Toxicological assessment of a particulate yeast (1,3/1,6)-β- d-glucan in rats

This study investigates the toxicity of WGP ® 3–6, a yeast-derived β-glucan ingredient, during single-dose acute and sub-chronic toxicity studies in rats. For the acute study, Fisher-344 rats were administered WGP ® 3–6 via gavage at a dose of 2000 mg/kg body weight, and any evidence of toxicity was...

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Veröffentlicht in:Food and chemical toxicology 2007-09, Vol.45 (9), p.1719-1730
Hauptverfasser: Babíček, K., Čechová, I., Simon, R.R., Harwood, M., Cox, D.J.
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container_end_page 1730
container_issue 9
container_start_page 1719
container_title Food and chemical toxicology
container_volume 45
creator Babíček, K.
Čechová, I.
Simon, R.R.
Harwood, M.
Cox, D.J.
description This study investigates the toxicity of WGP ® 3–6, a yeast-derived β-glucan ingredient, during single-dose acute and sub-chronic toxicity studies in rats. For the acute study, Fisher-344 rats were administered WGP ® 3–6 via gavage at a dose of 2000 mg/kg body weight, and any evidence of toxicity was monitored over a 14-day period. WGP ® 3–6 was well tolerated, indicating that the LD 50 value is greater than 2000 mg/kg body weight. For the sub-chronic study, Fisher-344 rats (10/sex/group) were randomly allocated to receive daily gavage treatment with WGP ® 3–6 at doses of 0, 2, 33.3, or 100 mg/kg body weight. Control and high-dose satellite recovery groups of each sex also were included. Full toxicological monitoring and endpoint investigations were performed throughout and upon completion of the study. No negative effects on animal weights or food consumption attributable to WGP ® 3–6 were evident at any dose. In addition, no mortality, clinical pathology, functional/behavioral, microscopic, or gross observations indicating toxicity were observed. Sporadic changes in some biochemical and hematological parameters were observed; however, since the effects were within the physiological ranges in historical controls, were not dose–responsive, or were not observed in both sexes, they were determined to be of no toxicological significance. In conclusion, no adverse or toxic effects were observed after subchronic oral administration of 2, 33.3, or 100 mg/kg body weight/day of WGP ® 3–6 in Fisher-344 rats, and therefore, a no observed adverse effect level (NOAEL) of 100 mg/kg body weight/day, the highest dose tested, was determined.
doi_str_mv 10.1016/j.fct.2007.03.013
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Sporadic changes in some biochemical and hematological parameters were observed; however, since the effects were within the physiological ranges in historical controls, were not dose–responsive, or were not observed in both sexes, they were determined to be of no toxicological significance. 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Čechová, I. ; Simon, R.R. ; Harwood, M. ; Cox, D.J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c436t-6ba687dec77d226878b48d335af1199e1733ddc86b3dac2923d914d0645ecf363</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>(1,3)-β- d-Glucan</topic><topic>alkaloids</topic><topic>Analysis of Variance</topic><topic>Animals</topic><topic>anticarcinogenic activity</topic><topic>antinutritional factors</topic><topic>apoptosis</topic><topic>beta-Glucans - toxicity</topic><topic>Biological and medical sciences</topic><topic>Blood Chemical Analysis</topic><topic>Body Weight - drug effects</topic><topic>cell cycle</topic><topic>chemoprevention</topic><topic>cytotoxicity</topic><topic>cytotoxins</topic><topic>Dose-Response Relationship, Drug</topic><topic>enzyme activity</topic><topic>enzyme inhibition</topic><topic>enzymes</topic><topic>Female</topic><topic>Hematologic Tests</topic><topic>hepatoma</topic><topic>Intubation, Gastrointestinal</topic><topic>Lethal Dose 50</topic><topic>Male</topic><topic>Medical sciences</topic><topic>medicinal plants</topic><topic>No-Observed-Adverse-Effect Level</topic><topic>NOAEL</topic><topic>Random Allocation</topic><topic>Rat</topic><topic>Rats</topic><topic>Rats, Inbred F344</topic><topic>Saccharomyces cerevisiae - chemistry</topic><topic>Safety</topic><topic>seed extracts</topic><topic>seeds</topic><topic>strychnine</topic><topic>Strychnos nux-vomica</topic><topic>Toxicity</topic><topic>Toxicity Tests, Acute</topic><topic>Toxicity Tests, Chronic</topic><topic>Toxicology</topic><topic>Yeast</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Babíček, K.