Suppr超能文献

兔网织红细胞中的能量平衡及其受腺嘌呤核苷酸的调控。

Energy balance in rabbit reticulocytes and its control by adenine nucleotides.

作者信息

Augustin H W, Spengler V

出版信息

Biomed Biochim Acta. 1983;42(11-12):S223-8.

PMID:6675695
Abstract

Respiration, lactate formation and adenine nucleotide contents were measured in highly enriched rabbit reticulocytes using substrates and mitochondrial inhibitors to adjust different states of energy metabolism. With glucose as substrate rates of ATP synthesis generated via mitochondrial plus glycolytic ADP phosphorylation of 1,6 mumoles ATP/ml cells X min were calculated at cellular ATP/ADP ratios of 13 resp. phosphorylation potentials of about 8000 M-1. Titrations with inhibitors acting at different levels of mitochondrial ATP production (antimycin A, oligomycin, uncouplers 2,4 DNP or FCCP and combinations) revealed a stepwise decline of ATP/ADP ratios and phosphorylation potentials attaining values of 5 and lower, and 1100, respectively, comparable to observations without exogenous glucose. The inhibited phosphorylating respiration was compensated by apparently not fully stoichiometric stimulation of glycolysis resulting in calculated rates of ATP synthesis lowered towards 1,0 (oligomycin) and fluctuating between 1,3 and 2,0 (antimycin). Mutual linkages between ATP producing and consuming reactions obviously influenced by the inhibitory species themselves are suggested compatible with the assumption that multiple steady states in reticulocyte energy metabolism might be established.

摘要

使用底物和线粒体抑制剂来调节能量代谢的不同状态,对高度富集的兔网织红细胞中的呼吸、乳酸生成和腺嘌呤核苷酸含量进行了测量。以葡萄糖作为底物,在细胞ATP/ADP比率为13(分别为)时,计算出线粒体加糖酵解ADP磷酸化产生的ATP合成速率为1.6微摩尔ATP/毫升细胞×分钟,磷酸化电位约为8000 M-1。用作用于线粒体ATP产生不同水平的抑制剂(抗霉素A、寡霉素、解偶联剂2,4-二硝基苯酚或FCCP以及组合)进行滴定,结果显示ATP/ADP比率和磷酸化电位逐步下降,分别达到5及更低和1100,这与没有外源葡萄糖时的观察结果相当。受抑制的磷酸化呼吸通过糖酵解的明显非完全化学计量刺激得到补偿,导致计算出的ATP合成速率降至1.0(寡霉素),并在1.3至2.0之间波动(抗霉素)。ATP产生和消耗反应之间的相互联系显然受到抑制物质本身的影响,这表明与网织红细胞能量代谢中可能建立多个稳态的假设是相符的。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验