Department of Pharmacology and Nutritional Sciences University of Kentucky Lexington KY.
Department of Biomedical Sciences Cedars-Sinai Medical Center Los Angeles CA.
J Am Heart Assoc. 2019 Dec 3;8(23):e012309. doi: 10.1161/JAHA.119.012309. Epub 2019 Nov 22.
Background We have previously reported that female mice exposed to maternal separation and early weaning (MSEW), a model of early life stress, show exacerbated diet-induced obesity associated with hypertension. The goal of this study was to test whether MSEW promotes angiotensin II-dependent hypertension via activation of the renin-angiotensin system in adipose tissue. Methods and Results MSEW was achieved by daily separations from the dam and weaning at postnatal day 17, while normally reared controls were weaned at postnatal day 21. Female controls and MSEW weanlings were placed on a low-fat diet (LF, 10% kcal from fat) or high-fat diet (HF, 60% kcal from fat) for 20 weeks. MSEW did not change mean arterial pressure in LF-fed mice but increased it in HF-fed mice compared with controls (<0.05). In MSEW mice fed a HF, angiotensin II concentration in plasma and adipose tissue was elevated compared with controls (<0.05). In addition, angiotensinogen concentration was increased solely in adipose tissue from MSEW mice (<0.05), while angiotensin-converting enzyme protein expression and activity were similar between groups. Chronic enalapril treatment (2.5 mg/kg per day, drinking water, 7 days) reduced mean arterial pressure in both groups of mice fed a HF (<0.05) and abolished the differences due to MSEW. Acute angiotensin II-induced increases in mean arterial pressure (10 μg/kg SC) were attenuated in untreated MSEW HF-fed mice compared to controls (<0.05); however, this response was similar between groups in enalapril-treated mice. Conclusions The upregulation of angiotensinogen and angiotensin II in adipose tissue could be an important mechanism by which female MSEW mice fed a HF develop hypertension.
我们之前曾报道过,雌性小鼠暴露于母体分离和早期断奶(MSEW),这是一种早期生活压力模型,与高血压相关的饮食诱导肥胖加重。本研究的目的是测试 MSEW 是否通过激活脂肪组织中的肾素-血管紧张素系统促进血管紧张素 II 依赖性高血压。
通过每天与母鼠分离和在产后第 17 天断奶来实现 MSEW,而正常饲养的对照组则在产后第 21 天断奶。雌性对照组和 MSEW 断奶小鼠被置于低脂饮食(LF,10%的热量来自脂肪)或高脂肪饮食(HF,60%的热量来自脂肪)中 20 周。MSEW 并未改变 LF 喂养的小鼠的平均动脉压,但与对照组相比,HF 喂养的小鼠的平均动脉压升高(<0.05)。在 MSEW 喂养的 HF 小鼠中,血浆和脂肪组织中的血管紧张素 II 浓度升高(<0.05)。此外,仅在 MSEW 小鼠的脂肪组织中增加了血管紧张素原浓度(<0.05),而 ACE 蛋白表达和活性在两组之间相似。慢性依那普利治疗(2.5mg/kg/天,饮用水,7 天)降低了两组 HF 喂养小鼠的平均动脉压(<0.05),并消除了 MSEW 引起的差异。未经处理的 MSEW HF 喂养小鼠中,急性血管紧张素 II 诱导的平均动脉压升高(10μg/kg SC)较对照组减弱(<0.05);然而,在依那普利治疗的小鼠中,这种反应在两组之间相似。
脂肪组织中血管紧张素原和血管紧张素 II 的上调可能是 MSEW 喂养 HF 小鼠发生高血压的重要机制。