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创伤性脑损伤后的神经保护靶点。

Neuroprotection targets after traumatic brain injury.

作者信息

Wang Kevin K W, Larner Stephen F, Robinson Gillian, Hayes Ronald L

机构信息

Center for Neuroproteomics and Biomarkers Research, Department of Psychiatry, McKnight Brain Institute of the University of Florida, 100 S. Newell Drive, Box 100256, Gainesville, FL 32610, USA.

出版信息

Curr Opin Neurol. 2006 Dec;19(6):514-9. doi: 10.1097/WCO.0b013e3280102b10.

Abstract

PURPOSE OF REVIEW

The scarcity of pharmacological neuroprotective treatments for traumatic brain injury is a concern being targeted on various fronts. This review examines the latest treatments under investigation.

RECENT FINDINGS

In the last 12-18 months, no drug has completed phase III clinical trials as a clearly proven method to treat traumatic brain injury. While the drugs work in rodents, when they make it to clinical trial they have failed primarily due to negative side-effects. Those still in trial show promise, and even those rejected have undergone modifications and now show potential, e.g. second-generation N-methyl-D-aspartic acid and alpha-amino-3-hydroxy-methyl-4-isoxazolyl-propionic acid receptor antagonists, calpain inhibitors, and cyclosporine A analogues. Also, several drugs not previously given much attention, such as the antibiotic minocycline, estrogen and progesterone, and a drug already approved for other diseases, erythropoietin, are being examined. Finally, a treatment generating some controversy, but showing potential, is the application of hypothermia to the patients.

SUMMARY

Clearly, finding treatments for traumatic brain injury is not going to be easy and is evidently going to require numerous trials. The good news is that we are closer to finding one or more methods for treating traumatic brain injury patients.

摘要

综述目的

用于治疗创伤性脑损伤的神经保护药物匮乏,这一问题正受到多方面关注。本综述探讨了正在研究的最新治疗方法。

最新发现

在过去12至18个月中,尚无药物作为已明确证实的治疗创伤性脑损伤的方法完成III期临床试验。虽然这些药物在啮齿动物中有效,但进入临床试验后,主要因负面副作用而失败。仍在试验中的药物显示出前景,甚至那些被否决的药物也经过了改进,现在显示出潜力,例如第二代N-甲基-D-天冬氨酸和α-氨基-3-羟基-5-甲基-4-异恶唑丙酸受体拮抗剂、钙蛋白酶抑制剂和环孢素A类似物。此外,几种以前未受太多关注的药物,如抗生素米诺环素、雌激素和孕酮,以及一种已被批准用于其他疾病的药物促红细胞生成素,也正在接受研究。最后,一种引发了一些争议但显示出潜力的治疗方法是对患者进行低温治疗。

总结

显然,找到治疗创伤性脑损伤的方法并非易事,而且显然需要进行大量试验。好消息是,我们离找到一种或多种治疗创伤性脑损伤患者的方法更近了。

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