首页> 外文期刊>American Journal of Physiology >Sex differences in adaptive downregulation of pre-macula densa sodium transporters with ANG II infusion in mice.
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Sex differences in adaptive downregulation of pre-macula densa sodium transporters with ANG II infusion in mice.

机译:小鼠ANG II输注在黄斑前DENSA钠转运蛋白的适应性下调中的性别差异。

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摘要

An increase in blood pressure (BP) due to angiotensin II (ANG II) infusion or other means is associated with adaptive pressure natriuresis due to reduced sodium reabsorption primarily in proximal tubule (PT) and thick ascending limb (TAL). We tested the hypothesis that male and female mice would show differential response to ANG II infusion with regard to the regulation of the protein abundance of sodium transporters in the PT and TAL and that these responses would be modulated by aging. Young (approximately 3 mo) and old (approximately 21 mo) male and female mice were infused with ANG II at 800 ng x kg body wt(-1) x min(-1) by osmotic minipump for 7 days or received a sham operation. ANG II increased mean arterial pressure (MAP), measured by radiotelemetry, significantly more in male mice of both ages (increased approximately 30-40 mmHg), compared with females (increased approximately 15-25 mmHg). On day 1, MAP was also significantly increased in old mice, relative to young (P = 0.01). ANG II infusion was associated with a significant decline in plasma testosterone (to <30% of control male) in male mice and rise in young female mice (to 478% of control female). No sex differences were found in the upregulation of the sodium hydrogen exchanger abundance on Western blots observed with ANG II infusion or the downregulation of the sodium phosphate cotransporter; however, aging did impact on some of these changes. Male mice (especially young) also had significantly reduced levels of the TAL bumetanide-sensitive Na-K-2Cl cotransporter (to 60% of male control), while young females showed an increase (to 126% of female control) with ANG II infusion. These sex differences do not support impaired pressure natriuresis in male mice, but might reflect a greater need and attempt to mount an appropriately BP-metered natriuretic response by additional downregulation of TAL sodium reabsorption.
机译:由于血管紧张素II(ANG II)输注或其他方式引起的血压升高(BP)与适应性压力钠尿有关,这主要是由于近端小管(PT)和上肢粗大上升(TAL)中钠的重吸收减少所致。我们测试了这样的假设,即雄性和雌性小鼠在PT和TAL中钠转运蛋白的蛋白质调节方面会表现出对ANG II输注的不同反应,并且这些反应会因衰老而受到调节。通过渗透微型泵将ANG II以800 ng x kg体重(-1)x min(-1)注入ANG II,对年轻(约3 mo)和年老(约21 mo)雄性和雌性小鼠进行7天或进行假手术。 ANG II增加了通过无线电遥测法测得的平均动脉压(MAP),与雌性(增加了约15-25 mmHg)相比,两个年龄段的雄性小鼠均增加了约30-40 mmHg。在第1天,与年幼的小鼠相比,老年小鼠的MAP也显着增加(P = 0.01)。 ANG II输注与雄性小鼠血浆睾丸激素显着下降(降至对照组雄性的30%)和雌性小鼠幼年升高(至雌性对照组的478%)有关。在通过ANG II输注观察到的Western印迹上,氢交换钠的丰度上调或磷酸钠共转运蛋白的下调均未发现性别差异。但是,老化确实影响了其中一些变化。雄性小鼠(尤其是年轻小鼠)的TAL布美他尼敏感Na-K-2Cl协同转运蛋白水平也显着降低(至雄性对照的60%),而雌性年轻的ANG II输注小鼠则升高(至雌性对照的126%) 。这些性别差异不支持雄性小鼠压力性钠尿功能受损,但可能反映了更大的需求,并试图通过进一步下调TAL钠重吸收来建立适当的BP计量的钠尿反应。

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