Acute and 90-day subchronic toxicity studies of Silk peptide E5K6, in Sprague–Dawley rats
► We performed acute and 90-day subchronic oral toxicity studies of Silk peptide E5K6. ► Acute oral ALD of E5K6 was considered to be higher than 5000mg/kg in rats. ► Subchronic oral NOAEL of E5K6 was considered to be higher than 2000mg/kg in rats. ► The target organ was not identified in subchronic...
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creator | Han, Zhong-Ze Koo, Kyo-Hwan Kim, Kwang-Ho Bae, Jin-Sook Shin, Seo-Ho Kim, Hak-Soo Kim, Ji-Hoon Heo, Hyun-Suk Gil, Ki-Hyun Lee, Joo-Young Kim, Kap-Ho Kang, Boo-Hyon Lee, Hyun-Kul Choi, Ho-Young Li, Yong-Chun Yeon, Seong-Ho Lee, Jeong-Yong Song, Si-Whan |
description | ► We performed acute and 90-day subchronic oral toxicity studies of Silk peptide E5K6. ► Acute oral ALD of E5K6 was considered to be higher than 5000mg/kg in rats. ► Subchronic oral NOAEL of E5K6 was considered to be higher than 2000mg/kg in rats. ► The target organ was not identified in subchronic toxicity study.
Acute and 90-day subchronic oral toxicity studies of Silk peptide E5K6 were performed in Sprague–Dawley rats. In the acute toxicity study, Silk peptide E5K6 was administered orally to male and female rats at a single dose of 2000 and 5000mg/kg. Mortality, clinical signs and body weight changes were monitored for 14days. There were no treatment-related changes in these parameters. Therefore, the Approximate Lethal Dose (ALD) of Silk peptide E5K6 in male and female rats is higher than 5000mg/kg. In the subchronic toxicity study, Silk peptide E5K6 was administered orally to male and female rats for 90days at a single dose of 500, 1000, and 2000mg/kg. There were no toxicologically significant changes in clinical signs, body weight, food and water consumptions, ophthalmoscopic examination, urinalysis, hematological and serum biochemical examinations, necropsy findings, organ weights and histopathological examination of all of the animals treated with Silk peptide E5K6. These results suggest that the oral No Observed Adverse-Effect Level (NOAEL) of Silk peptide E5K6 is greater than 2000mg/kg/day in both sexes and the target organs were not established. |
doi_str_mv | 10.1016/j.fct.2011.06.058 |
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Acute and 90-day subchronic oral toxicity studies of Silk peptide E5K6 were performed in Sprague–Dawley rats. In the acute toxicity study, Silk peptide E5K6 was administered orally to male and female rats at a single dose of 2000 and 5000mg/kg. Mortality, clinical signs and body weight changes were monitored for 14days. There were no treatment-related changes in these parameters. Therefore, the Approximate Lethal Dose (ALD) of Silk peptide E5K6 in male and female rats is higher than 5000mg/kg. In the subchronic toxicity study, Silk peptide E5K6 was administered orally to male and female rats for 90days at a single dose of 500, 1000, and 2000mg/kg. There were no toxicologically significant changes in clinical signs, body weight, food and water consumptions, ophthalmoscopic examination, urinalysis, hematological and serum biochemical examinations, necropsy findings, organ weights and histopathological examination of all of the animals treated with Silk peptide E5K6. These results suggest that the oral No Observed Adverse-Effect Level (NOAEL) of Silk peptide E5K6 is greater than 2000mg/kg/day in both sexes and the target organs were not established.