首页> 外文期刊>Brain research >Protective effects of brief intra- and delayed postischemic hypothermia in a transient focal ischemia model in the neonatal rat.
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Protective effects of brief intra- and delayed postischemic hypothermia in a transient focal ischemia model in the neonatal rat.

机译:短暂的局部缺血后和低温后低温对新生大鼠局灶性局部缺血模型的保护作用。

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摘要

Hypothermia provides neuroprotection in virtually all animal models of ischemia, including adult stroke models and the neonatal hypoxic-ischemic (HI) model. In these studies, brief periods of hypothermia are examined in a neonatal model employing transient focal ischemia in a 7-day-old rat pup. Pups underwent permanent middle cerebral artery (MCA) occlusion coupled with a temporary (1 h) occlusion of the ipsilateral common carotid artery (CCA). This study included five treatment groups: (1) normothermic (Normo)-brain temperature was maintained at 37 degrees C; (2) intraischemic hypothermia (IntraH)-28 degrees C during the 1-h ischemic period only; (3) postischemic hypothermia (PostH)-28 degrees C for the second hour of reperfusion only; (4) late-onset postischemic hypothermia (LPostH) cooled to 28 degrees C for the fifth and sixth hours of reperfusion only; and (5) Shams. After various times (3 days-6 weeks), the lesion was assessed using 2,3,5-triphenyltetrazolium chloride (TTC) or hematoxylin and eosin (H&E) stains. Intraischemic hypothermia resulted in significant protection in terms of survival, lesion size, and histology. Postischemic hypothermia was not effective in reducing lesion size early after ischemia, but significantly reduced the eventual long-term damage (2-6 weeks). Late-onset postischemic hypothermia did not reduce infarct volume. Therefore, both intraischemic and postischemic hypothermia provided neuroprotection in the neonatal rat, but with different effects on the degenerative time course. While there were no observable differences in simple behaviors or growth, all hypothermic conditions significantly reduced mortality rates. While the protection resulting from intraischemic hypothermia is similar to what is observed in other models, the degree of long-term ischemic protection observed after 1 h of postischemic hypothermia was remarkable and distinct from what has been observed in other adult or neonatal models.
机译:体温过低实际上可在所有缺血的动物模型中提供神经保护,包括成年中风模型和新生儿缺氧缺血(HI)模型。在这些研究中,在7天大的幼仔中采用短暂局灶性局部缺血的新生儿模型中检查了短暂的低温。幼犬接受永久性大脑中动脉(MCA)阻塞,同时暂时(1 h)阻塞同侧颈总动脉(CCA)。该研究包括五个治疗组:(1)正常体温(Normo)-脑温保持在37摄氏度; (2)仅在局部缺血1小时内局部缺血性低温(IntraH)-28摄氏度; (3)缺血后体温过低(PostH)-28摄氏度,仅用于再灌注的第二个小时; (4)仅在再灌注的第五和第六小时将迟发性缺血后体温过低(LPostH)冷却至28°C; (5)短毛。在不同的时间(3天至6周)后,使用2,3,5-三苯基氯化四唑(TTC)或苏木精和曙红(H&E)染色评估病变。缺血内低温治疗在生存率,病变大小和组织学方面均提供了重要的保护。缺血后体温过低不能有效减少缺血后早期的病变大小,但可以显着减少最终的长期损害(2-6周)。迟发性缺血后体温过低并不能减少梗死面积。因此,缺血内和缺血后低温都对新生大鼠提供了神经保护作用,但是对退行性时程的影响不同。虽然在简单的行为或生长方面没有可观察到的差异,但是所有低温条件都可以显着降低死亡率。虽然由缺血内低温引起的保护与在其他模型中观察到的相似,但缺血后低温1小时后观察到的长期缺血保护程度显着,并且与在其他成人或新生儿模型中观察到的不同。

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