Imai M
Eur J Pharmacol. 1977 Feb 21;41(4):409-16. doi: 10.1016/0014-2999(77)90261-8.
Direct effects of bumetanide and furosemide on the thick ascending limb of Henle's loop (TALH) were compared by using the isolated tubules of rabbits and rats perfused in vitro. Both drugs, applied to the lumen, reversibly suppressed the lumen positive potential (PDt) of the rabbit TALH. Bumetanide also suppressed the PDt in the absence of Na+ where the NaCl of the artificial solutions was replaced by choline chloride. The efflux of 36Cl was also reduced by the addition of bumetanide to the perfusate. The dose-response analysis disclosed that bumetanide was 14 times as potent as furosemide. The onset and duration of bumetanide action was significantly longer than that of furosemide. Bumetanide also suppressed the PDt of the rat TALH when it was added to the perfusate.
通过使用体外灌注的兔和大鼠的离体肾小管,比较了布美他尼和呋塞米对亨氏袢升支粗段(TALH)的直接作用。两种药物应用于管腔时,均可可逆性地抑制兔TALH的管腔正电位(PDt)。在无Na⁺的情况下,当人工溶液中的NaCl被氯化胆碱取代时,布美他尼也可抑制PDt。向灌流液中添加布美他尼也可减少³⁶Cl的外流。剂量反应分析表明,布美他尼的效力是呋塞米的14倍。布美他尼作用的起效时间和持续时间明显长于呋塞米。当将布美他尼添加到灌流液中时,它也可抑制大鼠TALH的PDt。