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首页> 外文期刊>American Journal of Physiology >Activation of the systemic and adipose renin-angiotensin system in rats with diet-induced obesity and hypertension.
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Activation of the systemic and adipose renin-angiotensin system in rats with diet-induced obesity and hypertension.

机译:饮食诱发的肥胖和高血压大鼠体内系统性和脂肪性肾素-血管紧张素系统的激活。

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In obesity-related hypertension, activation of the renin-angiotensin system (RAS) has been reported despite marked fluid volume expansion. Adipose tissue expresses components of the RAS and is markedly expanded in obesity. This study evaluated changes in components of the adipose and systemic RAS in diet-induced obese hypertensive rats. RAS was quantified in adipose tissue and compared with primary sources for the circulating RAS. Male Sprague-Dawley rats were fed either a low-fat (LF; 11% kcal as fat) or moderately high-fat (32% kcal as fat) diet for 11 wk. After 8 wk, rats fed the moderately high-fat diet segregated into obesity-prone (OP) and obesity-resistant (OR) groups based on their body weight gain (body weight: OR, 566 +/- 10; OP, 702 +/- 20 g; P < 0.05). Mean arterial blood pressure was increased in OP rats (LF: 97 +/- 2; OR: 97 +/- 2; OP: 105 +/- 1 mmHg; P < 0.05). Quantification of mRNA expression by real-time PCR demonstrated a selective increase (2-fold) in angiotensinogen gene expressionin retroperitoneal adipose tissue from OP vs. OR and LF rats. Similarly, plasma angiotensinogen concentration was increased in OP rats (LF: 390 +/- 48; OR: 355 +/- 24; OP: 530 +/- 22 ng/ml; P < 0.05). In contrast, other components of the RAS were not altered in OP rats. Marked increases in the plasma concentrations of angiotensin peptides were observed in OP rats (angiotensin II: LF: 95 +/- 31; OR: 59 +/- 20; OP: 295 +/- 118 pg/ml; P < 0.05). These results demonstrate increased activity of the adipose and systemic RAS in obesity-related hypertension.
机译:在肥胖相关的高血压中,尽管体液量明显增加,但据报道肾素-血管紧张素系统(RAS)激活。脂肪组织表达RAS的成分,并在肥胖中显着扩展。这项研究评估了饮食诱导的肥胖高血压大鼠的脂肪和全身RAS成分的变化。 RAS在脂肪组织中定量,并与循环RAS的主要来源进行比较。给雄性Sprague-Dawley大鼠喂低脂(LF; 11%大卡作为脂肪)或中度高脂(32%大卡作为脂肪)的饮食11周。 8周后,根据体重增加将高脂饮食的大鼠分为肥胖易感(OP)和抗肥胖(OR)组(体重:OR,566 +/- 10; OP,702 + 20g; P <0.05)。 OP大鼠的平均动脉血压升高(LF:97 +/- 2; OR:97 +/- 2; OP:105 +/- 1 mmHg; P <0.05)。通过实时PCR定量mRNA的表达证明了OP,OR和LF大鼠腹膜后脂肪组织中血管紧张素原基因表达的选择性增加(2倍)。同样,OP大鼠血浆中血管紧张素原浓度增加(LF:390 +/- 48; OR:355 +/- 24; OP:530 +/- 22 ng / ml; P <0.05)。相反,在OP大鼠中RAS的其他成分没有改变。在OP大鼠中观察到血管紧张素肽的血浆浓度显着增加(血管紧张素II:LF:95 +/- 31; OR:59 +/- 20; OP:295 +/- 118 pg / ml; P <0.05)。这些结果表明,在肥胖相关性高血压中,脂肪和全身RAS的活性增加。

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