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内质网应激抑制在糖尿病大鼠脊髓损伤模型中保护血脊髓屏障的完整性。

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

机构信息

Molecular Pharmacology Research Center, School of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, Zhejiang, 325035, China.

Department of Orthopaedics Surgery, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, 325035, China.

出版信息

Sci Rep. 2017 Aug 9;7(1):7661. doi: 10.1038/s41598-017-08052-4.

Abstract

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.

摘要

血-脊髓屏障(BSCB)在脊髓损伤(SCI)后的恢复中起着重要作用,糖尿病(DM)会损害内皮细胞功能和 BSCB 的完整性。内质网(ER)应激发生在 SCI 的早期阶段,会影响预后和细胞存活。然而,ER 应激与糖尿病大鼠 SCI 后 BSCB 完整性之间的关系尚不清楚。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 天出现 Evans Blue(EB)染料外渗增加,以及内皮细胞和周细胞丢失。糖尿病还会诱导 ER 应激的激活。在人脑血管内皮细胞中也观察到了类似的作用。内质网应激抑制剂 4-苯丁酸(4-PBA)降低了糖尿病对 SCI 的不良影响,减少了 EB 染料外渗,并限制了内皮细胞和周细胞的丢失。此外,4-PBA 治疗在体内和体外部分逆转了紧密连接和黏附连接的降解。总之,糖尿病通过诱导 ER 应激加重了 SCI 后 BSCB 的破坏,而 4-PBA 抑制 ER 应激可能对糖尿病 SCI 大鼠 BSCB 的完整性发挥有益作用,从而改善预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84ce/5550423/8a5cfc537cb5/41598_2017_8052_Fig1_HTML.jpg

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