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本文引用的文献

1
A Selective Staining Method for the Basic Proteins of Cell Nuclei.一种细胞核碱性蛋白质的选择性染色方法。
Proc Natl Acad Sci U S A. 1953 Oct;39(10):991-9. doi: 10.1073/pnas.39.10.991.
2
Protein measurement with the Folin phenol reagent.使用福林酚试剂进行蛋白质测定。
J Biol Chem. 1951 Nov;193(1):265-75.
3
THE CARBON MONOXIDE-BINDING PIGMENT OF LIVER MICROSOMES. II. SOLUBILIZATION, PURIFICATION, AND PROPERTIES.肝微粒体的一氧化碳结合色素。II. 增溶、纯化及性质
J Biol Chem. 1964 Jul;239:2379-85.
4
Microsomal triphosphopyridine nucleotide-cytochrome c reductase of liver.肝脏微粒体三磷酸吡啶核苷酸-细胞色素c还原酶
J Biol Chem. 1962 Feb;237:587-95.
5
A study of the conditions and mechanism of the diphenylamine reaction for the colorimetric estimation of deoxyribonucleic acid.用于比色法测定脱氧核糖核酸的二苯胺反应的条件及机制研究。
Biochem J. 1956 Feb;62(2):315-23. doi: 10.1042/bj0620315.
6
An electron microscopic study of the fenestrated endothelial lining of rat liver sinusoids.大鼠肝血窦有孔内皮衬里的电子显微镜研究。
J Ultrastruct Res. 1970 Apr;31(1):125-50. doi: 10.1016/s0022-5320(70)90150-4.
7
Drug metabolism in tumor-bearing rats. I. Activities of NADPH-linked electron transport and drug-metabolizing enzyme systems in liver microsomes of tumor-bearing rats.荷瘤大鼠的药物代谢。I. 荷瘤大鼠肝微粒体中与NADPH相关的电子传递和药物代谢酶系统的活性。
Jpn J Pharmacol. 1968 Jun;18(2):224-44.
8
Modification of hexobarbital metabolism by Morris hepatoma 5123tc.莫里斯肝癌5123tc对己巴比妥代谢的影响
Can J Physiol Pharmacol. 1967 Nov;45(6):975-83. doi: 10.1139/y67-115.
9
The effect of phenobarbital on drug metabolic enzyme activity, ultrastructure and growth of a "minimal deviation" hepatoma (Morris 7800).苯巴比妥对“微小偏离”肝癌(莫里斯7800)药物代谢酶活性、超微结构及生长的影响
J Pharmacol Exp Ther. 1967 Jul;157(1):227-44.
10
Abnormal microsomal cytochromes and electron transport in Morris hepatomas.莫里斯肝癌中异常的微粒体细胞色素和电子传递
J Biol Chem. 1974 Mar 25;249(6):1980-7.

人类和大鼠肝脏肿瘤附近肝脏内增强的药物代谢能力。

Enhanced drug-metabolizing capacity within liver adjacent to human and rat liver tumors.

作者信息

Sultatos L G, Vesell E S

出版信息

Proc Natl Acad Sci U S A. 1980 Jan;77(1):600-3. doi: 10.1073/pnas.77.1.600.

DOI:10.1073/pnas.77.1.600
PMID:6244568
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC348322/
Abstract

Cytochrome P-450 content (nmol/g of liver) differed within regions of rat liver according to proximity to intrahepatically implanted Morris hepatoma 7795 or 5123D. Liver adjacent to tumor had higher microsomal cytochrome P-450 content, decreased DNA content (mg/g of liver), and unaltered cytochrome c reductase activity compared to histologically indistinguishable liver far-removed from the tumor. Liver either adjacent to or far-removed from tumor contained markedly more cytochrome P-450 and higher cytochrome c reductase activity but less DNA than transplanted Morris hepatomas 7795 and 5123D that were grown intrahepatically. Compared to intramuscular implants of these same tumors, intrahepatically implanted Morris hepatomas 7795 and 5123D had increased cytochrome P-450 content. Tumor-containing liver from two human subjects revealed regional changes in cytochrome P-450-mediated monooxygenases similar to those observed in rats. These results suggest that histomorphically nontumorous mammalian liver directly adjacent to intrahepatic tumors exhibits previously unsuspected biochemical alterations.

摘要

根据与肝内植入的莫里斯肝癌7795或5123D的接近程度,大鼠肝脏各区域的细胞色素P - 450含量(nmol/g肝脏)有所不同。与组织学上无法区分的远离肿瘤的肝脏相比,靠近肿瘤的肝脏微粒体细胞色素P - 450含量更高,DNA含量(mg/g肝脏)降低,细胞色素c还原酶活性未改变。与肝内生长的移植性莫里斯肝癌7795和5123D相比,无论是靠近肿瘤还是远离肿瘤的肝脏,其细胞色素P - 450含量明显更高,细胞色素c还原酶活性更高,但DNA含量更低。与这些相同肿瘤的肌肉内植入相比,肝内植入的莫里斯肝癌7795和5123D的细胞色素P - 450含量增加。来自两名人类受试者的含肿瘤肝脏显示出细胞色素P - 450介导的单加氧酶的区域变化,类似于在大鼠中观察到的变化。这些结果表明,与肝内肿瘤直接相邻的组织形态学上无肿瘤的哺乳动物肝脏表现出以前未被怀疑的生化改变。