Effect of chlorpromazine on rat placenta development
We examined the sequential histopathological changes in the placentas from rats exposed to chlorpromazine. Chlorpromazine was intraperitoneally administered on GD 14 at 50 and 100mg/kg and the placentas were sampled on GDs 14.5, 15, 17 and 21. The incidence of dams with complete fetal resorption was...
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Veröffentlicht in: | Experimental and toxicologic pathology : official journal of the Gesellschaft für Toxikologische Pathologie 2014-01, Vol.66 (1), p.41-47 |
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creator | Furukawa, Satoshi Hayashi, Seigo Abe, Masayoshi Hagio, Souichiro Irie, Kota Kuroda, Yusuke Ogawa, Izumi Sugiyama, Akihiko |
description | We examined the sequential histopathological changes in the placentas from rats exposed to chlorpromazine. Chlorpromazine was intraperitoneally administered on GD 14 at 50 and 100mg/kg and the placentas were sampled on GDs 14.5, 15, 17 and 21. The incidence of dams with complete fetal resorption was increased from GD 17 up to 20% at 50mg/kg and 44.4% at 100mg/kg. The embryo/fetal weights reduced on GDs 15 and 17 at 50mg/kg and during GDs 15–21 at 100mg/kg. The placental weights reduced on GD 17 at 50mg/kg and during GDs 14.5–21 at 100mg/kg. Histopathologically, in the labyrinth zone, apoptotic cells were scattered in the trophoblastic septa without inhibition of cell proliferation on GDs 14.5 and 15 at 50 and 100mg/kg in a dose-dependent manner. A decrease in trophoblasts led to labyrinth zone hypoplasia. In the basal zone, apoptotic cells were scattered on GDs 14.5 and 15 at 100mg/kg, and most of them appeared to be glycogen cells. A decrease in glycogen cells induced the delayed development of glycogen cell islands and the subsequent remaining glycogen cell islands, and led to the cystic degeneration of glycogen cells. In addition, failure of development of the glycogen cell islands led to the impaired interstitial invasion of the glycogen cells, and then metrial gland hypoplasia occurred. |
doi_str_mv | 10.1016/j.etp.2013.08.002 |
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Chlorpromazine was intraperitoneally administered on GD 14 at 50 and 100mg/kg and the placentas were sampled on GDs 14.5, 15, 17 and 21. The incidence of dams with complete fetal resorption was increased from GD 17 up to 20% at 50mg/kg and 44.4% at 100mg/kg. The embryo/fetal weights reduced on GDs 15 and 17 at 50mg/kg and during GDs 15–21 at 100mg/kg. The placental weights reduced on GD 17 at 50mg/kg and during GDs 14.5–21 at 100mg/kg. Histopathologically, in the labyrinth zone, apoptotic cells were scattered in the trophoblastic septa without inhibition of cell proliferation on GDs 14.5 and 15 at 50 and 100mg/kg in a dose-dependent manner. A decrease in trophoblasts led to labyrinth zone hypoplasia. In the basal zone, apoptotic cells were scattered on GDs 14.5 and 15 at 100mg/kg, and most of them appeared to be glycogen cells. A decrease in glycogen cells induced the delayed development of glycogen cell islands and the subsequent remaining glycogen cell islands, and led to the cystic degeneration of glycogen cells. In addition, failure of development of the glycogen cell islands led to the impaired interstitial invasion of the glycogen cells, and then metrial gland hypoplasia occurred.</description><identifier>ISSN: 0940-2993</identifier><identifier>EISSN: 1618-1433</identifier><identifier>DOI: 10.1016/j.etp.2013.08.002</identifier><identifier>PMID: 24139509</identifier><language>eng</language><publisher>Germany: Elsevier GmbH</publisher><subject>Animals ; Antipsychotic Agents - toxicity ; Basal zone ; Chlorpromazine ; Chlorpromazine - toxicity ; Cystic degeneration ; Embryo, Mammalian - drug effects ; Female ; Fetal Weight - drug effects ; Fetus - drug effects ; Glycogen cell ; In Situ Nick-End Labeling ; Placenta - drug effects ; Placenta - pathology ; Pregnancy ; Rat ; Rats ; Rats, Wistar</subject><ispartof>Experimental and toxicologic pathology : official journal of the Gesellschaft für Toxikologische Pathologie, 2014-01, Vol.66 (1), p.41-47</ispartof><rights>2013 Elsevier GmbH</rights><rights>Copyright © 2013 Elsevier GmbH. