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联合补充肌醇对合并代谢综合征和肥胖的妊娠孕妇代谢状况的影响。

The effect of combined inositol supplementation on maternal metabolic profile in pregnancies complicated by metabolic syndrome and obesity.

作者信息

Ferrari Francesca, Facchinetti Fabio, Ontiveros Alejandra E, Roberts Robyn P, Saade Mia M, Blackwell Sean C, Sibai Baha M, Refuerzo Jerrie S, Longo Monica

机构信息

Division of Maternal-Fetal Medicine, Department of Obstetrics, Gynecology, and Reproductive Sciences, University of Texas Health Science Center at Houston, Houston, Texas; Department of Obstetrics and Gynecology, University of Modena and Reggio Emilia, Modena, Italy.

Department of Obstetrics and Gynecology, University of Modena and Reggio Emilia, Modena, Italy.

出版信息

Am J Obstet Gynecol. 2016 Oct;215(4):503.e1-8. doi: 10.1016/j.ajog.2016.05.038. Epub 2016 May 30.

Abstract

BACKGROUND

Myoinositol and D-chiroinositol improve insulin resistance in women with obesity and gestational diabetes and in postmenopausal women with metabolic syndrome. We previously reported that offspring born to hypertensive dams lacking endothelial nitric oxide synthase and fed a high-fat diet develop metabolic-like syndrome phenotype.

OBJECTIVE

The objective of the study was to investigate the effect of a mixture of myoinositol/D-chiroinositol supplementation during pregnancy on the maternal metabolic profile in pregnancies complicated by the metabolic-like syndrome and obesity using a pregnant mouse model.

STUDY DESIGN

Female heterozygous endothelial nitric oxide synthase(-/+) mice with moderate hypertension were placed on a high-fat diet for 4 weeks to induce a metabolic-like syndrome phenotype. Similarly, wild-type C57BL/6 mice were placed on a high-fat diet for 4 weeks to induce a murine obesity model. Mice were then bred with wild-type males. On gestational day 1, dams were randomly allocated to receive either a mixture of myoinositol/D-chiroinositol in water (7.2/0.18 mg/mL, respectively) or water as control (placebo). At term (gestational day 18), maternal weights, systolic blood pressure, and a glucose tolerance test were obtained. Dams were then killed; pups and placentas were weighed and maternal blood collected. Serum levels of metabolic biomarkers relevant to diabetes and obesity (ghrelin, gastric inhibitory peptide, glucagon-like peptide 1, glucagon, insulin, leptin, resistin) were measured by a multiplex enzyme-linked immunosorbent assay. Analysis was done comparing metabolic-like syndrome-myoinositol/D-chiroinositol-treated vs metabolic-like syndrome-nontreated mice and obese-myoinositol/D-chiroinositol-treated vs obese nontreated mice.

RESULTS

Mean systolic blood pressure was lower in metabolic-like syndrome pregnant mice treated with myoinositol/D-chiroinositol compared with placebo (P = .04), whereas there was no difference in systolic blood pressure between treated and placebo-treated obese pregnant mice. Pregnant metabolic-like syndrome mice treated with myoinositol/D-chiroinositol showed lower glucose values during the glucose tolerance test and in the area under the curve (myoinositol/D-chiroinositol: 17512.5 ± 3984.4 vs placebo: 29687.14 ± 8258.7; P = .003), but no differences were seen in the obese pregnant mice. Leptin serum levels were lower in the metabolic-like syndrome-myoinositol/D-chiroinositol-treated mice compared with the placebo group (myoinositol/D-chiroinositol: 16985 ± 976.4 pg/dL vs placebo: 24181.9 ± 3128.2 pg/dL, P = .045). No other differences were seen in any of the remaining serum metabolic biomarkers studied in metabolic-like syndrome and in obese pregnant mice. Maternal weight gain was not different in the pregnant metabolic-like syndrome dams, whereas it was lower in the obese myoinositol/D-chiroinositol-treated dams compared with the placebo group (myoinositol/D-chiroinositol: 10.9 ± 0.5 g vs 12.6 ± 0.6 g, P = .04). Fetal and placental weights did not differ between myoinositol/D-chiroinositol-treated and nontreated pregnant dams with metabolic-like syndrome and obesity.

