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葡萄球菌α毒素的抑制作用。芳香族聚磺酸对小鼠α毒素致死作用的影响。

Inhibition of staphylococcal alpha-toxin. The effect of aromatic polysulphonic acids on the lethal effect of alpha-toxin in mice.

作者信息

Arbuthnott J P, Lominski I R, Wright M R

出版信息

Biochem J. 1968 Jun;108(1):49-55. doi: 10.1042/bj1080049.

Abstract
  1. Certain aromatic polysulphonic acids, previously tested for inhibition of the haemolytic activity of staphylococcal alpha-toxin, together with some additional related compounds, were tested as possible inhibitors of alpha-toxin in mice. 2. Compounds that inhibited the haemolytic activity of alpha-toxin at concentrations of 0.16mm or less [compounds (I), (II), (IV), (V), (VII) and (VIII)] were found to inhibit the lethal effect of alpha-toxin. 3. With the exception of compound (VIII), amounts of 1mg. were required to inhibit 4 LD(50) of toxin when the test compounds were premixed with alpha-toxin before injection; comparable inhibition with 0.3mg. of compound (VIII) was achieved without prolonged premixing. 4. Mixtures of alpha-toxin and compounds (I) and (II) containing an excess of test compound showed markedly diminished inhibitory activities. 5. The ;half-molecule' analogues of group 1 [compounds (III) and (XVIII)] were non-inhibitory. 6. Compounds (I)-(V), when administered separately from alpha-toxin by the same route (intraperitoneal), were active only when injected almost simultaneously with toxin, whereas compounds (VII) and (VIII) were strikingly inhibitory when injected 15min. before or after the toxin. 7. Compound (VIII) failed to inhibit the lethal effect of alpha-toxin when injected by a different route (intravenous).
摘要
  1. 某些先前已测试过对葡萄球菌α毒素溶血活性抑制作用的芳香族聚磺酸,连同一些额外的相关化合物,作为小鼠体内α毒素的可能抑制剂进行了测试。2. 发现在浓度为0.16毫米或更低时能抑制α毒素溶血活性的化合物(化合物(I)、(II)、(IV)、(V)、(VII)和(VIII))能抑制α毒素的致死作用。3. 除化合物(VIII)外,当测试化合物在注射前与α毒素预混合时,需要1毫克的量来抑制4个半数致死量的毒素;在不进行长时间预混合的情况下,0.3毫克的化合物(VIII)能达到类似的抑制效果。4. 含有过量测试化合物的α毒素与化合物(I)和(II)的混合物显示出明显降低的抑制活性。5. 第1组的“半分子”类似物(化合物(III)和(XVIII))无抑制作用。6. 化合物(I) - (V)通过相同途径(腹腔内)与α毒素分开给药时,仅在几乎与毒素同时注射时才有活性,而化合物(VII)和(VIII)在毒素注射前15分钟或后注射时具有显著的抑制作用。7. 当通过不同途径(静脉内)注射时,化合物(VIII)未能抑制α毒素的致死作用。

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