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[1] Tai KK, Jin WQ, Chan TYK, et al. Characterization of [3H]U69593 binding sites in the rat heart by receptor binding assays [J]. J Mol Cell Cardiol, 1991, 23(11): 1297-1302.
[2] 毕辉,朱妙章,王跃民,等.U50488H对大鼠血压的影响及机制[J]. 医学研究生学报, 2004, 17(5): 404-407.
[3] 孙 新,臧益民,王跃民,等. U50488H对大鼠肺动脉的舒张作用及机制[J].心脏杂志, 2004,16(6):513-516.
[4] Sun X, Ma S, Zang YM, et al. Vasorelaxing effect of U50488H in pulmonary artery and underlying mechanism in rats [J]. Life Sci, 2006, 78(21):2516-2522.
[5] Pei JM, Sun X, Guo HT, et al.U50488H depresses pulmonary pressure in the rats subjected to chronic hypoxia [J]. J Cardiovasc Pharmacol, 2006, 47(4):594-598.
[6] Pei JM, Chen M, Wang YM, et al. kappaopioid receptor stimulation contributes to aortic artery dilation through activation of K(ATP) channel in the rats [J]. sheng Li xue Bao, 2003, 55(1): 91-95.
[7] 陈迈, 裴建明, 李兰荪, 等. U50488H对腹主动脉的舒张作用及其机制[J].第四军医大学学报,2001, 22(1):29-32.