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慢性渗透应激恢复过程中胶质细胞代谢的变化。

Alterations in glial cell metabolism during recovery from chronic osmotic stress.

作者信息

Flögel U, Leibfritz D

机构信息

Institut für Organische Chemie, Universität Bremen, Germany.

出版信息

Neurochem Res. 1998 Dec;23(12):1553-61. doi: 10.1023/a:1020984105448.

DOI:10.1023/a:1020984105448
PMID:9821161
Abstract

NMR spectroscopy of F98 glioma cell extracts showed that chronic hypertonic conditions largely increased the intracellular content of small, osmotically active molecules. Moreover, hypertonic stress decreased the incorporation of 13C-labeled amino acids into the cellular proteins albeit their cytosolic concentrations were increased, which reflects an inhibition of protein synthesis under these conditions. Reincubation with isotonic medium restored almost completely the control values for the cytosolic metabolites but not for amino acid incorporation into the protein. An increased amount of 13C label was found in the phospholipids, which indicates stimulation of membrane synthesis processes due to the recovery-induced cell swelling. On the other hand, chronic hypotonic conditions largely decreased the steady state concentration and synthesis of small, cytosolic molecules, whereas the effect on the incorporation of 13C-labeled amino acids into the cellular proteins was variable. Reincubation with isotonic medium partially restored the depressed cytosolic metabolite content and also the incorporation of labeled amino acids into cellular protein, but induced an inhibition of phospholipid synthesis. The results verify that 'readaptation' of glial cell metabolism during recovery from chronic osmotic stress is impaired or at least seriously retarded.

摘要

对F98胶质瘤细胞提取物进行的核磁共振光谱分析表明,长期高渗条件下,细胞内小分子渗透活性物质的含量大幅增加。此外,尽管细胞溶质中13C标记氨基酸的浓度有所增加,但高渗应激仍降低了其掺入细胞蛋白质的量,这反映出在此条件下蛋白质合成受到抑制。用等渗培养基再孵育后,细胞溶质代谢物的对照值几乎完全恢复,但氨基酸掺入蛋白质的情况并未恢复。在磷脂中发现13C标记量增加,这表明恢复诱导的细胞肿胀刺激了膜合成过程。另一方面,长期低渗条件下,细胞溶质中小分子的稳态浓度和合成大幅降低,而对13C标记氨基酸掺入细胞蛋白质的影响则各不相同。用等渗培养基再孵育可部分恢复降低的细胞溶质代谢物含量以及标记氨基酸掺入细胞蛋白质的情况,但会抑制磷脂合成。结果证实,胶质细胞在从慢性渗透应激恢复过程中的代谢“再适应”受损或至少严重受阻。

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本文引用的文献

1
Determination of de novo synthesized amino acids in cellular proteins revisited by 13C NMR spectroscopy.通过13C核磁共振光谱法重新测定细胞蛋白质中从头合成的氨基酸
NMR Biomed. 1997 Apr;10(2):50-8. doi: 10.1002/(sici)1099-1492(199704)10:2<50::aid-nbm450>3.0.co;2-1.
2
Adaptation of cellular metabolism to anisosmotic conditions in a glial cell line, as assessed by 13C-NMR spectroscopy.
Dev Neurosci. 1996;18(5-6):449-59. doi: 10.1159/000111440.
3
Effects of hypernatraemia in the central nervous system and its therapy in rats and rabbits.高钠血症对大鼠和家兔中枢神经系统的影响及其治疗
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Reinduction of hyponatremia improves survival in rats with myelinolysis-related neurologic symptoms.低钠血症的再次诱导可改善患有脱髓鞘相关神经症状大鼠的存活率。
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Mechanism and regulation of swelling-activated inositol efflux in brain glial cells.脑胶质细胞中肿胀激活型肌醇外流的机制与调节
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Taurine transport in rat astrocytes adapted to hyperosmotic conditions.适应高渗条件的大鼠星形胶质细胞中的牛磺酸转运
Brain Res. 1993 Jun 4;613(1):10-5. doi: 10.1016/0006-8993(93)90447-u.
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Neurochem Res. 1994 Mar;19(3):331-8. doi: 10.1007/BF00971582.
8
Channels for amino acids and metabolites activated by cell volume regulation.通过细胞容积调节激活的氨基酸和代谢物通道。
Jpn J Physiol. 1994;44 Suppl 2:S37-42.
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Taurine efflux and cell volume regulation in cerebral cortical slices during chronic hypernatraemia.
Neurosci Lett. 1995 Feb 6;185(1):56-9. doi: 10.1016/0304-3940(94)11224-7.
10
Role of organic osmolytes in myelinolysis. A topographic study in rats after rapid correction of hyponatremia.有机渗透溶质在髓鞘溶解中的作用。低钠血症快速纠正后大鼠的一项局部解剖学研究。
J Clin Invest. 1995 Apr;95(4):1579-86. doi: 10.1172/JCI117831.