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药物诱导低温对小鼠脑出血模型的急性和迟发性保护作用。

Acute and delayed protective effects of pharmacologically induced hypothermia in an intracerebral hemorrhage stroke model of mice.

机构信息

Department of Anesthesiology, Emory University School of Medicine, Atlanta, GA 30322, United States.

出版信息

Neuroscience. 2013 Nov 12;252:489-500. doi: 10.1016/j.neuroscience.2013.07.052. Epub 2013 Jul 30.

Abstract

Hemorrhagic stroke, including intracerebral hemorrhage (ICH), is a devastating subtype of stroke; yet, effective clinical treatment is very limited. Accumulating evidence has shown that mild to moderate hypothermia is a promising intervention for ischemic stroke and ICH. Current physical cooling methods, however, are less efficient and often impractical for acute ICH patients. The present investigation tested pharmacologically induced hypothermia (PIH) using the second-generation neurotensin receptor (NTR) agonist HPI-201 (formerly known as ABS-201) in an adult mouse model with ICH. Acute or delayed administrations of HPI-201 (2mg/kg bolus injection followed by 2 injections of 1mg/kg, i.p.) were initiated at 1 or 24h after ICH. HPI-201 induced mild hypothermia within 30 min and body and brain temperatures were maintained at 32.7 ± 0.4°C for at least 6h without causing observable shivering. With the 1-h delayed treatment, HPI-201-induced PIH significantly reduced ICH-induced cell death and brain edema compared to saline-treated ICH animals. When HPI-201-induced hypothermia was initiated 24h after the onset of ICH, it still significantly attenuated brain edema, cell death and blood-brain barrier breakdown. HPI-201 significantly decreased the expression of matrix metallopeptidase-9 (MMP-9), reduced caspase-3 activation, and increased Bcl-2 expression in the ICH brain. Moreover, ICH mice received 1-h delayed HPI-201 treatment performed significantly better in the neurological behavior test 48 h after ICH. All together, these data suggest that systemic injection of HPI-201 is an effective hypothermic strategy that protects the brain from ICH injury with a wide therapeutic window. The protective effect of this PIH therapy is partially mediated through the alleviation of apoptosis and neurovascular damage. We suggest that pharmacological hypothermia using the newly developed neurotensin analogs is a promising therapeutic treatment for ICH.

摘要

出血性脑卒中,包括脑出血 (ICH),是一种破坏性很强的脑卒中亚型;然而,有效的临床治疗方法非常有限。越来越多的证据表明,轻度至中度低温是缺血性卒中和 ICH 的一种有前途的干预措施。然而,目前的物理降温方法对于急性 ICH 患者效率较低,且往往不切实际。本研究在 ICH 成年小鼠模型中测试了第二代神经降压素受体 (NTR) 激动剂 HPI-201(以前称为 ABS-201)的药物诱导性低温 (PIH)。在 ICH 后 1 或 24 小时开始进行 HPI-201 的急性或延迟给药(2mg/kg 推注后腹腔内给予 1mg/kg 的 2 次注射)。HPI-201 在 30 分钟内引起轻度低温,体温和脑部温度至少维持在 32.7±0.4°C 6 小时,而不会引起明显的颤抖。在 1 小时延迟治疗中,与盐水治疗的 ICH 动物相比,HPI-201 诱导的 PIH 显著减少了 ICH 诱导的细胞死亡和脑水肿。当 HPI-201 诱导的低温在 ICH 发作后 24 小时开始时,它仍能显著减轻脑水肿、细胞死亡和血脑屏障破裂。HPI-201 显著降低了 ICH 大脑中基质金属蛋白酶-9 (MMP-9)的表达,降低了半胱天冬酶-3 的激活,并增加了 Bcl-2 的表达。此外,ICH 小鼠在 ICH 后 48 小时接受 1 小时延迟 HPI-201 治疗后,在神经行为测试中表现明显更好。总之,这些数据表明,全身注射 HPI-201 是一种有效的低温策略,可通过减轻细胞凋亡和神经血管损伤来保护大脑免受 ICH 损伤,具有广泛的治疗窗。这种 PIH 治疗的保护作用部分是通过减轻细胞凋亡和神经血管损伤来实现的。我们建议使用新开发的神经降压素类似物进行药物诱导性低温是治疗 ICH 的一种有前途的治疗方法。

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