Department of Physiology, Tulane University School of Medicine, New Orleans, Louisiana, United States.
Department of Pharmacology, Tulane University School of Medicine, New Orleans, Louisiana, United States.
Am J Physiol Heart Circ Physiol. 2023 Jun 1;324(6):H762-H775. doi: 10.1152/ajpheart.00638.2022. Epub 2023 Mar 17.
Plasma soluble prorenin receptor (sPRR) displays sexual dimorphism and is higher in women with type 2 diabetes mellitus (T2DM). However, the contribution of plasma sPRR to the development of vascular complications in T2DM remains unclear. We investigated if plasma sPRR contributes to sex differences in the activation of the systemic renin-angiotensin-aldosterone system (RAAS) and vascular damage in a model of high-fat diet (HFD)-induced T2DM. Male and female C57BL/6J mice were fed either a normal fat diet (NFD) or an HFD for 28 wk to assess changes in blood pressure, cardiometabolic phenotype, plasma prorenin/renin, sPRR, and ANG II. After completing dietary protocols, tissues were collected from males to assess vascular reactivity and aortic reactive oxygen species (ROS). A cohort of male mice was used to determine the direct contribution of increased systemic sPRR by infusion. To investigate the role of ovarian hormones, ovariectomy (OVX) was performed at 32 wk in females fed either an NFD or HFD. Significant sex differences were found after 28 wk of HFD, where only males developed T2DM and increased plasma prorenin/renin, sPRR, and ANG II. T2DM in males was accompanied by nondipping hypertension, carotid artery stiffening, and aortic ROS. sPRR infusion in males induced vascular thickening instead of material stiffening caused by HFD-induced T2DM. While intact females were less prone to T2DM, OVX increased plasma prorenin/renin, sPRR, and systolic blood pressure. These data suggest that sPRR is a novel indicator of systemic RAAS activation and reflects the onset of vascular complications during T2DM regulated by sex. High-fat diet (HFD) for 28 wk leads to type 2 diabetes mellitus (T2DM) phenotype, concomitant with increased plasma soluble prorenin receptor (sPRR), nondipping blood pressure, and vascular stiffness in male mice. HFD-fed female mice exhibiting a preserved cardiometabolic phenotype until ovariectomy revealed increased plasma sPRR and blood pressure. Plasma sPRR may indicate the status of systemic renin-angiotensin-aldosterone system (RAAS) activation and the onset of vascular complications during T2DM in a sex-dependent manner.
血浆可溶性肾素原受体(sPRR)表现出性别二态性,在 2 型糖尿病(T2DM)女性中更高。然而,血浆 sPRR 对 T2DM 血管并发症发展的贡献仍不清楚。我们研究了高脂饮食(HFD)诱导的 T2DM 模型中,血浆 sPRR 是否导致系统性肾素-血管紧张素-醛固酮系统(RAAS)激活和血管损伤的性别差异。雄性和雌性 C57BL/6J 小鼠分别喂食正常脂肪饮食(NFD)或 HFD 28 周,以评估血压、心脏代谢表型、血浆肾素/血管紧张素原、sPRR 和 ANG II 的变化。完成饮食方案后,从雄性小鼠中收集组织以评估血管反应性和主动脉活性氧(ROS)。一组雄性小鼠用于通过输注确定系统性 sPRR 增加的直接贡献。为了研究卵巢激素的作用,在喂食 NFD 或 HFD 的雌性小鼠中,在第 32 周进行卵巢切除术(OVX)。HFD 28 周后发现了显著的性别差异,只有雄性小鼠发生 T2DM 并增加了血浆肾素/血管紧张素原、sPRR 和 ANG II。雄性 T2DM 伴有非杓型高血压、颈动脉僵硬和主动脉 ROS。sPRR 输注在雄性小鼠中引起血管增厚而不是 HFD 诱导的 T2DM 引起的物质僵硬。尽管完整的雌性小鼠不太容易发生 T2DM,但 OVX 会增加血浆肾素/血管紧张素原、sPRR 和收缩压。这些数据表明,sPRR 是系统性 RAAS 激活的新指标,反映了 T2DM 期间血管并发症的发生,这一过程受性别调节。28 周的高脂饮食(HFD)导致 2 型糖尿病(T2DM)表型,同时伴有雄性小鼠血浆可溶性肾素原受体(sPRR)增加、非杓型血压和血管僵硬。直到卵巢切除术的 HFD 喂养雌性小鼠表现出保留的心脏代谢表型,显示出增加的血浆 sPRR 和血压。血浆 sPRR 可能以依赖于性别的方式指示系统性肾素-血管紧张素-醛固酮系统(RAAS)激活的状态和 T2DM 期间血管并发症的发生。