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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Veröffentlicht in:Food and chemical toxicology 2011-09, Vol.49 (9), p.2408-2414
Hauptverfasser: 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
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container_end_page 2414
container_issue 9
container_start_page 2408
container_title Food and chemical toxicology
container_volume 49
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. 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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. 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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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source MEDLINE; Access via ScienceDirect (Elsevier)
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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