首页> 外文期刊>Journal of Cerebral Blood Flow and Metabolism: Official Journal of the International Society of Cerebral Blood Flow and Metabolism >The adverse pial arteriolar and axonal consequences of traumatic brain injury complicated by hypoxia and their therapeutic modulation with hypothermia in rat.
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The adverse pial arteriolar and axonal consequences of traumatic brain injury complicated by hypoxia and their therapeutic modulation with hypothermia in rat.

机译:创伤性脑损伤并缺氧对大鼠小动脉和轴突的不利影响及其对体温过低的治疗调节作用。

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摘要

This study examined the effect of posttraumatic hypoxia on cerebral vascular responsivity and axonal damage, while also exploring hypothermia's potential to attenuate these responses. Rats were subjected to impact acceleration injury (IAI) and equipped with cranial windows to assess vascular reactivity to topical acetylcholine, with postmortem analyses using antibodies to amyloid precursor protein to assess axonal damage. Animals were subjected to hypoxia alone, IAI and hypoxia, IAI and hypoxia before induction of moderate hypothermia (33 degrees C), IAI and hypoxia induced during hypothermic intervention, and IAI and hypoxia initiated after hypothermia. Hypoxia alone had no impact on vascular reactivity or axonal damage. Acceleration injury and posttraumatic hypoxia resulted in dramatic axonal damage and altered vascular reactivity. When IAI and hypoxia were followed by hypothermic intervention, no axonal or vascular protection ensued. However, when IAI was followed by hypoxia induced during hypothermia, axonal and vascular protection followed. When this same hypoxic insult followed the use of hypothermia, no benefit ensued. These studies show that early hypoxia and delayed hypoxia exert damaging axonal and vascular consequences. Although this damage is attenuated by hypothermia, this follows only when hypoxia occurs during hypothermia, with no benefit found if the hypoxic insult proceeds or follows hypothermia.
机译:这项研究检查了创伤后缺氧对脑血管反应性和轴突损伤的影响,同时还探讨了低温治疗减弱这些反应的潜力。对大鼠进行冲击加速损伤(IAI),并配备颅窗以评估其对局部乙酰胆碱的血管反应性,并使用淀粉样前体蛋白抗体进行死后分析以评估轴突损伤。在中度低温(33摄氏度)诱导之前,动物接受了单独的低氧,IAI和低氧,IAI和低氧,低温干预期间诱导了IAI和低氧,低温后开始了IAI和低氧。单独的缺氧对血管反应性或轴突损伤没有影响。加速损伤和创伤后缺氧导致严重的轴突损伤和血管反应性改变。当IAI和缺氧后再进行低温干预时,则不会出现轴突或血管保护。但是,当IAI继之以在体温过低期间引起的缺氧时,轴突和血管保护随之而来。如果在使用低温治疗后发生了同样的缺氧损伤,则没有任何好处。这些研究表明,早期缺氧和延迟缺氧会对轴突和血管造成损害。尽管这种损害会因体温过低而减弱,但只有在体温过低时发生缺氧,这种损害才会随之发生,而如果低氧侮辱继续进行或继体温过低,则无益。

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