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Early L-T4 intervention improves fetal heart development in pregnant rats with subclinical hypothyroidism rats by activating BMP4/Smad4 signaling pathway

机译:早期的L-T4干预通过激活BMP4 / SMAD4信号通路,改善了亚临床甲状腺功能亢进大鼠胎儿心脏病的胎儿心脏发育

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It is unclear whether the offspring of subclinical hypothyroidism (SCH) pregnant rats still have abnormal cardiac development, and whether early intervention with L-T4 can improve the abnormality of these offspring. Therefore, the aim of this study was to investigate the effect of early L-T4 intervention on the heart development of offspring of SCH pregnant rats and its possible molecular mechanism. Eighty female Wistar rats were randomly divided into Sham group (placebo control), SCH group, LT4-E10 group (L-T4 treatment started on the 10th day of gestation), and LT4-E13 group (L-T4 treatment started on the 13th day of gestation). Each group was further divided into E16 (16th day of gestation), E18 (18th day of gestation), P5 (5th day postnatal day), and P10 (10th day postnatal day) subgroups. The levels of serum TT4 and TSH, the ratio of heart weight to body weight of offspring rats, the expression of metabolic enzymes, and the histopathology of cardiomyocytes were determined. To elucidate the effects of L-T4 on cardiac development of offspring of SCH pregnant rats, the expression levels of GATA4, Nkx2–5 and proteins involved in BMP4/Smad4 signaling pathway were detected by immunohistochemistry, real time quantitative polymerase chain reaction and Western blotting to elucidate the molecular mechanism of L-T4 regulating the heart development of the offspring of SCH pregnant rats. Compared with Sham group, serum TSH was significantly increased in SCH pregnant rats. Moreover, early L-T4 intervention significantly reduced the levels of serum TSH. Compared with the offspring in the SCH group, early L-T4 intervention significantly increased the heart weight, heart weight to body weight ratio, the activities of succinate dehydrogenase (SDH), Na /K -ATPase and Ca2 -ATPase, but reduced myocardial cell shrinkage and nuclear staining, hyperemia/congestion and vacuolar degeneration. In addition, early L-T4 intervention not only significantly increased the mRNA and protein expression of Gata4 and Nkx2–5, but also increased the protein expression involved in BMP4/Smad4 signal pathway in myocardium of the offspring of SCH pregnant rats. Early L-T4 intervention can regulate the cardiac development of the offspring of SCH pregnant rats by activating BMP4/Smad4 signaling pathway and increasing the expression of Gata4 and Nkx2–5 proteins.
机译:目前尚不清楚亚临床甲状腺功能减退症(SCH)孕鼠的后代仍然具有异常心脏发育,以及L-T4的早期干预是否可以改善这些后代的异常。因此,本研究的目的是探讨早期L-T4干预对Sch怀孕大鼠后代心脏发育的影响及其可能的分子机制。将八十雌性Wistar大鼠随机分为假组(安慰剂对照),Sch组,LT4-E10组(在妊娠第10天开始,LT4-E13组(L-T4治疗开始于13日妊娠日)。每组进一步分为E16(妊娠第16天),E18(妊娠第18天),P5(第5天)和P10(第10天后期后日期)亚组。确定血清TT4和TSH的水平,确定后代大鼠体重的心脏重量与体重,代谢酶的表达和心肌细胞的组织病理学。为了阐明L-T4对Sch怀孕大鼠后代的心脏发育的影响,通过免疫组化,实时定量聚合酶链反应和Western印迹检测到BMP4 / Smad4信号传导途径的GATA4,NKX2-5和蛋白质的表达水平阐明L-T4调节Sch怀孕大鼠后代心脏发育的分子机制。与Sham组相比,Sch怀孕大鼠的血清TSH显着增加。此外,早期的L-T4干预显着降低了血清TSH的水平。与Sch组中的后代相比,早期的L-T4干预显着增加了心脏重量,心脏重量,体重比,琥珀酸脱氢酶(SDH),Na / K -ATPase和Ca2 -ATP酶的活性,但减少了心肌细胞收缩和核染色,充血/充血和真空变性。此外,早期的L-T4干预不仅显着增加了GATA4和NKX2-5的mRNA和蛋白质表达,而且还增加了SCH孕鼠后代的BMP4 / SMAD4信号途径中涉及的蛋白质表达。早期L-T4干预可以通过激活BMP4 / SMAD4信号通路并增加GATA4和NKX2-5蛋白的表达来调节SCH孕鼠后代的心脏发育。

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