Tashiro S, Matsumura F
Arch Environ Contam Toxicol. 1978;7(1):113-27. doi: 10.1007/BF02332042.
The metabolic fate of trans-nonachlor and heptachlor in rats was studied in vivo and in vitro by using microsomal preparations of the liver. During in vivo studies the rate of excretion into urine and feces was monitored. The major metabolic products were collected from the feces and their chemical structures were determined by using various chromatographic and spectroscopic techniques. The immediate major metabolic product of transnonachlor is trans-chlordane which is further converted to 1,2-dichlorochlordene and to oxychlordane. From the latter metabolite, two major stable products, 1-hydroxy-2-chlorochlordene and 1-hydroxy-2-chloro-2,3-epoxy-chlordene are formed. Another route of metabolism is a direct formation of chlordene chlorohydrin which acts as a precursor for 1,2-trans-dihydroxydi-hydrochlordene. The major metabolic products of heptachlor were heptachlor epoxide, 1-exo-hydroxyheptachlor epoxide and 1,2-dihydroxy-dihydrochlordene.
利用大鼠肝脏微粒体制剂,对反式九氯和七氯在大鼠体内和体外的代谢命运进行了研究。在体内研究过程中,监测了尿液和粪便中的排泄速率。从粪便中收集主要代谢产物,并使用各种色谱和光谱技术确定其化学结构。反式九氯的直接主要代谢产物是反式氯丹,其进一步转化为1,2-二氯氯丹和氧氯丹。从后一种代谢产物中,形成了两种主要的稳定产物,即1-羟基-2-氯氯丹和1-羟基-2-氯-2,3-环氧氯丹。另一条代谢途径是直接形成氯丹氯醇,它是1,2-反式二羟基二氢氯丹的前体。七氯的主要代谢产物是七氯环氧化物、1-外向羟基七氯环氧化物和1,2-二羟基二氢氯丹。