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c452t-3b7271d85a6b4d12bfd5c1764fbaa8c40542d07575dd11278c09dd4a9c5b4aa23</citedby><cites>FETCH-LOGICAL-c452t-3b7271d85a6b4d12bfd5c1764fbaa8c40542d07575dd11278c09dd4a9c5b4aa23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.etp.2013.08.002$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27922,27923,45993</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24139509$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Furukawa, Satoshi</creatorcontrib><creatorcontrib>Hayashi, Seigo</creatorcontrib><creatorcontrib>Abe, Masayoshi</creatorcontrib><creatorcontrib>Hagio, Souichiro</creatorcontrib><creatorcontrib>Irie, Kota</creatorcontrib><creatorcontrib>Kuroda, Yusuke</creatorcontrib><creatorcontrib>Ogawa, Izumi</creatorcontrib><creatorcontrib>Sugiyama, Akihiko</creatorcontrib><title>Effect of chlorpromazine on rat placenta development</title><title>Experimental and toxicologic pathology : official journal of the Gesellschaft für Toxikologische Pathologie</title><addtitle>Exp Toxicol Pathol</addtitle><description>We examined the sequential histopathological changes in the placentas from rats exposed to chlorpromazine. Chlorpromazine was intraperitoneally administered on GD 14 at 50 and 100mg/kg and the placentas were sampled on GDs 14.5, 15, 17 and 21. The incidence of dams with complete fetal resorption was increased from GD 17 up to 20% at 50mg/kg and 44.4% at 100mg/kg. The embryo/fetal weights reduced on GDs 15 and 17 at 50mg/kg and during GDs 15–21 at 100mg/kg. The placental weights reduced on GD 17 at 50mg/kg and during GDs 14.5–21 at 100mg/kg. Histopathologically, in the labyrinth zone, apoptotic cells were scattered in the trophoblastic septa without inhibition of cell proliferation on GDs 14.5 and 15 at 50 and 100mg/kg in a dose-dependent manner. A decrease in trophoblasts led to labyrinth zone hypoplasia. In the basal zone, apoptotic cells were scattered on GDs 14.5 and 15 at 100mg/kg, and most of them appeared to be glycogen cells. A decrease in glycogen cells induced the delayed development of glycogen cell islands and the subsequent remaining glycogen cell islands, and led to the cystic degeneration of glycogen cells. In addition, failure of development of the glycogen cell islands led to the impaired interstitial invasion of the glycogen cells, and then metrial gland hypoplasia occurred.</description><subject>Animals</subject><subject>Antipsychotic Agents - toxicity</subject><subject>Basal zone</subject><subject>Chlorpromazine</subject><subject>Chlorpromazine - toxicity</subject><subject>Cystic degeneration</subject><subject>Embryo, Mammalian - drug effects</subject><subject>Female</subject><subject>Fetal Weight - drug effects</subject><subject>Fetus - drug effects</subject><subject>Glycogen cell</subject><subject>In Situ Nick-End Labeling</subject><subject>Placenta - drug effects</subject><subject>Placenta - pathology</subject><subject>Pregnancy</subject><subject>Rat</subject><subject>Rats</subject><subject>Rats, Wistar</subject><issn>0940-2993</issn><issn>1618-1433</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1LxDAQhoMo7rr6A7xIj15aM2nStHiSZf2ABS96DmkyxS5tU5Pugv56s-zq0dMw8LwvMw8h10AzoFDcbTKcxoxRyDNaZpSyEzKHAsoUeJ6fkjmtOE1ZVeUzchHCJgK0EnBOZoxDXglazQlfNQ2aKXFNYj4650fvev3dDpi4IfF6SsZOGxwmnVjcYefGPi6X5KzRXcCr41yQ98fV2_I5Xb8-vSwf1qnhgk1pXksmwZZCFzW3wOrGCgOy4E2tdWk4FZxZKoUU1gIwWRpaWct1ZUTNtWb5gtweeuNVn1sMk-rbYLDr9IBuGxQIKKSgUhYRhQNqvAvBY6NG3_bafymgai9LbVSUpfayFC1VdBEzN8f6bd2j_Uv82onA_QHA-OSuRa-CaXEwaFsfpSnr2n_qfwDD-nle</recordid><startdate>201401</startdate><enddate>201401</enddate><creator>Furukawa, Satoshi</creator><creator>Hayashi, Seigo</creator><creator>Abe, Masayoshi</creator><creator>Hagio, Souichiro</creator><creator>Irie, Kota</creator><creator>Kuroda, Yusuke</creator><creator>Ogawa, Izumi</creator><creator>Sugiyama, Akihiko</creator><general>Elsevier GmbH</general><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>201401</creationdate><title>Effect of chlorpromazine on rat