A 90-day oral (dietary) toxicity study of the 2R,4R-isomer of monatin salt in Sprague–Dawley rats

► No toxicologically relevant clinical or histopathological findings in any of the R,R-monatin salt-treated groups. ► Significantly lower cumulative body weight gains were noted in the 35,000ppm group. ► Mean bw in the 35,000ppm group males and females were 7% and 12% lower, respectively, than contr...

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Veröffentlicht in:Food and chemical toxicology 2011-12, Vol.49 (12), p.3249-3257
Hauptverfasser: Hlywka, J., Brathwaite, W.A., Rihner, M.O., Nikiforov, A.I., Eapen, A.K.
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container_issue 12
container_start_page 3249
container_title Food and chemical toxicology
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creator Hlywka, J.
Brathwaite, W.A.
Rihner, M.O.
Nikiforov, A.I.
Eapen, A.K.
description ► No toxicologically relevant clinical or histopathological findings in any of the R,R-monatin salt-treated groups. ► Significantly lower cumulative body weight gains were noted in the 35,000ppm group. ► Mean bw in the 35,000ppm group males and females were 7% and 12% lower, respectively, than controls at study week 13. ► Based on bw observations, the dietary NOAEL of R,R-monatin salt was 20,000ppm in female rats (approximately 1544mg/kgbw/day). ► Dietary NOAEL of R,R-monatin salt was 35,000ppm in male rats (approximately 2368mg/kgbw/day). The root bark of Sclerochitin ilicifolius contains an intensely sweet substance analytically identified as isomers of 2-hydroxy-2-(indol-3-ylmethyl)-4-aminoglutaric acid and generically coined “monatin.” Groups of male and female Crl:CD(SD) rats were fed 0 (control), 5000, 10,000, 20,000 or 35,000ppm R,R-monatin salt in the diet for 90days. There were no toxicologically relevant clinical or histopathological findings in any of the test article-treated groups. Significantly lower cumulative body weight gains were noted in the 35,000ppm group. Mean body weights in the 35,000ppm group males and females were 7% and 12% lower, respectively, than the control group at study week 13. In the absence of other observations associated with systemic toxicity and lower food consumption, the magnitude of the body weight difference in the 35,000ppm group females relative to the control group exceeded 10%, which indicated attainment of a maximum tolerated dose (MTD) level. Based on the results of this study, and conservatively assuming the body weight observations at the MTD to be indicative of an adverse effect, the dietary no-observed-adverse-effect level (NOAEL) of R,R-monatin salt for 90days was 20,000ppm in female rats (approximately 1544mg/kgbw/day) and 35,000ppm in male rats (approximately 2368mg/kgbw/day).
doi_str_mv 10.1016/j.fct.2011.09.004
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The root bark of Sclerochitin ilicifolius contains an intensely sweet substance analytically identified as isomers of 2-hydroxy-2-(indol-3-ylmethyl)-4-aminoglutaric acid and generically coined “monatin.” Groups of male and female Crl:CD(SD) rats were fed 0 (control), 5000, 10,000, 20,000 or 35,000ppm R,R-monatin salt in the diet for 90days. There were no toxicologically relevant clinical or histopathological findings in any of the test article-treated groups. Significantly lower cumulative body weight gains were noted in the 35,000ppm group. Mean body weights in the 35,000ppm group males and females were 7% and 12% lower, respectively, than the control group at study week 13. In the absence of other observations associated with systemic toxicity and lower food consumption, the magnitude of the body weight difference in the 35,000ppm group females relative to the control group exceeded 10%, which indicated attainment of a maximum tolerated dose (MTD) level. 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The root bark of Sclerochitin ilicifolius contains an intensely sweet substance analytically identified as isomers of 2-hydroxy-2-(indol-3-ylmethyl)-4-aminoglutaric acid and generically coined “monatin.” Groups of male and female Crl:CD(SD) rats were fed 0 (control), 5000, 10,000, 20,000 or 35,000ppm R,R-monatin salt in the diet for 90days. There were no toxicologically relevant clinical or histopathological findings in any of the test article-treated groups. Significantly lower cumulative body weight gains were noted in the 35,000ppm group. Mean body weights in the 35,000ppm group males and females were 7% and 12% lower, respectively, than the control group at study week 13. In the absence of other observations associated with systemic toxicity and lower food consumption, the magnitude of the body weight difference in the 35,000ppm group females relative to the control group exceeded 10%, which indicated attainment of a maximum tolerated dose (MTD) level. 