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首页> 外文期刊>Biological & pharmaceutical bulletin >Analysis of Angiotensin II Mediated COX-2 Downregulation in Angiotensin II- or Aldosterone-INfused Hypertensive Rat
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Analysis of Angiotensin II Mediated COX-2 Downregulation in Angiotensin II- or Aldosterone-INfused Hypertensive Rat

机译:血管紧张素II或醛固酮治疗的高血压大鼠中血管紧张素II介导的COX-2下调的分析

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摘要

The renin-angiotensin cascade plays an important role in blood pressure control and sodium homeostasis. This study investigated whether cyclooxygenase-2 expression is regulated in the kidney, in an angiotensin II- and aldosterone-induced hypertension model. For this purpose, we treated male Sprague-Dawley rats (n = 8 per group) with angiotensin II (9 mg/h, subcutaneously) for 14 d and aldosterone (0.75 mg/h, subcutaneously) for 42 d. Systolic blood pressure was significantly increased by angiotensin II (p < 0.001) and by aldosterone (p < 0.001). We found that angiotensin II downregulated cyclooxygenase-2 protein in the kidney cortex, whereas aldosterone showed no effect. These results indicate that angiotensin II may act directly to inhibit kidney cortex cyclooxygenase-2 protein expression, rather than acting via stimulation of aldosterone.
机译:肾素-血管紧张素级联在血压控制和钠稳态中起重要作用。这项研究调查了在血管紧张素II和醛固酮诱导的高血压模型中,肾脏中是否调节了环氧合酶2的表达。为此,我们用血管紧张素II(皮下注射9 mg / h)和醛固酮(皮下注射0.75 mg / h)治疗42天,对雄性Sprague-Dawley大鼠(每组8只)治疗14 d。血管紧张素II(p <0.001)和醛固酮(p <0.001)使收缩压显着升高。我们发现,血管紧张素II下调了肾皮质中的环氧合酶2蛋白,而醛固酮没有作用。这些结果表明,血管紧张素II可能直接起到抑制肾皮质环氧合酶2蛋白表达的作用,而不是通过刺激醛固酮起作用。

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