Ishikawa T, Murakami M, Seo Y
Department of Molecular Physiology, National Institute for Physiological Sciences, Okazaki, Japan.
Pflugers Arch. 1994 Oct;428(5-6):516-25. doi: 10.1007/BF00374573.
The involvement of large-conductance, voltage- and Ca(2+)-activated K+ channels (maxi-K+ channels) in basolateral Ca(2+)-dependent K(+)-efflux pathways and fluid secretion by the rat submandibular gland was investigated. Basolateral K+ efflux was monitored by measuring the change in K+ concentration in the perfusate collected from the vein of the isolated, perfused rat submandibular gland every 30 s. Under conditions in which the Na+/K(+)-ATPase and Na(+)-K(+)-2Cl- cotransporter were inhibited by ouabain (1 mmol/l) and bumetanide (50 mumol/l) respectively, continuous stimulation with acetylcholine (ACh) (1 mumol/l) caused a transient large net K+ efflux, followed by a smaller K+ efflux, which gradually returned to the basal level within 10 min. These two components of the K+ efflux appear to be dependent on an increase in cytosolic Ca2+ concentration. The initial transient K+ efflux was not affected by charybdotoxin (100 nmol/l) or tetraethylammonium (TEA) (5 mmol/l) but the smaller second component was strongly and reversibly inhibited by charybdotoxin (100 nmol/l) and TEA (0.1 and 5 mmol/l). The initial K+ efflux transient induced by ACh was inhibited by quinine (0.1-3 mmol/l), quinidine (1-3 mmol/l) and Ba2+ (5 mmol/l), but not by verapamil (0.1 mmol/l), lidocaine (1 mmol/l), 4-aminopyridine (1 mmol/l) or apamin (1 mumol/l). Ca(2+)-dependent transient large K+ effluxes induced by substance P (0.01 mumol/l) and A23187 (3 mumol/l) were not inhibited by TEA (5 mmol/l or 10 mmol/l). A23187 (3 mumol/l) evoked a biphasic fluid-secretory response, which was not inhibited by TEA (5 mmol/l). Patch-clamp studies confirmed that the whole-cell outward K+ current attributable to maxi-K+ channels obtained from rat submandibular endpiece cells was strongly inhibited by the addition of TEA (1-10 mmol/l) to the bath. It is concluded that maxi-K+ channels are not responsible for the major part of the Ca(2+)-dependent basolateral K+ efflux and fluid secretion by the rat submandibular gland.
研究了大电导、电压和Ca(2+)激活的K+通道(大电导K+通道)在大鼠下颌下腺基底外侧Ca(2+)依赖性K+外流途径及液体分泌中的作用。通过每隔30秒测量从分离灌注的大鼠下颌下腺静脉收集的灌流液中K+浓度的变化来监测基底外侧K+外流。在毒毛花苷(1 mmol/L)和布美他尼(50 μmol/L)分别抑制Na+/K(+)-ATP酶和Na(+)-K(+)-2Cl-共转运体的条件下,用乙酰胆碱(ACh)(1 μmol/L)持续刺激会引起短暂的大量净K+外流,随后是较小的K+外流,在10分钟内逐渐恢复到基础水平。K+外流的这两个成分似乎依赖于胞质Ca2+浓度的升高。最初的短暂K+外流不受蝎毒素(100 nmol/L)或四乙铵(TEA)(5 mmol/L)的影响,但较小的第二个成分受到蝎毒素(100 nmol/L)和TEA(0.1和5 mmol/L)的强烈且可逆的抑制。ACh诱导的初始K+外流短暂变化受到奎宁(0.1 - 3 mmol/L)、奎尼丁(1 - 3 mmol/L)和Ba2+(5 mmol/L)的抑制,但不受维拉帕米(0.1 mmol/L)、利多卡因(1 mmol/L)、4-氨基吡啶(1 mmol/L)或蜂毒明肽(1 μmol/L)的抑制。P物质(0.01 μmol/L)和A23187(3 μmol/L)诱导的Ca(2+)依赖性短暂大量K+外流不受TEA(5 mmol/L或10 mmol/L)的抑制。A23187(3 μmol/L)引发双相液体分泌反应,该反应不受TEA(5 mmol/L)的抑制。膜片钳研究证实,向浴槽中加入TEA(1 - 10 mmol/L)会强烈抑制从大鼠下颌下腺终末细胞获得的归因于大电导K+通道的全细胞外向K+电流。结论是,大电导K+通道不负责大鼠下颌下腺Ca(2+)依赖性基底外侧K+外流和液体分泌的主要部分。