Zoltán Spolarics , István Mucha , József Mandl , Raymund Machovich , Gábor Bánhegyi , Ferenc Antonio, Tamáas Garzó
{"title":"Prostanoid synthesis in isolated parenchymal and nonparenchymal mouse liver cells in the presence of arachioonic acid","authors":"Zoltán Spolarics , István Mucha , József Mandl , Raymund Machovich , Gábor Bánhegyi , Ferenc Antonio, Tamáas Garzó","doi":"10.1016/0262-1746(87)90001-1","DOIUrl":null,"url":null,"abstract":"<div><p>Prostanoid synthesis was investigated in suspensions of isolated mouse hepatocytes and nonparenchymal liver cells. A stable metabolite of thromboxane A<sub>2</sub> (TXB<sub>2</sub>) of prostacyclin (6-keto PGF<sub>1∝</sub>) and one of the prostaglandins (PGF<sub>2∝</sub>) was detected by radio-immuno-assay (RIA). Hepatocytes synthesized mainly TXB<sub>2</sub>, while smaller amounts of 6-keto PGF<sub>1∝</sub> and PGF<sub>2∝</sub> were detected during 60 min incubation. Homogenization of hepatocytes caused a slight increase in TXB<sub>2</sub> production and provoked the synthesis of PGF<sub>2∝</sub> and 6-keto PGF<sub>1∝</sub>. Theaddition ofarachidonate to hepatocytes did not influence prostanoid production at concentrations below 10<sup>−5</sup> M. Higher concentrations further increased TXB<sub>2</sub> production and also increased the synthesis of 6-keto PGF<sub>1∝</sub> and PGF<sub>2∝</sub>. Nonparenchymal cells synthesized all the three types of prostanoids and homogenization of these cells did not result in a marked change. The addition of 10<sup>−7</sup>−10<sup>−5</sup>M arachidonate increased the TXB<sub>2</sub>, 6-keto PGF<sub>1∝</sub> and PGF<sub>2∝</sub> synthesis in nonparenchymal cells. No further increase was found at higher concentrations.</p></div>","PeriodicalId":20720,"journal":{"name":"Prostaglandins, leukotrienes, and medicine","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"1987-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0262-1746(87)90001-1","citationCount":"10","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Prostaglandins, leukotrienes, and medicine","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0262174687900011","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 10
Abstract
Prostanoid synthesis was investigated in suspensions of isolated mouse hepatocytes and nonparenchymal liver cells. A stable metabolite of thromboxane A2 (TXB2) of prostacyclin (6-keto PGF1∝) and one of the prostaglandins (PGF2∝) was detected by radio-immuno-assay (RIA). Hepatocytes synthesized mainly TXB2, while smaller amounts of 6-keto PGF1∝ and PGF2∝ were detected during 60 min incubation. Homogenization of hepatocytes caused a slight increase in TXB2 production and provoked the synthesis of PGF2∝ and 6-keto PGF1∝. Theaddition ofarachidonate to hepatocytes did not influence prostanoid production at concentrations below 10−5 M. Higher concentrations further increased TXB2 production and also increased the synthesis of 6-keto PGF1∝ and PGF2∝. Nonparenchymal cells synthesized all the three types of prostanoids and homogenization of these cells did not result in a marked change. The addition of 10−7−10−5M arachidonate increased the TXB2, 6-keto PGF1∝ and PGF2∝ synthesis in nonparenchymal cells. No further increase was found at higher concentrations.