Pliss Lioudmila, Jatania Urvi, Patel Mulchand S
Department of Biochemistry, School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, NY 14214, USA.
Department of Exercise and Nutrition, School of Public Health and Health Professions, University at Buffalo, Buffalo, NY 14214, USA.
Mol Genet Metab Rep. 2016 Apr 22;7:78-86. doi: 10.1016/j.ymgmr.2016.03.012. eCollection 2016 Jun.
Pyruvate dehydrogenase complex (PDC) deficiency is a major inborn error of oxidative metabolism of pyruvate in the mitochondria causing congenital lactic acidosis and primarily structural and functional abnormalities of the central nervous system. To provide an alternate source of acetyl-CoA derived from ketone bodies to the developing brain, a formula high in fat content is widely employed as a treatment. In the present study we investigated efficacy of a high-fat diet given to mothers during pregnancy and lactation on lessening of the impact of PDC deficiency on brain development in PDC-deficient female progeny.
A murine model of systemic PDC deficiency by interrupting the X-linked Pdha1 gene was employed in this study.
Maternal consumption of a high-fat diet during pregnancy and lactation had no effect on number of live-birth, body growth, tissue PDC activity levels, as well as the in vitro rates of glucose oxidation and fatty acid biosynthesis by the developing brain of PDC-deficient female offspring during the postnatal age 35 days, as compared to the PDC-deficient progeny born to dams on a chow diet. Interestingly, brain weight was normalized in PDC-deficient progeny of high fat-fed mothers with improvement in impairment in brain structure deficit whereas brain weight was significantly decreased and was associated with greater cerebral structural defects in progeny of chow-fed mothers as compared to control progeny of mothers fed either a chow or high fat diet.
The findings provide for the first time experimental support for beneficial effects of a ketogenic diet during the prenatal and early postnatal periods on the brain development of PDC-deficient mammalian progeny.
丙酮酸脱氢酶复合体(PDC)缺乏症是线粒体中丙酮酸氧化代谢的一种主要先天性缺陷,可导致先天性乳酸酸中毒,并主要引起中枢神经系统的结构和功能异常。为了给发育中的大脑提供源自酮体的乙酰辅酶A的替代来源,高脂肪含量的配方奶被广泛用作一种治疗方法。在本研究中,我们调查了孕期和哺乳期母亲食用高脂饮食对减轻PDC缺乏对PDC缺乏雌性后代大脑发育影响的效果。
本研究采用通过中断X连锁的Pdha1基因建立的全身性PDC缺乏的小鼠模型。
与食用普通饮食的母鼠所生的PDC缺乏后代相比,孕期和哺乳期母鼠食用高脂饮食对活产数量、身体生长、组织PDC活性水平,以及出生后35天内PDC缺乏雌性后代发育中的大脑的体外葡萄糖氧化率和脂肪酸生物合成率均无影响。有趣的是,高脂饮食喂养的母亲所生的PDC缺乏后代的脑重恢复正常,脑结构缺陷损伤得到改善,而与食用普通饮食或高脂饮食的母亲的对照后代相比,普通饮食喂养的母亲所生后代的脑重显著降低,且伴有更严重的脑结构缺陷。
这些发现首次为产前和产后早期生酮饮食对PDC缺乏的哺乳动物后代大脑发育的有益作用提供了实验支持。