Zheng Yang, Wang Xiaoming
Department of Radiology, Shengjing Hospital of China Medical University, No. 36, Sanhao Street, Shenyang, China.
Quant Imaging Med Surg. 2021 Oct;11(10):4408-4417. doi: 10.21037/qims-21-250.
The normal regulation of brain pH is particularly critical for protein structure and enzymatic catalysis in the brain. This study aimed to investigate the regulation mechanism of brain pH after hypoxic-ischemic brain injury (HIBI) through the combination of amide proton transfer (APT) imaging, the analysis of brain pH levels, and the analysis of voltage-gated proton channel (Hv1) expression in piglets with HIBI.
A total of 59 healthy piglets (age range, 3-5 days after birth; body weight, 1-1.5 kg) were selected. Six piglets were excluded due to death, modeling failure, or motion artifacts, leaving a total of 10 animals in the control group and 43 animals in the HIBI model group. At different time points (0-2, 2-6, 6-12, 12-24, 24-48, and 48-72 hours) after HIBI, brain pH, Hv1 expression, and APT values were measured and analyzed. The statistical analysis of data was performed using the independent samples t-test, analysis of variance, and Spearman rank correlation analysis. A P value less than 0.05 indicated statistical significance.
As shown by the immunofluorescent staining results after HIBI, Hv1 protein expression in the basal ganglia reached a peak value at 0-2 hours, with a statistically significant difference between 0-2 hours and other time points (P<0.001). In piglets, the APT value reached a trough at 0-2 hours after HIBI, and subsequently, it gradually increased, and there was a significant difference between the control group and all HIBI model subgroups (P<0.001) except for the 2-6 hours subgroup (P=0.602). Brain pH decreased after HIBI and reached a trough at 0-2 hours, then gradually increased. Hv1 protein expression, pH, and APT values were all correlated (P<0.001).
After HIBI, values of brain pH, APT, and the expression of Hv1 changed over time and had a linear correlation. This suggests that there was a shift in brain hydrogen ions (H) in the neural network and a change in brain pH after hypoxic-ischemic (HI) injury.
脑pH值的正常调节对脑内蛋白质结构和酶催化作用尤为关键。本研究旨在通过酰胺质子转移(APT)成像、脑pH值分析以及缺氧缺血性脑损伤(HIBI)仔猪电压门控质子通道(Hv1)表达分析相结合的方法,探讨HIBI后脑pH值的调节机制。
选取59只健康仔猪(出生后3 - 5天;体重1 - 1.5千克)。6只仔猪因死亡、建模失败或运动伪影被排除,最终对照组共10只动物,HIBI模型组共43只动物。在HIBI后的不同时间点(0 - 2、2 - 6、6 - 12、12 - 24、24 - 48和48 - 72小时),测量并分析脑pH值、Hv1表达和APT值。数据采用独立样本t检验、方差分析和Spearman等级相关分析进行统计分析。P值小于0.05表示具有统计学意义。
HIBI后的免疫荧光染色结果显示,基底节区Hv1蛋白表达在0 - 2小时达到峰值,0 - 2小时与其他时间点之间存在统计学显著差异(P<0.001)。在仔猪中,APT值在HIBI后0 - 2小时达到最低点,随后逐渐升高,除2 - 6小时亚组外(P = 0.602),对照组与所有HIBI模型亚组之间均存在显著差异(P<0.001)。HIBI后脑pH值下降,在0 - 2小时达到最低点,然后逐渐升高。Hv1蛋白表达、pH值和APT值均具有相关性(P<0.001)。
HIBI后,脑pH值、APT值和Hv1表达随时间变化且呈线性相关。这表明缺氧缺血(HI)损伤后神经网络中脑氢离子(H)发生了转移,脑pH值发生了变化。