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肌浆网钙释放通道和ATP合成活性是犬快速心室起搏所致心力衰竭的早期心肌标志物。

Sarcoplasmic reticulum Ca-release channel and ATP-synthesis activities are early myocardial markers of heart failure produced by rapid ventricular pacing in dogs.

作者信息

O'Brien P J, Moe G W, Nowack L M, Grima E A, Armstrong P W

机构信息

Department of Pathology, Ontario Veterinary College, University of Guelph, Canada.

出版信息

Can J Physiol Pharmacol. 1994 Sep;72(9):999-1006. doi: 10.1139/y94-139.

Abstract

The contraction-relaxation cycle of the heart is dependent on a cycle of ATP production and utilization and a cycle of Ca uptake and Ca release by the sarcoplasmic reticulum (SR). Heart failure (HF) is associated with abnormalities of myocardial Ca and ATP cycling, but the time course of their development is unknown. This study tested the hypothesis that, compared with ATP-utilizing and Ca-uptake activities, decreases in ATP-synthesis and Ca-release activities occurred earlier in the development of HF and persisted longer during recovery from HF. HF was induced by right ventricular pacing of dogs at 250 beats/min. Dogs were studied after 1 week of pacing (n = 8, early HF), at HF (n = 11, severe HF), and 4 weeks after cessation of pacing (n = 9) and were compared with dogs not subjected to pacing. At early HF, there were decreased activities (p < 0.05) of the SR Ca-release channel (rate constant from 199 +/- 36 x 10(-4) to 90 +/- 16 x 10(-4) s-1), mitochondrial ATP synthesis (from 11.2 +/- 2.4 to 7.0 +/- 2.2 international units (IU)/g), and creatine kinase (CK) from 2028 +/- 266 to 1811 +/- 79 IU/g). The decreased Ca-channel activity was due to a 32% decrease in maximal activity (rate constant from 249 +/- 50 x 10(-4) to 170 +/- 29 x 10(-4) s-1) and to a 2-fold increase (from 19.1 +/- 12.4 to 42.0 +/- 14.2%) in inhibition of maximal channel activity (p < 0.05).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

心脏的收缩 - 舒张周期依赖于ATP生成与利用的循环以及肌浆网(SR)对钙的摄取与释放循环。心力衰竭(HF)与心肌钙和ATP循环异常相关,但其发展的时间进程尚不清楚。本研究检验了以下假设:与ATP利用和钙摄取活动相比,ATP合成和钙释放活动的降低在HF发展过程中更早出现,并且在从HF恢复过程中持续更长时间。通过以250次/分钟的频率对犬进行右心室起搏诱导HF。在起搏1周后(n = 8,早期HF)、处于HF时(n = 11,重度HF)以及起搏停止4周后(n = 9)对犬进行研究,并与未接受起搏的犬进行比较。在早期HF时,肌浆网钙释放通道的活性降低(速率常数从199±36×10⁻⁴降至90±16×10⁻⁴ s⁻¹,p < 0.05),线粒体ATP合成(从11.2±2.4降至7.0±2.2国际单位(IU)/g),肌酸激酶(CK)从2028±266降至1811±79 IU/g。钙通道活性降低是由于最大活性降低32%(速率常数从249±50×10⁻⁴降至170±29×10⁻⁴ s⁻¹)以及最大通道活性抑制增加2倍(从19.1±12.4%增至42.0±14.2%,p < 0.05)。(摘要截断于250字)

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