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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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. 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).</description><identifier>ISSN: 0278-6915</identifier><identifier>EISSN: 1873-6351</identifier><identifier>DOI: 10.1016/j.fct.2011.09.004</identifier><identifier>PMID: 21925562</identifier><identifier>CODEN: FCTOD7</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>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</subject><ispartof>Food and chemical toxicology, 2011-12, Vol.49 (12), p.3249-3257</ispartof><rights>2011 Elsevier Ltd</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2011 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c481t-8826dc4bf9c9587631f822fd10bff8ecc65f90ba9aa86e1ddf151e94ed677ff23</citedby><cites>FETCH-LOGICAL-c481t-8826dc4bf9c9587631f822fd10bff8ecc65f90ba9aa86e1ddf151e94ed677ff23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.fct.2011.09.004$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=25251574$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21925562$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hlywka, J.</creatorcontrib><creatorcontrib>Brathwaite, W.A.</creatorcontrib><creatorcontrib>Rihner, M.O.</creatorcontrib><creatorcontrib>Nikiforov, A.I.</creatorcontrib><creatorcontrib>Eapen, A.K.</creatorcontrib><title>A 90-day oral (dietary) toxicity study of the 2R,4R-isomer of monatin salt in Sprague–Dawley rats</title><title>Food and chemical toxicology</title><addtitle>Food Chem Toxicol</addtitle><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).</description><subject>Administration, Oral</subject><subject>adverse effects</subject><subject>Animals</subject><subject>bark</subject><subject>Biological and medical sciences</subject><subject>Body Weight - drug effects</subject><subject>Diet</subject><subject>Dose-Response Relationship, Drug</subject><subject>Female</subject><subject>females</subject><subject>Glutamic Acid - administration & dosage</subject><subject>Glutamic Acid - analogs & derivatives</subject><subject>Glutamic Acid - toxicity</subject><subject>histopathology</subject><subject>Indoles - administration & dosage</subject><subject>Indoles - toxicity</subject><subject>isomers</subject><subject>Male</subject><subject>males</subject><subject>Medical sciences</subject><subject>No-Observed-Adverse-Effect Level</subject><subject>Oral</subject><subject>Organ Size - drug effects</subject><subject>R,R-monatin</subject><subject>Rat</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Sex Factors</subject><subject>Subchronic toxicity</subject><subject>Sweetener</subject><subject>Toxicity Tests, Subchronic - methods</subject><subject>Toxicology</subject><subject>weight gain</subject><issn>0278-6915</issn><issn>1873-6351</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kUtuFDEQhi0EIkPgAGzAGwRIdOPytN1tZRWFR5AiISVkbXnscvCoH4PtDsyOO-SGnASPZoAdq5Lsr35XfSbkKbAaGMi369rbXHMGUDNVM9bcIwvo2mUllwLukwXjbVdJBeKIPEppzRhroZUPyREHxYWQfEHsKVWscmZLp2h6-soFzCZuX9M8_Qg25C1NeXbl1tP8FSm_fNNcViFNA8bd2TCNJoeRJtNnWurVJpqbGX_9vHtnvve4pdHk9Jg88KZP-ORQj8n1h_dfzs6ri88fP52dXlS26SBXXcels83KK6tE18ol-I5z74CtvO_QWim8YiujjOkkgnMeBKBq0Mm29Z4vj8nLfe4mTt9mTFkPIVnsezPiNCetAECCbNpCwp60cUopotebGIaytwamd2r1Whe1eqdWM6WL2tLz7JA-rwZ0fzv-uCzAiwNgkjW9j2a0If3jBBcg2l3Q8z3nzaTNTSzM9VV5STAG5X8YK8TJnsBi6zZg1MkGHC26ELGM5abwn0F_A2lun6Q</recordid><startdate>20111201</startdate><enddate>20111201</enddate><creator>Hlywka, J.</creator><creator>Brathwaite, W.A.</creator><creator>Rihner, M.O.</creator><creator>Nikiforov, A.I.</creator><creator>Eapen, A.K.</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><scope>FBQ</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7U7</scope><scope>C1K</scope></search><sort><creationdate>20111201</creationdate><title>A 90-day oral (dietary) toxicity study of the 2R,4R-isomer of monatin salt in Sprague–Dawley rats</title><author>Hlywka, J. ; 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 & dosage</topic><topic>Glutamic Acid - analogs & derivatives</topic><topic>Glutamic Acid - toxicity</topic><topic>histopathology</topic><topic>Indoles - administration & 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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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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