The influence of porphyrogenic drugs on the glyoxalase enzymes.

R Van Brummelen, S Myburgh, S H Bissbort
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Abstract

A variety of drugs, known to induce acute attacks in porphyric patients has been found to inhibit the glyoxalase pathway. Glyoxalase I is competitively inhibited by sulphadimidine, oxytetracycline, chloramphenicol, etc. Allylisopropyl acetamide (AIA) seems to inhibit glyoxalase II. This inhibition could play a contributing role in the overproduction of porphyrins in porphyria and thus help explain the mechanism of induction of porphyric attacks. The results indicate, that the Heme pathway and the glyoxalase cycle are closely connected.

致卟啉药物对乙二醛酶的影响。
多种已知可诱导卟啉症患者急性发作的药物已被发现可抑制乙二醛酶途径。乙二醛酶I被磺胺、土霉素、氯霉素等竞争性抑制。烯丙基异丙基乙酰胺(AIA)似乎抑制乙醛酶II。这种抑制作用可能在卟啉症中卟啉的过量产生中起促进作用,从而有助于解释诱导卟啉发作的机制。结果表明,血红素途径与乙二醛酶循环密切相关。
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