Lindenbaum J, Maulitz R M, Butler V P
Gastroenterology. 1976 Sep;71(3):399-404.
The effect of the administration of the antibiotic neomycin sulfate on the absorption of digoxin was assessed in crossover studies in normal human volunteers. Doses of neomycin (1 and 3 g) markedly depressed serum digoxin concentrations, the areas under the serum concentration-time curves, and cumulative 6-day urinary digoxin excretion after the oral ingestion of 0.5 mg of the cardiac glycoside in tablet form. Neomycin also prolonged the mean time at which peak serum digoxin levels were attained by 1.7 to 3 hr. The inhibition of digoxin absorption was also seen: (1) when the antibiotic was given 3 or 6 hr before the cardiac glycoside, (2) with digoxin tablets of varying dissolution rate, (3) when digoxin or neomycin solutions were used instead of tablets, and (4) in a patient who had had a total gastrectomy. When neomycin was administered with maintenance doses of digoxin, steady state serum digoxin concentrations were significantly reduced. When neomycin was given after a 9-day period of digitalization, the terminal serum digoxin half-life was not significantly shortened. Single doses of neomycin did not interfere with the extent of absorption of d-xylose. In vitro, neomycin did not affect the movement of digoxin across dialysis membranes, nor did it precipitate digoxin out of human bile or intestinal fluid. Neomycin thus clearly depresses the rate and extent of digoxin absorption in man. The mechanism of this effect remains to be established.
在正常人类志愿者的交叉研究中评估了抗生素硫酸新霉素给药对地高辛吸收的影响。新霉素剂量为1克和3克时,显著降低了血清地高辛浓度、血清浓度-时间曲线下面积以及口服0.5毫克片剂形式的强心苷后6天的地高辛累积尿排泄量。新霉素还使达到血清地高辛峰值水平的平均时间延长了1.7至3小时。还观察到地高辛吸收受到抑制:(1)在强心苷给药前3或6小时给予抗生素时;(2)使用不同溶出速率的地高辛片剂时;(3)使用地高辛或新霉素溶液而非片剂时;(4)在一名全胃切除患者中。当新霉素与维持剂量的地高辛一起给药时,稳态血清地高辛浓度显著降低。在数字化9天后给予新霉素时,血清地高辛终末半衰期没有显著缩短。单次剂量的新霉素不干扰d-木糖的吸收程度。在体外,新霉素不影响地高辛穿过透析膜的移动,也不会使地高辛从人胆汁或肠液中沉淀出来。因此,新霉素明显降低了人体内地高辛的吸收速率和程度。这种作用的机制尚待确定。