placenta development</title><author>Furukawa, Satoshi ; Hayashi, Seigo ; Abe, Masayoshi ; Hagio, Souichiro ; Irie, Kota ; Kuroda, Yusuke ; Ogawa, Izumi ; Sugiyama, Akihiko</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c452t-3b7271d85a6b4d12bfd5c1764fbaa8c40542d07575dd11278c09dd4a9c5b4aa23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Animals</topic><topic>Antipsychotic Agents - toxicity</topic><topic>Basal zone</topic><topic>Chlorpromazine</topic><topic>Chlorpromazine - toxicity</topic><topic>Cystic degeneration</topic><topic>Embryo, Mammalian - drug effects</topic><topic>Female</topic><topic>Fetal Weight - drug effects</topic><topic>Fetus - drug effects</topic><topic>Glycogen cell</topic><topic>In Situ Nick-End Labeling</topic><topic>Placenta - drug effects</topic><topic>Placenta - pathology</topic><topic>Pregnancy</topic><topic>Rat</topic><topic>Rats</topic><topic>Rats, Wistar</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Furukawa, Satoshi</creatorcontrib><creatorcontrib>Hayashi, Seigo</creatorcontrib><creatorcontrib>Abe, Masayoshi</creatorcontrib><creatorcontrib>Hagio, Souichiro</creatorcontrib><creatorcontrib>Irie, Kota</creatorcontrib><creatorcontrib>Kuroda, Yusuke</creatorcontrib><creatorcontrib>Ogawa, Izumi</creatorcontrib><creatorcontrib>Sugiyama, Akihiko</creatorcontrib><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>Experimental and toxicologic pathology : official journal of the Gesellschaft für Toxikologische Pathologie</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Furukawa, Satoshi</au><au>Hayashi, Seigo</au><au>Abe, Masayoshi</au><au>Hagio, Souichiro</au><au>Irie, Kota</au><au>Kuroda, Yusuke</au><au>Ogawa, Izumi</au><au>Sugiyama, Akihiko</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of chlorpromazine on rat placenta development</atitle><jtitle>Experimental and toxicologic pathology : official journal of the Gesellschaft für Toxikologische Pathologie</jtitle><addtitle>Exp Toxicol Pathol</addtitle><date>2014-01</date><risdate>2014</risdate><volume>66</volume><issue>1</issue><spage>41</spage><epage>47</epage><pages>41-47</pages><issn>0940-2993</issn><eissn>1618-1433</eissn><abstract>We examined the sequential histopathological changes in the placentas from rats exposed to chlorpromazine. Chlorpromazine was intraperitoneally administered on GD 14 at 50 and 100mg/kg and the placentas were sampled on GDs 14.5, 15, 17 and 21. The incidence of dams with complete fetal resorption was increased from GD 17 up to 20% at 50mg/kg and 44.4% at 100mg/kg. The embryo/fetal weights reduced on GDs 15 and 17 at 50mg/kg and during GDs 15–21 at 100mg/kg. The placental weights reduced on GD 17 at 50mg/kg and during GDs 14.5–21 at 100mg/kg. Histopathologically, in the labyrinth zone, apoptotic cells were scattered in the trophoblastic septa without inhibition of cell proliferation on GDs 14.5 and 15 at 50 and 100mg/kg in a dose-dependent manner. A decrease in trophoblasts led to labyrinth zone hypoplasia. In the basal zone, apoptotic cells were scattered on GDs 14.5 and 15 at 100mg/kg, and most of them appeared to be glycogen cells. A decrease in glycogen cells induced the delayed development of glycogen cell islands and the subsequent remaining glycogen cell islands, and led to the cystic degeneration of glycogen cells. In addition, failure of development of the glycogen cell islands led to the impaired interstitial invasion of the glycogen cells, and then metrial gland hypoplasia occurred.</abstract><cop>Germany</cop><pub>Elsevier GmbH</pub><pmid>24139509</pmid><doi>10.1016/j.etp.2013.08.002</doi><tpages>7</tpages></addata></record> |
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subjects | Animals Antipsychotic Agents - toxicity Basal zone Chlorpromazine Chlorpromazine - toxicity Cystic degeneration Embryo, Mammalian - drug effects Female Fetal Weight - drug effects Fetus - drug effects Glycogen cell In Situ Nick-End Labeling Placenta - drug effects Placenta - pathology Pregnancy Rat Rats Rats, Wistar |
title | Effect of chlorpromazine on rat placenta development |
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