Chen Guoxun, Zhang Yan, Lu Danhong, Li Nan-Qian, Ross A Catharine
Department of Nutrition, University of Tennessee at Knoxville, Knoxville, TN 37996, U.S.A.
Biochem J. 2009 May 1;419(3):645-53. doi: 10.1042/BJ20082368.
Hepatic GK (glucokinase) plays a key role in maintaining glucose homoeostasis. Many stimuli regulate GK activity by controlling its gene transcription. We hypothesized that endogenous lipophilic molecules modulate hepatic Gck expression. Lipophilic molecules were extracted from rat livers, saponified and re-constituted as an LE (lipophilic extract). LE synergized with insulin to induce primary hepatocyte, but not beta-cell, Gck expression in an SREBP-1c (sterol-regulatory-element-binding protein-1c)-independent manner. The dramatic induction of Gck mRNA resulted in a significant increase in GK activity. Subsequently, the active molecules were identified as retinol and retinal by MS after the purification of the active LE fractions. Retinoids synergized with insulin to induce Gck expression by the activation of both RAR [RA (retinoic acid) receptor] and RXR (retinoid X receptor). Inhibition of RAR activation completely abolished the effect of retinal. The hepatic GK specific activity and Gck mRNA levels of Zucker lean rats fed with a VAD [VA (vitamin A)-deficient] diet were significantly lower than those of rats fed with VAS (VA-sufficient) diet. Additionally, the hepatic Gck mRNA expression of Sprague-Dawley rats fed with a VAD diet was lower than that of rats fed with VA-marginal, -adequate or -supplemented diets. The reduced expression of Gck mRNA was increased after an intraperitoneal dose of RA in VAD rats. Furthermore, an intravenous injection of RA rapidly raised hepatic Gck expression in rats fed with a VAS control diet. Understanding the underlying mechanism that mediates the synergy may be helpful for developing a treatment strategy for patients with diabetes.
肝脏葡萄糖激酶(GK)在维持葡萄糖稳态中起关键作用。许多刺激通过控制其基因转录来调节GK活性。我们推测内源性亲脂性分子可调节肝脏Gck表达。从大鼠肝脏中提取亲脂性分子,皂化后重新构建为亲脂性提取物(LE)。LE与胰岛素协同作用,以不依赖固醇调节元件结合蛋白1c(SREBP-1c)的方式诱导原代肝细胞而非β细胞的Gck表达。Gck mRNA的显著诱导导致GK活性显著增加。随后,在纯化活性LE组分后,通过质谱鉴定出活性分子为视黄醇和视黄醛。类视黄醇与胰岛素协同作用,通过激活维甲酸受体(RAR)和类视黄醇X受体(RXR)来诱导Gck表达。抑制RAR激活完全消除了视黄醛的作用。喂食维生素A缺乏(VAD)饮食的Zucker瘦大鼠的肝脏GK比活性和Gck mRNA水平显著低于喂食维生素A充足(VAS)饮食的大鼠。此外,喂食VAD饮食的Sprague-Dawley大鼠的肝脏Gck mRNA表达低于喂食维生素A边缘、充足或补充饮食的大鼠。在VAD大鼠腹腔注射维甲酸后,Gck mRNA表达的降低有所增加。此外,静脉注射维甲酸可迅速提高喂食VAS对照饮食大鼠的肝脏Gck表达。了解介导这种协同作用的潜在机制可能有助于为糖尿病患者制定治疗策略。