Acute toxicity of gymnodimine to mice

被引:110
作者
Munday, R
Towers, NR
Mackenzie, L
Beuzenberg, V
Holland, PT
Miles, CO
机构
[1] AgRes, Ruakura Agr Res Ctr, Hamilton, New Zealand
[2] Cawthron Inst, Nelson, New Zealand
关键词
gymnodimine; acute toxicity; intraperitoneal injection; oral administration;
D O I
10.1016/j.toxicon.2004.05.017
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The acute toxicity of the phycotoxin gymnodimine to female Swiss mice by intraperitoneal injection and by oral administration has been determined. Gymnodimine was highly toxic by injection, the LD50 being only 96 mug/kg. Animals either died within 10 min of injection or made a full recovery with no perceptible long-term effects. Gymnodimine was also toxic after ;oral administration by gavage (LD50 755 mug/kg), but was much less toxic when administered with food. No signs of toxicity were seen in mice voluntarily ingesting food containing gymnodimine at a level sufficient to give a dose of similar to7500 mug/kg. Pre-treatment with physostigmine or neostigmine protected against injected gymnodimine, suggesting that the latter exerts its toxic effects via blockade of nicotinic receptors at the neuromuscular junction. The low toxicity of gymnodimine when ingested with food suggests that this compound is of low risk to humans, a conclusion that is consonant with anecdotal evidence for the absence of harmful effects in individuals consuming shellfish contaminated with gymnodimine. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:173 / 178
页数:6
相关论文
共 29 条
[1]  
Biré R, 2002, J NAT TOXINS, V11, P269
[2]  
BOKDAWALA F, 1969, REV CAN BIOL EXPTL, V28, P267
[3]  
Brown AP, 2000, CONTEMP TOP LAB ANIM, V39, P17
[4]   A COMPARISON OF THE ANTAGONISMS BY NEOSTIGMINE AND DIAMINOPYRIDINE AGAINST THE NEUROMUSCULAR BLOCK CAUSED BY COBROTOXIN AND (+)-TUBOCURARINE [J].
CHANG, CC ;
SU, MJ ;
HONG, SJ ;
SHIEH, BH ;
CHIOU, LC .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1986, 38 (02) :153-155
[5]  
DAWSON RMC, 1987, DATA BIOCH RES, P417
[6]   Toxicological comparison of a muscarinic agonist given to rats by gavage or in the diet [J].
Dethloff, LA ;
Chang, T ;
Courtney, CL .
FOOD AND CHEMICAL TOXICOLOGY, 1996, 34 (04) :407-+
[7]   Clinical pharmacology of neuromuscular blocking agents [J].
Fisher, DM .
AMERICAN JOURNAL OF HEALTH-SYSTEM PHARMACY, 1999, 56 (11) :S4-S9
[8]   Neural injury biomarkers of novel shellfish toxins, spirolides: A pilot study using immunochemical and transcriptional analysis [J].
Gill, S ;
Murphy, M ;
Clausen, J ;
Richard, D ;
Quilliam, M ;
MacKinnon, S ;
LaBlanc, P ;
Mueller, R ;
Pulido, O .
NEUROTOXICOLOGY, 2003, 24 (4-5) :593-604
[9]  
HAYWOOD AJ, 2004, IN PRESS NZ J PHYCOL
[10]   SPIROLIDE-B AND SPIROLIDE-D, 2 NOVEL MACROCYCLES ISOLATED FROM THE DIGESTIVE GLANDS OF SHELLFISH [J].
HU, TM ;
CURTIS, JM ;
OSHIMA, Y ;
QUILLIAM, MA ;
WALTER, JA ;
WATSONWRIGHT, WM ;
WRIGHT, JLC .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1995, (20) :2159-2161