</description><identifier>ISSN: 0278-6915</identifier><identifier>EISSN: 1873-6351</identifier><identifier>DOI: 10.1016/j.fct.2011.06.058</identifier><identifier>PMID: 21729733</identifier><identifier>CODEN: FCTOD7</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>90-Day subchronic oral toxicity ; Acute oral toxicity ; acute toxicity ; Animals ; Biological and medical sciences ; blood serum ; body weight changes ; Dose-Response Relationship, Drug ; Female ; histopathology ; Insect Proteins - toxicity ; lethal dose ; Male ; Medical sciences ; mortality ; necropsy ; no observed adverse effect level ; oral administration ; Organ Size - drug effects ; Rats ; Rats, Sprague-Dawley ; Silk - chemistry ; Silk peptide E5K6 ; Sprague–Dawley rats ; subchronic toxicity ; toxicity testing ; Toxicology ; urinalysis</subject><ispartof>Food and chemical toxicology, 2011-09, Vol.49 (9), p.2408-2414</ispartof><rights>2011</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2011. Published by Elsevier Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c438t-acafaabfa6946bec8bbe20ea915bb16b14d78fe882ecde865619816c3e88f21c3</citedby><cites>FETCH-LOGICAL-c438t-acafaabfa6946bec8bbe20ea915bb16b14d78fe882ecde865619816c3e88f21c3</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.2011.06.058$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27928,27929,45999</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24523779$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21729733$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Han, Zhong-Ze</creatorcontrib><creatorcontrib>Koo, Kyo-Hwan</creatorcontrib><creatorcontrib>Kim, Kwang-Ho</creatorcontrib><creatorcontrib>Bae, Jin-Sook</creatorcontrib><creatorcontrib>Shin, Seo-Ho</creatorcontrib><creatorcontrib>Kim, Hak-Soo</creatorcontrib><creatorcontrib>Kim, Ji-Hoon</creatorcontrib><creatorcontrib>Heo, Hyun-Suk</creatorcontrib><creatorcontrib>Gil, Ki-Hyun</creatorcontrib><creatorcontrib>Lee, Joo-Young</creatorcontrib><creatorcontrib>Kim, Kap-Ho</creatorcontrib><creatorcontrib>Kang, Boo-Hyon</creatorcontrib><creatorcontrib>Lee, Hyun-Kul</creatorcontrib><creatorcontrib>Choi, Ho-Young</creatorcontrib><creatorcontrib>Li, Yong-Chun</creatorcontrib><creatorcontrib>Yeon, Seong-Ho</creatorcontrib><creatorcontrib>Lee, Jeong-Yong</creatorcontrib><creatorcontrib>Song, Si-Whan</creatorcontrib><title>Acute and 90-day subchronic toxicity studies of Silk peptide E5K6, in Sprague–Dawley rats</title><title>Food and chemical toxicology</title><addtitle>Food Chem Toxicol</addtitle><description>► We performed acute and 90-day subchronic oral toxicity studies of Silk peptide E5K6. ► Acute oral ALD of E5K6 was considered to be higher than 5000mg/kg in rats. ► Subchronic oral NOAEL of E5K6 was considered to be higher than 2000mg/kg in rats. ► The target organ was not identified in subchronic toxicity study.
Acute and 90-day subchronic oral toxicity studies of Silk peptide E5K6 were performed in Sprague–Dawley rats. In the acute toxicity study, Silk peptide E5K6 was administered orally to male and female rats at a single dose of 2000 and 5000mg/kg. Mortality, clinical signs and body weight changes were monitored for 14days. There were no treatment-related changes in these parameters. Therefore, the Approximate Lethal Dose (ALD) of Silk peptide E5K6 in male and female rats is higher than 5000mg/kg. In the subchronic toxicity study, Silk peptide E5K6 was administered orally to male and female rats for 90days at a single dose of 500, 1000, and 2000mg/kg. There were no toxicologically significant changes in clinical signs, body weight, food and water consumptions, ophthalmoscopic examination, urinalysis, hematological and serum biochemical examinations, necropsy findings, organ weights and histopathological examination of all of the animals treated with Silk peptide E5K6. These results suggest that the oral No Observed Adverse-Effect Level (NOAEL) of Silk peptide E5K6 is greater than 2000mg/kg/day in both sexes and the target organs were not established.