Dib Abdallah, Payen Cyrielle, Bourreau Jennifer, Munier Mathilde, Grimaud Linda, Fajloun Ziad, Loufrani Laurent, Henrion Daniel, Fassot Céline
UMR Centre National de la Recherche Scientifique 6015, INSERM U1083, MITOVASC, University of Angers, Angers, France.
University Hospital of Angers, Angers, France.
Front Physiol. 2018 Apr 4;9:350. doi: 10.3389/fphys.2018.00350. eCollection 2018.
exposure to maternal diabetes increases the risk of developing hypertension and cardiovascular disorders during adulthood. We have previously shown that this is associated with changes in vascular tone in favor of a vasoconstrictor profile, which is involved in the development of hypertension. This excessive constrictor tone has also a strong impact on vascular structure. Our objective was to study the impact of exposure to maternal diabetes on vascular structure and remodeling induced by chronic changes in hemodynamic parameters. We used an animal model of rats exposed to maternal hyperglycemia (DMO), which developed hypertension at 6 months of age. At a pre-hypertensive stage (3 months of age), we observed deep structural modifications of the vascular wall without any hemodynamic perturbations. Indeed, in basal conditions, resistance arteries of DMO rats are smaller than those of control mother offspring (CMO) rats; in addition, large arteries like thoracic aorta of DMO rats have an increase of smooth muscle cell attachments to elastic lamellae. In an isolated perfused kidney, we also observed a leftward shift of the flow/pressure relationship, suggesting a rise in renal peripheral vascular resistance in DMO compared to CMO rats. In this context, we studied vascular remodeling in response to reduced blood flow by mesenteric arteries ligation. In DMO rats, inward remodeling induced by a chronic reduction in blood flow (1 or 3 weeks after ligation) did not occur by contrast to CMO rats in which arterial diameter decreased from 428 ± 17 μm to 331 ± 20 μm (at 125 mmHg, = 0.001). In these animals, the transglutaminase 2 (TG2) pathway, essential for inward remodeling development in case of flow perturbations, was not activated in low-flow (LF) mesenteric arteries. Finally, in old hypertensive DMO rats (18 months of age), we were not able to detect a pressure-induced remodeling in thoracic aorta. Our results demonstrate for the first time that exposure to maternal diabetes induces deep changes in the vascular structure. Indeed, the early narrowing of the microvasculature and the structural modifications of conductance arteries could be a pre-emptive adaptation to fetal programming of hypertension.
暴露于母体糖尿病会增加成年后患高血压和心血管疾病的风险。我们之前已经表明,这与血管张力的变化有关,有利于血管收缩剂的分布,而这与高血压的发展有关。这种过度的收缩张力也对血管结构有很大影响。我们的目的是研究暴露于母体糖尿病对血流动力学参数慢性变化引起的血管结构和重塑的影响。我们使用了暴露于母体高血糖(DMO)的大鼠动物模型,这些大鼠在6个月大时患上了高血压。在高血压前期阶段(3个月大),我们观察到血管壁有深度结构改变,且没有任何血流动力学扰动。事实上,在基础条件下,DMO大鼠的阻力动脉比对照母鼠后代(CMO)大鼠的小;此外,DMO大鼠的大动脉,如胸主动脉,平滑肌细胞与弹性膜的附着增加。在一个离体灌注肾中,我们还观察到流量/压力关系向左移位,这表明与CMO大鼠相比,DMO大鼠的肾外周血管阻力增加。在此背景下,我们通过结扎肠系膜动脉来研究对血流减少的血管重塑反应。与CMO大鼠不同,DMO大鼠在结扎后1周或3周因血流慢性减少而诱导的内向重塑并未发生,在CMO大鼠中,动脉直径从428±17μm降至331±20μm(在125mmHg时,P = 0.001)。在这些动物中,在低流量(LF)肠系膜动脉中,对于因流量扰动而发生内向重塑至关重要的转谷氨酰胺酶2(TG2)途径未被激活。最后,在老年高血压DMO大鼠(18个月大)中,我们未能在胸主动脉中检测到压力诱导的重塑。我们的结果首次证明,暴露于母体糖尿病会引起血管结构的深度变化。事实上,微血管的早期狭窄和传导动脉的结构改变可能是对高血压胎儿编程的一种先发适应。