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氯沙坦治疗可改善创伤性脑损伤小鼠的预后。

Losartan Treatment Could Improve the Outcome of TBI Mice.

作者信息

Xiong Jianhua, Gao Yalong, Li Xiaotian, Li Kai, Li Qifeng, Shen Jun, Han Zhenying, Zhang Jianning

机构信息

Department of Neurosurgery, Tianjin Medical University General Hospital, Tianjin, China.

出版信息

Front Neurol. 2020 Oct 15;11:992. doi: 10.3389/fneur.2020.00992. eCollection 2020.

DOI:10.3389/fneur.2020.00992
PMID:33178092
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7593661/
Abstract

Traumatic brain injury frequently leads to serious mortality and physical disability, yet effective treatments remains insufficient. TBI always leads to a series of secondary brain injuries including neuronal apoptosis, continuous inflammation, endoplasmic reticulum stress, and disruption of the blood-brain barrier. Sartans that block angiotensin II type 1 receptors are strongly neuroprotective, neurorestorative and anti-inflammatory. However, whether losartan, a FDA-approved and widely used drug for regulating blood pressure, is beneficial for improving the prognosis of TBI need more evidence. Through a controlled cortical impact injury mice model, we confirmed that losartan treatment could ameliorate CCI-induced secondary brain injury. We found that losartan treatment decreased brain lesion volume, neuronal apoptosis and ER stress protein ATF4 and eIF2α. Moreover, our results showed that losartan also improved neurological and motor function. It is worth pointing out that losartan increased the expression of tight junction proteins ZO-1 and alleviated brain edema and blood brain barrier leakage. Additionally, losartan inhibited pro-inflammatory factor TNF-α and improve anti-inflammatory factor IL-10. Taken together, our data demonstrated that losartan could improve the prognosis of TBI and may be a promising therapeutic method for mitigating TBI.

摘要

创伤性脑损伤常常导致严重的死亡率和身体残疾,但有效的治疗方法仍然不足。创伤性脑损伤总是会引发一系列继发性脑损伤,包括神经元凋亡、持续炎症、内质网应激以及血脑屏障破坏。阻断血管紧张素II 1型受体的沙坦类药物具有强大的神经保护、神经修复和抗炎作用。然而,氯沙坦作为一种经美国食品药品监督管理局批准且广泛用于调节血压的药物,对改善创伤性脑损伤的预后是否有益,还需要更多证据。通过控制皮质撞击损伤小鼠模型,我们证实氯沙坦治疗可减轻皮质撞击诱导的继发性脑损伤。我们发现氯沙坦治疗可减小脑损伤体积、减少神经元凋亡以及内质网应激蛋白ATF4和eIF2α。此外,我们的结果表明氯沙坦还可改善神经和运动功能。值得指出的是,氯沙坦可增加紧密连接蛋白ZO-1的表达,减轻脑水肿和血脑屏障渗漏。此外,氯沙坦可抑制促炎因子TNF-α并提高抗炎因子IL-10。综上所述,我们的数据表明氯沙坦可改善创伤性脑损伤的预后,可能是减轻创伤性脑损伤的一种有前景的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c95/7593661/68f2b61a36d5/fneur-11-00992-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c95/7593661/172b0f381609/fneur-11-00992-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c95/7593661/0c0a027145fc/fneur-11-00992-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c95/7593661/e0bd0434488c/fneur-11-00992-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c95/7593661/968b8860c5c1/fneur-11-00992-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c95/7593661/68f2b61a36d5/fneur-11-00992-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c95/7593661/172b0f381609/fneur-11-00992-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c95/7593661/0c0a027145fc/fneur-11-00992-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c95/7593661/e0bd0434488c/fneur-11-00992-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c95/7593661/968b8860c5c1/fneur-11-00992-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c95/7593661/68f2b61a36d5/fneur-11-00992-g0005.jpg

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