Cupples William A, Braam Branko
Centre for Biomedical Research and Dept. of Biology, Univ. of Victoria, PO Box 3020, STN CSC, Victoria, BC, Canada.
Am J Physiol Renal Physiol. 2007 Apr;292(4):F1105-23. doi: 10.1152/ajprenal.00194.2006. Epub 2007 Jan 16.
The kidney displays highly efficient autoregulation so that under steady-state conditions renal blood flow (RBF) is independent of blood pressure over a wide range of pressure. Autoregulation occurs in the preglomerular microcirculation and is mediated by two, perhaps three, mechanisms. The faster myogenic mechanism and the slower tubuloglomerular feedback contribute both directly and interactively to autoregulation of RBF and of glomerular capillary pressure. Multiple experiments have been used to study autoregulation and can be considered as variants of two basic designs. The first measures RBF after multiple stepwise changes in renal perfusion pressure to assess how a biological condition or experimental maneuver affects the overall pressure-flow relationship. The second uses time-series analysis to better understand the operation of multiple controllers operating in parallel on the same vascular smooth muscle. There are conceptual and experimental limitations to all current experimental designs so that no one design adequately describes autoregulation. In particular, it is clear that the efficiency of autoregulation varies with time and that most current techniques do not adequately address this issue. Also, the time-varying and nonadditive interaction between the myogenic mechanism and tubuloglomerular feedback underscores the difficulty of dissecting their contributions to autoregulation. We consider the modulation of autoregulation by nitric oxide and use it to illustrate the necessity for multiple experimental designs, often applied iteratively.
肾脏表现出高效的自身调节功能,因此在稳态条件下,肾血流量(RBF)在很宽的血压范围内与血压无关。自身调节发生在肾小球前微循环中,由两种(可能三种)机制介导。较快的肌源机制和较慢的肾小管-肾小球反馈直接或交互地对RBF和肾小球毛细血管压力的自身调节起作用。多项实验已被用于研究自身调节,可被视为两种基本设计的变体。第一种是在肾灌注压多次逐步变化后测量RBF,以评估生物状态或实验操作如何影响整体压力-流量关系。第二种使用时间序列分析来更好地理解在同一血管平滑肌上并行运行的多个控制器的运作。所有当前的实验设计都存在概念和实验上的局限性,因此没有一种设计能充分描述自身调节。特别是,很明显自身调节的效率随时间变化,而大多数当前技术并未充分解决这个问题。此外,肌源机制和肾小管-肾小球反馈之间随时间变化且非相加的相互作用突出了剖析它们对自身调节贡献的难度。我们考虑一氧化氮对自身调节的调节作用,并以此来说明通常需反复应用多种实验设计的必要性。