首页> 外文期刊>American Journal of Physiology >Differential effects of polyunsaturated fatty acids on sterol synthesis rates in adult and fetal tissues of the hamster: consequence of altered sterol balance.
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Differential effects of polyunsaturated fatty acids on sterol synthesis rates in adult and fetal tissues of the hamster: consequence of altered sterol balance.

机译:多不饱和脂肪酸对仓鼠成年和胎儿组织中固醇合成速率的不同影响:固醇平衡改变的结果。

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Cholesterol is necessary for the proper growth and development of the fetus. Consequently, disruptions in cholesterol biosynthesis lead to abnormal fetal development. It has been shown that in cells exposed to polyunsaturated fatty acids (PUFA), the expressions of genes and activities of enzymes involved in cholesterol synthesis are reduced. Similarly, we found that adult male hamsters fed PUFA-enriched diets had an approximately 60% reduction in in vivo hepatic sterol synthesis rates. If fetal tissues respond to PUFA in the same manner as do adult livers, then maternal dietary PUFA could lead to a reduction in fetal sterol synthesis rates and possibly abnormal development. To investigate the impact of maternal dietary fatty acids on fetal sterol synthesis rates, female hamsters were fed diets enriched in various fatty acids before and throughout gestation. In vivo sterol synthesis rates were measured in fetuses at mid- and late gestation. At both gestational stages, dietary PUFA had no effect on fetalsterol synthesis rates. This lack of effect was not a consequence of a lack of PUFA enrichment in fetal fatty acids or the lack of PUFA receptor expression in the fetus. We hypothesize that the fetus may experience a dysregulation of sterol synthesis as the result of the fetus being in a negative sterol balance; the PUFA-induced suppression of sterol synthesis in the adult male hamster liver was ablated by creating a net negative sterol balance across the adult hepatocyte.
机译:胆固醇对于胎儿的正常生长和发育必不可少。因此,胆固醇生物合成的破坏导致胎儿发育异常。已经表明,在暴露于多不饱和脂肪酸(PUFA)的细胞中,参与胆固醇合成的基因表达和酶活性降低。同样,我们发现,饲喂富含PUFA的饮食的成年雄性仓鼠体内肝脏甾醇的合成速率降低了约60%。如果胎儿组织对PUFA的反应方式与成人肝脏相同,则母体饮食PUFA可能导致胎儿固醇合成率降低,并可能导致异常发育。为了研究母体饮食脂肪酸对胎儿固醇合成速率的影响,在妊娠之前和整个妊娠期间,给雌性仓鼠饲喂富含多种脂肪酸的饮食。在妊娠中期和晚期测量胎儿体内甾醇的合成速率。在两个妊娠阶段,饮食中的PUFA对胎儿甾醇的合成率均没有影响。这种缺乏效果不是由于胎儿脂肪酸中缺乏PUFA富集或胎儿中PUFA受体表达不足所致。我们假设,由于胎儿的固醇平衡处于负值,胎儿可能会发生固醇合成异常。通过在整个成年肝细胞中产生净的甾醇负平衡来消除PUFA诱导的成年雄性仓鼠肝脏中固醇合成的抑制。

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