</description><subject>90-Day subchronic oral toxicity</subject><subject>Acute oral toxicity</subject><subject>acute toxicity</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>blood serum</subject><subject>body weight changes</subject><subject>Dose-Response Relationship, Drug</subject><subject>Female</subject><subject>histopathology</subject><subject>Insect Proteins - toxicity</subject><subject>lethal dose</subject><subject>Male</subject><subject>Medical sciences</subject><subject>mortality</subject><subject>necropsy</subject><subject>no observed adverse effect level</subject><subject>oral administration</subject><subject>Organ Size - drug effects</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Silk - chemistry</subject><subject>Silk peptide E5K6</subject><subject>Sprague–Dawley rats</subject><subject>subchronic toxicity</subject><subject>toxicity testing</subject><subject>Toxicology</subject><subject>urinalysis</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>eNp9kL-O1DAQhy0E4paDB6ABN4iGBE-ysR1RnY7jjziJYrmKwpo448NLNgm2A2zHO_CGPAk-7QId1Uij7zfz08fYQxAlCJDPt6WzqawEQClkKRp9i61Aq7qQdQO32UpUSheyheaE3YtxK4RQoORddlKBqlpV1yv28cwuiTiOPW9F0eOex6Wzn8I0esvT9N1bn_IuLb2nyCfHN374zGeak--JXzTv5DPuR76ZA14v9OvHz5f4baA9D5jifXbH4RDpwXGesqtXFx_O3xSX71-_PT-7LOy61qlAiw6xcyjbtezI6q6jShDm3l0HsoN1r7QjrSuyPWnZSGg1SFvnlavA1qfs6eHuHKYvC8Vkdj5aGgYcaVqiaUVVq1ZqmUk4kDZMMQZyZg5-h2FvQJgbpWZrslJzo9QIabLSnHl0vL50O-r_Jv44zMCTI4DR4uACjtbHf9y6ye9Vm7nHB87hZPA6ZOZqkz81QoCCpoVMvDgQlG199RRMtJ5GS70PlGv1k_9P0d-Oy53j</recordid><startdate>20110901</startdate><enddate>20110901</enddate><creator>Han, Zhong-Ze</creator><creator>Koo, Kyo-Hwan</creator><creator>Kim, Kwang-Ho</creator><creator>Bae, Jin-Sook</creator><creator>Shin, Seo-Ho</creator><creator>Kim, Hak-Soo</creator><creator>Kim, Ji-Hoon</creator><creator>Heo, Hyun-Suk</creator><creator>Gil, Ki-Hyun</creator><creator>Lee, Joo-Young</creator><creator>Kim, Kap-Ho</creator><creator>Kang, Boo-Hyon</creator><creator>Lee, Hyun-Kul</creator><creator>Choi, Ho-Young</creator><creator>Li, Yong-Chun</creator><creator>Yeon, Seong-Ho</creator><creator>Lee, Jeong-Yong</creator><creator>Song, Si-Whan</creator><general>Elsevier Ltd</general><general>Elsevier</general><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>20110901</creationdate><title>Acute and 90-day subchronic toxicity studies of Silk peptide E5K6, in Sprague–Dawley rats</title><author>Han, Zhong-Ze ; Koo, Kyo-Hwan ; Kim, Kwang-Ho ; Bae, Jin-Sook ; Shin, Seo-Ho ; Kim, Hak-Soo ; Kim, Ji-Hoon ; Heo, Hyun-Suk ; Gil, Ki-Hyun ; Lee, Joo-Young ; Kim, Kap-Ho ; Kang, Boo-Hyon ; Lee, Hyun-Kul ; Choi, Ho-Young ; Li, Yong-Chun ; Yeon, Seong-Ho ; Lee, Jeong-Yong ; Song, Si-Whan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c438t-acafaabfa6946bec8bbe20ea915bb16b14d78fe882ecde865619816c3e88f21c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>90-Day subchronic oral toxicity</topic><topic>Acute oral toxicity</topic><topic>acute toxicity</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>blood serum</topic><topic>body weight changes</topic><topic>Dose-Response Relationship, Drug</topic><topic>Female</topic><topic>histopathology</topic><topic>Insect Proteins - toxicity</topic><topic>lethal dose</topic><topic>Male</topic><topic>Medical sciences</topic><topic>mortality</topic><topic>necropsy</topic><topic>no observed adverse effect level</topic><topic>oral administration</topic><topic>Organ Size - drug effects</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Silk - chemistry</topic><topic>Silk peptide E5K6</topic><topic>Sprague–Dawley rats</topic><topic>subchronic toxicity</topic><topic>toxicity