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首页> 外文期刊>American Journal of Physiology >Maturation of the Na+/H+ antiporter (NHE3) in the proximal tubule of the hypothyroid adrenalectomized rat.
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Maturation of the Na+/H+ antiporter (NHE3) in the proximal tubule of the hypothyroid adrenalectomized rat.

机译:甲减肾上腺切除的大鼠近端小管中Na + / H +反转运蛋白(NHE3)的成熟。

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In previous studies examining the role of glucocorticoids and thyroid hormone on the maturation of the Na(+)/H(+) antiporter (NHE3), we found attenuation in the maturational increase in proximal tubule apical Na(+)/H(+) antiporter activity but no change in NHE3 mRNA abundance in either glucocorticoid-deficient or hypothyroid rats. In addition, prevention of the maturational increase in either hormone failed to totally prevent the maturational increase in Na(+)/H(+) antiporter activity. We hypothesized that one hormone played a compensatory role when the other was deficient. The present study examined whether combined deficiency of thyroid and glucocorticoid hormones would completely prevent the maturation of the Na(+)/H(+) antiporter. Adrenalectomy was performed in 9-day-old hypothyroid Sprague-Dawley rats, a time before the normal postnatal maturational increase in these hormones occurs. Nine- and 30-day-old adrenalectomized (ADX), hypothyroid rats had comparable NHE3 mRNA abundance, which was 5- to 10-fold less than 30-day-old ADX, hypothyroid rats that received corticosterone-thyroxine replacement and 30-day-old sham control rats (P < 0.05). Brush-border membrane NHE3 protein abundance was comparable in 9- and 30-day-old ADX, hypothyroid groups and approximately 20-fold lower than both the 30-day replacement and 30-day sham groups (P < 0.05). Similarly, the replacement and sham groups had higher sodium-dependent proton secretion than 9- and 30-day-old ADX, hypothyroid groups (P < 0.05). We conclude that combined deficiency of both hormones totally prevents the maturational increase in NHE3 mRNA and protein abundance and Na(+)/H(+) antiporter activity.
机译:在以前的研究中,研究了糖皮质激素和甲状腺激素对Na(+)/ H(+)反转运蛋白(NHE3)成熟的作用,我们发现近端肾小管根尖Na(+)/ H(+)的成熟增加导致衰减糖皮质激素缺乏或甲状腺功能减退大鼠的抗转运蛋白活性但NHE3 mRNA丰度没有变化。此外,任何一种激素的成熟增加的预防都不能完全阻止Na(+)/ H(+)反转运蛋白活性的成熟增加。我们假设一种激素在另一种激素缺乏时起补偿作用。本研究检查了甲状腺和糖皮质激素激素的联合缺乏是否会完全阻止Na(+)/ H(+)反转运蛋白的成熟。在9天大的甲状腺功能减退的Sprague-Dawley大鼠中进行肾上腺切除术,当时这些激素在正常的出生后成熟增加。九岁和30天大的肾上腺切除术(ADX)的甲状腺功能减退大鼠的NHE3 mRNA丰度相当,比30天大的ADX少了5至10倍,甲状腺功能减退的大鼠接受皮质酮-甲状腺素替代和30天假对照组(P <0.05)。刷边界膜NHE3蛋白的丰度在9和30天的ADX组,甲状腺功能减退组中是相当的,比30天的替代组和30天的假组低约20倍(P <0.05)。同样,置换组和假手术组的钠依赖性质子分泌水平均高于9和30天的ADX甲状腺功能减退组(P <0.05)。我们得出结论,两种激素的联合缺乏完全阻止了NHE3 mRNA和蛋白质丰度以及Na(+)/ H(+)反转运蛋白活性的成熟增加。

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