|1.||Haleen, Stephen J: 1 article (08/2002)|
|2.||Coceani, Flavio: 1 article (08/2002)|
|3.||Liu, You-An: 1 article (08/2002)|
|4.||Coe, Yashu: 1 article (08/2002)|
|5.||Welch, Kathleen M: 1 article (08/2002)|
|6.||Johengen, M J: 1 article (02/2001)|
|7.||Black, S M: 1 article (02/2001)|
|8.||McMullan, D M: 1 article (02/2001)|
|9.||Gerrets, R: 1 article (02/2001)|
|10.||Fineman, J R: 1 article (02/2001)|
07/01/1996 - "In myocardial infarction studies, micropigs received either saline vehicle (n = 7) or PD 156707 (n = 8) at a loading dose of 10 mg/kg/1 hr, followed by a maintenance dose of 7 mg/kg/hr. Coinciding with the start of the maintenance dose, the left anterior descending coronary artery was occluded for 1 hr followed by 3 hr of reperfusion. "
|2.||Pulmonary Hypertension (Ayerza Syndrome)
02/01/2001 - "The objectives of this study were to determine the effects of inhaled NO on endogenous ET-1 production in vivo in the intact lamb and to determine the potential role of ET-1 in the rebound pulmonary hypertension associated with the withdrawal of inhaled NO. Seven 1-mo-old vehicle-treated control lambs and six PD-156707 (an ET(A) receptor antagonist)-treated lambs were mechanically ventilated. "
01/01/1999 - "Three nephrectomized groups that did not undergo ischemia but that received infusions of saline (N = 6), PD 156707 (N = 6), and SB 209670 (N = 6), respectively, were also studied. "
01/01/1999 - "Twenty-four hours after renal ischemia, one of two ETR antagonists, PD 156707 (N = 7) or SB 209670 (N = 8), was administered. "
08/01/2002 - "Consistent with findings in vivo, when using isolated pulmonary resistance arteries from term fetal lamb, PD 156707 curtailed the hypoxia- but not the ONO-11113-induced constriction. "
08/01/2002 - "We conclude that PD 156707 and PD 180988 are selective inhibitors of pulmonary vasoconstriction resulting from hypoxia. "