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高龄产妇对子代成年大鼠心血管功能的性别特异性影响。

Sex-specific effects of advanced maternal age on cardiovascular function in aged adult rat offspring.

机构信息

Department of Obstetrics and Gynecology, University of Alberta , Edmonton, Alberta , Canada.

Women and Children's Health Research Institute, University of Alberta , Edmonton, Alberta , Canada.

出版信息

Am J Physiol Heart Circ Physiol. 2018 Dec 1;315(6):H1724-H1734. doi: 10.1152/ajpheart.00375.2018. Epub 2018 Oct 5.

Abstract

Pregnancy at an advanced maternal age has an increased risk of complications for both the mothers and their offspring. We have previously shown that advanced maternal age in a rat model leads to poor fetal outcomes, maternal vascular dysfunction, and hypertension, concordant with findings in humans. Moreover, offspring from aged dams had sex-specific cardiovascular dysfunction in young adulthood. However, the detrimental impact of aging on the cardiovascular system of the offspring in this model is unknown. We hypothesized that offspring born to aged dams (9.5-10 mo old) would have impaired cardiovascular function at 12 mo of age. Echocardiographic data revealed signs of mild left ventricular diastolic dysfunction in only male offspring from aged dams [isovolumetric relaxation time: 34.27 ± 2.04 in the young dam group vs. 27.61 ± 0.99 ms in the aged dam group, P < 0.01; mitral annular velocity ratio ( E'/ A'): 1.08 ± 0.04 in the young dam group vs. 0.96 ± 0.02 in the aged dam group, P < 0.05]. We have previously shown that in young adulthood (4 mo of age), male, but not female, offspring born to aged dams had impaired recovery from ischemia-reperfusion injury. Aging did not alter the susceptibility of female offspring to ischemia-reperfusion injury. Interestingly, wire myography data revealed that male offspring from aged dams had enhanced vascular sensitivity to methacholine (negative log of EC: 7.4 ± 0.08 in young dams vs. 7.9 ± 0.11 in aged dams, P = 0.007) due, in part, to increased prostaglandin-mediated vasodilation. Despite intact endothelium-dependent relaxation, female offspring from aged dams had elevated systolic blood pressure (125.3 ± 4.2 mmHg in young dams vs. 144.0 ± 6.9 mmHg in aged dams, P = 0.03). These data highlight sex-specific mechanisms underlying cardiovascular programming in offspring born to dams of advanced age. NEW & NOTEWORTHY Our study demonstrated that adult male and female offspring (12 mo old) born to aged dams had impaired cardiac diastolic function and increased blood pressure, respectively, signifying sex-specific differential cardiovascular effects of advanced maternal age.

摘要

高龄产妇妊娠会增加母婴并发症的风险。我们之前的研究表明,在大鼠模型中,高龄产妇会导致胎儿发育不良、母体血管功能障碍和高血压,与人类的发现一致。此外,来自高龄母体的后代在成年早期会出现特定于性别的心血管功能障碍。然而,在这种模型中,衰老对后代心血管系统的有害影响尚不清楚。我们假设高龄母体(9.5-10 个月龄)所生的后代在 12 个月龄时会出现心血管功能障碍。超声心动图数据显示,只有高龄母体所生雄性后代存在轻度左心室舒张功能障碍的迹象[等容舒张时间:年轻母体组为 34.27±2.04ms,高龄母体组为 27.61±0.99ms,P<0.01;二尖瓣环速度比(E'/A'):年轻母体组为 1.08±0.04,高龄母体组为 0.96±0.02,P<0.05]。我们之前的研究表明,在成年早期(4 个月龄时),来自高龄母体的雄性后代,但不是雌性后代,其对缺血再灌注损伤的恢复能力受损。衰老并没有改变雌性后代对缺血再灌注损伤的易感性。有趣的是,血管张力测定数据显示,来自高龄母体的雄性后代对乙酰甲胆碱的血管敏感性增强(年轻母体组 EC 的负对数为 7.4±0.08,高龄母体组为 7.9±0.11,P=0.007),部分原因是前列腺素介导的血管舒张增加。尽管内皮依赖性舒张正常,但来自高龄母体的雌性后代的收缩压升高(年轻母体组为 125.3±4.2mmHg,高龄母体组为 144.0±6.9mmHg,P=0.03)。这些数据突出了高龄母体后代心血管编程的性别特异性机制。本研究表明,来自高龄母体的成年雄性和雌性后代(12 个月龄)分别出现心脏舒张功能障碍和血压升高,表明高龄产妇对后代的心血管影响具有性别特异性差异。

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