Koyama S, Yoshitomi K, Imai M
Department of Pharmacology, Jichi Medical School, Tochigi, Japan.
Am J Physiol. 1991 Jun;260(6 Pt 2):F839-47. doi: 10.1152/ajprenal.1991.260.6.F839.
To estimate the contribution of paracellular shunt pathway to the cation-selective permeability in the upper portion of the descending limb of long-looped nephron (LDLu) of hamsters, we observed the effect of protamine on salt-diffusion voltage (delta VT) and transmural resistance (RT). delta VT generated on reduction of lumen NaCl concentration was decreased from 12.0 +/- 1.4 to 7.3 +/- 1.2 mV when 100 micrograms/ml protamine were added to the lumen. Although the effect of protamine persisted after removal of the agent from the lumen, addition of 30 U/ml heparin reversed the delta VT toward the control level. The effect of protamine was dose dependent in the range from 3 to 1,000 micrograms/ml. Protamine was without effect from the bath. Studies on single salt dilution voltage revealed that 100 and 300 micrograms/ml protamine inhibited relative Na+ to Cl- permeability from 4.03 +/- 0.38 to 2.14 +/- 0.21 and from 3.75 +/- 0.37 to 1.36 +/- 0.09, respectively. Protamine markedly decreased the apparent transference number for Na+ but slightly increased the value for Cl-. Protamine also inhibited permeabilities for K+, Rb+, and Li+ relative to Cl-, indicating that the inhibitory effect of protamine was not confined to Na+ but was generalized to cations. Transmural cable analysis showed that 100 micrograms/ml protamine increased RT from 14.0 +/- 1.1 to 19.3 +/- 1.2 omega.cm2, with the effect being reversed by 30 U/ml heparin. Because the effect of protamine on RT was unaffected by ouabain in the bath, changes in RT may mainly represent those of the paracellular shunt resistance.(ABSTRACT TRUNCATED AT 250 WORDS)
为了评估旁细胞旁路途径对仓鼠长襻肾单位降支上段(LDLu)阳离子选择性通透的贡献,我们观察了鱼精蛋白对盐扩散电压(δVT)和跨膜电阻(RT)的影响。当向管腔内加入100微克/毫升鱼精蛋白时,因管腔内NaCl浓度降低而产生的δVT从12.0±1.4毫伏降至7.3±1.2毫伏。尽管从管腔内去除该药物后鱼精蛋白的作用仍持续存在,但加入30单位/毫升肝素可使δVT恢复至对照水平。鱼精蛋白的作用在3至1000微克/毫升范围内呈剂量依赖性。从浴槽侧加入鱼精蛋白则无作用。对单盐稀释电压的研究表明,100微克/毫升和300微克/毫升鱼精蛋白分别将相对Na⁺对Cl⁻的通透性从4.03±0.38抑制至2.14±0.21,以及从3.75±0.37抑制至1.36±0.09。鱼精蛋白显著降低了Na⁺的表观迁移数,但略微增加了Cl⁻的值。鱼精蛋白还抑制了相对于Cl⁻的K⁺、Rb⁺和Li⁺的通透性,表明鱼精蛋白的抑制作用不仅限于Na⁺,而是普遍针对阳离子。跨膜电缆分析显示,100微克/毫升鱼精蛋白使RT从14.0±1.1增加至19.3±1.2Ω·cm²,30单位/毫升肝素可逆转该作用。由于浴槽中哇巴因不影响鱼精蛋白对RT的作用,RT的变化可能主要代表旁细胞旁路电阻的变化。(摘要截断于250字)