Paulmichl M, Friedrich F, Lang F
Pflugers Arch. 1987 Apr;408(4):408-13. doi: 10.1007/BF00581137.
In the present study we have investigated the influence of bradykinin on the potential difference across the cell membrane (PD) of Madin Darby Canine Kidney (MDCK)-cells. In the absence of bradykinin PD averages -52.6 +/- 0.9 mV (n = 52). Increasing extracellular potassium concentration from 5.4 to 10 and 20 mmol/l depolarizes the cell membrane by +5.2 +/- 0.3 mV (n = 8) and +14.9 +/- 1.0 mV (n = 9), respectively. The application of 0.1 mumol/l bradykinin leads to a transient hyperpolarization of the cell membrane to -70.3 +/- 0.6 mV (n = 30). During this transient hyperpolarization increasing extracellular potassium concentration from 5.4 to 10 and 20 mmol/l depolarizes the cell membrane by +10.4 +/- 0.7 mV (n = 10) and +29.2 +/- 0.8 mV (n = 8) respectively. Application of fragments of bradykinin (0.1 mumol/l) are without significant effect on the potential difference across the cell membrane. 1 mmol/l barium depolarizes the cell membrane by +15.8 +/- 1.2 mV (n = 9) and abolishes the effect of step increase of extracellular potassium concentration from 5.4 to 10 mmol/l. In the presence of barium, bradykinin leads to a transient hyperpolarization by -24.7 +/- 1.3 mV (n = 7). During this transient hyperpolarization, the cell membrane is sensitive to extracellular potassium concentration despite the continued presence of barium. In the nominal absence of extracellular calcium, bradykinin leads to a transient hyperpolarization, which can be elicited only once. The transient hyperpolarization is not affected by the presence of verapamil or indomethacin. In conclusion, bradykinin hyperpolarizes MDCK-cells by increasing the apparent potassium conductance.(ABSTRACT TRUNCATED AT 250 WORDS)
在本研究中,我们研究了缓激肽对麦氏达比犬肾(MDCK)细胞跨细胞膜电位差(PD)的影响。在无缓激肽的情况下,PD平均值为-52.6±0.9 mV(n = 52)。将细胞外钾浓度从5.4 mmol/L增加到10 mmol/L和20 mmol/L时,细胞膜分别去极化+5.2±0.3 mV(n = 8)和+14.9±1.0 mV(n = 9)。应用0.1 μmol/L缓激肽会导致细胞膜短暂超极化至-70.3±0.6 mV(n = 30)。在这种短暂超极化期间,将细胞外钾浓度从5.4 mmol/L增加到10 mmol/L和20 mmol/L时,细胞膜分别去极化+10.4±0.7 mV(n = 10)和+29.2±0.8 mV(n = 8)。应用缓激肽片段(0.1 μmol/L)对跨细胞膜电位差无显著影响。1 mmol/L钡使细胞膜去极化+15.8±1.2 mV(n = 9),并消除细胞外钾浓度从5.4 mmol/L逐步增加到10 mmol/L的影响。在有钡存在的情况下,缓激肽导致短暂超极化-24.7±1.3 mV(n = 7)。在这种短暂超极化期间,尽管钡持续存在,细胞膜仍对细胞外钾浓度敏感。在名义上无细胞外钙的情况下,缓激肽导致短暂超极化,且只能诱发一次。这种短暂超极化不受维拉帕米或吲哚美辛存在的影响。总之,缓激肽通过增加表观钾电导使MDCK细胞超极化。(摘要截断于250字)