Tricarico D, Petruzzi R, Camerino D C
Unit of Pharmacology, Department of Pharmacobiology, Faculty of Pharmacy, University of Bari, via Orabona no. 4, I-70125 Bari, Italy.
Pflugers Arch. 1997 Nov;434(6):822-9. doi: 10.1007/s004240050471.
In the present work, we have investigated the effects of the aging process on Ca2+-activated K+ channels (KCa2+) of rat skeletal muscle fibres. KCa2+ channels of adult (5-7 months old) and aged (24-26 months old) rats were surveyed by the patch-clamp technique. In aged rats, KCa2+ channels were routinely detected on the surface membrane of the fibres in both cell-attached and inside-out configurations. Conversely, in adult rat fibres, KCa2+ channels were rarely detected. In the cell-attached configuration, the open probability of the aged rat KCa2+ channel, measured in the range of potentials from -60 mV to +20 mV, was about 1.5-2 times higher than that of the adult one. The number of functional channels was abnormally increased by aging. An average of three channels per patch/area was counted in the inside-out patches of aged rat fibres, whereas no more than one open channel per patch/area was detected in the adult rat fibres. The frequency of finding channels in the patches also increased with aging, i.e. 11.5% and 30.1% in the adult and in the aged rat fibres, respectively. However, no significant change in the single-channel conductance has been observed with aging: it was 227 pS and 231 pS for adult and aged rat channels, respectively. In detached patches, both the adult and aged rat channels showed a similar voltage dependence of open probability and a similar sensitivity to Ca2+ ions. The aging process did not alter the response of the single channel to charybdotoxin, or its modulation by nucleotides, MgATP and adenosine 5'-O-(3-thiotriphosphate) (ATP[gamma-S]). On the other hand, charybdotoxin reduced the abnormally high resting macroscopic K+ conductance of the aged rat fibres, recorded using the two-intracellular-microelectrode technique. These findings indicate that, in skeletal muscle, the activity of KCa2+ channels increases with advancing age.
在本研究中,我们研究了衰老过程对大鼠骨骼肌纤维钙激活钾通道(KCa2+)的影响。采用膜片钳技术对成年(5 - 7个月大)和老年(24 - 26个月大)大鼠的KCa2+通道进行了检测。在老年大鼠中,无论是在细胞贴附式还是外翻式膜片钳记录模式下,均可在纤维表面膜上常规检测到KCa2+通道。相反,在成年大鼠纤维中,很少检测到KCa2+通道。在细胞贴附式记录模式下,在 - 60 mV至 + 20 mV的电位范围内测量,老年大鼠KCa2+通道的开放概率比成年大鼠的高约1.5 - 2倍。衰老使功能性通道的数量异常增加。在老年大鼠纤维的外翻式膜片中,每个膜片/面积平均计数到三个通道,而在成年大鼠纤维中,每个膜片/面积检测到的开放通道不超过一个。在膜片中发现通道的频率也随衰老而增加,即在成年和老年大鼠纤维中分别为11.5%和30.1%。然而,未观察到单通道电导随衰老有显著变化:成年和老年大鼠通道的单通道电导分别为227 pS和231 pS。在分离的膜片中,成年和老年大鼠通道均表现出相似的开放概率电压依赖性以及对Ca2+离子的相似敏感性。衰老过程并未改变单通道对蝎毒素的反应,也未改变其受核苷酸、MgATP和腺苷5'-O-(3-硫代三磷酸)(ATP[γ-S])的调节。另一方面,蝎毒素降低了老年大鼠纤维异常高的静息宏观钾电导,该电导是用双细胞内微电极技术记录的。这些发现表明,在骨骼肌中,KCa2+通道的活性随年龄增长而增加。