Exercise training attenuates remodeling of CaL channel in cerebral artery of aging hypertensive rats
Author:
Affiliation:

Department of Exercise Physiology, Beijing Sport University, Beijing 100084, China)

Clc Number:

R363

  • Article
  • | |
  • Metrics
  • |
  • Reference [29]
  • | | | |
  • Comments
    Abstract:

    Aim To investigate the effects of exercise training on the function of the CaL channels in cerebral arterial smooth muscle cells of aging spontaneously hypertensive rats. Methods 18 3-month-old male Wistar-Kyoto (WKY) rats and 18 spontaneously hypertensive rats (SHR) were used, besides, 16-month-old male WKY and SHR were randomly assigned into either a sedentary group or an exercise-trained group, each group contained 18 rats. The rats in exercise-trained groups ran on a motor treadmill (60 min/d, 5 d/w) at 16~18 m/min for 8 weeks. After 8 weeks training, body weight and heart weight among these groups were measured. The CaL channel function and the expression of CaL channel α1C protein in cerebral artery were measured by whole-cell patch-clamp technique and Western blot. Results(1)Aging effects:Both heart rate and systolic blood pressure in SHR were much higher than those of the same age WKY rats, the systolic blood pressure in 16-month-old rats were significantly higher than the same strain in 3-month-old rats; The CaL channel current density and CaL channel α1C protein expression in young SHR were extremely increased compared with WKY, whereas aging markedly decreased CaL channel current density and CaL channel α1C protein expression in both hypertensive and normotensive rats with no significant differences between them. (2) Exercise effects:The heart weight index (heart weight/ body weight) in aging exercise-trained groups were markedly higher than those in sedentary strains; Exercise training greatly lowered the systolic blood pressure, and increased CaL channel current density and CaL channel α1C protein expression in SHR. Conclusion Aging reduced CaL channel function of cerebral artery from SHR, while exercise training attenuated remodeling of CaL channel.

