三磷酸核苷和无机磷酸盐在离体灌注大鼠肝脏中核磁共振弛豫时间的温度依赖性。对Pi区隔的影响

Sylvie Dufour, Eric Thiaudière, Giovanni Vidal, Jean-Louis Gallis, Nicole Rousse, Paul Canioni
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引用次数: 16

摘要

在9.4 t温度下研究温度对离体灌注大鼠肝脏31p NMR谱的影响,测定三磷酸核苷(NTP)和无机磷酸盐(Pi)在37、25、15和4℃时的弛豫时间(t1和t2)。在低温条件下,观察到π谱区出现了意想不到的明显线锐化,并明显出现了额外的π共振。这个额外的信号被分配给线粒体Pi。细胞质和线粒体Pi在4°C时的t1值分别为1.14±0.24 s (n= 5)和0.71±0.18 s (n= 5)。37°C时未观察到线粒体对Pi共振的显著贡献。通过比较灌注肝脏光谱和相应的高氯酸提取物光谱,定量37°C和4°C时Pi和NTP肝脏含量。在低外部Pi (0.12 mM)的实验条件下,细胞内Pi在4℃和37℃下完全可见。电镜观察到,在4°C时,线粒体Pi信号的观察结果很好地解释了基质内Pi水平的增加,这是对低温引起的线粒体肿胀的反应。37°C和4°C时胞浆Pi值分别为17±4 ms (n= 8)和22±4 ms (n= 10)。与实测线宽的比较表明,主要磷酸化代谢物(包括基质pi)的线宽是b0场不均匀性的结果。在4°C和37°C时细胞质Pi共振的额外拓宽归因于肝脏内pH的异质性。
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Temperature Dependence of NMR Relaxation Times of Nucleoside Triphosphates and Inorganic Phosphate in the Isolated Perfused Rat Liver. Effect on Pi Compartmentation

The effect of temperature on31P NMR spectra from isolated perfused rat livers was studied at 9.4 T. Relaxation times (T1andT2) of nucleoside triphosphates (NTP) and inorganic phosphate (Pi) were determined at 37, 25, 15, and 4°C. Under hypothermic conditions, an unexpected apparent line sharpening in the Pi spectral region and a clear emergence of an additional Pi resonance were observed. This additional signal was assigned to mitochondrial Pi.T1values obtained for cytosolic and mitochondrial Pi at 4°C were 1.14 ± 0.24 s (n= 5) and 0.71 ± 0.18 s (n= 5), respectively. No significant mitochondrial contribution to the Pi resonance was observed at 37°C. Quantification of Pi and NTP liver contents at 37 and 4°C was performed by comparing the perfused liver spectrum and the corresponding perchloric acid extract spectrum. Under experimental conditions of low external Pi (0.12 mM), it was concluded that intracellular Pi was completely NMR-visible at 4 and 37°C. The observation of the mitochondrial Pi signal at 4°C was well explained by an increase in the Pi level within the matrix, in response to the mitochondrial swelling induced by hypothermia, as observed by electron microscopy.T2values for the cytosolic Pi at 37 and 4°C were 17 ± 4 ms (n= 8) and 22 ± 4 ms (n= 10), respectively. Comparison with measured linewidths indicated that line broadening for the main phosphorylated metabolites—including matrix Pi—was the result ofB0field inhomogeneity. The additional broadening of the cytosolic Pi resonance at 4 and 37°C was attributed to pH heterogeneity within the liver.

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