首页> 外文期刊>Japanese Journal of Pharmacology >REVERSIBLE EFFECTS OF MONOTHIOL (D-PENICILLAMINE) AND DITHIOL (DIMERCAPTOSUCCINIC ACID) CHELATING COMPOUNDS ON METHYLMERCURY-INHIBITED CHOLINE ACETYLTRANSFERASE ACTIVITY AND HIGH AFFINITY CHOLINE UPTAKE
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REVERSIBLE EFFECTS OF MONOTHIOL (D-PENICILLAMINE) AND DITHIOL (DIMERCAPTOSUCCINIC ACID) CHELATING COMPOUNDS ON METHYLMERCURY-INHIBITED CHOLINE ACETYLTRANSFERASE ACTIVITY AND HIGH AFFINITY CHOLINE UPTAKE

机译:单点(D-青霉胺)和二硫醇(二巯基琥珀酸)螯合化合物对甲基汞抑制胆碱乙酰转移酶活性和高亲和力胆碱摄取的可逆效应

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References(37) Cited-By(5) The effects of thiol compounds on methylmercury chloride (MMC)-inhibited choline acetyltransferase (ChAT) activity and MMCinhibited high affinity choline uptake of rat brain tissue were studied in vitro. D-penicillamine (D-Pc) and dimercaptosuccinic acid (DMS) reversed the MMC-inhibited ChAT activity dose-dependently. Equilibrium dialysis of MMC-inhibited ChAT against the buffer containing 10-3M D-Pc reversed the ChAT activity almost completely. The reversal effect of D-Pc (monothiol compound) on MMC-inhibited ChAT was significantly more potent than that of DMS (dithiol compound). D-Pc and DMS almost equally reversed the MMC-inhibited high affinity choline uptake by synaptosomes in a dose dependent fashion. Washing with a solution containing D-Pc or DMS equally reversed the MMC-inhibited high affinity choline uptake in a dosedependent fashion. Neither D-Pc nor DMS could reverse the hemicholinium-3-inhibited high affinity choline uptake.
机译:引用(37)在体外研究了(5)对甲基氯化甲醇化合物对甲基汞(MMC) - 抑制胆碱乙酰转移酶(聊天)活性和MM抑制的高亲和力胆碱的影响。 D-青霉胺(D-PC)和二巯基琥珀酸(DMS)依赖于MMC抑制的聊天活动。 MMC禁止聊天的平衡透析对含有10-3M D-PC的缓冲区几乎完全反转聊天活动。 D-PC(单点化合物)对MMC抑制聊天的反转效果显着高于DMS(二硫醇化合物)的效率。 D-PC和DMS几乎同样逆转MMC抑制的高亲和力胆碱,其在剂量依赖性时的时装。用含有D-PC或DMS的溶液洗涤同样逆转MMC抑制的高亲和力胆碱摄取,以依赖性的方式。 D-PC和DMS都不能逆转血清腺素-3抑制的高亲和力胆碱摄取。

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