Haque M S, Minokoshi Y, Hamai M, Iwai M, Horiuchi M, Shimazu T
Department of Medical Biochemistry, Ehime University School of Medicine, Shigenobu, Japan.
Diabetes. 1999 Sep;48(9):1706-12. doi: 10.2337/diabetes.48.9.1706.
Our previous study demonstrated that microinjection of leptin into the ventromedial hypothalamus (VMH) dramatically increased glucose uptake in the heart, brown adipose tissue (BAT), and skeletal muscles, but not in white adipose tissue (WAT) in conscious unrestrained rats, as assessed in vivo by the 2-[3H]deoxyglucose method. Here we examined the role of the sympathetic nervous system and insulin in enhanced glucose uptake by tissues after hypothalamic leptin injection. Pretreatment with guanethidine significantly suppressed the increased glucose uptake by the tissues in response to leptin injected into the VMH, whereas bilateral adrenal demedullation had no significant effect. Treatment with propranolol but not phenoxybenzamine also decreased significantly enhanced glucose uptake by the tissues. We further examined the interaction of the effects of hypothalamic leptin and insulin administered peripherally by clamping the glucose concentrations at a constant level. When leptin was injected into the VMH and a maximal dose of insulin was administered intravenously, the rates of glucose uptake by the heart, BAT, and skeletal muscles, but not by WAT, markedly increased beyond the values reached by insulin stimulation alone. Surgical sympathetic denervation of BAT abolished the enhancement of glucose uptake in this tissue, decreasing to the level stimulated by insulin alone. These results appear to indicate that leptin in the hypothalamus enhances glucose uptake in certain peripheral tissues through mediation of a beta-adrenergic mechanism for the sympathetic nerves innervating the tissues and that central leptin and peripheral insulin have a synergistic role in augmenting tissue glucose uptake.
我们之前的研究表明,在清醒自由活动的大鼠中,通过2-[³H]脱氧葡萄糖法在体内评估发现,向腹内侧下丘脑(VMH)微量注射瘦素可显著增加心脏、棕色脂肪组织(BAT)和骨骼肌的葡萄糖摄取,但白色脂肪组织(WAT)的葡萄糖摄取无明显变化。在此,我们研究了交感神经系统和胰岛素在下丘脑注射瘦素后组织葡萄糖摄取增强过程中的作用。胍乙啶预处理显著抑制了VMH注射瘦素后组织葡萄糖摄取的增加,而双侧肾上腺髓质切除则无显著影响。普萘洛尔治疗可显著降低组织葡萄糖摄取的增强,而苯苄胺则无此作用。我们通过将葡萄糖浓度维持在恒定水平,进一步研究了下丘脑瘦素和外周给予胰岛素的相互作用。当向VMH注射瘦素并静脉给予最大剂量胰岛素时,心脏、BAT和骨骼肌而非WAT的葡萄糖摄取速率显著高于单独胰岛素刺激所达到的值。对BAT进行手术交感神经去支配消除了该组织葡萄糖摄取的增强,降至单独胰岛素刺激的水平。这些结果似乎表明,下丘脑的瘦素通过支配组织的交感神经的β-肾上腺素能机制介导,增强某些外周组织的葡萄糖摄取,并且中枢瘦素和外周胰岛素在增强组织葡萄糖摄取方面具有协同作用。