首页> 外文期刊>Gerontology: International Journal of Experimental and Clinical Gerontology >Impaired lipid metabolism in aged mice as revealed by fasting-induced expression of apolipoprotein mRNAs in the liver and changes in serum lipids.
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Impaired lipid metabolism in aged mice as revealed by fasting-induced expression of apolipoprotein mRNAs in the liver and changes in serum lipids.

机译:空腹诱导的载脂蛋白mRNA在肝脏中的表达以及血清脂质的变化表明,老年小鼠的脂质代谢受损。

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BACKGROUND: Changes in apolipoprotein (Apo) metabolism can cause an increased incidence of diseases such as cardiovascular disorders and diabetes with advancing age. Limited reports are available on this topic, however. OBJECTIVE: To investigate age-related changes in mobilization of stored lipid, we studied the effects of fasting on the gene expression of Apos in the liver as well as serum triglyceride (TG) and cholesterol levels in the serum. METHODS: Using young (6- to 8-month-old) and old (24- to 28-month-old) fasted and re-fed mice, Northern blots of hepatic mRNAs for Apos A-I, A-IV, C-II, C-III, and liver-type fatty acid-binding protein and HPLC analyses of serum lipids were conducted. RESULTS: Fasting induced 4- and 20-fold increases in the mRNA of Apo C-II and A-IV, respectively, in young mice while only 1.1- and 7-fold increases, respectively, were detected in old mice. In contrast, the Apo C-III gene expression was significantly reduced by fasting in the young mice but the reduction was smallin the old. In view of the stimulating effect of Apo C-II and A-IV and the inhibiting effect of C-III on lipoprotein lipase (LPL), these findings suggest that the fasting-induced activation of LPL may be considerably decreased in old mice. The amount of TG in very low-density lipoprotein (VLDL), a major form of the transport of TG to peripheral tissues, was significantly greater in the young than in the old mice. Despite possible activation of LPL by fasting, the amount of TG in VLDL, a major form of the transport of TG to peripheral tissues, was significantly greater in the young mice than in the old. It is indicated that the synthesis of VLDL in the liver is high in the young but low in the old mice, which also may be true for the rate of transport of TG. CONCLUSION: The present findings suggest that mobilization of lipids is impaired in old animals due to decreased gene expression of Apos, possibly leading in the long run to excessive lipid accumulation in tissues such as the liver, adipose tissues and blood vessels even in normal feeding, and resulting in an increased incidence of age-related diseases.
机译:背景:随着年龄的增长,载脂蛋白(Apo)代谢的变化会导致诸如心血管疾病和糖尿病等疾病的发生率增加。但是,有关此主题的报告有限。目的:研究与年龄相关的脂质运动的变化,我们研究了禁食对肝脏中Apos基因表达以及血清甘油三酸酯(TG)和胆固醇水平的影响。方法:使用年轻(6至8个月大)和大龄(24至28个月大)的空腹和再喂养小鼠,对Apos AI,A-IV,C-II,进行了C-III,肝型脂肪酸结合蛋白和血清脂质的HPLC分析。结果:空腹诱导幼鼠Apo C-II和A-IV mRNA分别增加4倍和20倍,而老年小鼠分别仅检测到1.1和7倍。相反,幼鼠禁食可显着降低Apo C-III基因表达,而老年小鼠则减少。考虑到Apo C-II和A-IV的刺激作用以及C-III对脂蛋白脂肪酶(LPL)的抑制作用,这些发现表明,空腹诱导的LPL激活在老年小鼠中可能大大降低。极低密度脂蛋白(VLDL)中的TG含量是TG向外围组织运输的主要形式,在幼鼠中,TG的量明显大于老年小鼠。尽管可能通过禁食激活LPL,但VLDL中TG的量是TG向外围组织运输的主要形式,但在DLDL中,年轻小鼠的数量显着大于老年小鼠。结果表明,肝脏中VLDL的合成在年轻小鼠中较高,而在老年小鼠中较低,这对于TG的转运速率也可能是正确的。结论:本研究结果表明,由于Apos基因表达的下降,老年动物的脂质动员受到损害,从长远来看,甚至在正常喂养下,长期可能导致脂质在肝脏,脂肪组织和血管等组织中过度积聚,并导致与年龄有关的疾病的发生率增加。

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