High-salt diets during pregnancy increases renal vascular reactivity due to altered soluble guanylyl cyclase-related pathways in rat offspring

卷:28

Jiang, Lin ; Yin, Xiaohui ; He, Axin ; Li, Lingjun ; Bo, Le ; Zhou, Xiuwen ; Tang, Jiaqi ; Gu, Xiuxia ; Wu, Jue ; Gao, Qinqin ; Lv, Juanxiu ; Mao, Caiping ; Xu, Zhice

Soochow Univ

关键词: BKCa channels;    PKG;    Prenatal HS;    Renal interlobar arteries;    sGC;   

DOI  :  10.1016/j.jnutbio.2015.10.009

学科分类：食品科学和技术

【 摘 要 】

Adverse prenatal factors such as overtake of salt or fat food are potential risks for cardiovascular diseases in offspring. This study tested the hypothesis thatprenatal high-salt (HS) diets may influence renal vascular tone and attenuates signaling pathways related to soluble guanylyl cyclase (sGC) or/and large conductance Ca2+-activated K+ (BKca) channels in the offspring. Pregnant rats were fed either normal salt (NS) (1% NaCl) or HS (8% NaCl) diet for the whole gestation. Offspring were maintained on NS diets. Renal interlobar arteries in offspring were tested for vascular responses to phenylephrine (Phe), K+ channels and signal pathways related to sGC. Phe induced higher vessel tension in interlobar arteries of the HS offspring. Following pretreatment with BKca channel inhibitor iberiotoxin, Phe-mediated vasoconstrictions were decreased in HS offspring compared to NS. Phe-mediated constrictions following pretreatment with NO synthase inhibitor N(G)-nitro-Larginine methyl ester or sGC inhibitor 1H-1,2,4-oxadiazolo-4,3-quinoxalin-1-one in the HS offspring were less sensitive than NS. The whole-cell K+ currents and the component of BKca channels were not changed in smooth muscle cells from interlobar arteries, whereas the K+ currents stimulated by sGC activator BAY-412272 were reduced in the HS offspring. The protein expressions of sGC 131 and 132 in the interlobar arteries of HS offspring were reduced. The results showed that chronic overintake of salt during pregnancy could increase renal vascular tone in the offspring. The affected signal pathways included down-regulation of sGC function and expression. (C) 2015 Elsevier Inc. All rights reserved.