Hillgartner F B, Romsos D R
Department of Food Science and Human Nutrition, Michigan State University, East Lansing 48824-1224.
Am J Physiol. 1988 Jul;255(1 Pt 1):E54-8. doi: 10.1152/ajpendo.1988.255.1.E54.
Obese (ob/ob) mice exhibit impaired hepatic thyroid hormone action that is mediated, at least in part, by a reduced nuclear 3,5,3'-triiodothyronine (T3) receptor occupancy. The possibility that lowered occupancy in obese mice may be caused by decreased transport of T3 across the hepatic plasma membrane was examined by measuring the unidirectional influx of [125I]T3 into livers of 8- to 10-wk-old obese and lean mice using a tissue-sampling portal vein-injection technique. Influx of [125I]thyroxine (T4), a substrate for T4 5'-deiodinase, was also measured. Unidirectional clearance of T3 and T4 was 64 and 80% lower, respectively, in obese mice than in lean mice. Hepatic T3 and T4 uptake was nonsaturable in both lean and obese mice, suggesting that transport occurs by lipid-mediated free diffusion. Clearance of another lipid-soluble hormone, hydrocortisone, was also lower in obese mice than in lean mice. Decreased membrane permeability to the above hormones in obese mice may result from reported changes in membrane lipid composition. In conclusion, decreased hepatic thyroid hormone uptake may contribute to impaired thyroid hormone action and T3 production in livers of obese mice.
肥胖(ob/ob)小鼠表现出肝脏甲状腺激素作用受损,这至少部分是由核3,5,3'-三碘甲状腺原氨酸(T3)受体占有率降低介导的。通过使用组织采样门静脉注射技术测量[125I]T3向8至10周龄肥胖和瘦小鼠肝脏的单向流入,研究了肥胖小鼠中占有率降低可能是由T3跨肝细胞膜转运减少引起的可能性。还测量了[125I]甲状腺素(T4)(T4 5'-脱碘酶的底物)的流入。肥胖小鼠中T3和T4的单向清除率分别比瘦小鼠低64%和80%。在瘦小鼠和肥胖小鼠中,肝脏对T3和T4的摄取均不饱和,表明转运是通过脂质介导的自由扩散进行的。肥胖小鼠中另一种脂溶性激素氢化可的松的清除率也低于瘦小鼠。肥胖小鼠中上述激素的膜通透性降低可能是由于报道的膜脂质组成变化所致。总之,肝脏甲状腺激素摄取减少可能导致肥胖小鼠肝脏中甲状腺激素作用受损和T3生成减少。