小鼠脑微循环对cGMP部分反应的内皮依赖性。

W I Rosenblum, G H Nelson, P Weinbrecht
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引用次数: 0

摘要

用电视显微镜对小鼠脑表面直径30 ~ 40 μ m的小动脉进行图像分割监测。在血管内埃文斯蓝存在的情况下,氦氖激光损伤内皮细胞。这种方法先前被证明可以选择性地消除已知的内皮依赖性扩张剂的扩张,这种扩张剂会导致内皮细胞释放一种或多种放松因子(edrf)。局部应用8 Br cGMP和二丁基cAMP, 10(-5) m,使血管扩张,比较内皮损伤前和损伤后的反应。进行了两项独立的研究。其中,10只小鼠接受8br cGMP治疗,10只小鼠接受二丁基cAMP治疗。在第二项研究中,12只小鼠在内皮损伤前和损伤后分别接受每种核苷酸的治疗。在这两项研究中,只有对8 Br cGMP的反应受到内皮损伤的损害(p < 0.01)。这些数据表明,在这些小动脉中,一部分对GMP的反应,而不是对AMP的反应,是由内皮细胞控制的,这可能反映了鸟苷酸环化酶/GMP在EDRF的合成/释放中的作用。这将为内皮细胞中的鸟苷酸环化酶提供功能。鸟苷酸环化酶在这些细胞中的功能以前没有被定义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Endothelium dependence of a portion of the response to cGMP in brain microcirculation of mice.

The diameters of arterioles 30-40 microns on the surface of the mouse brain were monitored by TV microscopy with an image splitting technique. Endothelium was injured by light from a helium neon laser in the presence of intravascular Evans blue. This method was previously shown to selectively eliminate dilation by known endothelium dependent dilators which cause endothelial cells to release one or more relaxing factors (EDRFs). Dilation was produced by local application of 8 Br cGMP and dibutyryl cAMP, 10(-5) M. The response before endothelial damage was compared with the response after damage. Two separate studies were conducted. In one, 10 mice were treated with 8 Br cGMP and 10 with dibutyryl cAMP. In the second study 12 mice were treated with each nucleotide before endothelial injury and again after injury. In both studies only the response to 8 Br cGMP was impaired (p less than .01) by the endothelial injury. These data suggest that in these arterioles a portion of the response to GMP, but not to AMP, is controlled by endothelium and may reflect a role for guanylate cyclase/GMP in the synthesis/-release of an EDRF. This would provide a function for the guanylate cyclase in endothelial cells. The function of guanylate cyclase within these cells has not previously been defined.

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