Salt-sensitive hypertension after reversal of unilateral ureteral obstruction

被引:2
|
作者
Imig, John D. [1 ,2 ]
Khan, Md Abdul Hye [2 ]
Stavniichuk, Anna [2 ,3 ]
Jankiewicz, Wojciech K. [2 ]
Goorani, Samaneh [1 ,2 ]
Yeboah, Michael M. [4 ]
El-Meanawy, Ashraf [4 ]
机构
[1] Univ Arkansas Med Sci, Dept Pharmaceut Sci, Little Rock, AR 72205 USA
[2] Med Coll Wisconsin, Drug Discovery Ctr, Cardiovasc Ctr, Milwaukee, WI USA
[3] Univ Texas Hlth Sci Ctr Houston, Dept Integrat Biol & Pharmacol, Houston, TX USA
[4] Med Coll Wisconsin, Dept Med, Milwaukee, WI USA
关键词
Hypertension; Ureter obstruction; Kidney; Vascular density; Inflammation; ACUTE KIDNEY INJURY; SECONDARY RENAL-DISEASE; PROGRESSION; RECOVERY; PATHOPHYSIOLOGY; PATHOGENESIS; FAILURE; RELEASE; REPAIR; CELLS;
D O I
10.1016/j.bcp.2023.115438
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The incidence of ureter obstruction is increasing and patients recovering from this kidney injury often progress to chronic kidney injury. There is evidence that a long-term consequence of recovery from ureter obstruction is an increased risk for salt-sensitive hypertension. A reversal unilateral ureteral obstruction (RUUO) model was used to study long-term kidney injury and salt-sensitive hypertension. In this model, we removed the ureteral obstruction at day 10 in mice. Mice were divided into four groups: (1) normal salt diet, (2) high salt diet, (3) RUUO normal salt diet, and (4) RUUO high salt diet. At day 10, the mice were fed a normal or high salt diet for 4 weeks. Blood pressure was measured, and urine and kidney tissue collected. There was a progressive increase in blood pressure in the RUUO high salt diet group. RUUO high salt group had decreased sodium excretion and glomerular injury. Renal epithelial cell injury was evident in RUUO normal and high salt mice as assessed by neutrophil gelatinase-associated lipocalin (NGAL). Kidney inflammation in the RUUO high salt group involved an increase in F4/80 positive macrophages; however, CD3+ positive T cells were not changed. Importantly, RUUO normal and high salt mice had decreased vascular density. RUUO was also associated with renal fibrosis that was further elevated in RUUO mice fed a high salt diet. Overall, these findings demonstrate long-term renal tubular injury, inflammation, decreased vascular density, and renal fibrosis following reversal of unilateral ureter obstruction that could contribute to impaired sodium excretion and salt-sensitive hypertension.
引用
收藏
页数:10
相关论文
共 50 条
  • [1] REVERSAL OF UNILATERAL URETERAL OBSTRUCTION LEADS TO SALT-SENSITIVE HYPERTENSION
    Khan, Md
    Stavniichuk, Anna
    Savchuk, Olexiy
    Jankiewicz, Wojciech
    Imig, John
    FASEB JOURNAL, 2020, 34
  • [2] Relief of chronic partial ureteral obstruction attenuates salt-sensitive hypertension in rats
    Carlstrom, M.
    Wahlin, N.
    Skott, O.
    Persson, A. E. G.
    ACTA PHYSIOLOGICA, 2007, 189 (01) : 67 - 75
  • [3] Reversal of Genetic Salt-Sensitive Hypertension by Targeted Sympathetic Ablation
    Foss, Jason D.
    Fink, Gregory D.
    Osborn, John W.
    HYPERTENSION, 2013, 61 (04) : 806 - +
  • [4] SALT-SENSITIVE HYPERTENSION
    OPARIL, S
    CIRCULATION, 1993, 88 (04) : F - F
  • [5] SALT-SENSITIVE HYPERTENSION
    Wang Ji-Guang
    NEPHROLOGY, 2014, 19 : 9 - 9
  • [6] SALT-SENSITIVE HYPERTENSION AND HYPERLIPIDEMIA IN DAHL SALT-SENSITIVE RAT
    SHINAGAWA, T
    YAMAGUCHI, T
    IWAMI, K
    OGASAWARA, N
    DOI, Y
    KAMEI, T
    HYPERTENSION, 1995, 26 (03) : 556 - 556
  • [7] Salt-sensitive hypertension - Reply
    Johnson, RJ
    Herrera-Acosta, J
    Schreiner, GF
    Rodriguez-Iturbe, B
    NEW ENGLAND JOURNAL OF MEDICINE, 2002, 347 (06): : 448 - 449
  • [8] The brain and salt-sensitive hypertension
    Frans H. H. Leenen
    Marcel Ruzicka
    Bing S. Huang
    Current Hypertension Reports, 2002, 4 : 129 - 135
  • [9] Genetics of salt-sensitive hypertension
    Pasquale Strazzullo
    Ferruccio Galletti
    Current Hypertension Reports, 2007, 9
  • [10] Genetics of salt-sensitive hypertension
    Strazzullo, Pasquale
    Galletti, Ferruccio
    CURRENT HYPERTENSION REPORTS, 2007, 9 (01) : 25 - 32