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通过对组织提取物中谷氨酸进行1H核磁共振分析来测定大鼠心脏和骨骼肌中乙酰辅酶A的富集情况。

Determination of acetyl-CoA enrichment in rat heart and skeletal muscle by 1H nuclear magnetic resonance analysis of glutamate in tissue extracts.

作者信息

Jones J G, Hansen J, Sherry A D, Malloy C R, Victor R G

机构信息

Department of Radiology, UT Southwestern Medical Center, Dallas, Texas 75235, USA.

出版信息

Anal Biochem. 1997 Jul 1;249(2):201-6. doi: 10.1006/abio.1997.2172.

Abstract

The contribution of a 13C-enriched substrate to the acetyl-CoA pool in animal tissues is typically measured by analysis of glutamate enrichment from tissue extracts. 13C NMR analysis offers the advantages of minimal sample processing and high information content, but has a low analytical sensitivity compared to other methods of tracer analysis such as GC/MS. We present a sensitive, simple, and direct 1H NMR measurement of glutamate C4 enrichment from tissue extracts. The method is demonstrated with heart and hindlimb muscle tissue extracts of rats infused with [2,4,6,8-13C4]-octanoate, a source of [2-13C]acetyl-CoA. Glutamate C4 enrichment in extracts of individual hindlimb soleus muscles weighing approximately 150 mg and containing approximately 0.3 mumol of glutamate was quantified by 1H NMR within about 40 min. Glutamate C4 enrichment measurements by 1H NMR in heart and gastrocnemius muscle were also highly correlated with independent measurements obtained from 13C NMR isotopomer analysis.

摘要

富含13C的底物对动物组织中乙酰辅酶A库的贡献通常通过分析组织提取物中谷氨酸的富集情况来衡量。13C核磁共振分析具有样品处理最少和信息含量高的优点,但与其他示踪分析方法(如气相色谱/质谱法)相比,分析灵敏度较低。我们提出了一种灵敏、简单且直接的1H核磁共振法,用于测量组织提取物中谷氨酸C4的富集情况。该方法通过给大鼠注射[2,4,6,8-13C4]-辛酸(一种[2-13C]乙酰辅酶A的来源)后,对大鼠的心脏和后肢肌肉组织提取物进行了验证。通过1H核磁共振法,在约40分钟内对单个重量约为150毫克、含有约0.3微摩尔谷氨酸的后肢比目鱼肌提取物中的谷氨酸C4富集情况进行了定量分析。通过1H核磁共振法对心脏和腓肠肌中谷氨酸C4富集情况的测量结果也与通过13C核磁共振同位素异构体分析获得的独立测量结果高度相关。

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