Elmoselhi A B, Samson S E, Grover A K
Department of Biomedical Sciences, McMaster University, Hamilton, Ontario, Canada.
Am J Physiol. 1996 Nov;271(5 Pt 1):C1652-9. doi: 10.1152/ajpcell.1996.271.5.C1652.
Reactive oxygen species are known to decrease the action of agents that mobilize Ca2+ from sarcoplasmic reticulum (SR) in pig coronary artery smooth muscle. Potentially, this may be due to damage to the SR Ca2+ pump or to the myo-inositol 1,4,5-trisphosphate (IP3)-induced Ca2+ release channels. Here we report on the effects of peroxide and superoxide on the SR Ca2+ pump and the subsequent IP3-induced Ca2+ release. Smooth muscle cells cultured from pig left coronary arteries were permeabilized using saponin and then loaded with 45Ca2+ in the presence of an ATP-regenerating system and the mitochondrial Ca2+ uptake inhibitor sodium azide. IP3 caused a release of up to 65% of the loaded 45Ca2+, whereas the Ca2+ ionophore A-23187 caused a release of > 95%. The nature of the IP3-insensitive component of the Ca2+ uptake is not known. The IP3-induced Ca2+ release occurred at 0 or 37 degrees C and was complete in < 30 s. The 50% effective concentration for IP3 was 2.7 +/- 1.0 microM at pH 6.8 and 37 degrees C. At pH 7.4 the IP3-induced Ca2+ release was slightly lower than at pH 6.4-6.8. The IP3-induced release was also inhibited by Ca2+ concentration in the release medium. To investigate the effects of peroxide or superoxide, the cells were treated with these agents, washed, skinned, and then used to examine the IP3-sensitive and -insensitive Ca2+ pools under the conditions in which the IP3-sensitive pool was 60-65% of the total. Peroxide pretreatment was equipotent in inhibiting loading into the IP3-sensitive and -insensitive Ca2+ pools. In contrast, superoxide pretreatment inhibited loading into the IP3-sensitive pool but not into the IP3-insensitive pool. These data are consistent with a model in which the SR Ca2+ pumps are heterogeneous: those required to pump Ca2+ into the IP3-sensitive pool are inhibited by peroxide and superoxide, but those loading the IP3-insensitive pool are inhibited by peroxide only.
已知活性氧会降低猪冠状动脉平滑肌中从肌浆网(SR)动员Ca2+的药物的作用。这可能是由于SR Ca2+泵受损或肌醇1,4,5 -三磷酸(IP3)诱导的Ca2+释放通道受损。在此我们报告过氧化物和超氧化物对SR Ca2+泵以及随后IP3诱导的Ca2+释放的影响。从猪左冠状动脉培养的平滑肌细胞用皂素通透处理,然后在存在ATP再生系统和线粒体Ca2+摄取抑制剂叠氮化钠的情况下加载45Ca2+。IP3导致加载的45Ca2+释放高达65%,而Ca2+离子载体A - 23187导致释放>95%。Ca2+摄取中IP3不敏感成分的性质尚不清楚。IP3诱导的Ca2+释放在0或37℃时发生,且在<30秒内完成。在pH 6.8和37℃时,IP3的50%有效浓度为2.7±1.0 microM。在pH 7.4时,IP3诱导的Ca2+释放略低于pH 6.4 - 6.8时。释放介质中的Ca2+浓度也会抑制IP3诱导的释放。为了研究过氧化物或超氧化物的影响,用这些试剂处理细胞,洗涤,去皮,然后用于在IP3敏感池占总量60 - 65%的条件下检查IP3敏感和不敏感的Ca2+池。过氧化物预处理在抑制加载到IP3敏感和不敏感的Ca2+池中具有同等效力。相比之下,超氧化物预处理抑制加载到IP3敏感池中,但不抑制加载到IP3不敏感池中。这些数据与一个模型一致,即SR Ca2+泵是异质的:那些将Ca2+泵入IP3敏感池所需的泵被过氧化物和超氧化物抑制,但那些加载IP3不敏感池的泵仅被过氧化物抑制。