Zhao D Y, Dhalla N S
Division of Cardiovascular Sciences, St. Boniface General Hospital Research Centre, Winnipeg, Man., Canada.
Can J Physiol Pharmacol. 1989 Jun;67(6):546-52. doi: 10.1139/y89-088.
The effects of gramicidin S (GS), an antibiotic, on the rat heart membrane ATPases and contractile activity of the right ventricle strips were investigated. GS inhibited sarcolemmal Ca2+-stimulated ATPase (IC50 = 3 microM), Ca2+/Mg2+ ATPase which is activated by millimolar Ca2+ or Mg2+ (IC50 = 3.4 microM), and sarcoplasmic reticulum Ca2+-stimulated ATPase (IC50 = 6 microM). The type of inhibition for the sarcolemmal Ca2+/Mg2+ ATPase by GS was apparently uncompetitive, while that for Ca2+-stimulated ATPases in sarcolemma or sarcoplasmic reticulum was of mixed type. Other ATPases, including mitochondrial ATPase, sarcolemmal Na+-K+ ATPase, and myofibrillar ATPase, were not inhibited by this agent. GS also decreased the rat right ventricle maximum force development (half-maximal inhibitory concentration was 2-4 microM), maximum velocity of contraction, and maximum velocity of relaxation. The resting tension was increased by GS to over 200%. The contractile actions of GS were mostly irreversible upon washing the muscle 3 times over a 10-min period. Decreased Ca2+, Mg2+, Na+, K+ concentrations in the perfusate increased the effects of GS. These findings showed that GS was a potent inhibitor of divalent cation ATPases of heart sarcolemma and sarcoplasmic reticulum and it is suggested that these membrane effects may explain the cardiodepressant action of this agent.
研究了抗生素短杆菌肽S(GS)对大鼠心脏膜ATP酶及右心室条带收缩活性的影响。GS抑制肌膜Ca2+刺激的ATP酶(IC50 = 3 microM)、由毫摩尔浓度的Ca2+或Mg2+激活的Ca2+/Mg2+ ATP酶(IC50 = 3.4 microM)以及肌浆网Ca2+刺激的ATP酶(IC50 = 6 microM)。GS对肌膜Ca2+/Mg2+ ATP酶的抑制类型明显为非竞争性,而对肌膜或肌浆网中Ca2+刺激的ATP酶的抑制类型为混合型。其他ATP酶,包括线粒体ATP酶、肌膜Na+-K+ ATP酶和肌原纤维ATP酶,不受该药物抑制。GS还降低了大鼠右心室的最大力发展(半数最大抑制浓度为2 - 4 microM)、最大收缩速度和最大舒张速度。静息张力被GS提高到超过200%。在10分钟内将肌肉洗涤3次后,GS的收缩作用大多不可逆。灌注液中Ca2+、Mg2+、Na+、K+浓度降低会增强GS的作用。这些发现表明,GS是心脏肌膜和肌浆网二价阳离子ATP酶的有效抑制剂,提示这些膜效应可能解释了该药物的心脏抑制作用。