Department of Physiology, School of Pharmacy and Biochemistry, Universidad de Buenos Aires, IQUIMEFA-CONICET, Buenos Aires, Argentina.
Metabolism. 2013 Sep;62(9):1287-95. doi: 10.1016/j.metabol.2013.04.013. Epub 2013 May 22.
Hypothyroid state and aging are associated with impairment in water reabsorption and changes in aquaporin water channel type 2 (AQP2). Nitric oxide (NO) is involved in AQP2 trafficking to the apical plasma membrane in medullary collecting duct cells. The purpose of this study was to investigate whether aging and hypothyroidism alter renal function, and whether medullary NO and AQP2 are implicated in maintaining water homeostasis.
MATERIALS/METHODS: Sprague-Dawley rats aged 2 and 18months old were treated with 0.02% methimazole (w/v) during 28days. Renal function was examined and NO synthase (NOS) activity ([(14)C (U)]-L-arginine to [(14)C (U)]-L-citrulline assays), NOS, caveolin-1 and -3 and AQP2 protein levels were determined in medullary tissue (Western blot). Plasma membrane fraction and intracellular vesicle fraction of AQP2 were evaluated by Western blot and immunohistochemistry.
A divergent response was observed in hypothyroid rats: while young rats exhibited polyuria with decreased medullary NOS activity, adult rats exhibited a decrease in urine output with increased NOS activity. AQP2 was increased with hypothyroidism, but while young rats exhibited increased AQP2 in plasma membrane, adult rats did so in the cytosolic site.
Hypothyroidism contributes in a differential way to aging-induced changes in renal function, and medullary NO and AQP2 would be implicated in maintaining water homeostasis.
甲状腺功能减退症和衰老与水重吸收功能障碍以及水通道蛋白 2(AQP2)改变有关。一氧化氮(NO)参与了集合管细胞顶膜 AQP2 的运输。本研究旨在探讨衰老和甲状腺功能减退症是否改变肾功能,以及是否涉及髓质 NO 和 AQP2 以维持水稳态。
材料/方法:2 月龄和 18 月龄的 Sprague-Dawley 大鼠用 0.02%甲巯咪唑(w/v)处理 28 天。检测肾功能,用酶联免疫吸附法测定(14C(U))-L-精氨酸到(14C(U))-L-瓜氨酸(Western blot)测定一氧化氮合酶(NOS)活性,测定髓质组织中的 NOS、窖蛋白-1 和 -3 和 AQP2 蛋白水平。用 Western blot 和免疫组织化学法评估 AQP2 的质膜部分和细胞内囊泡部分。
甲状腺功能减退症的大鼠表现出不同的反应:年轻大鼠表现出多尿伴髓质 NOS 活性降低,成年大鼠表现出尿量减少伴 NOS 活性增加。AQP2 随着甲状腺功能减退而增加,但年轻大鼠的 AQP2 增加在质膜,而成年大鼠则在细胞质部位。
甲状腺功能减退症以不同的方式导致肾功能的衰老诱导变化,髓质 NO 和 AQP2 将参与维持水稳态。