Rappaport A M
Int Rev Physiol. 1980;21:1-63.
The study of the morphology of the hepatic circulation has given evidence that the liver consists of a large vascular delta formed by the confluence of the portal and arterial streams. Their arms, which subdivide the delta into lobar areas, start to run parallel and close to each other when they are still visible to the naked eye. Dwindled down to microscopic size, they become the scaffold of the parenchymal cell masses nestling between the microvessels. The arterioles, as they merge with the sinusoidal and portal channels, assume the role of organizing the microcirculation into units. These units are the vascular core of the structural and functional liver acini. It has now been demonstrated beyond doubt that a PO2 gradient exists in the hepatic vessels and tissues, decreasing from the site of the arteriolar rivulets joining the venous stream toward the site of their common egress via the terminal hepatic venules. The gradient permits the subdivision of the microscopic vascular units into three microcirculatory zones, each of them creating an appropriate microenvironment for specific enzymic and metabolic activity. The microcirculatory shifts in arterial flow from tide to ebb will cause change in the activity of the zones. These are essentially dynamic subdivisions of the metabolic activity in the large liver swamp. Here also start the tiny rivulets forming a green river, the bile stream, that runs in the opposite direction to the portal and hepatic arterial flow. It is to be expected that the quantity and quality of bile carrying important products back to the gastrointestinal area for digestion and absorption of fat are influenced by the tides in portal and arterial flow. All in all, it is evident that vascular morphology is the visual aspect of the dynamic blood flow, thus permitting us to perceive its functional orderliness, and to study the circulatory physiology in the hepatic delta. Means of measurement of hepatic blood flow have been reviewed and its methodological problems have been discussed. It was found that the term "estimated" hepatic blood flow is still justified. Also the relationship between hepatic blood flow and metabolism is not yet clear-cut. The role of the arterial and portal components of the hepatic circulation has been analyzed. There is a reciprocal relationship between arterial and portal volume flow; it is effectuated by the state of constriction or dilation of the mesenteric and hepatic arterioles, both under myogenic control. Portal blood delivers directly to the hepatocyte all water-soluble substances absorbed from the intestines or produced in the intestinal walls. The hepatic artery maintains an appropriate PO2 gradient between the acinar zones and flow of blood against increased tissue resistance; it assures a steady clearance of blood-borne substances, e.g., hormones and endogenous products. Regulation of arterial flow is less neural than neurohumoral; metabolites and bile salts exert additional effects on blood flow...
肝脏循环形态学的研究表明,肝脏由门静脉和动脉血流汇合形成的一个大的血管三角洲组成。它们的分支将三角洲细分为叶状区域,在肉眼仍可见时,这些分支开始相互平行且彼此靠近。当缩小到微观尺寸时,它们成为微血管之间实质细胞团的支架。小动脉在与窦状隙和门静脉通道汇合时,承担着将微循环组织成单位的作用。这些单位是肝脏结构和功能腺泡的血管核心。现已毫无疑问地证明,肝血管和组织中存在氧分压梯度,从汇入静脉血流的小动脉分支处向经终末肝静脉共同流出的部位逐渐降低。该梯度允许将微观血管单位细分为三个微循环区,每个微循环区为特定的酶活性和代谢活动创造适宜的微环境。动脉血流从潮式到ebb式的微循环变化将导致各区活性的改变。这些本质上是大肝脏区域代谢活动的动态细分。在这里还开始形成一条绿色河流的细小支流,即胆汁流,它与门静脉和肝动脉血流方向相反。可以预期,携带重要产物回到胃肠道区域以消化和吸收脂肪的胆汁的数量和质量会受到门静脉和动脉血流潮汐的影响。总而言之,很明显血管形态是动态血流的直观表现,从而使我们能够感知其功能的有序性,并研究肝脏三角洲的循环生理学。对肝血流的测量方法进行了综述,并讨论了其方法学问题。发现“估计的”肝血流这一术语仍然合理。肝血流与代谢之间的关系也尚不明确。分析了肝脏循环中动脉和门静脉成分的作用。动脉和门静脉容积流量之间存在相互关系;这种关系通过肠系膜和肝小动脉的收缩或扩张状态来实现,两者均受肌源性控制。门静脉血将从肠道吸收或在肠壁产生的所有水溶性物质直接输送给肝细胞。肝动脉在腺泡区之间维持适当的氧分压梯度,并在组织阻力增加时使血流保持稳定;它确保对血液中携带的物质,如激素和内源性产物进行稳定清除。动脉血流的调节神经调节作用小于神经体液调节作用;代谢产物和胆盐对血流有额外影响……