A 13-WEEK ORAL REPEATED DOSE TOXICITY STUDY OF A NEW ANTINEOPLASTIC AGENT S-1 IN RATS

S-1, an antineoplastic formulation of a fluorinated pyrimidine derivative containing tegafur (FT), CDHP, and potassium oxonate (Oxo) in a molar ratio of 1:0.4:1, was recently developed by Taiho Pharmaceutical Co., Ltd., with the aim of prolonging the effective plasma concentration of 5-fluorouracil...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of toxicological sciences 1996/11/27, Vol.21(SupplementIII), pp.505-526
Hauptverfasser: HAYASHI, Taiji, HASEGAWA, Hiroyuki, TANAKA, Gotaro, OHMAE, Sigeo
Format: Artikel
Sprache:eng
Schlagworte:
Rat
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 526
container_issue SupplementIII
container_start_page 505
container_title Journal of toxicological sciences
container_volume 21
creator HAYASHI, Taiji
HASEGAWA, Hiroyuki
TANAKA, Gotaro
OHMAE, Sigeo
description S-1, an antineoplastic formulation of a fluorinated pyrimidine derivative containing tegafur (FT), CDHP, and potassium oxonate (Oxo) in a molar ratio of 1:0.4:1, was recently developed by Taiho Pharmaceutical Co., Ltd., with the aim of prolonging the effective plasma concentration of 5-fluorouracil (5-FU) over that producted by FT alone and reducing its dose-limiting gastrointestinal toxicity. As a part of the S-1 toxicity study, a 13-week oral repeated dose toxicity study and a recovery study using male and female rats was conducted. Doses of S-1 were adjusted to deliver 1.5, 5, and 15 mg/kg/day as doses of FT, and FT wad given at 15mg/kg/day. The following results were obtained. 1. In clinical observation, edema of the limbs and face or swelling of the auricle of the ear and an anemic appearance were observed in both sexes in the 15 mg/kg/day group as dose of FT. Subsequently, ma1es in ithis group developed severe anemia, decrdased spontaneous motor activity, emaciation, and subnormal skin temperature, and many males died. In the survivors, keratosis of the palm, sole, or tail was observed, with necrosis and loss of the tail tip in the severe cases. 2. Body weight gain was suppressed from about week 2 of treatment in both sexes in the 15 mg/kg/day group as dose of FT, and there was almost no weight gain after week 4-5. Food consumption was consistently less than the control value for males in the 15 mg/kg/day group as dose of FT throughout the treatment period. 3. No marked changes were observed in water intake and on ophthalmologic examination. 4. In the fecal test for occult blood, a positive tendency was observed in both sexes in the 15 mg/kg/day group as dose of FT. 5. Urinalysis disclosed a slight increase in protein and decrease in sodium, potassium, and chloride in males, and an increase in protein in females in the 15 mg/kg/day group as dose of FT. 6. Hematologically, both sexes in the 15 mg/kg/day group as dose of FT showed decreases in red blood cell count, hemoglobin, and hematocrit, and increases in platelet count and fibrinogen, with a slight decrease in white blood cell count in males. 7. In the blood biochemical test, abnormal findings included increases in total cholesterol and free cholesterol, and decreases in non-esterified fatty acid and albumin in both sexes in the 15 mg/kg/day group as dose of FT. 8. In organ weight measurement, abnormal changes included a decrease in thymus weight in both sexes in the 5 mg/kg/day or higher dosage g
doi_str_mv 10.2131/jts.21.SupplementIII_505