    Reference
    [1] Zhu Y, Qiu H, Trzeciakowski J P, et al.Temporal analysis of vascular smooth muscle cell elasticity and adhesion reveals oscillation waveforms that differ with aging .Aging Cell, 2,1(5):741-750.
    [2] Sehgel N L, Zhu Y, Sun Z, et al.Increased vascular smooth muscle cell stiffness:a novel mechanism for aortic stiffness in hypertension .Am J Physiol Heart Circ Physiol, 3,5(9):H1 281-287.
    [3] Wamhoff B R, Bowles D K, Mcdonald O G, et al.L-type voltage-gated Ca2+ channels modulate expression of smooth muscle differentiation marker genes via a rho kinase/myocardin/SRF-dependent mechanism .Circ Res, 4,5(4):406-414.
    [4] Dimeo F, Pagonas N, Seibert F, et al.Aerobic exercise reduces blood pressure in resistant hypertension .Hypertension, 2,0(3):653-658.
    [5] Chen Y, Zhang H, Zhang Y, et al.Exercise intensity-dependent reverse and adverse remodeling of voltage-gated Ca(2+) channels in mesenteric arteries from spontaneously hypertensive rats .Hypertens Res, 5,8(10):656-665.
    [6] Wolf-Maier K, Cooper R S, Banegas J R, et al.Hypertension prevalence and blood pressure levels in 6 European countries, Canada, and the United States .JAMA, 3,9(18):2 363-369.
    [7] Kapur G, Ahmed M, Pan C, et al.Secondary hypertension in overweight and stage 1 hypertensive children:a Midwest Pediatric Nephrology Consortium report .J Clin Hypertens (Greenwich), 0,2(1):34-39.
    [8] Liao J, Zhang Y, Ye F, et al.Epigenetic regulation of L-type voltage-gated Ca2+ channels in mesenteric arteries of aging hypertensive rats .Hypertens Res, 7,0(5):441.
    [9] Sehgel N L, Sun Z, Hong Z, et al.Augmented vascular smooth muscle cell stiffness and adhesion when hypertension is superimposed on aging .Hypertension, 5,5(2):370-377.
    [10] Pratt P F, Bonnet S, Ludwig L M, et al.Upregulation of L-type Ca2+ channels in mesenteric and skeletal arteries of SHR .Hypertension, 2,0(2):214-219.
    [11] Wang W Z, Saada N, Dai B, et al.Vascular-specific increase in exon 1B-encoded CAV1.2 channels in spontaneously hypertensive rats .Am J Hypertens, 6,9(8):823-831.
    [12] Albinsson S, Sward K.Targeting smooth muscle microRNAs for therapeutic benefit in vascular disease .Pharmacol Res, 3,5:28-36.
    [13] Garcia-Palmieri M.Hypertension in old age .P R Health Sci J, 5,4(3):217-221.
    [14] Lu Y, Zhang Y, Wang N, et al.MicroRNA-328 contributes to adverse electrical remodeling in atrial fibrillation .Circulation, 0,2(23):2 378-387.
    [15] Arun K H, Kaul C L, Ramarao P.AT1 receptors and L-type calcium channels:functional coupling in supersensitivity to angiotensin II in diabetic rats .Cardiovasc Res, 5,5(2):374-386.
    [16] Fukuda T, Kuroda T, Kono M, et al.Attenuation of L-type Ca2+ channel expression and vasomotor response in the aorta with age in both Wistar-Kyoto and spontaneously hypertensive rats .PLoS One, 4,9(2):e88 975.
    [17] Pesic A, Madden J A, Pesic M, et al.High blood pressure upregulates arterial L-type Ca2+ channels is membrane depolarization the signal? .Circ Res, 4,4(10):e97-e104.
    [18] Ohya Y, Abe I, Fujii K, et al.Voltage-dependent Ca2+ channels in resistance arteries from spontaneously hypertensive rats .Circ Res, 3,3(6):1 090-099.
    [19] Kolwicz S C, Macdonnell S M, Renna B F, et al.Left ventricular remodeling with exercise in hypertension .Am J Physiol Heart Circ Physiol, 9,7(4):H1 361-368.
    [20] 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.
    [21] Zamo F D S, Barauna V G, Chiavegatto S, et al.The renin-angiotensin system is modulated by swimming training depending on the age of spontaneously hypertensive rats .Life Sci, 1,9(3):93-99.
    [22] Negrao C E, Irigoyen M C, Moreira E D, et al.Effect of exercise training on RSNA, baroreflex control, and blood pressure responsiveness .Am J Physiol, 3,5(2 Pt 2):R365-370.
    [23] Veras-Silva A S, Mattos K C, Gava N S, et al.Low-intensity exercise training decreases cardiac output and hypertension in spontaneously hypertensive rats .Am J Physiol, 7,3(6 Pt 2):H2 627-631.
    [24] Harder D R.Pressure-induced myogenic activation of cat cerebral arteries is dependent on intact endothelium .Circ Res, 7,0(1):102-107.
    [25] 陈渝, 石丽君.有氧运动抑制高血压诱导的肠系膜动脉 CaL 通道功能重构 .中国运动医学杂志, 5,4(4):341-346.
    [26] Heaps C L, Bowles D K, Sturek M, et al.Enhanced L-type Ca2+ channel current density in coronary smooth muscle of exercise-trained pigs is compensated to limit myoplasmic free Ca2+ accumulation .J Physiol, 0,8(Pt 3):435-445.
    [27] Guia A, Wan X, Courtemanche M, et al.Local Ca2+ entry through L-type Ca2+ channels activates Ca2+-dependent K+ channels in rabbit coronary myocytes .Circ Res, 9,4(9):1 032-042.
    [28] Albarwani S, Al-Siyabi S, Baomar H, et al.Exercise training attenuates ageing-induced BKCa channel downregulation in rat coronary arteries .Exp Physiol, 0,5(6):746-755.
    [29] Ghosh P, Solis F R M, Dominguez J M, et al.Exercise training reverses aging-induced impairment of myogenic constriction in skeletal muscle arterioles .J Appl Physiol (1985), 5,8(7):904-911.
    Related
    Cited by
    Comments
    Comments
    分享到微博
    Submit
Get Citation

CHEN Yu, SHI Li-Jun, WU Ying. Exercise training attenuates remodeling of CaL channel in cerebral artery of aging hypertensive rats[J]. Editorial Office of Chinese Journal of Arteriosclerosis,2018,26(4):353-360.

Copy
Share
Article Metrics
  • Abstract:877
  • PDF: 0
  • HTML: 0
  • Cited by: 0
History
  • Received:September 29,2017
  • Revised:October 25,2017
  • Online: May 04,2018
Article QR Code