Gottlieb Stephen S, Brater D Craig, Thomas Ignatius, Havranek Edward, Bourge Robert, Goldman Steven, Dyer Farere, Gomez Miguel, Bennett Donald, Ticho Barry, Beckman Evan, Abraham William T
University of Maryland School of Medicine and the D.V.A. Medical Center, Baltimore, Md, USA.
Circulation. 2002 Mar 19;105(11):1348-53. doi: 10.1161/hc1102.105264.
Adenosine may adversely affect renal function via its effects on renal arterioles and tubuloglomerular feedback, but effects of adenosine blockade in humans receiving furosemide and ACE inhibitors is unknown.
This was a randomized, double-blind, ascending-dose, crossover study evaluating 3 doses of BG9719 in 63 patients with congestive heart failure. Patients received placebo or 1 of 3 doses of BG9719 on 1 day and the same medication plus furosemide on a separate day. Renal function and electrolyte and water excretion were assessed. BG9719 alone caused an increase in urine output and sodium excretion (P<0.05). Although administration of furosemide alone caused a large diuresis, addition of BG9719 to furosemide increased diuresis, which was significant at the 0.75-microg/mL concentration. BG9719 alone improved glomerular filtration rate (GFR) at the 2 lower doses. Furosemide alone caused a decline in GFR. When BG9719 was added to furosemide, however, creatinine clearance remained at baseline at the 2 lower doses.
In patients with congestive heart failure on standard therapy, including ACE inhibitors, BG9719 increased both urine output and GFR. In these same patients, furosemide increased urine output at the expense of decreased GFR. When BG9719 was given in addition to furosemide, urine volume additionally increased and there was no deterioration in GFR. A1 adenosine antagonism might preserve renal function while simultaneously promoting natriuresis during treatment for heart failure.
腺苷可能通过对肾小动脉和肾小管-肾小球反馈的作用而对肾功能产生不利影响,但腺苷阻断剂对接受呋塞米和血管紧张素转换酶抑制剂治疗的患者的影响尚不清楚。
这是一项随机、双盲、剂量递增、交叉研究,评估了63例充血性心力衰竭患者使用3种剂量的BG9719的情况。患者在一天接受安慰剂或3种剂量的BG9719中的一种,在另一天接受相同药物加呋塞米。评估肾功能、电解质和水排泄情况。单独使用BG9719可导致尿量和钠排泄增加(P<0.05)。虽然单独使用呋塞米可引起大量利尿,但在呋塞米中加入BG9719可增加利尿,在0.75微克/毫升浓度时具有显著意义。单独使用BG9719在较低的两种剂量下可改善肾小球滤过率(GFR)。单独使用呋塞米可导致GFR下降。然而,当在呋塞米中加入BG9719时,在较低的两种剂量下肌酐清除率仍保持在基线水平。
在接受包括血管紧张素转换酶抑制剂在内的标准治疗的充血性心力衰竭患者中,BG9719可增加尿量和GFR。在这些相同的患者中,呋塞米增加尿量但以降低GFR为代价。当在呋塞米基础上给予BG9719时,尿量进一步增加且GFR没有恶化。A1腺苷拮抗作用可能在心力衰竭治疗期间保护肾功能,同时促进利钠作用。