Nagesetty R, Paul R J
Department of Physiology and Biophysics, University of Cincinnati, College of Medicine, OH 45267-0576.
Circ Res. 1994 Dec;75(6):990-8. doi: 10.1161/01.res.75.6.990.
During ischemia or hypoxia, alterations in pHi may play a significant role in alteration of vessel wall function. We studied the effects of altering pHi on isometric force and [Ca2+]i in porcine coronary artery. pHi was altered at constant pHo by use of NH4Cl and measured with the fluorescent dye BCECF. [Ca2+]i was monitored with fura 2 and ratiometric fluorescence measurements. Addition of NH4Cl elicited a concentration-dependent (2 to 30 mmol/L) sustained increase in isometric force in unstimulated tissues. In tissues stimulated with KCl (29 mmol/L) or U46619 (1 mumol/L), addition of NH4Cl elicited a rapid but transient decrease followed by a sustained increase in force above the initial stimulated levels. Removal of NH4Cl was associated with a transient decrease and increase followed by a prolonged depression of force and slow recovery to initial levels. Addition of NH4Cl elicited a rapid monotonic increase in pHi and then a slow recovery toward initial levels; washout of NH4Cl led to a rapid acidification followed by recovery. In contrast to the steady state effects of NH4Cl on force, its effects on [Ca2+i were in the opposite direction. During the sustained increase in force elicited by NH4Cl alkalinization, [Ca2+]i was substantially decreased, whereas when force was depressed during the acidification elicited by NH4Cl washout, [Ca2+i was increased to values observed before addition of NH4Cl. The initial transients in force elicited by NH4Cl addition or washout were also associated with opposite changes in [Ca2+]i. Thus, the effects on force of the NH4Cl-induced changes in pHi are associated with changes in the Ca2+ sensitivity of the contractile apparatus rather than mediated through changes in [Ca2+]i.
在缺血或缺氧期间,细胞内pH值(pHi)的改变可能在血管壁功能改变中起重要作用。我们研究了改变pHi对猪冠状动脉等长收缩力和细胞内钙离子浓度([Ca2+]i)的影响。通过使用氯化铵在恒定的细胞外pH值(pHo)条件下改变pHi,并使用荧光染料BCECF进行测量。[Ca2+]i通过fura 2和比率荧光测量进行监测。添加氯化铵会引起未受刺激组织中等长收缩力浓度依赖性(2至30 mmol/L)的持续增加。在用氯化钾(29 mmol/L)或U46619(1 μmol/L)刺激的组织中,添加氯化铵会引起快速但短暂的下降,随后力持续增加并超过初始刺激水平。去除氯化铵会导致短暂的下降和增加,随后是力的长时间降低,并缓慢恢复到初始水平。添加氯化铵会引起pHi快速单调增加,然后缓慢恢复到初始水平;冲洗氯化铵会导致快速酸化,随后恢复。与氯化铵对力的稳态影响相反,其对[Ca2+]i的影响方向相反。在氯化铵碱化引起的力持续增加期间,[Ca2+]i显著降低,而在氯化铵冲洗引起的酸化期间力降低时,[Ca2+]i增加到添加氯化铵之前观察到的值。添加或冲洗氯化铵引起的力的初始瞬变也与[Ca2+]i的相反变化相关。因此,氯化铵诱导的pHi变化对力的影响与收缩装置的Ca2+敏感性变化有关,而不是通过[Ca2+]i的变化介导的。