Lammerich A, Günther J, Pfitzer G, Storch E, Vetter R
Institute of Physiology, Humboldt-University, Berlin, Germany.
J Hypertens. 1995 Nov;13(11):1313-24. doi: 10.1097/00004872-199511000-00014.
Transport activities of cardiac sodium-calcium exchange and sarcoplasmic reticulum calcium ATPase were measured biochemically in spontaneously hypertensive rats (SHR) with hypertrophied myocardium and in normotensive Wistar-Kyoto (WKY) rats and it was tested whether possible differences have consequences for the contractile properties of papillary muscle.
Sarcolemmal sodium-dependent calcium transport via sodium-calcium exchange and oxalate-supported sarcoplasmic reticulum calcium uptake were measured in left ventricular membranes of 22-week-old rats. Postextrastimulatory potentiated contractions, postrest potentiated contractions, the twitch-to-twitch decay of those potentiations and the response to increasing stimulation frequency of left ventricular papillary muscles were analysed.
Compared with WKY rats we found in SHR: a significant increase in sodium-calcium exchange (65%) and in sarcoplasmic reticulum calcium uptake (24%); a steeper twitch-to-twitch decay in postextrastimulatory potentiated contractions and postrest potentiated contractions, suggesting a lower calcium fraction recirculating between myofilaments and sarcoplasmic reticulum and, consequently, a relatively higher calcium efflux via sodium-calcium exchange; a stronger rest-dependent decrease in recirculating calcium fraction in postrest potentiated contractions accompanied by accelerated relaxation, suggesting an increasing driving force for calcium extrusion via sodium-calcium exchange, probably caused by decreasing intracellular sodium during rest; a greater transient decrease in peak force of subsequent twitches after postrest potentiated contractions below pre-interventional level, indicating higher cellular calcium loss; and a smaller negative inotropic effect in response to doubling of stimulation rate as a manoeuvre to increase the intracellular sodium level.
In SHR, the contractile properties suggest an increased contribution of sodium-calcium exchange to cellular calcium removal, which is strongly supported by the enhanced sodium-calcium exchange activity in cardiac membrane vesicles.
通过生物化学方法测定自发性高血压大鼠(SHR)肥厚心肌以及正常血压的Wistar - Kyoto(WKY)大鼠心脏钠钙交换体和肌浆网钙ATP酶的转运活性,并检测可能存在的差异是否会对乳头肌的收缩特性产生影响。
测定22周龄大鼠左心室膜中通过钠钙交换体的肌膜钠依赖性钙转运以及草酸盐支持的肌浆网钙摄取。分析额外刺激后增强收缩、静息后增强收缩、这些增强收缩的单次抽搐衰减以及左心室乳头肌对增加刺激频率的反应。
与WKY大鼠相比,在SHR中我们发现:钠钙交换体显著增加(65%),肌浆网钙摄取增加(24%);额外刺激后增强收缩和静息后增强收缩中单次抽搐衰减更陡峭,提示在肌丝和肌浆网之间循环的钙部分较低,因此通过钠钙交换体的钙外流相对较高;静息后增强收缩中循环钙部分的静息依赖性降低更强,伴有舒张加速,提示通过钠钙交换体的钙外排驱动力增加,可能是由于静息时细胞内钠减少所致;静息后增强收缩后随后单次抽搐的峰值力出现更大的短暂下降至干预前水平以下,表明细胞钙丢失增加;以及作为增加细胞内钠水平的操作,对刺激频率加倍的负性肌力作用较小。
在SHR中,收缩特性表明钠钙交换体对细胞钙清除的贡献增加,这在心脏膜囊泡中增强的钠钙交换体活性中得到有力支持。