CONCLUSION

Combined inositol treatment during pregnancy improves blood pressure, glucose levels at the glucose tolerance test, and leptin levels in pregnant dams with metabolic-like syndrome phenotype but not in obese pregnant dams. In addition, inositol treatment was associated with lower gestational weight gain in the obese but not in the metabolic-like syndrome pregnant dams.

摘要

背景

肌醇和D-手性肌醇可改善肥胖和妊娠期糖尿病女性以及绝经后代谢综合征女性的胰岛素抵抗。我们之前报道,缺乏内皮型一氧化氮合酶且喂食高脂饮食的高血压母鼠所产后代会出现类似代谢综合征的表型。

目的

本研究的目的是利用妊娠小鼠模型,探讨孕期补充肌醇/D-手性肌醇混合物对合并类似代谢综合征和肥胖的妊娠母体代谢谱的影响。

研究设计

将患有中度高血压的雌性杂合子内皮型一氧化氮合酶(-/+)小鼠喂食高脂饮食4周,以诱导类似代谢综合征的表型。同样,将野生型C57BL/6小鼠喂食高脂饮食4周,以诱导小鼠肥胖模型。然后将小鼠与野生型雄性小鼠交配。在妊娠第1天,将母鼠随机分配接受水中的肌醇/D-手性肌醇混合物(分别为7.2/0.18 mg/mL)或水作为对照(安慰剂)。在足月时(妊娠第18天),测量母体体重、收缩压和葡萄糖耐量试验。然后处死母鼠;称量幼崽和胎盘重量,并采集母体血液。通过多重酶联免疫吸附测定法测量与糖尿病和肥胖相关的代谢生物标志物的血清水平(胃饥饿素、胃抑制肽、胰高血糖素样肽1、胰高血糖素、胰岛素、瘦素、抵抗素)。进行分析,比较类似代谢综合征-肌醇/D-手性肌醇治疗组与未治疗的类似代谢综合征小鼠,以及肥胖-肌醇/D-手性肌醇治疗组与未治疗的肥胖小鼠。

结果

与安慰剂相比,用肌醇/D-手性肌醇治疗的类似代谢综合征妊娠小鼠的平均收缩压较低(P = 0.04),而治疗组与安慰剂治疗组的肥胖妊娠小鼠的收缩压无差异。用肌醇/D-手性肌醇治疗的妊娠类似代谢综合征小鼠在葡萄糖耐量试验期间及曲线下面积的血糖值较低(肌醇/D-手性肌醇:17512.5±3984.4 vs安慰剂:29687.14±8258.7;P = 0.003),但肥胖妊娠小鼠未见差异。与安慰剂组相比,类似代谢综合征-肌醇/D-手性肌醇治疗组小鼠的瘦素血清水平较低(肌醇/D-手性肌醇:16985±976.4 pg/dL vs安慰剂:24181.9±3128.2 pg/dL,P = 0.045)。在类似代谢综合征和肥胖妊娠小鼠中研究的其余血清代谢生物标志物中未见其他差异。妊娠类似代谢综合征母鼠的母体体重增加无差异,而与安慰剂组相比,肥胖肌醇/D-手性肌醇治疗组母鼠的体重增加较低(肌醇/D-手性肌醇:10.9±0.5 g vs 12.6±0.6 g,P = 0.04)。在患有类似代谢综合征和肥胖的肌醇/D-手性肌醇治疗组与未治疗的妊娠母鼠之间,胎儿和胎盘重量无差异。

结论

孕期联合肌醇治疗可改善具有类似代谢综合征表型的妊娠母鼠的血压、葡萄糖耐量试验时的血糖水平和瘦素水平,但对肥胖妊娠母鼠无效。此外,肌醇治疗与肥胖妊娠母鼠而非类似代谢综合征妊娠母鼠的妊娠期体重增加较低有关。

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