Chechi Kanta, McGuire John J, Cheema Sukhinder K
Memorial Univesity, St. John's, NL, A1B 3X9, Canada.
Am J Physiol Regul Integr Comp Physiol. 2009 Apr;296(4):R1029-40. doi: 10.1152/ajpregu.90932.2008. Epub 2009 Feb 4.
We have previously shown that a maternal high-fat diet, rich in saturated fatty acids (SFA), alters the lipid metabolism of their adult offspring. The present study was designed to investigate 1) whether alterations in hepatic LDL-receptor (LDL-r) expression may serve as a potential mechanism of developmental programming behind the altered lipid metabolism of the offspring, 2) whether altered lipid metabolism leads to aortic vascular dysfunction in the offspring, 3) whether deleterious effects of SFA exposure preweaning are influenced by postweaning diet, and 4) whether gender-specific programming effects are observed. Female C57Bl/6 mice were fed a high-SFA diet or regular chow during gestation and lactation while their pups, both male and female, received either SFA or a chow diet after weaning. Male offspring obtained from mothers fed an SFA diet and those who continued on chow postweaning had higher plasma triglycerides and total cholesterol, whereas female offspring had higher plasma total and LDL cholesterol levels, lower hepatic LDL-r mRNA expression, and reduced aortic contractile responses compared with the offspring that were fed chow throughout the study. A comparison of the postweaning diet revealed significantly lower hepatic LDL-r expression along with significantly higher plasma LDL-cholesterol concentration in the female offspring that were obtained from mothers fed an SFA diet and who continued on an SFA diet postweaning, compared with the female offspring that were obtained from mothers fed an SFA diet but who continued on chow postweaning. In conclusion, we report a novel observation of hepatic LDL-r-mediated programming of altered lipid metabolism, along with aortic vascular dysfunction, in the female offspring of mothers fed a high-SFA diet. Male offspring only exhibited dyslipidemia, suggesting gender-mediated programming. This study further highlighted the role of postweaning diets in overriding the effects of maternal programming.
我们之前已经表明,富含饱和脂肪酸(SFA)的母体高脂饮食会改变其成年后代的脂质代谢。本研究旨在调查:1)肝脏低密度脂蛋白受体(LDL-r)表达的改变是否可能作为后代脂质代谢改变背后发育编程的潜在机制;2)脂质代谢改变是否会导致后代主动脉血管功能障碍;3)断奶前暴露于SFA的有害影响是否受断奶后饮食的影响;4)是否观察到性别特异性编程效应。雌性C57Bl/6小鼠在妊娠和哺乳期喂食高SFA饮食或常规饲料,而它们的幼崽,无论雄性还是雌性,在断奶后接受SFA或饲料饮食。与整个研究期间喂食饲料的后代相比,从喂食SFA饮食的母亲处获得且断奶后继续喂食饲料的雄性后代具有更高的血浆甘油三酯和总胆固醇,而雌性后代具有更高的血浆总胆固醇和低密度脂蛋白胆固醇水平、更低的肝脏LDL-r mRNA表达以及降低的主动脉收缩反应。断奶后饮食的比较显示,与从喂食SFA饮食但断奶后继续喂食饲料的母亲处获得的雌性后代相比,从喂食SFA饮食的母亲处获得且断奶后继续喂食SFA饮食的雌性后代肝脏LDL-r表达显著降低,同时血浆低密度脂蛋白胆固醇浓度显著升高。总之,我们报告了一项新的观察结果,即喂食高SFA饮食的母亲的雌性后代中存在肝脏LDL-r介导的脂质代谢改变编程以及主动脉血管功能障碍。雄性后代仅表现出血脂异常,表明存在性别介导的编程。这项研究进一步强调了断奶后饮食在克服母体编程影响方面的作用。