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1.
Food Chem ; 138(2-3): 751-6, 2013 Jun 01.
Article in English | MEDLINE | ID: mdl-23411171

ABSTRACT

The anti-inflammatory effects of an aqueous extract of Welsh onion green leaves (WOE) in mice was investigated. Administration of WOE, in the range of 0.25-1g/kg, showed a concentration dependent inhibition on paw edema development after carrageenan treatment in mice. The anti-inflammatory effects of WOE were closely attributed to decreased levels of tissue NO and tumor necrosis factor-α (TNF-α). Further evidence for WOE's protection is shown in the reduction of lipid oxidation and the increase of antioxidant enzyme activities, including catalase (CAT), superoxide dismutase (SOD), and glutathione peroxidase (GPX) in vivo. Further, WOE also decreased the number of acetic acid-induced writhing responses and formalin-induced pain in the late phase in mice. Overall, the results showed that WOE might serve as a natural source of anti-inflammatory compounds.


Subject(s)
Anti-Inflammatory Agents/administration & dosage , Edema/drug therapy , Onions/chemistry , Plant Extracts/administration & dosage , Animals , Edema/chemically induced , Edema/immunology , Humans , Male , Mice , Mice, Inbred ICR , Phytotherapy , Plant Leaves/chemistry , Tumor Necrosis Factor-alpha/immunology
2.
J Chromatogr A ; 1217(31): 5130-6, 2010 Jul 30.
Article in English | MEDLINE | ID: mdl-20591436

ABSTRACT

Spermine-graft-dextran (Spe-g-Dex) copolymer was synthesized and used as a non-covalent coating for the separation of proteins and neurotransmitters by capillary electrophoresis. The coating was obtained via flushing the capillary with 1.0% Spe-g-Dex copolymer solution for 2min. Electroosmotic flow (EOF) was strongly suppressed, ranging from -1.60x10(-9) to 3.65x10(-9)m(2)V(-1)s(-1). Effect of experimental conditions, such as the copolymer concentration, the concentration and pH of the background electrolyte (BGE), on the Spe-g-Dex coating was investigated. Separation of lysozyme, cytochrome c, ribonuclease A and alpha-chymotrypsinogen yielded high separation efficiencies ranging from 141000 to 303000plates/m and recoveries from 85.4% to 98.3% at pH 4.0 (284.0mM sodium acetate-acetic acid buffer, I=50mM). Run-to-run repeatabilities and day-to-day, and capillary-to-capillary reproducibilities were all below 1.7%. In addition, Spe-g-Dex coating allowed the successful separation of five neurotransmitters, 5-hydroxytryptamine, dopamine, epinephrine, isoprenaline, dobuamine at pH 4.0 with high separation efficiencies of 290000-449000plates/m.


Subject(s)
Electrophoresis, Capillary/instrumentation , Electrophoresis, Capillary/methods , Neurotransmitter Agents/isolation & purification , Polymers/chemistry , Proteins/isolation & purification , Animals , Dextrans/chemistry , Neurotransmitter Agents/analysis , Protein Binding , Proteins/analysis , Spermine/chemistry
3.
Shokuhin Eiseigaku Zasshi ; 44(1): 49-53, 2003 Feb.
Article in English | MEDLINE | ID: mdl-12749197

ABSTRACT

The effect of exogenous polyamines (cadaverine, putrescine, norspermidine, spermidine, and spermine) on the growth, toxicity, and toxin profile of the dinoflagellate Alexandrium minutum T1 was examined. It was found that cadaverine at concentrations of 0.1-2.0 mumol/L enhanced the growth of A. minutum T1. Putrescine and norspermidine at a low level (0.1 mumol/L) also promoted the algal growth. Spermidine depressed the algal growth. However, the cell toxicity levels of A. minutum T1 cultured with or without cadaverine, putrescine, norspermidine, and spermidine were almost the same. The toxic components of A. minutum T1 were GTXs 1-4 only, and GTXs 1 and 4 were predominant (74.6 +/- 7.1%) in all cultures. On the other hand, spermine did not effect the growth of A. minutum T1, though it decreased the cell toxicity and the ratio of GTX 2 + GTX 3 (15.0 +/- 6.6%).


Subject(s)
Dinoflagellida/drug effects , Dinoflagellida/growth & development , Marine Toxins/biosynthesis , Polyamines/pharmacology , Spermidine/analogs & derivatives , Animals , Cadaverine/pharmacology , Putrescine/pharmacology , Spermidine/pharmacology , Spermine/pharmacology
4.
Toxicon ; 41(4): 529-33, 2003 Mar.
Article in English | MEDLINE | ID: mdl-12657324

ABSTRACT

The toxins in the new gastropods Oliva miniacea, O. mustelina and O. nirasei implicated in a food paralytic poisoning incident in South Taiwan in February 2002 were studied. It was found that the three species of gastropods contained moderate amounts of toxin in edible portion only, and the highest toxicity score was 18 MU/g for O. miniacea, 10 MU/g for O. mustelina, and 27 MU/g for O. nirasei. The toxin was partially purified from the toxic specimens of each species by ultrafiltration using a YM-1 membrane, followed by chromatography on Bio-Gel P-2 column. Analyses by HPLC, GC-MS and LC-MS showed that the toxin from O. miniacea, O. nirasei and O. mustelina contained TTX, and related compounds 4-epi TTX and anhydro-TTX. The paralytic shellfish poisons were not found.


