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迟缓真杆菌培养物将地高辛还原为20R-二氢地高辛。

Reduction of digoxin to 20R-dihydrodigoxin by cultures of Eubacterium lentum.

作者信息

Robertson L W, Chandrasekaran A, Reuning R H, Hui J, Rawal B D

出版信息

Appl Environ Microbiol. 1986 Jun;51(6):1300-3. doi: 10.1128/aem.51.6.1300-1303.1986.

Abstract

The anaerobic bacterium Eubacterium lentum, a common constituent of the intestinal microflora, inactivates digoxin by reducing the unsaturated lactone ring. Reduction of the cardiac glycoside by growing cultures of E. lentum ATCC 25559 proceeded in a stereospecific manner, with the 20R-dihydrodigoxin constituting more than 99% of the product formed. This is in contrast to the 3:1 ratio of 20R and 20S epimers formed in the chemical catalytic hydrogenation. Formation of the reduced glycosides proceeded quantitatively when an overall concentration of 10 micrograms/ml was added to the cultures. E. lentum did not hydrolyze the digitoxose sugars from C-3 of the parent glycoside. However, the synthetically prepared sugar-hydrolyzed metabolites (digoxigenin, digoxigenin monodigitoxoside, and digoxigenin bisdigitoxoside) were reduced to the corresponding dihydro metabolites. Repetition of the experiments with a feces sample from a volunteer who was known to be a converter of digoxin to dihydrodigoxin gave results identical to those obtained with pure E. lentum cultures.

摘要

迟缓真杆菌是肠道微生物群的常见组成部分,属于厌氧菌,它通过还原不饱和内酯环使地高辛失活。迟缓真杆菌ATCC 25559的培养物在生长过程中对强心苷的还原具有立体特异性,生成的产物中20R - 二氢地高辛占比超过99%。这与化学催化氢化反应中形成的20R和20S差向异构体3:1的比例形成对比。当向培养物中添加的总浓度为10微克/毫升时,还原糖苷的形成是定量的。迟缓真杆菌不会从母体糖苷的C - 3位水解洋地黄毒糖。然而,合成制备的糖水解代谢产物(地高辛配基、地高辛配基单洋地黄毒糖苷和地高辛配基双洋地黄毒糖苷)会被还原为相应的二氢代谢产物。用已知会将地高辛转化为二氢地高辛的志愿者的粪便样本重复实验,得到的结果与用纯迟缓真杆菌培养物得到的结果相同。

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本文引用的文献

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Urinary excretion of reduced metabolites of digoxin.地高辛还原代谢产物的尿排泄
Am J Med. 1981 Jul;71(1):67-74. doi: 10.1016/0002-9343(81)90260-6.
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Digoxigenin biotransformation.洋地黄毒苷元生物转化
Clin Pharmacol Ther. 1982 Jun;31(6):695-704. doi: 10.1038/clpt.1982.98.
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