31P nuclear magnetic resonance measurements of muscle glucose-6-phosphate. Evidence for reduced insulin-dependent muscle glucose transport or phosphorylation activity in non-insulin-dependent diabetes mellitus.
31P nuclear magnetic resonance measurements of muscle glucose-6-phosphate. Evidence for reduced insulin-dependent muscle glucose transport or phosphorylation activity in non-insulin-dependent diabetes mellitus.
复制标题
肌肉葡萄糖-6-磷酸的 31P 核磁共振测量。
DOI:
10.1172/jci115686
复制
发表时间:
1992
期刊:
影响因子:
--
通讯作者:
Shulman,GI
中科院分区:
文献类型:
--
作者:
Rothman,DL;Shulman,RG;Shulman,GI
To assess the rate-limiting step in muscle glycogen synthesis in non-insulin-dependent diabetes mellitus (NIDDM), the concentration of glucose-6-phosphate (G6P) was measured by 31P nuclear magnetic resonance (NMR) during a hyperglycemic-hyperinsulinemic clamp. Six subjects with NIDDM and six age weight-matched controls were studied at similar steady-state plasma concentrations of insulin (approximately 450 pmol/liter) and glucose (11 mmol/liter). The concentration of G6P in the gastrocnemius muscle was measured by 31P NMR. Whole-body oxidative and nonoxidative glucose metabolism was determined by the insulin-glucose clamp technique in conjunction with indirect calorimetry. Nonoxidative glucose metabolism which under these conditions is a measure of muscle glycogen synthesis (1990. N. Engl. J. Med. 322:223-228), was 31 +/- 7 mumol/(kg body wt-min) in the normal subjects and 13 +/- 3 mumol/(kg body wt-min) in the NIDDM subjects (P less than 0.05). The concentration of G6P was higher (0.24 +/- 0.02 mmol/kg muscle) in the normal subjects than in the NIDDM subjects (0.17 +/- 0.02, P less than 0.01). Increasing insulin concentrations to insulin 8,500 pmol/liter in four NIDDM subjects restored the glucose uptake rate and G6P concentrations to normal levels. In conclusion, the lower concentration of G6P in the diabetic subjects despite a decreased rate of nonoxidative glucose metabolism is consistent with a defect in muscle glucose transport or phosphorylation reducing the rate of muscle glycogen synthesis.
登录
查看更多内容
影响因子:
158.5
作者:
SHULMAN, GI;ROTHMAN, DL;SHULMAN, RG
通讯作者:
SHULMAN, RG
影响因子:
4
作者:
R. E. Gordon
通讯作者:
R. E. Gordon
DOI:
--
发表时间:
1979
期刊:
影响因子:
--
作者:
D. Gadian;G. Radda;R. Richards;P. Seeley
通讯作者:
P. Seeley
影响因子:
7.7
作者:
H. Yki;K. Sahlin;J. Ren;V. Koivisto
通讯作者:
V. Koivisto
DOI:
10.1172/jci113069
发表时间:
1987
期刊:
The Journal of clinical investigation
影响因子:
--
作者:
Hannele Yki;David M. Mott;Andrew A. Young;K. Stone;Clifton Bogardus
通讯作者:
Clifton Bogardus