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_1468873326</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3159152031</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3345-27a80404eca3582cd284a048abe0c16c9378a2470f3691208fa523ff919c08803</originalsourceid><addsrcrecordid>eNptkMtOwzAURC0EEqXwD5ZYp_iRh7O0UrdYREnVuCoVC8sYBxr1EZJ0wd-TqqibsrqzmDOjOwBAjEYEU_xUdW0vRsWhrjdu63adlFIHKLgCA8wY8mjM4mswQJQxD9MA3YK7tq0QIhEK_AFYcIiptxTiBeZznsK5mAmuxBiO80JAlb_KRKoVLNRivIL5BHKYiSXkmZKZyGcpL5RMIJ-KTMHCw1BmcM5VcQ9uSrNp3cPfHYLFRKjk2UvzqUx46llK_cAjkWHIR76zhgaM2A_CfIN8Zt4dsji0MY2YIX6EShrGmCBWmoDQsoxxbFH_HB2Cx1Nu3ey_D67tdLU_NLu-UmM_ZCyilIS9i51cttm3beNKXTfrrWl-NEb6OKLuR-yFvhixR99OaNV25tOdQdN0a7txRxDHUXgJ_5d2puyXabTb0V848YIu</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1468873326</pqid></control><display><type>article</type><title>A 13-WEEK ORAL REPEATED DOSE TOXICITY STUDY OF A NEW ANTINEOPLASTIC AGENT S-1 IN RATS</title><source>J-STAGE Free</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Free Full-Text Journals in Chemistry</source><creator>HAYASHI, Taiji ; HASEGAWA, Hiroyuki ; TANAKA, Gotaro ; OHMAE, Sigeo</creator><creatorcontrib>HAYASHI, Taiji ; HASEGAWA, Hiroyuki ; TANAKA, Gotaro ; OHMAE, Sigeo</creatorcontrib><description>S-1, an antineoplastic formulation of a fluorinated pyrimidine derivative containing tegafur (FT), CDHP, and potassium oxonate (Oxo) in a molar ratio of 1:0.4:1, was recently developed by Taiho Pharmaceutical Co., Ltd., with the aim of prolonging the effective plasma concentration of 5-fluorouracil (5-FU) over that producted by FT alone and reducing its dose-limiting gastrointestinal toxicity. As a part of the S-1 toxicity study, a 13-week oral repeated dose toxicity study and a recovery study using male and female rats was conducted. Doses of S-1 were adjusted to deliver 1.5, 5, and 15 mg/kg/day as doses of FT, and FT wad given at 15mg/kg/day. The following results were obtained. 1. In clinical observation, edema of the limbs and face or swelling of the auricle of the ear and an anemic appearance were observed in both sexes in the 15 mg/kg/day group as dose of FT. Subsequently, ma1es in ithis group developed severe anemia, decrdased spontaneous motor activity, emaciation, and subnormal skin temperature, and many males died. In the survivors, keratosis of the palm, sole, or tail was observed, with necrosis and loss of the tail tip in the severe cases. 2. Body weight gain was suppressed from about week 2 of treatment in both sexes in the 15 mg/kg/day group as dose of FT, and there was almost no weight gain after week 4-5. Food consumption was consistently less than the control value for males in the 15 mg/kg/day group as dose of FT throughout the treatment period. 3. No marked changes were observed in water intake and on ophthalmologic examination. 4. In the fecal test for occult blood, a positive tendency was observed in both sexes in the 15 mg/kg/day group as dose of FT. 5. Urinalysis disclosed a slight increase in protein and decrease in sodium, potassium, and chloride in males, and an increase in protein in females in the 15 mg/kg/day group as dose of FT. 6. Hematologically, both sexes in the 15 mg/kg/day group as dose of FT showed decreases in red blood cell count, hemoglobin, and hematocrit, and increases in platelet count and fibrinogen, with a slight decrease in white blood cell count in males. 7. In the blood biochemical test, abnormal findings included increases in total cholesterol and free cholesterol, and decreases in non-esterified fatty acid and albumin in both sexes in the 15 mg/kg/day group as dose of FT. 8. In organ weight measurement, abnormal changes included a decrease in thymus weight in both sexes in the 5 mg/kg/day or higher dosage groups and a decrease in the testis weight in mdles and an increase in the liver weight in females in the 15mg/kg/day group as dose of FT. 9. Histopathologically, both sexes in the 15 mg/kg/day group as dose of FT showed a decrease in the red pulp of the bone marrow; atrophy of the thymus, white pulp of the spleen, and testes, degeneration of the renal tubules, and ulcerative changes of the skin or oral mucosa. 