Department of Anatomy and Histology, School of Basic Medical Sciences, Peking University, Beijing, 100191, China.
Beijing Key Lab of Magnetic Resonance Imaging Technology, Beijing, 100191, China.
Neurosci Lett. 2019 Jun 21;704:189-194. doi: 10.1016/j.neulet.2019.04.025. Epub 2019 Apr 10.
In this study, the protective effects of 3,4-dihydroxyphenyl lactic acid (DLA) on blood-brain barrier (BBB) injury following subarachnoid hemorrhage (SAH) has been explored.
Male Sprague-Dawley rats (weight 300-350 g) were used to establish the SAH model using the endovascular perforation method. The animals were randomly divided into four groups: sham (n = 40), SAH (n = 46), SAH + vehicle (n = 44), and SAH + DLA (n = 40) treatment groups. At 1 h after SAH, either DLA (10 mg/kg) or normal saline (vehicle) was administered by femoral vein injection. The effects of DLA on mortality, neurological function, brain water content, and BBB were observed. Additionally, immunohistochemistry and western blot techniques were applied to investigate the mechanism of action of DLA.
We found that the administration of DLA (10 mg/kg) following SAH could improve neurological functions, reduce brain water content, and maintain BBB integrity. The expression of pro-inflammatory and pro-apoptotic factors such as toll-like receptor 4 (TLR4), NF-κB (p-p65), tumor necrosis factor-α, p-p38 MAPK, p-p53, and caspase-3 were significantly increased after SAH. These same factors were markedly attenuated following treatment with DLA.
These findings showed that DLA can alleviate BBB injury following SAH through its anti-inflammatory and anti-apoptotic effects via suppression of TLR4 and its downstream NF-κB and p38 MAPK pathways.
本研究旨在探讨 3,4-二羟基苯乳酸(DLA)对蛛网膜下腔出血(SAH)后血脑屏障(BBB)损伤的保护作用。
采用血管内穿针法建立雄性 Sprague-Dawley 大鼠(体重 300-350g)SAH 模型。动物随机分为四组:假手术组(n=40)、SAH 组(n=46)、SAH+载体组(n=44)和 SAH+DLA 治疗组(n=40)。SAH 后 1h,通过股静脉注射 DLA(10mg/kg)或生理盐水(载体)。观察 DLA 对死亡率、神经功能、脑水含量和 BBB 的影响。此外,应用免疫组织化学和 Western blot 技术探讨 DLA 的作用机制。
我们发现,SAH 后给予 DLA(10mg/kg)可改善神经功能,降低脑水含量,维持 BBB 完整性。SAH 后,促炎和促凋亡因子如 toll 样受体 4(TLR4)、核因子-κB(p-p65)、肿瘤坏死因子-α、p-p38 MAPK、p-p53 和 caspase-3 的表达明显增加。而 DLA 治疗后,这些因子的表达明显减弱。
这些发现表明,DLA 通过抑制 TLR4 及其下游 NF-κB 和 p38 MAPK 通路,发挥抗炎和抗凋亡作用,减轻 SAH 后 BBB 损伤。