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Inhibition of Endoplasmic Reticulum Stress Preserves the Integrity of Blood-Spinal Cord Barrier in Diabetic Rats Subjected to Spinal Cord Injury

机译:内质网应激的抑制保留了脊髓损伤的糖尿病大鼠的血脊髓屏障的完整性。

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摘要

The blood-spinal cord barrier (BSCB) plays significance roles in recovery following spinal cord injury (SCI), and diabetes mellitus (DM) impairs endothelial cell function and integrity of BSCS. Endoplasmic reticulum (ER) stress occurs in the early stages of SCI and affects prognosis and cell survival. However, the relationship between ER stress and the integrity of BSCB in diabetic rats after SCI remains unclear. Here we observed that diabetic rats showed increased extravasation of Evans Blue (EB) dye, and loss of endothelial cells and pericytes 1 day after SCI compared to non-diabetic rats. Diabetes was also shown to induce activation of ER stress. Similar effects were observed in human brain microvascular endothelial cells. 4-phenylbutyric acid (4-PBA), an ER stress inhibitor lowered the adverse effect of diabetes on SCI, reduced EB dye extravasation, and limited the loss of endothelial cells and pericytes. Moreover, 4-PBA treatment partially reversed the degradation of tight junction and adherens junction both in vivo and in vitro. In conclusion, diabetes exacerbates the disruption of BSCB after SCI via inducing ER stress, and inhibition of ER stress by 4-PBA may play a beneficial role on the integrity of BSCB in diabetic SCI rats, leading to improved prognosis.
机译:脊髓脊髓损伤(SCI)后的恢复过程中,血脊髓屏障(BSCB)发挥着重要作用,而糖尿病(DM)则损害了BSCS的内皮细胞功能和完整性。内质网(ER)应激发生在SCI的早期阶段,影响预后和细胞存活。但是,尚不清楚SCI后糖尿病大鼠的内质网应激与BSCB完整性之间的关系。在这里,我们观察到,与非糖尿病大鼠相比,糖尿病大鼠在SCI后1天表现出增加的Evans Blue(EB)染料外渗,以及内皮细胞和周细胞的丢失。糖尿病也显示出诱导ER应激的激活。在人脑微血管内皮细胞中观察到类似的作用。 ER应激抑制剂4-苯基丁酸(4-PBA)降低了糖尿病对SCI的不利影响,减少了EB染料的外渗,并限制了内皮细胞和周细胞的损失。此外,4-PBA处理在体内和体外均部分逆转了紧密连接和粘附连接的降解。总之,糖尿病通过诱导ER应激加剧SCI后BSCB的破坏,而4-PBA抑制ER应激可能对糖尿病SCI大鼠BSCB的完整性起有益作用,从而改善预后。

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