10. The findings were unremarkable in the FT group. 11. During the recovery study, all the toxic effects tended to reverse. 12. The NOAEL of S-1 was estimated to be 1.5 mg/kg/day as dose of FT for both sexes.</description><identifier>ISSN: 0388-1350</identifier><identifier>EISSN: 1880-3989</identifier><identifier>DOI: 10.2131/jts.21.SupplementIII_505</identifier><language>eng</language><publisher>Suita: The Japanese Society of Toxicology</publisher><subject>Rat</subject><ispartof>The Journal of Toxicological Sciences, 1996/11/27, Vol.21(SupplementIII), pp.505-526</ispartof><rights>The Japanese Society of Toxicology Headquarters</rights><rights>Copyright Japan Science and Technology Agency 1996</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3345-27a80404eca3582cd284a048abe0c16c9378a2470f3691208fa523ff919c08803</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,1883,4024,27923,27924,27925</link.rule.ids></links><search><creatorcontrib>HAYASHI, Taiji</creatorcontrib><creatorcontrib>HASEGAWA, Hiroyuki</creatorcontrib><creatorcontrib>TANAKA, Gotaro</creatorcontrib><creatorcontrib>OHMAE, Sigeo</creatorcontrib><title>A 13-WEEK ORAL REPEATED DOSE TOXICITY STUDY OF A NEW ANTINEOPLASTIC AGENT S-1 IN RATS</title><title>Journal of toxicological sciences</title><description>S-1, an antineoplastic formulation of a fluorinated pyrimidine derivative containing tegafur (FT), CDHP, and potassium oxonate (Oxo) in a molar ratio of 1:0.4:1, was recently developed by Taiho Pharmaceutical Co., Ltd., with the aim of prolonging the effective plasma concentration of 5-fluorouracil (5-FU) over that producted by FT alone and reducing its dose-limiting gastrointestinal toxicity. As a part of the S-1 toxicity study, a 13-week oral repeated dose toxicity study and a recovery study using male and female rats was conducted. Doses of S-1 were adjusted to deliver 1.5, 5, and 15 mg/kg/day as doses of FT, and FT wad given at 15mg/kg/day. The following results were obtained. 1. In clinical observation, edema of the limbs and face or swelling of the auricle of the ear and an anemic appearance were observed in both sexes in the 15 mg/kg/day group as dose of FT. Subsequently, ma1es in ithis group developed severe anemia, decrdased spontaneous motor activity, emaciation, and subnormal skin temperature, and many males died. In the survivors, keratosis of the palm, sole, or tail was observed, with necrosis and loss of the tail tip in the severe cases. 2. Body weight gain was suppressed from about week 2 of treatment in both sexes in the 15 mg/kg/day group as dose of FT, and there was almost no weight gain after week 4-5. Food consumption was consistently less than the control value for males in the 15 mg/kg/day group as dose of FT throughout the treatment period. 3. No marked changes were observed in water intake and on ophthalmologic examination. 4. In the fecal test for occult blood, a positive tendency was observed in both sexes in the 15 mg/kg/day group as dose of FT. 5. Urinalysis disclosed a slight increase in protein and decrease in sodium, potassium, and chloride in males, and an increase in protein in females in the 15 mg/kg/day group as dose of FT. 6. Hematologically, both sexes in the 15 mg/kg/day group as dose of FT showed decreases in red blood cell count, hemoglobin, and hematocrit, and increases in platelet count and fibrinogen, with a slight decrease in white blood cell count in males. 