</creatorcontrib><creatorcontrib>Čechová, I.</creatorcontrib><creatorcontrib>Simon, R.R.</creatorcontrib><creatorcontrib>Harwood, M.</creatorcontrib><creatorcontrib>Cox, D.J.</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><jtitle>Food and chemical toxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Babíček, K.</au><au>Čechová, I.</au><au>Simon, R.R.</au><au>Harwood, M.</au><au>Cox, D.J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Toxicological assessment of a particulate yeast (1,3/1,6)-β- d-glucan in rats</atitle><jtitle>Food and chemical toxicology</jtitle><addtitle>Food Chem Toxicol</addtitle><date>2007-09-01</date><risdate>2007</risdate><volume>45</volume><issue>9</issue><spage>1719</spage><epage>1730</epage><pages>1719-1730</pages><issn>0278-6915</issn><eissn>1873-6351</eissn><coden>FCTOD7</coden><abstract>This study investigates the toxicity of WGP ® 3–6, a yeast-derived β-glucan ingredient, during single-dose acute and sub-chronic toxicity studies in rats. For the acute study, Fisher-344 rats were administered WGP ® 3–6 via gavage at a dose of 2000 mg/kg body weight, and any evidence of toxicity was monitored over a 14-day period. WGP ® 3–6 was well tolerated, indicating that the LD 50 value is greater than 2000 mg/kg body weight. For the sub-chronic study, Fisher-344 rats (10/sex/group) were randomly allocated to receive daily gavage treatment with WGP ® 3–6 at doses of 0, 2, 33.3, or 100 mg/kg body weight. Control and high-dose satellite recovery groups of each sex also were included. Full toxicological monitoring and endpoint investigations were performed throughout and upon completion of the study. No negative effects on animal weights or food consumption attributable to WGP ® 3–6 were evident at any dose. In addition, no mortality, clinical pathology, functional/behavioral, microscopic, or gross observations indicating toxicity were observed. Sporadic changes in some biochemical and hematological parameters were observed; however, since the effects were within the physiological ranges in historical controls, were not dose–responsive, or were not observed in both sexes, they were determined to be of no toxicological significance. In conclusion, no adverse or toxic effects were observed after subchronic oral administration of 2, 33.3, or 100 mg/kg body weight/day of WGP ® 3–6 in Fisher-344 rats, and therefore, a no observed adverse effect level (NOAEL) of 100 mg/kg body weight/day, the highest dose tested, was determined.</abstract><cop>Oxford</cop><cop>New York, NY</cop><pub>Elsevier Ltd</pub><pmid>17493735</pmid><doi>10.1016/j.fct.2007.03.013</doi><tpages>12</tpages></addata></record>
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subjects (1,3)-β- d-Glucan
alkaloids
Analysis of Variance
Animals
anticarcinogenic activity
antinutritional factors
apoptosis
beta-Glucans - toxicity
Biological and medical sciences
Blood Chemical Analysis
Body Weight - drug effects
cell cycle
chemoprevention
cytotoxicity
cytotoxins
Dose-Response Relationship, Drug
enzyme activity
enzyme inhibition
enzymes
Female
Hematologic Tests
hepatoma
Intubation, Gastrointestinal
Lethal Dose 50
Male
Medical sciences
medicinal plants
No-Observed-Adverse-Effect Level
NOAEL
Random Allocation
Rat
Rats
Rats, Inbred F344
Saccharomyces cerevisiae - chemistry
Safety
seed extracts
seeds
strychnine
Strychnos nux-vomica
Toxicity
Toxicity Tests, Acute
Toxicity Tests, Chronic
Toxicology
Yeast
title Toxicological assessment of a particulate yeast (1,3/1,6)-β- d-glucan in rats
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