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呋喃唑酮在海水养殖沉积物中的归宿及微生物学效应

Fate and microbiological effects of furazolidone in a marine aquaculture sediment.

作者信息

Samuelsen O B, Solheim E, Lunestad B T

机构信息

Department of Pharmacology and Toxicology, School of Medicine, University of Bergen, Norway.

出版信息

Sci Total Environ. 1991 Oct 15;108(3):275-83. doi: 10.1016/0048-9697(91)90364-k.

DOI:10.1016/0048-9697(91)90364-k
PMID:1754880
Abstract

Furazolidone is used in the treatment of bacterial diseases in farmed fish. During application a large proportion of the administered drug reaches the environment directly or via feces. The persistence and metabolism of furazolidone in sediment from a Norwegian salmon farm is described. Furazolidone, in contrast to oxytetracycline and oxolinic acid, is actively metabolized by microorganisms in the sediment. The main metabolite is 3-(4-cyano-2-oxobutylidene-amino)-2-oxazolidone. This is a well known metabolite of the degradation of furazolidone in mammals, fish and Escherichia coli. 3-(4-Cyano-2-oxobutylideneamino)-2- oxazolidone had no detectable antibacterial activity. The half-life of furazolidone in the sediment at 4 degrees C was calculated to be 18 h.

摘要

呋喃唑酮用于治疗养殖鱼类的细菌性疾病。在使用过程中,很大一部分施用的药物直接或通过粪便进入环境。本文描述了呋喃唑酮在挪威鲑鱼养殖场沉积物中的持久性和代谢情况。与土霉素和恶喹酸不同,呋喃唑酮在沉积物中会被微生物积极代谢。主要代谢产物是3-(4-氰基-2-氧代丁烯基)-氨基-2-恶唑烷酮。这是呋喃唑酮在哺乳动物、鱼类和大肠杆菌中降解的一种众所周知的代谢产物。3-(4-氰基-2-氧代丁烯基)-氨基-2-恶唑烷酮没有可检测到的抗菌活性。在4摄氏度下,呋喃唑酮在沉积物中的半衰期经计算为18小时。

相似文献

1
Fate and microbiological effects of furazolidone in a marine aquaculture sediment.呋喃唑酮在海水养殖沉积物中的归宿及微生物学效应
Sci Total Environ. 1991 Oct 15;108(3):275-83. doi: 10.1016/0048-9697(91)90364-k.
2
Disposition of 3-(4-cyano-2-oxobutylidene amino)-2-oxazolidone, a cyano-metabolite of furazolidone, in furazolidone-treated grouper.
Food Addit Contam. 2003 Mar;20(3):229-36. doi: 10.1080/0265203021000043930.
3
[The residue behavior of the furazolidone metabolite 3-(4-cyano-2-oxobutylideneamino)-2-oxazolidone in trout].[呋喃唑酮代谢物3-(4-氰基-2-氧代丁叉氨基)-2-恶唑烷酮在鳟鱼体内的残留行为]
Z Lebensm Unters Forsch. 1990 Oct-Nov;191(4-5):319-21. doi: 10.1007/BF01202435.
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The elimination of furazolidone and its open-chain cyano-derivative from adult swine.成年猪体内呋喃唑酮及其开链氰基衍生物的消除情况。
Xenobiotica. 1987 Dec;17(12):1427-35. doi: 10.3109/00498258709044003.
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Metabolism in vivo of furazolidone: evidence for formation of an open-chain carboxylic acid and alpha-ketoglutaric acid from the nitrofuran in rats.呋喃唑酮在大鼠体内的代谢:硝基呋喃在大鼠体内形成开链羧酸和α-酮戊二酸的证据。
Arch Biochem Biophys. 1984 Oct;234(1):112-6. doi: 10.1016/0003-9861(84)90330-8.
6
Reductive metabolism of furazolidone by Escherichia coli and rat liver in vitro.呋喃唑酮在体外经大肠杆菌和大鼠肝脏的还原代谢。
Drug Metab Dispos. 1984 Nov-Dec;12(6):732-41.
7
Determinations of residual furazolidone and its metabolite, 3-amino-2-oxazolidinone (AOZ), in fish feeds by HPLC-UV and LC-MS/MS, respectively.分别采用高效液相色谱-紫外检测法(HPLC-UV)和液相色谱-串联质谱法(LC-MS/MS)测定鱼饲料中残留的呋喃唑酮及其代谢物3-氨基-2-恶唑烷酮(AOZ)。
J Agric Food Chem. 2007 Feb 21;55(4):1144-9. doi: 10.1021/jf062902a.
8
Identification of a reactive intermediate of furazolidone formed by swine liver microsomes.猪肝脏微粒体形成的呋喃唑酮反应中间体的鉴定。
Chem Biol Interact. 1987;64(1-2):167-79. doi: 10.1016/0009-2797(87)90069-x.
9
Reversible interaction of a reactive intermediate derived from furazolidone with glutathione and protein.
Toxicol Appl Pharmacol. 1988 Aug;95(1):53-60. doi: 10.1016/s0041-008x(88)80007-3.
10
Identification of a furazolidone metabolite responsible for the inhibition of amino oxidases.鉴定一种负责抑制氨基酸氧化酶的呋喃唑酮代谢物。
Xenobiotica. 2003 Feb;33(2):153-67. doi: 10.1080/0049825021000038459.

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