7. In the blood biochemical test, abnormal findings included increases in total cholesterol and free cholesterol, and decreases in non-esterified fatty acid and albumin in both sexes in the 15 mg/kg/day group as dose of FT. 8. In organ weight measurement, abnormal changes included a decrease in thymus weight in both sexes in the 5 mg/kg/day or higher dosage groups and a decrease in the testis weight in mdles and an increase in the liver weight in females in the 15mg/kg/day group as dose of FT. 9. Histopathologically, both sexes in the 15 mg/kg/day group as dose of FT showed a decrease in the red pulp of the bone marrow; atrophy of the thymus, white pulp of the spleen, and testes, degeneration of the renal tubules, and ulcerative changes of the skin or oral mucosa. 10. The findings were unremarkable in the FT group. 11. During the recovery study, all the toxic effects tended to reverse. 12. The NOAEL of S-1 was estimated to be 1.5 mg/kg/day as dose of FT for both sexes.</description><subject>Rat</subject><issn>0388-1350</issn><issn>1880-3989</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><recordid>eNptkMtOwzAURC0EEqXwD5ZYp_iRh7O0UrdYREnVuCoVC8sYBxr1EZJ0wd-TqqibsrqzmDOjOwBAjEYEU_xUdW0vRsWhrjdu63adlFIHKLgCA8wY8mjM4mswQJQxD9MA3YK7tq0QIhEK_AFYcIiptxTiBeZznsK5mAmuxBiO80JAlb_KRKoVLNRivIL5BHKYiSXkmZKZyGcpL5RMIJ-KTMHCw1BmcM5VcQ9uSrNp3cPfHYLFRKjk2UvzqUx46llK_cAjkWHIR76zhgaM2A_CfIN8Zt4dsji0MY2YIX6EShrGmCBWmoDQsoxxbFH_HB2Cx1Nu3ey_D67tdLU_NLu-UmM_ZCyilIS9i51cttm3beNKXTfrrWl-NEb6OKLuR-yFvhixR99OaNV25tOdQdN0a7txRxDHUXgJ_5d2puyXabTb0V848YIu</recordid><startdate>1996</startdate><enddate>1996</enddate><creator>HAYASHI, Taiji</creator><creator>HASEGAWA, Hiroyuki</creator><creator>TANAKA, Gotaro</creator><creator>OHMAE, Sigeo</creator><general>The Japanese Society of Toxicology</general><general>Japan Science and Technology Agency</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7ST</scope><scope>7U7</scope><scope>C1K</scope><scope>SOI</scope></search><sort><creationdate>1996</creationdate><title>A 13-WEEK ORAL REPEATED DOSE TOXICITY STUDY OF A NEW ANTINEOPLASTIC AGENT S-1 IN RATS</title><author>HAYASHI, Taiji ; HASEGAWA, Hiroyuki ; TANAKA, Gotaro ; OHMAE, Sigeo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3345-27a80404eca3582cd284a048abe0c16c9378a2470f3691208fa523ff919c08803</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Rat</topic><toplevel>online_resources</toplevel><creatorcontrib>HAYASHI, Taiji</creatorcontrib><creatorcontrib>HASEGAWA, Hiroyuki</creatorcontrib><creatorcontrib>TANAKA, Gotaro</creatorcontrib><creatorcontrib>OHMAE, Sigeo</creatorcontrib><collection>CrossRef</collection><collection>Environment Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Environment Abstracts</collection><jtitle>Journal of toxicological sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>HAYASHI, Taiji</au><au>HASEGAWA, Hiroyuki</au><au>TANAKA, Gotaro</au><au>OHMAE, Sigeo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A 13-WEEK ORAL REPEATED DOSE TOXICITY STUDY OF A NEW ANTINEOPLASTIC AGENT S-1 IN RATS</atitle><jtitle>Journal of toxicological sciences</jtitle><date>1996</date><risdate>1996</risdate><volume>21</volume><issue>SupplementIII</issue><spage>505</spage><epage>526</epage><pages>505-526</pages><issn>0388-1350</issn><eissn>1880-3989</eissn><abstract>S-1, an antineoplastic formulation of a fluorinated pyrimidine derivative containing tegafur (FT), CDHP, and potassium oxonate (Oxo) in a molar ratio of 1:0.4:1, was recently developed by Taiho Pharmaceutical Co., Ltd., with the aim of prolonging the effective plasma concentration of 5-fluorouracil (5-FU) over that producted by FT alone and reducing its dose-limiting gastrointestinal toxicity. As a part of the S-1 toxicity study, a 13-week oral repeated dose toxicity study and a recovery study using male and female rats was conducted. Doses of S-1 were adjusted to deliver 1.5, 5, and 15 mg/kg/day as doses of FT, and FT wad given at 15mg/kg/day. The following results were obtained. 