Zammit Victor A
Cell Biochemistry, Hannah Research Institute, Ayr KA6 5HL, Scotland, United Kingdom.
Ann N Y Acad Sci. 2002 Jun;967:52-65. doi: 10.1111/j.1749-6632.2002.tb04263.x.
Observations on humans, on rats in vivo, and on isolated perfused rat livers indicate that insulin stimulates hepatic very-low-density lipoprotein (VLDL)-TAG secretion when the liver is chronically exposed to the hormone. They suggest that frequent stimulation of insulin secretion throughout the diurnal cycle may result in a chronic stimulation of VLDL secretion and increased delivery of acyl moieties to the periphery, particularly to muscle, the most important site of insulin-sensitive glucose disposal. If acyl groups are provided in excess of the oxidative needs of the tissue, this may lead to induction of insulin resistance, irrespective of whether obesity is established concomitantly. Dietary factors that stimulate hepatic VLDL secretion may have the same effect and contribute to the induction of a vicious spiral leading to the development of the full-blown Metabolic Syndrome and its pathological consequences, including type-2 diabetes, stroke, and cardiovascular disease.
对人类、活体大鼠以及离体灌注大鼠肝脏的观察表明,当肝脏长期暴露于胰岛素时,胰岛素会刺激肝脏极低密度脂蛋白(VLDL)-甘油三酯的分泌。这些观察结果提示,在整个昼夜周期频繁刺激胰岛素分泌可能会导致VLDL分泌的慢性刺激,并增加酰基部分向周围组织,特别是向肌肉的输送,而肌肉是胰岛素敏感的葡萄糖代谢的最重要部位。如果提供的酰基超过组织的氧化需求,这可能会导致胰岛素抵抗的诱导,无论是否同时伴有肥胖。刺激肝脏VLDL分泌的饮食因素可能具有相同的作用,并有助于引发恶性循环,导致全面发展的代谢综合征及其病理后果,包括2型糖尿病、中风和心血管疾病。