{"title":"三乙基铅降低体外大鼠小脑中枢苯二氮卓受体结合","authors":"Hannu Komulainen , Arto Keränen , Veijo Saano","doi":"10.1016/0926-6917(95)00013-5","DOIUrl":null,"url":null,"abstract":"<div><p>Effect of triethyllead on the specific [<sup>3</sup>H]flunitrazepam binding was studied in rat cortical and cerebellar P<sub>2</sub> fractions in vitro and in tissue homogenates of several rat brain regions ex vivo after 5 daily subcutaneous doses of 1.9 mg/kg triethyllead acetate to rats. Up to concentration of 100 μM, triethyllead did not significantly the specific [<sup>3</sup>H]flunitrazepam binding but attenuated marginally (14–18%) the GABA<sub>A</sub> receptor agonist, muscimol-induced elevation of [<sup>3</sup>H]flunitrazepam binding in cerebellar tissue. After the subacute treatment of rats with triethyllead, the specific [<sup>3</sup>H]flunitrazepam binding was 27% lower in cerebellum compared to control animals. In other brain regions the receptor binding was not changed. The data suggest that triethyllead modified the cerebellar GABA<sub>A</sub> receptor complex causing decreased binding in the benzodiazepine site. Such an inhibitory effect in the GABA<sub>A</sub> receptor complex may decrease cerebellarinhibitory output and augment the triethyllead induced convulsions and tremor.</p></div>","PeriodicalId":100501,"journal":{"name":"European Journal of Pharmacology: Environmental Toxicology and Pharmacology","volume":"293 2","pages":"Pages 167-171"},"PeriodicalIF":0.0000,"publicationDate":"1995-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0926-6917(95)00013-5","citationCount":"8","resultStr":"{\"title\":\"Triethyllead decreases central benzodiazepine receptor binding in rat cerebellum ex vivo\",\"authors\":\"Hannu Komulainen , Arto Keränen , Veijo Saano\",\"doi\":\"10.1016/0926-6917(95)00013-5\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Effect of triethyllead on the specific [<sup>3</sup>H]flunitrazepam binding was studied in rat cortical and cerebellar P<sub>2</sub> fractions in vitro and in tissue homogenates of several rat brain regions ex vivo after 5 daily subcutaneous doses of 1.9 mg/kg triethyllead acetate to rats. Up to concentration of 100 μM, triethyllead did not significantly the specific [<sup>3</sup>H]flunitrazepam binding but attenuated marginally (14–18%) the GABA<sub>A</sub> receptor agonist, muscimol-induced elevation of [<sup>3</sup>H]flunitrazepam binding in cerebellar tissue. After the subacute treatment of rats with triethyllead, the specific [<sup>3</sup>H]flunitrazepam binding was 27% lower in cerebellum compared to control animals. In other brain regions the receptor binding was not changed. The data suggest that triethyllead modified the cerebellar GABA<sub>A</sub> receptor complex causing decreased binding in the benzodiazepine site. Such an inhibitory effect in the GABA<sub>A</sub> receptor complex may decrease cerebellarinhibitory output and augment the triethyllead induced convulsions and tremor.</p></div>\",\"PeriodicalId\":100501,\"journal\":{\"name\":\"European Journal of Pharmacology: Environmental Toxicology and Pharmacology\",\"volume\":\"293 2\",\"pages\":\"Pages 167-171\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1995-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/0926-6917(95)00013-5\",\"citationCount\":\"8\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"European Journal of Pharmacology: Environmental Toxicology and Pharmacology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/0926691795000135\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Journal of Pharmacology: Environmental Toxicology and Pharmacology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0926691795000135","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Triethyllead decreases central benzodiazepine receptor binding in rat cerebellum ex vivo
Effect of triethyllead on the specific [3H]flunitrazepam binding was studied in rat cortical and cerebellar P2 fractions in vitro and in tissue homogenates of several rat brain regions ex vivo after 5 daily subcutaneous doses of 1.9 mg/kg triethyllead acetate to rats. Up to concentration of 100 μM, triethyllead did not significantly the specific [3H]flunitrazepam binding but attenuated marginally (14–18%) the GABAA receptor agonist, muscimol-induced elevation of [3H]flunitrazepam binding in cerebellar tissue. After the subacute treatment of rats with triethyllead, the specific [3H]flunitrazepam binding was 27% lower in cerebellum compared to control animals. In other brain regions the receptor binding was not changed. The data suggest that triethyllead modified the cerebellar GABAA receptor complex causing decreased binding in the benzodiazepine site. Such an inhibitory effect in the GABAA receptor complex may decrease cerebellarinhibitory output and augment the triethyllead induced convulsions and tremor.