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犬缺血诱导的肌膜(钠,钾)-ATP酶、钾-pNPP酶、唾液酸和磷脂的变化以及尼索地平与氯丙嗪治疗的影响。

Ischemia-induced changes in sarcolemmal (Na+, K+)-ATPase, K+-pNPPase, sialic acid, and phospholipid in the dog and effects of the nisoldipine and chlorpromazine treatment.

作者信息

Takahashi K, Kako K J

出版信息

Biochem Med. 1984 Jun;31(3):271-86. doi: 10.1016/0006-2944(84)90083-8.

Abstract

This work was undertaken to study functional and structural changes of the cardiac sarcolemmal membrane which was isolated from the ischemic lesion in the dog. The sarcolemmal fraction was prepared, by adopting the method devised by Reeves and Sutko , from the right ventricle and the subendocardial and subepicardial layers of the left ventricle. Ischemic lesion was produced by occlusion of a branch of the left anterior descending coronary artery for a period of 1.5 hr in the thoracotomized dog, followed by release of the occlusion for 3 hr. Nisoldipine, 5 micrograms/kg, was given twice intravenously, and chlorpromazine was infused at a rate of 10 micrograms/kg X min, in addition to the administration of twice bolus doses of 400 micrograms/kg each. Nisoldipine significantly decreased the incidence of premature ventricular contractions and microvascular hemorrhage. Sarcolemmal purity was monitored by using enzyme and chemical markers; the results indicated that the membrane preparation was tenfold purified over the homogenate. Although the activities of ouabain-sensitive (Na+, K+)-ATPase and ouabain-sensitive K+-p-nitrophenylphosphatase ( pNPPase ) of the sarcolemmal preparation isolated from the subendocardial layer were similar to those from the subepicardial layer in the nonischemic left ventricle, a significant decrease in these activities was observed only when the sarcolemmal fraction isolated from the subendocardial layer of ischemic area was compared with that from the subendocardial layer of nonischemic area. In contrast, the sialic acid content of the sarcolemma from the ischemic subendocardial layer was significantly increased compared to that of the nonischemic subendocardial layer. No such changes occurred in sarcolemma prepared from the ischemic subepicardial layer. The total phospholipid content as well as phosphatidylcholine and -ethanolamine contents of the sarcolemmal membrane prepared from the subendocardial layer of ischemic area were significantly decreased compared to nonischemic area. Nisoldipine prevented the ischemia-induced alterations in sarcolemmal (Na+, K+)-ATPase, pNPPase , sialic acid and phospholipids of the subendocardial layer. Chlorpromazine showed a less consistent effect than did Nisoldipine under our experimental conditions. Our study thus demonstrates that the lipid component and function of cardiac sarcolemmal membrane are altered in the early ischemic lesion and that these alterations are nonuniform in distribution and are alleviated by some pharmacological intervention.

摘要

本研究旨在探讨从犬缺血性病变部位分离出的心肌肌膜的功能和结构变化。采用Reeves和Sutko设计的方法,从右心室以及左心室的心内膜下层和心外膜下层制备肌膜组分。通过在开胸犬身上阻断左前降支冠状动脉分支1.5小时,然后松开阻断3小时来制造缺血性病变。静脉注射两次5微克/千克的尼索地平,除了两次推注剂量各400微克/千克外,还以10微克/千克·分钟的速率输注氯丙嗪。尼索地平显著降低了室性早搏和微血管出血的发生率。通过使用酶和化学标记物监测肌膜纯度;结果表明,与匀浆相比,膜制剂的纯度提高了10倍。虽然从非缺血左心室的心内膜下层分离出的肌膜制剂中哇巴因敏感的(Na +,K +)-ATP酶和哇巴因敏感的K + -对硝基苯磷酸酶(pNPPase)的活性与心外膜下层的相似,但仅当将从缺血区域的心内膜下层分离出的肌膜组分与非缺血区域的心内膜下层的进行比较时,才观察到这些活性显著降低。相比之下,缺血心内膜下层的肌膜唾液酸含量与非缺血心内膜下层相比显著增加。从缺血心外膜下层制备的肌膜未发生此类变化。与非缺血区域相比,从缺血区域的心内膜下层制备的肌膜总磷脂含量以及磷脂酰胆碱和乙醇胺含量显著降低。尼索地平可预防缺血引起的心内膜下层肌膜(Na +,K +)-ATP酶、pNPPase、唾液酸和磷脂的改变。在我们的实验条件下,氯丙嗪的作用不如尼索地平一致。因此,我们的研究表明,在早期缺血性病变中,心肌肌膜的脂质成分和功能会发生改变,且这些改变分布不均,并可通过一些药物干预得到缓解。

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