Effects of Low-dose Morphine on Nitric Oxide Concentration and Angiogenesis in Two-kidney One Clip Hypertensive Rats

被引:0
作者
Pourshanazari, Aliasghar [1 ]
Allahtavakoli, Mohammad [1 ]
Hassanshahi, GHGholamhossein [2 ]
机构
[1] Rafsanjan Univ Med Sci, Physiol & Pharmacol Res Ctr, Rafsanjan, Iran
[2] Rafsanjan Univ Med Sci, Mol Med Res Ctr, Rafsanjan, Iran
关键词
Angiogenesis; Blood pressure; Morphine; Nitric oxide; Renin activity; OPIOID RECEPTOR; ENDOTHELIAL-CELLS; PROGENITOR CELLS; BLOOD-PRESSURE; MODULATION; EXPRESSION; GROWTH; CARDIOPROTECTION; PERMEABILITY; DYSFUNCTION;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Objective(s) We investigated the effects of low-dose morphine on nitric oxide (NO) and angiogenesis in two-kidney one clip hypertensive (2K1C) rats. Materials and Methods Male rats were divided into two groups: sham-clip operated and 2K1C. Each group subdivided into saline and morphine (3 mg/kg i.p. 8 weeks) groups. Blood pressure, heart rate, plasma renin activity (PRA), NO concentration and murine matrigel angiogenesis were evaluated. Results Morphine had no effects on blood pressures and HR in sham normotensive rats but attenuated diastolic blood pressure (DBP) (P< 0.01) and mean arterial pressure (MAP) (P< 0.01) in 2K1C compared with saline. PRA level was significantly higher in 2K1C compared with sham groups (P< 0.01) but morphine decreased it in 2K1C compared with saline (P< 0.01). After clipping, NO in 2K1C hypertensive rats was decreased (P< 0.01) and morphine increased it compared with saline (P< 0.01). Morphine promoted angiogenesis in both sham (P< 0.01) and 2K1C (P< 0.0001) groups. Conclusion Low-dose morphine stimulated angiogenesis in two-kidney one clip hypertensive rats probably via NO pathways.
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页码:560 / 567
页数:8
相关论文
共 43 条
  • [1] ARENDT RM, 1995, J PHARMACOL EXP THER, V272, P1
  • [2] Angiogenesis assays: A critical overview
    Auerbach, R
    Lewis, R
    Shinners, B
    Kubai, L
    Akhtar, N
    [J]. CLINICAL CHEMISTRY, 2003, 49 (01) : 32 - 40
  • [3] Morphine-mediated alteration of hypertension-related gene expression in human white blood cells and multilineage progenitor cells
    Banach, M.
    Casares, F. M.
    Kream, R. M.
    Gluba, A.
    Rysz, J.
    Stefano, G. B.
    [J]. JOURNAL OF HUMAN HYPERTENSION, 2010, 24 (11) : 713 - 720
  • [4] Morphine-induced macrophage apoptosis: oxidative stress and strategies for modulation
    Bhat, RS
    Bhaskaran, M
    Mongia, A
    Hitosugi, N
    Singhal, PC
    [J]. JOURNAL OF LEUKOCYTE BIOLOGY, 2004, 75 (06) : 1131 - 1138
  • [5] Vascular System: Role of Nitric Oxide in Cardiovascular Diseases
    Bian, Ka
    Doursout, Marie-Francoise
    Murad, Ferid
    [J]. JOURNAL OF CLINICAL HYPERTENSION, 2008, 10 (04) : 304 - 310
  • [6] Morphine stimulates vascular endothelial growth factor-like signaling in mouse retinal endothelial cells
    Chen, Chunsheng
    Farooqui, Mariya
    Gupta, Kalpna
    [J]. CURRENT NEUROVASCULAR RESEARCH, 2006, 3 (03) : 171 - 180
  • [7] Reduced basal NO-mediated dilation and decreased endothelial NO-synthase expression in coronary vessels of spontaneously hypertensive rats
    Crabos, M
    Coste, P
    Paccalin, M
    Tariosse, L
    Daret, D
    Besse, P
    BonoronAdele, S
    [J]. JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1997, 29 (01) : 55 - 65
  • [8] Effect of supplementation with antioxidants upon long-term risk of hypertension in the SU.VI.MAX study:: association with plasma antioxidant levels
    Czernichow, Sebastien
    Bertrais, Sandrine
    Blacher, Jacques
    Galan, Pilar
    Briancon, Serge
    Favier, Alain
    Safar, Michel
    Hercberg, Serge
    [J]. JOURNAL OF HYPERTENSION, 2005, 23 (11) : 2013 - 2018
  • [9] de Gasparo Marc, 2002, Heart Fail Rev, V7, P347
  • [10] DELLE M, 1990, J PHARMACOL EXP THER, V253, P646