Tanaka Sarasa, Yamamoto Hironori, Nakahashi Otoki, Ishiguro Mariko, Takei Yuichiro, Masuda Masashi, Kozai Mina, Ikeda Shoko, Taketani Yutaka, Miyamoto Ken-ichi, Takeda Eiji
Department of Clinical Nutrition, Institute of Health Biosciences, the University of Tokushima Graduate School.
J Med Invest. 2013;60(3-4):191-6. doi: 10.2152/jmi.60.191.
The type IIa sodium-dependent phosphate co-transporter (Npt2a) is important to maintain renal inorganic phosphate (Pi) homeostasis and the plasma Pi levels. It has reported that disorder of Pi metabolism in kidney can be risk factors for cardiovascular disease as well as hypercholesterolemia. However, the relationship between Pi and cholesterol metabolism has not been clarified. The current study investigated the effects of Npt2a gene ablation that is known as hypophosphatemia model on cholesterol metabolism in mice. Npt2a deficient (Npt2a(-/-)) mice and wild type mice were fed diets with or without 2% cholesterol for 12 days. Plasma lipid and lipoprotein profile analysis revealed that plasma lipid levels (total, LDL and HDL cholesterol) were significantly higher in Npt2a(-/-) mice than wild type (WT) mice. Interestingly, high cholesterol diet markedly increased plasma levels of total, LDL and HDL cholesterol in WT mice, but not Npt2a(-/-) mice. On the other hand, there were no differences in body and liver weight, intake and hepatic lipid accumulation between WT and Npt2a(-/-) mice. These results suggest that ablation of Npt2a gene induces hypercholesterolemia and affects the ability to respond normally to dietary cholesterol.
IIa型钠依赖性磷酸盐共转运蛋白(Npt2a)对于维持肾脏无机磷酸盐(Pi)稳态和血浆Pi水平至关重要。据报道,肾脏中Pi代谢紊乱可能是心血管疾病以及高胆固醇血症的危险因素。然而,Pi与胆固醇代谢之间的关系尚未阐明。当前研究调查了已知为低磷血症模型的Npt2a基因敲除对小鼠胆固醇代谢的影响。给Npt2a基因缺陷(Npt2a(-/-))小鼠和野生型小鼠喂食含或不含2%胆固醇的饮食12天。血浆脂质和脂蛋白谱分析显示,Npt2a(-/-)小鼠的血浆脂质水平(总胆固醇、低密度脂蛋白胆固醇和高密度脂蛋白胆固醇)显著高于野生型(WT)小鼠。有趣的是,高胆固醇饮食显著增加了WT小鼠的血浆总胆固醇、低密度脂蛋白胆固醇和高密度脂蛋白胆固醇水平,但对Npt2a(-/-)小鼠没有影响。另一方面,WT小鼠和Npt2a(-/-)小鼠在体重、肝脏重量、摄入量和肝脏脂质积累方面没有差异。这些结果表明,Npt2a基因敲除会诱导高胆固醇血症,并影响对饮食胆固醇正常反应的能力。