Takahashi A, Sudo M, Minokoshi Y, Shimazu T
Department of Neuropsychopharmacology, Gunma University School of Medicine, Tsumura, Japan.
Am J Physiol. 1992 Dec;263(6 Pt 2):R1228-34. doi: 10.1152/ajpregu.1992.263.6.R1228.
Electrical stimulation of the ventromedial hypothalamus (VMH) increased the rate constant of glucose uptake in rat heart and brown adipose tissue (BAT), as measured in vivo by the 2-deoxy-D-[3H]glucose method. The increase in glucose uptake in BAT was abolished by local sympathetic denervation. To analyze the mechanism of this hypothalamic modulation, the effects of VMH stimulation and insulin treatment on the number and dissociation constant (Kd) of glucose transporters in the plasma and microsomal membranes were examined by means of [3H]cytochalasin B binding. VMH stimulation did not alter either the number or Kd value of glucose transporters in plasma and microsomal membranes prepared from heart and BAT, whereas insulin treatment increased the number of glucose transporters in the plasma membranes and decreased those in the microsomal membranes. D-Glucose transport activity was also measured with the same plasma membrane vesicles. An apparent functional activity of transporters was detected to be increased in the heart and BAT plasma membranes after VMH stimulation but not after insulin treatment. These results suggest that VMH stimulation enhances glucose utilization in heart and BAT via sympathetic innervation and that the mechanism by which VMH stimulation increases tissue glucose uptake is different from that of insulin, possibly causing an activation of glucose transporters present in the plasma membrane.
通过2-脱氧-D-[3H]葡萄糖法在体内测量发现,电刺激腹内侧下丘脑(VMH)可提高大鼠心脏和棕色脂肪组织(BAT)中葡萄糖摄取的速率常数。局部交感神经去神经支配可消除BAT中葡萄糖摄取的增加。为了分析这种下丘脑调节的机制,通过[3H]细胞松弛素B结合法检测了VMH刺激和胰岛素治疗对血浆和微粒体膜中葡萄糖转运体数量和解离常数(Kd)的影响。VMH刺激并未改变从心脏和BAT制备的血浆和微粒体膜中葡萄糖转运体的数量或Kd值,而胰岛素治疗增加了质膜中葡萄糖转运体的数量,并减少了微粒体膜中的葡萄糖转运体数量。还用相同的质膜囊泡测量了D-葡萄糖转运活性。在VMH刺激后,在心脏和BAT质膜中检测到转运体的表观功能活性增加,但在胰岛素治疗后未增加。这些结果表明,VMH刺激通过交感神经支配增强心脏和BAT中的葡萄糖利用,并且VMH刺激增加组织葡萄糖摄取的机制与胰岛素不同,可能导致质膜中存在的葡萄糖转运体激活。