (P < 0.05). Conclusion: The results imply that high expression of AQP4 may play a key role in ischemic brain edema. It is, certainly, one of the important reasons of the DWI molecular biologic mechanism in the cerebral ischemia.展开更多
基金Supported by the National Natural Science Foundation of China(No.30070247)
文摘Objective: To study the correlation between aquaporin-4 ( AQP4) expression and diffusion-weighted imaging ( DWI) in the process of ischemic brain edema for the molecular biologic mechanism of DWI. Methods: A total of 34 Wistar rats were divided into 8 groups randomly: Non-operated group (n = 4) , sham-operated group (n = 6) , and operated group, receiving right middle cerebral artery occlusion ( MCAO) for 15 and 30 min, and 1,3,6 and 24 h respectively (6 subgroups, n =4). All groups were imaged with DWI and T2WI. The apparent diffusion coefficient (ADC) , relevant density (rd) and relevant area (rs) of hyperintensity of the lesions on DWI and T2WI were measured. Relevant ADC (rADC) , relevant area of immunohistochemical staining for AQP4 (rS) , optical density of AQP4 hybridization (a) were calculated. After that the animals were sacrificed and perfused at different time intervals, correlations between DWI, ADC, and AQP4 expression (rS, a) in ischemic tissue was made. Results: There was a significant correlation between rS and a ( r = 0. 949 ). The abnormal high intensity was found in DWI of the ipsilateral MAC territory at 15 min after MCAO. The ADC value decreased quickly within 1 h after MCAO, the rd and rs of DWI increased rapidly and the expression of AQP4 increased quickly, too. However, there was no change on the T2WI. In the period of time (15 min - 1 h) , the AQP4 expression( a) had a strong relation to the rd and rs( r = 0. 914, 0. 895). With the progress of the time, the ADC value of MCAO decreased further to (2.1±0.6)×10-4 mm2/s at 3 h, and then followed an increased slowly till 24 h, but the rd and the rs as well as the expression of AQP4 continuously increased during the stage. The T2WI detected the lesion at the average time (1.4 h) after MCAO, and the rs of T2WI was less than that of DWI at the same time in the same layer (P < 0.05). Conclusion: The results imply that high expression of AQP4 may play a key role in ischemic brain edema. It is, certainly, one of the important reasons of the DWI molecular biologic mechanism in the cerebral ischemia.