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Brathwaite, W.A. ; Rihner, M.O. ; Nikiforov, A.I. ; Eapen, A.K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c481t-8826dc4bf9c9587631f822fd10bff8ecc65f90ba9aa86e1ddf151e94ed677ff23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Administration, Oral</topic><topic>adverse effects</topic><topic>Animals</topic><topic>bark</topic><topic>Biological and medical sciences</topic><topic>Body Weight - drug effects</topic><topic>Diet</topic><topic>Dose-Response Relationship, Drug</topic><topic>Female</topic><topic>females</topic><topic>Glutamic Acid - administration &amp; dosage</topic><topic>Glutamic Acid - analogs &amp; derivatives</topic><topic>Glutamic Acid - toxicity</topic><topic>histopathology</topic><topic>Indoles - administration &amp; dosage</topic><topic>Indoles - toxicity</topic><topic>isomers</topic><topic>Male</topic><topic>males</topic><topic>Medical sciences</topic><topic>No-Observed-Adverse-Effect Level</topic><topic>Oral</topic><topic>Organ Size - drug effects</topic><topic>R,R-monatin</topic><topic>Rat</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Sex Factors</topic><topic>Subchronic toxicity</topic><topic>Sweetener</topic><topic>Toxicity Tests, Subchronic - methods</topic><topic>Toxicology</topic><topic>weight gain</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hlywka, J.</creatorcontrib><creatorcontrib>Brathwaite, W.A.</creatorcontrib><creatorcontrib>Rihner, M.O.</creatorcontrib><creatorcontrib>Nikiforov, A.I.</creatorcontrib><creatorcontrib>Eapen, A.K.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><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><jtitle>Food and chemical toxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hlywka, J.</au><au>Brathwaite, W.A.</au><au>Rihner, M.O.</au><au>Nikiforov, A.I.</au><au>Eapen, A.K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A 90-day oral (dietary) toxicity study of the 2R,4R-isomer of monatin salt in Sprague–Dawley rats</atitle><jtitle>Food and chemical toxicology</jtitle><addtitle>Food Chem Toxicol</addtitle><date>2011-12-01</date><risdate>2011</risdate><volume>49</volume><issue>12</issue><spage>3249</spage><epage>3257</epage><pages>3249-3257</pages><issn>0278-6915</issn><eissn>1873-6351</eissn><coden>FCTOD7</coden><abstract>► No toxicologically relevant clinical or histopathological findings in any of the R,R-monatin salt-treated groups. ► Significantly lower cumulative body weight gains were noted in the 35,000ppm group. ► Mean bw in the 35,000ppm group males and females were 7% and 12% lower, respectively, than controls at study week 13. ► Based on bw observations, the dietary NOAEL of R,R-monatin salt was 20,000ppm in female rats (approximately 1544mg/kgbw/day). ► Dietary NOAEL of R,R-monatin salt was 35,000ppm in male rats (approximately 2368mg/kgbw/day). The root bark of Sclerochitin ilicifolius contains an intensely sweet substance analytically identified as isomers of 2-hydroxy-2-(indol-3-ylmethyl)-4-aminoglutaric acid and generically coined “monatin.” Groups of male and female Crl:CD(SD) rats were fed 0 (control), 5000, 10,000, 20,000 or 35,000ppm R,R-monatin salt in the diet for 90days. There were no toxicologically relevant clinical or histopathological findings in any of the test article-treated groups. Significantly lower cumulative body weight gains were noted in the 35,000ppm group. Mean body weights in the 35,000ppm group males and females were 7% and 12% lower, respectively, than the control group at study week 13. In the absence of other observations associated with systemic toxicity and lower food consumption, the magnitude of the body weight difference in the 35,000ppm group females relative to the control group exceeded 10%, which indicated attainment of a maximum tolerated dose (MTD) level. Based on the results of this study, and conservatively assuming the body weight observations at the MTD to be indicative of an adverse effect, the dietary no-observed-adverse-effect level (NOAEL) of R,R-monatin salt for 90days was 20,000ppm in female rats (approximately 1544mg/kgbw/day) and 35,000ppm in male rats (approximately 2368mg/kgbw/day).</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>21925562</pmid><doi>10.1016/j.fct.2011.09.004</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; ScienceDirect Journals (5 years ago - present)
subjects Administration, Oral
adverse effects
Animals
bark
Biological and medical sciences
Body Weight - drug effects
Diet
Dose-Response Relationship, Drug
Female
females
Glutamic Acid - administration & dosage
Glutamic Acid - analogs & derivatives
Glutamic Acid - toxicity
histopathology
Indoles - administration & dosage
Indoles - toxicity
isomers
Male
males
Medical sciences
No-Observed-Adverse-Effect Level
Oral
Organ Size - drug effects
R,R-monatin
Rat
Rats
Rats, Sprague-Dawley
Sex Factors
Subchronic toxicity
Sweetener
Toxicity Tests, Subchronic - methods
Toxicology
weight gain
title A 90-day oral (dietary) toxicity study of the 2R,4R-isomer of monatin salt in Sprague–Dawley rats
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