Sex differences in dietary sodium evoked NCC regulation and blood pressure in male and female Sprague-Dawley, Dahl salt-resistant, and Dahl salt-sensitive rats.

Kiyoung Kim, Kayla M Nist, Franco Puleo, James McKenna, Richard D Wainford
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Abstract

Hypertension affects approximately one in two United States adults and sex plays an important role in the pathogenesis of hypertension. The Na+-Cl- cotransporter (NCC), regulated by a kinase network including with-no-lysine kinase (WNK)1 and WNK4, STE20/SPS1-related proline alanine-rich kinase (SPAK), and oxidative stress response 1 (OxSR1), is critical to Na+ reabsorption and blood pressure regulation. Dietary salt differentially modulates NCC in salt-sensitive and salt-resistant rats, in part by modulation of WNK/SPAK/OxSR1 signaling. In this study, we tested the hypothesis that sex-dependent differences in NCC regulation contribute to the development of the salt sensitivity of blood pressure using male and female Sprague-Dawley (SD), Dahl salt-resistant (DSR), and Dahl salt-sensitive (DSS) rats. In normotensive salt-resistant SD and DSR rats, a high-salt diet evoked significant decreases in NCC activity, expression, and phosphorylation. In males, these changes were associated with no change in WNK1 expression, a decrease in WNK4 levels, and suppression of SPAK/OxSR1 expression and phosphorylation. In contrast, in females, there was decreased NCC activity associated with suppression of SPAK/OxSR1 expression and phosphorylation. In hypertensive DSS rats, the ability of females to suppress NCC (in opposition to males) via a SPAK/OxSR1 mechanism likely contributes to their lower magnitude of salt-sensitive hypertension. Collectively, our findings support the existence of sex differences in male versus female rats with NCC regulation during dietary salt intake involving suppression of WNK4 expression in male rats only and the involvement of SPAK/OxSR1 signaling in both males and females.NEW & NOTEWORTHY NCC regulation is sex dependent. In normotensive male and female Sprague-Dawley and Dahl salt-resistant rats, which exhibit dietary Na+-evoked NCC suppression, male rats exhibit decreased WNK4 expression and decreased SPAK and OxSR1 levels, whereas female rats only suppress SPAK and OxSR1. In hypertensive Dahl salt-sensitive rats, the ability of females to suppress NCC (in opposition to males) via a SPAK/OxSR1 mechanism likely contributes to their lower magnitude of salt-sensitive hypertension.

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雌雄 Sprague Dawley 大鼠、耐达尔盐大鼠和对达尔盐敏感大鼠饮食钠诱发的 NCC 调节和血压的性别差异。
大约每两个美国成年人中就有一人患有高血压,而性别在高血压的发病机制中起着重要作用。 氯化钠共转运体(NCC)由一个激酶网络调控,该激酶网络包括无赖氨酸激酶(WNK)1 和 WNK4、STE20/SPS1 相关富脯氨酸丙氨酸激酶(SPAK)和氧化应激反应 1(OxSR1),对钠的重吸收和血压调节至关重要。膳食盐对盐敏感大鼠和盐耐受大鼠的 NCC 有不同的调节作用,部分原因是 WNK/SPAK/OxSR1 信号的调节。在这些研究中,我们使用雄性和雌性 Sprague Dawley 大鼠、达尔耐盐大鼠(DSR)和达尔盐敏感大鼠(DSS)测试了 NCC 调节的性别差异有助于血压盐敏感性发展的假设。在血压正常的耐盐 SD 和 DSR 大鼠中,高盐饮食导致 NCC 活性、表达和磷酸化显著下降。在雄性大鼠中,这些变化与 WNK1 表达无变化、WNK4 水平下降以及 SPAK/OxSR1 表达和磷酸化受抑制有关。相反,在雌性大鼠中,NCC 活性的降低与 SPAK/OxSR1 表达和磷酸化的抑制有关。在高血压 DSS 大鼠中,雌性大鼠通过 SPAK/OxSR1 机制抑制 NCC 的能力(与雄性相反)很可能是其盐敏感性高血压程度较低的原因。总之,我们的研究结果表明,雄性大鼠与雌性大鼠存在性别差异,在饮食摄入盐分期间,NCC的调节只涉及雄性大鼠WNK4表达的抑制,而SPAK/OxSR1信号传导在雄性和雌性大鼠中均有参与。
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