Zhang Z, Huang J M, Turner M R, Rhinehart K L, Pallone T L
Division of Nephrology, University of Maryland School of Medicine, Baltimore, Maryland 21201-1595, USA.
Am J Physiol Regul Integr Comp Physiol. 2001 Jun;280(6):R1878-86. doi: 10.1152/ajpregu.2001.280.6.R1878.
We investigated the dependence of ANG II (10(-8) M)-induced constriction of outer medullary descending vasa recta (OMDVR) on membrane potential (Psim) and chloride ion. ANG II depolarized OMDVR, as measured by fully loading them with the voltage-sensitive dye bis[1,3-dibutylbarbituric acid-(5)] trimethineoxonol [DiBAC(4)(3)] or selectively loading their pericytes. ANG II was also observed to depolarize pericytes from a resting value of -55.6 +/- 2.6 to -26.2 +/- 5.4 mV when measured with gramicidin D-perforated patches. When measured with DiBAC(4)(3) in unstimulated vessels, neither changing extracellular Cl(-) concentration ([Cl(-)]) nor exposure to the chloride channel blocker indanyloxyacetic acid 94 (IAA-94; 30 microM) affected Psim. In contrast, IAA-94 repolarized OMDVR pretreated with ANG II. Neither IAA-94 (30 microM) nor niflumic acid (30 microM, 1 mM) affected the vasoactivity of unstimulated OMDVR, whereas both dilated ANG II-preconstricted vessels. Reduction of extracellular [Cl(-)] from 150 to 30 meq/l enhanced ANG II-induced constriction. Finally, we identified a Cl(-) channel in OMDVR pericytes that is activated by ANG II or by excision into extracellular buffer. We conclude that constriction of OMDVR by ANG II involves pericyte depolarization due, in part, to increased activity of chloride channels.
我们研究了血管紧张素II(10⁻⁸ M)诱导的外髓质降支直小血管(OMDVR)收缩对膜电位(Psim)和氯离子的依赖性。通过用电压敏感染料双[1,3 - 二丁基巴比妥酸 - (5)]三甲川氧杂菁[DiBAC(4)(3)]完全加载OMDVR或选择性加载其周细胞来测量,血管紧张素II使OMDVR去极化。当用短杆菌肽D穿孔膜片测量时,还观察到血管紧张素II使周细胞从静息值 - 55.6±2.6 mV去极化至 - 26.2±5.4 mV。在用DiBAC(4)(3)测量未刺激的血管时,改变细胞外Cl⁻浓度([Cl⁻])或暴露于氯离子通道阻滞剂茚满氧基乙酸94(IAA - 94;30 μM)均不影响Psim。相反,IAA - 94使预先用血管紧张素II处理的OMDVR复极化。IAA - 94(30 μM)和氟尼辛(30 μM,1 mM)均不影响未刺激的OMDVR的血管活性,而两者都使血管紧张素II预收缩的血管舒张。将细胞外[Cl⁻]从150降低至30 meq/l可增强血管紧张素II诱导的收缩。最后,我们在OMDVR周细胞中鉴定出一种氯离子通道,该通道可被血管紧张素II激活或通过切除进入细胞外缓冲液而激活。我们得出结论,血管紧张素II引起的OMDVR收缩涉及周细胞去极化,部分原因是氯离子通道活性增加。