Measurement of muscle protein synthesis by positron emission tomography with L-[methyl-11C]methionine:: Effects of transamination and transmethylation
Measurement of muscle protein synthesis by positron emission tomography with L-[methyl-11C]methionine:: Effects of transamination and transmethylation
复制标题
DOI:
10.1097/00005373-199908000-00021
复制
发表时间:
1999-08-01
影响因子:
--
通讯作者:
Fischman, AJ
中科院分区:
文献类型:
--
作者:
Carter, EA;Yu, YM;Fischman, AJ
Background: Positron emission tomography with L-[methyl-(11)C]methionine provides a measure of regional protein synthesis rate (PSR) in skeletal muscle. However, the validity of the method depends on incorporation of methionine into protein with minimal transamination, transmethylation, or both. To test directly these assumptions, uptake of L-[methyl-(14)C]methionine in skeletal muscle was measured in control and cycloheximide-treated rats.Methods: Normal and cycloheximide-treated rats (n = 8/group) were injected with 50 mu Ci of L-[methyl-(14)C]methionine and arterial blood sampled over 90 minutes. After killing, thigh muscle was homogenized, centrifuged, and treated with trichloroacetic acid. PSR from circulating methionine was estimated from trichloroacetic acid-precipitable radioactivity, arterial time-activity curves, and plasma methionine concentrations.Results: In normal rats, similar to 70% of the tissue radioactivity was precipitated with trichloroacetic acid. In normal animals, PSR was 0.22 nmoles.min(-1).g(-1), in excellent agreement with previous results. In the cyclohexamide-treated group, PSR was 0.0032 nmoles.min(-1).g(-1); similar to 98% reduction compared with controls.Conclusion: These studies support the hypothesis that L-[methyl-(11(14))C]methionine accumulates in skeletal muscle as (11(14))C-labeled protein.