Potassium-39 nuclear magnetic resonance observation of intracellular potassium without chemical shift reagents during metabolic inhibition in the isolated perfused rat heart.
Potassium-39 nuclear magnetic resonance observation of intracellular potassium without chemical shift reagents during metabolic inhibition in the isolated perfused rat heart.
复制标题
离体灌注大鼠心脏代谢抑制过程中不使用化学位移试剂的 Potass-39 核磁共振观察细胞内钾。
DOI:
10.1161/01.res.67.2.401
复制
发表时间:
1990
影响因子:
20.1
通讯作者:
Y. Kawashima
中科院分区:
文献类型:
--
作者:
S. Kuki;E. Suzuki;H. Watari;H. Takami;H. Matsuda;Y. Kawashima
The intracellular potassium content of perfused rat heart was measured by potassium-39 nuclear magnetic resonance (NMR) spectroscopy at 33 degrees C with an inversion recovery technique based on the fact that the spin-lattice relaxation time (T1) of the intracellular potassium (8.3 msec at 8.45 T) is much faster than that of the extracellular potassium (68 msec). Intracellular potassium decreased to 60.2 +/- 4.3% of the control level (mean +/- SEM, n = 6) at 40 minutes from the start of metabolic inhibition (2 mM cyanide, 0 mM glucose). Removal of cyanide restored intracellular potassium to 94.2 +/- 3.9% at 30 minutes from the restart of oxidative metabolism. The cumulative potassium loss was determined from the flow rate and potassium concentration of the coronary effluent, which reached 139 +/- 12 mumol/g dry wt during 40 minutes of metabolic inhibition. This value was calculated as 41.8% of intracellular potassium in the control heart and agreed with the decrement of intracellular potassium measured by NMR. During the metabolic inhibition and recovery period, a linear correlation was observed between the changes in 39K NMR-observed intracellular potassium and the cumulative potassium loss. The present results evaluate the inversion recovery technique as a method to successfully monitor the myocardial intracellular potassium.
DOI:
10.1152/ajpheart.1987.252.6.h1138
发表时间:
1987
期刊:
The American journal of physiology
影响因子:
--
作者:
Burstein,D;Fossel,ET
通讯作者:
Fossel,ET
影响因子:
37.8
作者:
Watanabe,I;Johnson,TA;Buchanan,J;Engle,CL;Gettes,LS
通讯作者:
Gettes,LS
DOI:
10.1152/ajpheart.1982.243.2.h318
发表时间:
1982
期刊:
The American journal of physiology
影响因子:
--
作者:
Weiss,J;Shine,KI
通讯作者:
Shine,KI