1. In clinical observation, edema of the limbs and face or swelling of the auricle of the ear and an anemic appearance were observed in both sexes in the 15 mg/kg/day group as dose of FT. Subsequently, ma1es in ithis group developed severe anemia, decrdased spontaneous motor activity, emaciation, and subnormal skin temperature, and many males died. In the survivors, keratosis of the palm, sole, or tail was observed, with necrosis and loss of the tail tip in the severe cases. 2. Body weight gain was suppressed from about week 2 of treatment in both sexes in the 15 mg/kg/day group as dose of FT, and there was almost no weight gain after week 4-5. Food consumption was consistently less than the control value for males in the 15 mg/kg/day group as dose of FT throughout the treatment period. 3. No marked changes were observed in water intake and on ophthalmologic examination. 4. In the fecal test for occult blood, a positive tendency was observed in both sexes in the 15 mg/kg/day group as dose of FT. 5. Urinalysis disclosed a slight increase in protein and decrease in sodium, potassium, and chloride in males, and an increase in protein in females in the 15 mg/kg/day group as dose of FT. 6. Hematologically, both sexes in the 15 mg/kg/day group as dose of FT showed decreases in red blood cell count, hemoglobin, and hematocrit, and increases in platelet count and fibrinogen, with a slight decrease in white blood cell count in males. 7. In the blood biochemical test, abnormal findings included increases in total cholesterol and free cholesterol, and decreases in non-esterified fatty acid and albumin in both sexes in the 15 mg/kg/day group as dose of FT. 8. In organ weight measurement, abnormal changes included a decrease in thymus weight in both sexes in the 5 mg/kg/day or higher dosage groups and a decrease in the testis weight in mdles and an increase in the liver weight in females in the 15mg/kg/day group as dose of FT. 9. Histopathologically, both sexes in the 15 mg/kg/day group as dose of FT showed a decrease in the red pulp of the bone marrow; atrophy of the thymus, white pulp of the spleen, and testes, degeneration of the renal tubules, and ulcerative changes of the skin or oral mucosa. 10. The findings were unremarkable in the FT group. 11. During the recovery study, all the toxic effects tended to reverse. 12. The NOAEL of S-1 was estimated to be 1.5 mg/kg/day as dose of FT for both sexes.</abstract><cop>Suita</cop><pub>The Japanese Society of Toxicology</pub><doi>10.2131/jts.21.SupplementIII_505</doi><tpages>22</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0388-1350
ispartof The Journal of Toxicological Sciences, 1996/11/27, Vol.21(SupplementIII), pp.505-526
issn 0388-1350
1880-3989
language eng
recordid cdi_proquest_journals_1468873326
source J-STAGE Free; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Free Full-Text Journals in Chemistry
subjects Rat
title A 13-WEEK ORAL REPEATED DOSE TOXICITY STUDY OF A NEW ANTINEOPLASTIC AGENT S-1 IN RATS
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T15%3A02%3A29IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%2013-WEEK%20ORAL%20REPEATED%20DOSE%20TOXICITY%20STUDY%20OF%20A%20NEW%20ANTINEOPLASTIC%20AGENT%20S-1%20IN%20RATS&rft.jtitle=Journal%20of%20toxicological%20sciences&rft.au=HAYASHI,%20Taiji&rft.date=1996&rft.volume=21&rft.issue=SupplementIII&rft.spage=505&rft.epage=526&rft.pages=505-526&rft.issn=0388-1350&rft.eissn=1880-3989&rft_id=info:doi/10.2131/jts.21.SupplementIII_505&rft_dat=%3Cproquest_cross%3E3159152031%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1468873326&rft_id=info:pmid/&rfr_iscdi=true