Research Institute for Sport & Exercise Sciences, Liverpool John Moores University, Tom Reilly Building, Byrom Street, Liverpool, L3 3AF, UK.
Department of Medicine, University of Minnesota, Minneapolis, MN, USA.
Lipids Health Dis. 2024 Apr 2;23(1):94. doi: 10.1186/s12944-024-02079-z.
Insulin-stimulated glucose uptake into skeletal muscle occurs via translocation of GLUT4 from intracellular storage vesicles to the plasma membrane. Elevated free fatty acid (FFA) availability via a lipid infusion reduces glucose disposal, but this occurs in the absence of impaired proximal insulin signalling. Whether GLUT4 localisation to the plasma membrane is subsequently affected by elevated FFA availability is not known.
Trained (n = 11) and sedentary (n = 10) individuals, matched for age, sex and body mass index, received either a 6 h lipid or glycerol infusion in the setting of a concurrent hyperinsulinaemic-euglycaemic clamp. Sequential muscle biopsies (0, 2 and 6 h) were analysed for GLUT4 membrane localisation and microvesicle size and distribution using immunofluorescence microscopy.
At baseline, trained individuals had more small GLUT4 spots at the plasma membrane, whereas sedentary individuals had larger GLUT4 spots. GLUT4 localisation with the plasma membrane increased at 2 h (P = 0.04) of the hyperinsulinemic-euglycemic clamp, and remained elevated until 6 h, with no differences between groups or infusion type. The number of GLUT4 spots was unchanged at 2 h of infusion. However, from 2 to 6 h there was a decrease in the number of small GLUT4 spots at the plasma membrane (P = 0.047), with no differences between groups or infusion type.
GLUT4 localisation with the plasma membrane increases during a hyperinsulinemic-euglycemic clamp, but this is not altered by elevated FFA availability. GLUT4 appears to disperse from small GLUT4 clusters located at the plasma membrane to support glucose uptake during a hyperinsulinaemic-euglycaemic clamp.
胰岛素刺激骨骼肌摄取葡萄糖是通过将 GLUT4 从细胞内储存小泡易位到质膜来实现的。通过脂质输注增加游离脂肪酸 (FFA) 的可用性会降低葡萄糖的清除率,但这种情况发生在胰岛素信号转导没有受损的情况下。FFA 可用性增加是否随后影响 GLUT4 向质膜的定位尚不清楚。
受过训练的(n=11)和久坐的(n=10)个体,年龄、性别和体重指数匹配,在同时进行高胰岛素-正常血糖钳夹的情况下接受 6 小时的脂质或甘油输注。使用免疫荧光显微镜分析序贯肌肉活检(0、2 和 6 小时)中 GLUT4 膜定位和微泡大小和分布。
在基线时,训练有素的个体在质膜上有更多的小 GLUT4 斑点,而久坐不动的个体有更大的 GLUT4 斑点。高胰岛素-正常血糖钳夹 2 小时(P=0.04)时 GLUT4 向质膜的定位增加,并且直到 6 小时仍保持升高,两组之间或输注类型之间没有差异。输注 2 小时时 GLUT4 斑点的数量没有变化。然而,从 2 小时到 6 小时,质膜上的小 GLUT4 斑点数量减少(P=0.047),两组之间或输注类型之间没有差异。
在高胰岛素-正常血糖钳夹期间,GLUT4 向质膜的定位增加,但 FFA 可用性的增加不会改变这一点。GLUT4 似乎从位于质膜的小 GLUT4 簇分散出来,以支持高胰岛素-正常血糖钳夹期间的葡萄糖摄取。