Haase E B, Shoukas A A
Department of Biomedical Engineering, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
Am J Physiol. 1992 Dec;263(6 Pt 2):H1939-45. doi: 10.1152/ajpheart.1992.263.6.H1939.
This series of experiments quantified the role of the rat small intestinal arterioles in capacity changes during bilateral carotid occlusion (BCO) and compared them with previous venular studies. We also determined the role of autoregulation in arteriolar constriction during BCO. First-order, second-order, and third-order arteriolar diameter changes were measured during changes in arteriolar pressure and/or sympathetic activity (via BCO). The results indicated that an arteriolar pressure drop caused an immediate significant transient diameter decrease of 14% (P < 0.001), followed by an average steady-state diameter increase of 11% (P < 0.001) over control because of autoregulation. During BCO, the arterioles demonstrated an initial 8-22% decrease in diameter (P < 0.05). The largest first-order vessels were the least responsive to changes in pressure and BCO, while the smallest third-order vessels were the most responsive. Apparently autoregulation, and not sympathetic activity, was responsible for most of the arteriolar constriction during BCO. We also developed an anatomic model of the rat intestinal vasculature which revealed that venules hold 70% of the microcirculatory volume and are responsible for 80% of the total blood shift during BCO. Venular constriction and, to a minor degree, arteriolar constriction result in a 14% decrease in microcirculatory intestinal blood volume during BCO.
本系列实验量化了大鼠小肠小动脉在双侧颈动脉闭塞(BCO)期间容量变化中的作用,并将其与先前关于小静脉的研究进行了比较。我们还确定了自动调节在BCO期间小动脉收缩中的作用。在小动脉压力和/或交感神经活动变化(通过BCO)期间,测量了一级、二级和三级小动脉直径的变化。结果表明,小动脉压力下降导致直径立即显著短暂降低14%(P<0.001),随后由于自动调节,平均稳态直径比对照增加11%(P<0.001)。在BCO期间,小动脉直径最初下降8-22%(P<0.05)。最大的一级血管对压力和BCO变化的反应最小,而最小的三级血管反应最大。显然,自动调节而非交感神经活动是BCO期间大部分小动脉收缩的原因。我们还建立了大鼠肠道血管系统的解剖模型,该模型显示小静脉容纳70%的微循环容积,并且在BCO期间负责80%的总血容量转移。在BCO期间,小静脉收缩以及在较小程度上小动脉收缩导致肠道微循环血容量减少14%。