Lalo U, Voitenko N, Kostyuk P
Bogomoletz Institute of Physiology, National Academy of Sciences of Ukraine, Bogomoletz St., 4, 252024 Kyiv-24, Ukraine.
Brain Res. 1998 Jul 20;799(2):285-91. doi: 10.1016/s0006-8993(98)00486-7.
ATP receptor-mediated Ca2+ concentration changes were recorded from neocortical neurones in brain slices from 2 week-old rats. To measure the cytoplasmic concentration of Ca2+ ([Ca2+]i) slices were incubated with fura-2/AM, and the microfluorimetry system was focused on an individual cell. During transients the intracellular level of [Ca2+]i in the majority of neocortical neurones (98 of 102) varied in the concentration range of ATP 5-2000 microM between 41. 3+/-5 and 163+/-7 nM. The rank order of efficacy for purinoreceptor agonists in concentration 100 microM was: ATPgammaS>ATP>ADP>>AMP approximately Adenosine approximately alpha,beta-methylene ATP>UTP. 10 microM PPADS, a P2-purinoreceptor antagonist, reduced the ATP-induced [Ca2+]i response by 26%+/-4%. After elimination of calcium from extracellular solution the first ATP-induced [Ca2+]i transient decreased to 65+/-8%, suggesting the participation of metabotropic P2y triggered Ca-release in the generation of the transient. Elevation of cytosolic Ca2+ by activation of plasmalemmal Ca2+ channels failed to potentiate such release indicating the absence of effective reloading of the corresponding stores. No Ca2+-induced Ca2+-release has been observed in the investigated neurons.
在2周龄大鼠脑片的新皮质神经元中记录了ATP受体介导的Ca2+浓度变化。为了测量Ca2+的细胞质浓度([Ca2+]i),将脑片与fura-2/AM一起孵育,然后将显微荧光测定系统聚焦于单个细胞。在瞬变期间,大多数新皮质神经元(102个中的98个)的细胞内[Ca2+]i水平在ATP浓度为5 - 2000 microM时,在41.3±5至163±7 nM之间变化。100 microM浓度下嘌呤受体激动剂的效能排序为:ATPγS > ATP > ADP >> AMP ≈ 腺苷 ≈ α,β-亚甲基ATP > UTP。10 microM的PPADS,一种P2嘌呤受体拮抗剂,使ATP诱导的[Ca2+]i反应降低了26%±4%。从细胞外溶液中去除钙后,第一个ATP诱导的[Ca2+]i瞬变降至65%±8%,这表明代谢型P2y触发的Ca2+释放参与了瞬变的产生。通过激活质膜Ca2+通道升高胞质Ca2+未能增强这种释放,这表明相应的储存库没有有效的再填充。在所研究的神经元中未观察到Ca2+诱导的Ca2+释放。