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Sodium recirculation and isotonic transport in toad small intestine.

机译:蟾蜍小肠中的钠再循环和等渗运输。

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Isolated small intestine of toad (Bufo bufo) was mounted on glass tubes for perfusion studies with oxygenated amphibian Ringer's solution containing glucose and acetate. Under open-circuit conditions (Vt = -3.9 +/- 1.8 mV, N = 14) the preparation generated a net influx of 134Cs+. The time course of unidirectional 134Cs+-fluxes was mono-exponential with similar rate constants for influx and outflux when measured in the same preparation. The flux-ratio was time invariant from the beginning of appearance of the tracers to steady state was achieved. Thus, just a single pathway, the paracellular pathway, is available for transepithelial transport of Cs+. From the ratio of unidirectional Cs+-fluxes the paracellular force was calculated to be, 18.2 +/- 1.5 mV (N = 6), which is directed against the small transepithelial potential difference. The paracellular netflux of cesium ions, therefore, is caused by solvent drag. The flux of 134Cs+ entering and trapped by the cells was of a magnitude similar to that passing the paracellular route. Therefore, independent of the convective flux of 134Cs+, every second 134Cs+ ion flowing into the lateral space was pumped into the cells rather than proceeding, via the low resistance pathway, to the serosal bath. It is thus indicated that the paracellular convective flow of 134Cs+ is driven by lateral Na+/K+-pumps. Transepithelial unidirectional 42K+ fluxes did not reach steady state within an observation period of 70 min, indicating that components of the fluxes in both directions pass the large cellular pool of potassium ions. The ratio of unidirectional 24Na+ fluxes was time-variant and declined from an initial value of 3.66 +/- 0.34 to a significantly smaller steady-state value of 2.57 +/- 0.26 (P < 0.001, N = 5 paired observations), indicating that sodium ions pass the epithelium both via the paracellular and the cellular pathway. Quantitatively, the larger ratio of paracellular Na+ fluxes, as compared to that of paracellular Cs+ fluxes, is compatible with convective flow of the two alkali metal ions through the same population of water-filled pores. With a new set of equations, the fraction of the sodium flux passing the basement membrane barrier of the lateral space that is recirculated through the cellular compartment is estimated. This fraction was, on average, 0.72 +/- 0.03 (N = 5). It is concluded that isotonicity of the transportate can be maintained by producing a hypertonic fluid emerging from the lateral space combined with reuptake of salt via the cells.
机译:将分离的蟾蜍小肠(Bufo bufo)安装在玻璃管上,用含葡萄糖和乙酸盐的含氧两栖林格氏液进行灌注研究。在开路条件下(Vt = -3.9 +/- 1.8 mV,N = 14),该制剂产生的净流入量为134Cs +。当在同一制剂中测量时,单向134Cs +助焊剂的时间过程是单指数的,流入和流出的速率常数相似。从示踪剂开始出现到达到稳态,通量比是时间不变的。因此,仅有一个途径,即细胞旁途径,可用于Cs +的跨上皮运输。根据单向Cs +助焊剂的比例,计算细胞旁力为18.2 +/- 1.5 mV(N = 6),这与较小的跨上皮电位差有关。因此,铯离子的细胞旁净通量是由溶剂阻力引起的。进入细胞并被细胞捕获的134Cs +流量与通过旁细胞途径的流量相似。因此,与134Cs +的对流无关,流入侧面空间的每秒134Cs +离子被泵入细胞,而不是通过低阻力途径进入浆膜浴。因此表明134Cs +的细胞旁对流是由侧向Na + / K +泵驱动的。跨上皮单向42K +通量在70分钟的观察期内未达到稳定状态,表明双向通量的成分都通过了较大的钾离子细胞池。单向24Na +通量的比率是随时间变化的,并且从初始值3.66 +/- 0.34下降到显着较小的稳态值2.57 +/- 0.26(P <0.001,N = 5个配对观测值),表明钠离子既通过细胞旁途径又通过细胞途径通过上皮。从数量上讲,与旁细胞Cs +通量相比,旁细胞Na +通量的更大比例与两种碱金属离子通过相同的充满水孔的对流流动是相容的。使用一组新的方程式,可以估算出通过横向空间的基底膜屏障并通过细胞室再循环的钠通量的比例。该分数平均为0.72 +/- 0.03(N = 5)。结论是,可以通过产生从侧面空间出现的高渗流体并结合盐经由细胞的再摄取来维持转运体的等渗性。

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