Louis T M, Meng W, Bari F, Errico R A, Busija D W
Department of Anatomy and Cell Biology, East Carolina University, Medical School, Greenville, NC 27858, USA.
Stroke. 1996 Jan;27(1):134-8; discussion 139. doi: 10.1161/01.str.27.1.134.
Effects of anoxic stress on cerebrovascular responses to calcitonin gene-related peptide (CGRP) have not been examined previously. We determined the effects of total global ischemia on cerebral arteriolar responses to CGRP in newborn pigs.
Piglets were anesthetized and ventilated with a respirator. Pial arteriolar diameter was determined using a closed cranial window and intravital microscopy. Baseline arteriolar diameters ranged from 80 to 100 microns. Arteriolar responses to 10(-9) and 10(-8) mmol/L CGRP applied topically were determined before and 1, 2, and 4 hours after a 10-minute period of total global ischemia. Ischemia was caused by increasing intracranial pressure.
Before ischemia, CGRP dilated arterioles by 14 +/- 2% (n = 6) and 24 +/- 3% (n = 7) at 10(-9) and 10(-8) mmol/L, respectively. However, after ischemia, arteriolar responses to 10(-9) mmol/L CGRP were reduced at 1 hour to 4 +/- 1%, at 2 hours to 3 +/- 2%, and at 4 hours to 5 +/- 4% (P < .05 for all comparisons). Similarly, arteriolar responses to 10(-8) mmol/L CGRP were reduced to 5 +/- 2% at 1 hour, 5 +/- 2% at 2 hours, and 10 +/- 6% at 4 hours (P < .05 for all comparisons). In time control animals, arteriolar responses to CGRP did not change over time. In other animals, we examined effects of pretreatment with indomethacin (5 mg/kg IV) on ischemia-induced decreases in arteriolar responses to CGRP. Indomethacin administration did not preserve arteriolar dilation to CGRP at 1 hour after ischemia, but responses were normal at 2 hours.
Total global ischemia leads to prolonged attenuated dilator responses of cerebral arterioles to CGRP. In addition, indomethacin treatment alters effects of ischemia on CGRP-induced dilation.
以往尚未研究缺氧应激对脑血管对降钙素基因相关肽(CGRP)反应的影响。我们测定了全脑缺血对新生猪脑小动脉对CGRP反应的影响。
仔猪麻醉后用呼吸机通气。使用闭合式颅窗和活体显微镜测定软脑膜小动脉直径。小动脉基线直径范围为80至100微米。在10分钟全脑缺血之前以及缺血后1、2和4小时,测定局部应用10⁻⁹和10⁻⁸mmol/L CGRP时的小动脉反应。缺血由颅内压升高引起。
缺血前,10⁻⁹和10⁻⁸mmol/L CGRP分别使小动脉扩张14±2%(n = 6)和24±3%(n = 7)。然而,缺血后,对10⁻⁹mmol/L CGRP的小动脉反应在1小时时降至4±1%,2小时时降至3±2%,4小时时降至5±4%(所有比较P <.05)。同样,对10⁻⁸mmol/L CGRP的小动脉反应在1小时时降至5±2%,2小时时降至5±2%,4小时时降至10±6%(所有比较P <.05)。在时间对照动物中,小动脉对CGRP的反应未随时间变化。在其他动物中,我们研究了用吲哚美辛(5mg/kg静脉注射)预处理对缺血诱导的小动脉对CGRP反应降低的影响。吲哚美辛给药在缺血后1小时并未维持小动脉对CGRP的扩张,但在2小时时反应正常。
全脑缺血导致脑小动脉对CGRP的扩张反应长期减弱。此外,吲哚美辛治疗改变了缺血对CGRP诱导的扩张的影响。