The role of CaN/NFAT signaling pathway in aerobic exercise-induced upregulation of KV2.1 channels in vascular smooth muscle cells in hypertension rat
CSTR:
Author:
Affiliation:

Key Laboratory of Physical Fitness and Exercise, Ministry of Education, Beijing Sport University, Beijing 100084, China)

Clc Number:

R363

  • Article
  • | |
  • Metrics
  • |
  • Reference [20]
  • |
  • Related [20]
  • | | |
  • Comments
    Abstract:

    Aim To investigate the role of calcineurin/nuclear factor of activated T cells (CaN/NFAT) signaling pathway in aerobic exercise-induced increased expression of KV2.1 channel in mesenteric artery vascular smooth muscle cell from spontaneously hypertensive rats (SHR). Methods Male SHR and Wistar-Kyoto rats (WKY), 12 weeks age, were randomly divided into control groups (WKY-SED, SHR-SED), and exercise groups (WKY-EX, SHR-EX). Exercise groups were subjected to a 12-week treadmill training protocol:20 m/min, 60 min/day, 5 d/w. After 12 weeks, heart rate (HR) and blood pressure (BP) was acquired in each group. Immunocytochemistry was used to observe the distribution and changing of KV2.1 and CaN in mesenteric artery (MA). Western blot was applied to examine the expression levels of KV2.1, CaN, NFATc3, p-NFATc3, A-kinase anchoring protein (AKAP150) and calmodulin (CaM) protein in MA. Results (1)After 12 weeks of exercise, HR, systolic blood pressure (SBP)and mean blood pressure (MBP) in SHR-EX group was significantly lower than that in SHR-SED group (P<0.01); SBP in WKY-EX group was lower than that in WKY-SED group (P<0.05). (2) The distribution and protein expression of KV2.1 in SHR-SED group was significantly lower than that in WKY-SED group (P<0.01); Exercise training markedly increased the expression of KV2.1 in SHR-EX group (P<0.01). (3) Compared with the WKY-SED group, the distribution and protein expression of CaN was significantly increased, but the protein expression of p-NFATc3 was significantly lower in SHR-SED group(P<0.01); Exercise training markedly inhibited the distribution and expression of CaN and increased the expression of p-NFATc3 in SHR-EX group (P<0.01). (4) The protein expression of AKAP150 in SHR-SED group was significantly higher than that of WKY-SED group (P<0.01); aerobic exercise obviously decreased the upregulation protein expression of AKAP150 in hypertension(P<0.01). (5) The protein expression of CaM in SHR-SED group was significantly higher than that of WKY-SED group (P<0.01); Compared with the SHR-SED group, the protein expression of CaM was significantly decreased in SHR-EX group (P<0.01); Compared with the WKY-SED group, the protein expression of CaM was significantly increased in WKY-EX group (P<0.05). Conclusion The increased CaN/NFAT signaling pathway may induce the KV2.1 expression downregulation, however, aerobic exercise can effectively inhibit such effects, which may be the mechanism of exercise restoring cardiovascular function.

