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由冰岛青霉分离出的环氯素所诱导的肝损伤。

Liver injuries induced by cyclochlorotine isolated from Penicillium islandicum.

作者信息

Terao K, Ito E, Tatsuno T

出版信息

Arch Toxicol. 1984 Mar;55(1):39-46. doi: 10.1007/BF00316584.

DOI:10.1007/BF00316584
PMID:6732503
Abstract

Sequential morphological changes in murine liver induced by cyclochlorotine (CC), a secondary metabolite of Penicillium islandicum were investigated by transmission electron microscopy and scanning electron microscopy. Within 15 min after the administration of CC there was a marked dilatation of Disse's space around the portal triads, and the exudates then poured out into the space which was formed by the invagination of the hepatocyte plasma membrane. Shortly after the invagination was completed, the connection between Disse's space and the invaginated space was pinched off, so that this space became a membrane-bound vacuole. After dehydration, the vacuoles became granular. The liver injuries induced by CC were influenced by various pretreatments. The results indicate that drug-metabolizing systems mediated by cytochrome p-450 in the hepatocytes may play an important role in the hepatotoxicity of CC.

摘要

通过透射电子显微镜和扫描电子显微镜研究了由冰岛青霉的次生代谢产物环氯素(CC)诱导的小鼠肝脏的连续形态变化。给予CC后15分钟内,门三联周围的狄氏间隙明显扩张,渗出物随后倒入由肝细胞质膜内陷形成的间隙中。内陷完成后不久,狄氏间隙与内陷间隙之间的连接被掐断,使得这个间隙变成一个膜结合的液泡。脱水后,液泡变成颗粒状。CC诱导的肝损伤受各种预处理的影响。结果表明,肝细胞中由细胞色素p-450介导的药物代谢系统可能在CC的肝毒性中起重要作用。

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本文引用的文献

1
Liver cirrhosis induced by metabolites of Penicillium islandicum Sopp.
Acta Pathol Jpn. 1959 Nov;9(Suppl):785-90. doi: 10.1111/j.1440-1827.1959.tb02966.x.
2
EFFECT OF DRUGS ON THE FORMATION OF SMOOTH ENDOPLASMIC RETICULUM AND DRUG-METABOLIZING ENZYMES.药物对滑面内质网形成及药物代谢酶的影响
Ann N Y Acad Sci. 1965 Mar 12;123:79-97. doi: 10.1111/j.1749-6632.1965.tb12247.x.
3
MORPHOLOGICAL CHANGES IN THE LIVER ACCOMPANYING STIMULATION OF MICROSOMAL DRUG METABOLIZING ENZYME ACTIVITY BY PHENOBARBITAL, CHLORDANE, BENZPYRENE OR METHYL-CHOLANTHRENE IN RATS.苯巴比妥、氯丹、苯并芘或甲基胆蒽刺激大鼠微粒体药物代谢酶活性时肝脏的形态学变化
J Pharmacol Exp Ther. 1965 Jan;147:112-9.
4
[STUDIES ON THE TOXIC EFFECTS OF A CHLORINE-CONTAINING PEPTIDE (ISLANDITOXIN) PRODUCED BY PENICILLIUM ISLANDICUM SOPP GROWN ON YELLOW RICE. 1. EXPERIMENTAL STUDY ON ACUTE LIVER INJURIES CAUSED BY ISLANDITOXIN].
Tokyo Igaku Zasshi. 1964 Jun;72:136-53.
5
DRUG-INDUCED CHANGES IN THE LIVER ENDOPLASMIC RETICULUM: ASSOCIATION WITH DRUG-METABOLIZING ENZYMES.药物诱导的肝脏内质网变化:与药物代谢酶的关联
Science. 1963 Dec 27;142(3600):1657-8. doi: 10.1126/science.142.3600.1657.
6
Changes in the fine structure of rat liver cells brought about by dimethylnitrosamine.二甲基亚硝胺引起的大鼠肝细胞精细结构的变化。
J Biophys Biochem Cytol. 1960 Apr;7(2):393-6. doi: 10.1083/jcb.7.2.393.
7
Study of the toxic principle in yellow rice.黄米中毒素原理的研究。
Pharm Bull. 1955 Dec;3(6):476-7. doi: 10.1248/cpb1953.3.476.
8
Zonal changes in the rat liver following an acute dose of phenobarbitone: an ultrastructural, morphometric and biochemical correlation.急性给予苯巴比妥后大鼠肝脏的区域变化:超微结构、形态计量学及生化相关性研究
Chem Biol Interact. 1981 Feb;34(1):31-8. doi: 10.1016/0009-2797(81)90087-9.
9
Different tissue responses of mixed function oxidases and detoxifying enzymes to aflatoxin B1 administration in the rat.大鼠体内混合功能氧化酶和解毒酶对黄曲霉毒素B1给药的不同组织反应。
Br J Exp Pathol. 1980 Dec;61(6):611-6.
10
Toxicologic enhancement by a combination of drugs which deplete hepatic glutathione: acetaminophen and doxorubicin (adriamycin).通过联合使用消耗肝脏谷胱甘肽的药物实现的毒理学增强作用:对乙酰氨基酚和阿霉素(多柔比星)。
Toxicol Appl Pharmacol. 1980 Jun 30;54(2):197-209. doi: 10.1016/0041-008x(80)90187-8.