Pabello Nina G, Tracy Seth J, Keller Richard W
Center for Neuropharmacology and Neuroscience, Albany Medical College MC-136, 47 New Scotland Avenue, Albany, NY 12208, USA.
Brain Res. 2004 Jan 2;995(1):29-38. doi: 10.1016/j.brainres.2003.09.065.
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.
体温过低在几乎所有缺血性动物模型中都具有神经保护作用,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,在一个新生大鼠模型中研究了短暂的体温过低情况,该模型采用7日龄大鼠幼崽的短暂局灶性缺血。幼崽接受永久性大脑中动脉(MCA)闭塞,并伴有同侧颈总动脉(CCA)的临时(1小时)闭塞。本研究包括五个治疗组:(1)正常体温(Normo)——脑温维持在37摄氏度;(2)缺血期低温(IntraH)——仅在1小时缺血期内为28摄氏度;(3)缺血后低温(PostH)——仅在再灌注的第二个小时为28摄氏度;(4)迟发性缺血后低温(LPostH)——仅在再灌注的第五和第六个小时冷却至28摄氏度;以及(5)假手术组。在不同时间(3天至6周)后,使用氯化三苯基四氮唑(TTC)或苏木精和伊红(H&E)染色评估损伤情况。缺血期低温在生存、损伤大小和组织学方面产生了显著的保护作用。缺血后低温在缺血早期对减小损伤大小无效,但显著减少了最终的长期损伤(2至6周)。迟发性缺血后低温并未减少梗死体积。因此,缺血期和缺血后低温在新生大鼠中均提供了神经保护作用,但对退变时间进程有不同影响。虽然在简单行为或生长方面没有观察到差异,但所有低温条件均显著降低了死亡率。虽然缺血期低温产生的保护作用与其他模型中观察到的相似,但缺血后1小时低温观察到的长期缺血保护程度显著,且与其他成年或新生模型中观察到的不同。