Subject(s)
Foodborne Diseases/parasitology , Meat/parasitology , Snails/chemistry , Snails/classification , Tetrodotoxin/analysis , Animals , Humans , Taiwan , Tetrodotoxin/adverse effects , Tetrodotoxin/isolation & purification , Tetrodotoxin/toxicity
5.
J Food Prot ; 66(1): 110-4, 2003 Jan.
Article in English | MEDLINE | ID: mdl-12540189

ABSTRACT

Outbreaks of paralytic snail poisoning have recently occurred in Asia, especially in China. The epidemiological characteristics of this disease from an outbreak in Zhoushan City, China, were recorded. Forty-two outbreaks of paralytic snail poisoning, involving 309 cases of illness, occurred from 1977 to 2001. Sixteen people (5.2%) died, 48 people (15.5%) required intubations, and 140 people (45.3%) required emergency hospital treatment as a result of these outbreaks. Outbreaks involved multiple marine snail species and occurred primarily during the summer (from June to August) on 11 islands with high population densities. Peak numbers of outbreaks and amounts of snail toxicity occurred from 1978 to 1979, from 1985 to 1987, and from 1992 to 1994. Toxicity varied depending on specimen, region, and season. The toxin involved was identified as tetrodotoxin. The data obtained in this study suggest that snails should not be eaten unless they are certified to be nontoxic.


Subject(s)
Foodborne Diseases , Snails/metabolism , Tetrodotoxin/toxicity , Animals , China/epidemiology , Disease Outbreaks , Humans , Paralysis/etiology , Population Density , Retrospective Studies , Seasons , Tetrodotoxin/isolation & purification
6.
J Nat Toxins ; 11(4): 315-22, 2002 Dec.
Article in English | MEDLINE | ID: mdl-12503874

ABSTRACT

Attempts were made to elucidate the different responses of shellfish to paralytic shellfish poison (PSP) and the PSP donor Alexandrium minutum T1. Five species of edible bivalves (Crassostrea gigas, Meretrix lusoria, Mytilus edulis, Ruditapes philippinarum, and Soletellina diphos) were collected and examined for susceptibility to PSP and PSP donor. It was determined that all five bivalves had low susceptibility to PSP following an intramuscular injection (> 300 MU/20 g). The abnormal effects on bivalves were species-specific and varied with the concentration of A. minutum T1. Judging from the LC50 data (medium lethal concentration), the resistance of bivalves to the toxic dinoflagellate was as follows (least to most resistant): C. gigas < R. philippinarum < M. lusoria < M. edulis, S. diphos. With the exception of S. diphos, the bivalves accumulated very little toxin (< 2 MU/g edible tissue) when they were exposed to 10(7) cells/L of A. minutum for four days. The toxin levels in S. diphos increased with exposure time to the toxic dinoflagellates and accumulated primarily in the digestive gland (88-100%), followed by the gill (0-10%), and other organs (0-8%). Although the concentrations of toxin components in the digestive gland were found to be variable during the exposure period, the toxin profile in the digestive gland of S. diphos during the early exposure period was similar to that of A. minutum. Moreover, toxin components in the gills and in other organs were retained at near constant concentrations during the exposure period.


Subject(s)
Bivalvia/drug effects , Dinoflagellida/chemistry , Marine Toxins/toxicity , Saxitoxin/analogs & derivatives , Saxitoxin/toxicity , Shellfish/standards , Animals , Biotransformation , Bivalvia/metabolism , Chromatography, High Pressure Liquid , Dinoflagellida/metabolism , Food Chain , Injections, Intramuscular , Lethal Dose 50 , Marine Toxins/isolation & purification , Marine Toxins/pharmacokinetics , Saxitoxin/isolation & purification , Saxitoxin/pharmacokinetics , Species Specificity , Taiwan , Tissue Distribution
7.
J Food Prot ; 65(8): 1341-4, 2002 Aug.
Article in English | MEDLINE | ID: mdl-12182492

ABSTRACT

The toxin in the gastropods (snails) Zeuxis sufflatus and Niotha clathrata implicated in a food poisoning incident in northern Taiwan in April 2001 was studied. The symptoms exhibited by four victims were general paresthesia, paralysis of the phalanges and the extremities, paralysis, coma, vomiting, and aphasia. The remaining gastropods were assayed for toxicity in the form of tetrodotoxin (TTX). The ranges of specimen toxicity were 345 to 1,640 mouse units (MU) for Z sufflatus and 190 to 643 MU for N. clathrata. The toxicities of the digestive gland and for other parts of the gastropod were 1,120 +/- 477 MU and 497 +/- 238 MU, respectively, for Z sufflatus and 683 +/- 113 MU and 289 +/- 169 MU, respectively, for N. clathrata. The toxin from the methanolic extract of the gastropods was partially purified by ultrafiltration and Bio-Gel P-2 column chromatography. Cellulose acetate membrane electrophoresis, thin-layer chromatography, high-performance liquid chromatography, and gas chromatography-mass spectrometry analyses demonstrated that the toxin consisted of TTX. It was concluded that the causative agent of the food poisoning in question was TTX.


Subject(s)
Foodborne Diseases/etiology , Snails/chemistry , Tetrodotoxin/poisoning , Animals , Disease Outbreaks , Humans , Marine Toxins , Taiwan/epidemiology , Tetrodotoxin/analysis
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