Tricarico D, Petruzzi R, Conte Camerino D C
Department of Pharmacobiology, Faculty of Pharmacy, University of Bari, Italy.
Eur J Pharmacol. 1997 Mar 5;321(3):369-78. doi: 10.1016/s0014-2999(96)00965-x.
We have described here the changes of the biophysical and pharmacological properties of the sarcolemmal ATP-sensitive K+ channels (KATP) of rat skeletal muscle fibres, occurring from an early postnatal period (5 days) to adulthood (210 days). The age-dependent changes of the mean current of the KATP channel (channel activity) and the effects of the blockers, ATP and glybenclamide, were examined by using the patch-clamp technique. Measurements of the single channel conductance, open probability and channel density were also performed. Excision of cell-attached patches into an ATP-free solution dramatically increased the KATP channel activity; however, the intensity of this activity was age dependent. The relative activity was low at 5-6 days of postnatal life, increased to a plateau at 12-13 days, then declined toward adult values after 37 days. Two distinct types of the KATP channel complex could be distinguished. The early developmental period (5-6 days) was dominated by a KATP channel having a conductance of 66 pS, a high open probability of 0.602, and an IC50 for ATP and glybenclamide of 123.1 microM and 3.97 microM, respectively. This type of channel disappeared with maturation of the muscle to be replaced by the adult form of the KATP channel. The later developmental period (from 56 days) was dominated by a KATP channel having a 71 pS conductance, but a low open probability of 0.222. This adult channel was also 3.2 and 73.5 times more sensitive to ATP and glybenclamide, respectively. We have also observed that the sensitivity of the KATP channel to ATP and glybenclamide develops differently. Indeed, the greater increase in the sensitivity of the channel to ATP was observed between 5 and 12 days of age. Conversely, the greater enhancement of the sensitivity of the channel to glybenclamide occurred between 12 and 37 days. A further increase of this parameter was also observed between 37 and 56 days of age. The differential age-dependent acquisition of the sensitivity of KATP channels to ATP and glybenclamide poses the hypothesis that in rat skeletal muscle the ATP regulatory site and sulfonylurea site are located on different subunits of the KATP channel complex. The intense KATP channel activity recorded between 12 and 37 days of postnatal life sustains the high resting macroscopic K+ conductance characteristic of the early postnatal development.
我们在此描述了大鼠骨骼肌纤维肌膜ATP敏感性钾通道(KATP)从出生后早期(5天)到成年期(210天)生物物理和药理特性的变化。采用膜片钳技术研究了KATP通道平均电流(通道活性)的年龄依赖性变化以及阻滞剂、ATP和格列本脲的作用。还进行了单通道电导、开放概率和通道密度的测量。将细胞贴附膜片切除到无ATP溶液中可显著增加KATP通道活性;然而,这种活性的强度是年龄依赖性的。出生后5 - 6天相对活性较低,12 - 13天增加到平台期,37天后向成年值下降。可以区分出两种不同类型的KATP通道复合物。发育早期(5 - 6天)以一种KATP通道为主,其电导为66 pS,高开放概率为0.602,ATP和格列本脲的IC50分别为123.1 microM和3.97 microM。这种类型的通道随着肌肉成熟而消失,被成年形式的KATP通道取代。发育后期(从56天开始)以一种电导为71 pS但开放概率低至0.222的KATP通道为主。这种成年通道对ATP和格列本脲的敏感性分别也是前者的3.2倍和73.5倍。我们还观察到KATP通道对ATP和格列本脲的敏感性发育方式不同。实际上,在5至12日龄之间观察到通道对ATP敏感性的更大增加。相反,通道对格列本脲敏感性的更大增强发生在12至37日龄之间。在37至56日龄之间也观察到该参数的进一步增加。KATP通道对ATP和格列本脲敏感性的年龄依赖性差异获得提出了这样一种假说,即在大鼠骨骼肌中,ATP调节位点和磺酰脲位点位于KATP通道复合物的不同亚基上。出生后12至37天记录到的强烈KATP通道活性维持了出生后早期发育特有的高静息宏观钾电导。