testing</topic><topic>Toxicology</topic><topic>urinalysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Han, Zhong-Ze</creatorcontrib><creatorcontrib>Koo, Kyo-Hwan</creatorcontrib><creatorcontrib>Kim, Kwang-Ho</creatorcontrib><creatorcontrib>Bae, Jin-Sook</creatorcontrib><creatorcontrib>Shin, Seo-Ho</creatorcontrib><creatorcontrib>Kim, Hak-Soo</creatorcontrib><creatorcontrib>Kim, Ji-Hoon</creatorcontrib><creatorcontrib>Heo, Hyun-Suk</creatorcontrib><creatorcontrib>Gil, Ki-Hyun</creatorcontrib><creatorcontrib>Lee, Joo-Young</creatorcontrib><creatorcontrib>Kim, Kap-Ho</creatorcontrib><creatorcontrib>Kang, Boo-Hyon</creatorcontrib><creatorcontrib>Lee, Hyun-Kul</creatorcontrib><creatorcontrib>Choi, Ho-Young</creatorcontrib><creatorcontrib>Li, Yong-Chun</creatorcontrib><creatorcontrib>Yeon, Seong-Ho</creatorcontrib><creatorcontrib>Lee, Jeong-Yong</creatorcontrib><creatorcontrib>Song, Si-Whan</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><jtitle>Food and chemical toxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Han, Zhong-Ze</au><au>Koo, Kyo-Hwan</au><au>Kim, Kwang-Ho</au><au>Bae, Jin-Sook</au><au>Shin, Seo-Ho</au><au>Kim, Hak-Soo</au><au>Kim, Ji-Hoon</au><au>Heo, Hyun-Suk</au><au>Gil, Ki-Hyun</au><au>Lee, Joo-Young</au><au>Kim, Kap-Ho</au><au>Kang, Boo-Hyon</au><au>Lee, Hyun-Kul</au><au>Choi, Ho-Young</au><au>Li, Yong-Chun</au><au>Yeon, Seong-Ho</au><au>Lee, Jeong-Yong</au><au>Song, Si-Whan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Acute and 90-day subchronic toxicity studies of Silk peptide E5K6, in Sprague–Dawley rats</atitle><jtitle>Food and chemical toxicology</jtitle><addtitle>Food Chem Toxicol</addtitle><date>2011-09-01</date><risdate>2011</risdate><volume>49</volume><issue>9</issue><spage>2408</spage><epage>2414</epage><pages>2408-2414</pages><issn>0278-6915</issn><eissn>1873-6351</eissn><coden>FCTOD7</coden><abstract>► We performed acute and 90-day subchronic oral toxicity studies of Silk peptide E5K6. ► Acute oral ALD of E5K6 was considered to be higher than 5000mg/kg in rats. ► Subchronic oral NOAEL of E5K6 was considered to be higher than 2000mg/kg in rats. ► The target organ was not identified in subchronic toxicity study.
Acute and 90-day subchronic oral toxicity studies of Silk peptide E5K6 were performed in Sprague–Dawley rats. In the acute toxicity study, Silk peptide E5K6 was administered orally to male and female rats at a single dose of 2000 and 5000mg/kg. Mortality, clinical signs and body weight changes were monitored for 14days. There were no treatment-related changes in these parameters. Therefore, the Approximate Lethal Dose (ALD) of Silk peptide E5K6 in male and female rats is higher than 5000mg/kg. In the subchronic toxicity study, Silk peptide E5K6 was administered orally to male and female rats for 90days at a single dose of 500, 1000, and 2000mg/kg. There were no toxicologically significant changes in clinical signs, body weight, food and water consumptions, ophthalmoscopic examination, urinalysis, hematological and serum biochemical examinations, necropsy findings, organ weights and histopathological examination of all of the animals treated with Silk peptide E5K6. These results suggest that the oral No Observed Adverse-Effect Level (NOAEL) of Silk peptide E5K6 is greater than 2000mg/kg/day in both sexes and the target organs were not established.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>21729733</pmid><doi>10.1016/j.fct.2011.06.058</doi><tpages>7</tpages></addata></record> |
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subjects | 90-Day subchronic oral toxicity Acute oral toxicity acute toxicity Animals Biological and medical sciences blood serum body weight changes Dose-Response Relationship, Drug Female histopathology Insect Proteins - toxicity lethal dose Male Medical sciences mortality necropsy no observed adverse effect level oral administration Organ Size - drug effects Rats Rats, Sprague-Dawley Silk - chemistry Silk peptide E5K6 Sprague–Dawley rats subchronic toxicity toxicity testing Toxicology urinalysis |
title | Acute and 90-day subchronic toxicity studies of Silk peptide E5K6, in Sprague–Dawley rats |
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