    Reference
    [1] 孙东东, 王佐广, 温绍君.难治性高血压临床治疗进展.心肺血管病杂志, 7,6(3):182-4,9.
    [2] Gregory CA, Charles FR, Manuel FN, et al.NFATc3 regulates Kv2.1 expression in arterial smooth muscle.J Biol Chem, 4,9(45):47326-47334.
    [3] Nystoriak MA, Nieves-Cintron M, Nygren PJ, et al.AKAP150 contributes to enhanced vascular tone by facilitating large-conductance Ca2+-activated K+ channel remodeling in hyperglycemia and diabetes mellitus.Circ Res, 4,4(4):607-615.
    [4] Martens JR, Gelband CH.Alterations in rat interlobar artery membrane potential and K+ channels in genetic and nongenetic hypertension.Circ Res, 6,9:295-301.
    [5] Cox RH, Folandar K, Swanson R.Differential expression of voltage-gated K+ channel genes in arteries from spontaneously hypertensive and Wistar-Kyoto rats.Hypertension, 1,7 (5):1315-1322.
    [6] Hirsch AT.Vascular disease, hypertension, and prevention:“from endothelium to clinical events”.J Am Coll Cardiol, 3,2(2):377-379.
    [7] Marques CM, Nascimento FA, Mandarim-de-Lacerda CA, et al.Exercise training attenuates cardiovascular adverse remodeling in adult ovariectomized spontaneously hypertensive rats.Menopause, 6,3(1):87-95.
    [8] Shahzad M, Benyu J, Antoine G, et al.Exercise reduces arterial pressure augmentation through vasodilation of muscular arteries in humans.Am J Physiol Heart Circ Physiol, 8,4:H1645-H1650.
    [9] Lien PT, Hua C, Ann B, et al.Effects of low-intensity exercise conditioning on blood pressure, heart rate, and autonomic modulation of heart rate in men and women with hypertension.Biol Res Nurs, 9,1:129-143.
    [10] Sherri S, Stutzman C.The effects of exercise conditioning in normal and overweight pregnant women on blood pressure and heart rate variability.Biol Res Nurs, 0,2:137-148.
    [11] Pescatello LS, Franklin BA, Fagard R, et al.Exercise and hypertension.Med Sci Sports Exerc, 4,6(3):533-553.
    [12] Ivy J, Withers R, Van HP, et al.Muscle respiratory capacity and fiber type as determinants of the lactate threshold.J Appl Physiol, 0,8(3):523-527.
    [13] 邱方, 熊开宇, 石丽君.褪黑素在有氧运动改善自发性高血压大鼠血压和肠系膜动脉功能中的作用.中国动脉硬化杂志, 5,3(12):1229-1235.
    [14] Constantino PB, Dionisio TJ, Duchatsch F, et al.Exercise attenuates dexamethasone-induced hypertension through an improvement of baroreflex activity independently of the renin-angiotensin system.Steroids, 7,1(18):007.
    [15] 叶芳, 吴迎, 曾凡星, 等.有氧运动抑制老年高血压大鼠血管功能重塑的氧化应激机制.中国动脉硬化杂志, 7,5(7):679-687.
    [16] Masson GS, Michelini LC.Experimental evidences supporting training-induced benefits in spontaneously hypertensive rats.Adv Exp Med Biol, 7,9:287-306.
    [17] Huang YF, Liu ML, Dong MQ, et al.Effects of sodium tanshinone II A sulphonate on hypoxic pulmonary hypertension in rats in vivo and on Kv2.1 expression in pulmonary artery smooth muscle cells in vitro.J Ethnopharmacol, 9,5(3):436-443.
    [18] Gregory CA, Luis FS.Kv2 channels oppose myogenic constriction of rat cerebral arteries.Am J Physiol Cell Physiol, 6,1(2):C348-356.
    [19] Guan S, Huang Y, Feng Z, et al.The toxic effects of benzopyrene on activated mouse T cells in vitro.Immunopharmacol Immunotoxicol, 7,9(3):117-123.
    [20] Madeline NC, Matthew AN, Maria PP, et al.Selective down-regulation of KV2.1 function contributes to enhanced arterial tone during diabetes.J Biol Chem, 5,0(12):7918-7929.
    Cited by
    Comments
    Comments
    分享到微博
    Submit
Get Citation

LI Shanshan, BAI Ping, WU Ying, LI Li, ZENG Fanxing, SHI Lijun. The role of CaN/NFAT signaling pathway in aerobic exercise-induced upregulation of KV2.1 channels in vascular smooth muscle cells in hypertension rat[J]. Editorial Office of Chinese Journal of Arteriosclerosis,2018,26(8):767-773.

Copy
Share
Article Metrics
  • Abstract:1249
  • PDF: 853
  • HTML: 0
  • Cited by: 0
History
  • Received:February 09,2018
  • Revised:March 21,2018
  • Online: July 17,2018
Article QR Code