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钠氢交换调节因子 1(NHERF1)在衰老的高血压雄性和雌性模型中均赋予盐敏感性。

Sodium-hydrogen exchanger regulatory factor-1 (NHERF1) confers salt sensitivity in both male and female models of hypertension in aging.

机构信息

Department of Physiology, University of Louisville, Louisville, KY, United States of America.

Department of Physiology and Biophysics, Howard University College of Medicine, Washington, DC, United States of America.

出版信息

Life Sci. 2020 Feb 15;243:117226. doi: 10.1016/j.lfs.2019.117226. Epub 2020 Jan 3.

Abstract

Hypertension is a risk factor for premature death and roughly 50% of hypertensive patients are salt-sensitive. The incidence of salt-sensitive hypertension increases with age. However, the mechanisms of salt-sensitive hypertension are not well understood. We had demonstrated decreased renal sodium‑hydrogen exchanger regulatory factor 1 (NHERF1) expression in old salt-resistant F344 rats. Based on those studies we hypothesized that NHERF1 expression is required for the development of some forms of salt-sensitive hypertension. To address this hypothesis, we measured blood pressure in NHERF1 expressing salt-sensitive 4-mo and 24-mo-old male and female Fischer Brown Norway (FBN) rats male and female 18-mo-old NHERF1 knock-out (NHERF1) mice and wild-type (WT) littermates on C57BL/6J background after feeding high salt (8% NaCl) diet for 7 days. Our data demonstrate that 8% salt diet increased blood pressure in both male and female 24-mo-old FBN rats but not in 4-mo-old FBN rats and in 18-mo-old male and female WT mice but not in NHERF1 mice. Renal dopamine 1 receptor (D1R) expression was decreased in 24-mo-old rats, compared with 4-mo-old FBN rats. However, sodium chloride cotransporter (NCC) expression increased in 24-mo-old FBN rats. In FBN rats, age had no effect on NaK ATPase α1 and NKCC2 expression. By contrast, high salt diet increased the renal expressions of NKCC2, and NCC in 24-mo-old FBN rats. High salt diet also increased NKCC2 and NCC expression in WT mice but not NHERF1 mice. Our data suggest that renal NHERF1 expression confers salt sensitivity with aging, associated with increased expression of sodium transporters.

摘要

高血压是导致早逝的一个风险因素,大约有 50%的高血压患者对盐敏感。盐敏感性高血压的发病率随年龄增长而增加。然而,盐敏感性高血压的发病机制尚不清楚。我们已经证明,在老年盐抵抗 F344 大鼠中,肾脏钠-氢交换调节因子 1(NHERF1)的表达减少。基于这些研究,我们假设 NHERF1 的表达是某些类型盐敏感性高血压发展所必需的。为了验证这一假设,我们测量了在摄入高盐(8%NaCl)饮食 7 天后,NHERF1 表达的盐敏感性 4 月龄和 24 月龄雄性和雌性 Fischer 棕褐色挪威(FBN)大鼠、18 月龄 NHERF1 敲除(NHERF1)小鼠和野生型(WT)同窝仔鼠的血压。我们的数据表明,8%盐饮食可使 24 月龄雄性和雌性 FBN 大鼠的血压升高,但不能使 4 月龄 FBN 大鼠和 18 月龄雄性和雌性 WT 小鼠的血压升高,而 NHERF1 小鼠则不受影响。与 4 月龄 FBN 大鼠相比,24 月龄大鼠的肾脏多巴胺 1 受体(D1R)表达减少。然而,24 月龄 FBN 大鼠的氯化钠共转运蛋白(NCC)表达增加。在 FBN 大鼠中,年龄对 NaK ATPaseα1 和 NKCC2 的表达没有影响。相比之下,高盐饮食增加了 24 月龄 FBN 大鼠肾脏中 NKCC2 和 NCC 的表达。高盐饮食还增加了 WT 小鼠肾脏中 NKCC2 和 NCC 的表达,但 NHERF1 小鼠没有。我们的数据表明,肾脏 NHERF1 的表达赋予了衰老时的盐敏感性,与钠转运体表达增加有关。

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