Grasemann C, Herrmann R, Starschinova J, Gertsen M, Palmert M R, Grasemann H
Pediatric Endocrinology and Diabetology, Kinderklinik II, Universitätsklinikum Essen and University of Duisburg-Essen, Essen, Germany.
Division of Neonatology, Kinderklinik I, Universitätsklinikum Essen and University of Duisburg-Essen, Essen, Germany.
Nutr Diabetes. 2017 Feb 20;7(2):e244. doi: 10.1038/nutd.2016.56.
BACKGROUND/OBJECTIVES: Alterations in the L-arginine/nitric oxide (NO) metabolism contribute to diseases such as obesity, metabolic syndrome and airway dysfunction. The impact of early-life exposures on the L-arginine/NO metabolism in lung later in life is not well understood. The objective of this work was to study the effects of intrauterine exposures to maternal hyperglycemia and high-fat diet (HFD) on pulmonary L-arginine/NO metabolism in mice.
We used two murine models of intrauterine exposures to maternal (a) hyperglycemia and (b) HFD to study the effects of these exposures on the L-arginine/NO metabolism in lung in normal chow-fed offspring.
Both intrauterine exposures resulted in NO deficiency in the lung of the offspring at 6 weeks of age. However, each of the exposures leading to different metabolic phenotypes caused a distinct alteration in the L-arginine/NO metabolism. Maternal hyperglycemia leading to impaired glucose tolerance but no obesity in the offspring resulted in increased levels of asymmetric dimethylarginine and impairment of NO synthases. Although maternal HFD led to obesity without impairment in glucose tolerance in the offspring, it resulted in increased expression and activity of arginase in the lung of the normal chow-fed offspring.
These data suggest that maternal hyperglycemia and HFD can cause alterations in the pulmonary L-arginine/NO metabolism in offspring.
背景/目的:L-精氨酸/一氧化氮(NO)代谢的改变与肥胖、代谢综合征和气道功能障碍等疾病有关。早年暴露对后期肺部L-精氨酸/NO代谢的影响尚不清楚。本研究旨在探讨宫内暴露于母体高血糖和高脂饮食(HFD)对小鼠肺L-精氨酸/NO代谢的影响。
我们使用两种宫内暴露于母体(a)高血糖和(b)HFD的小鼠模型,研究这些暴露对正常饮食喂养后代肺L-精氨酸/NO代谢的影响。
两种宫内暴露均导致6周龄后代肺中NO缺乏。然而,每种导致不同代谢表型的暴露都会引起L-精氨酸/NO代谢的明显改变。母体高血糖导致后代葡萄糖耐量受损但无肥胖,导致不对称二甲基精氨酸水平升高和一氧化氮合酶受损。虽然母体HFD导致后代肥胖但葡萄糖耐量未受损,但它导致正常饮食喂养后代肺中精氨酸酶的表达和活性增加。
这些数据表明,母体高血糖和HFD可导致后代肺L-精氨酸/NO代谢改变。