Dipak V. parmar, Gazala Ahmed, Milind A. Khandkar, Surendra S. Katyare
{"title":"线粒体atp酶:对乙酰氨基酚引起的肝毒性的靶点","authors":"Dipak V. parmar, Gazala Ahmed, Milind A. Khandkar, Surendra S. Katyare","doi":"10.1016/0926-6917(95)00021-6","DOIUrl":null,"url":null,"abstract":"<div><p>We examined the effect of paracetamol treatment (650 mg/kg) on the function of the ATPase from rat hepatic mitochondria. The drug treatment caused an overall 35% decrease in ATPase activity, with a complete loss of the high affinity component as determined by substrate kinetic studies. The <em>K</em><sub>m</sub> for the intermediate and low affinity components decreased by about 30% without change in <em>V</em><sub>max</sub>, which may represent a compensatory mechanism. The drug treatment also resulted in a dramatic decrease in the phase transition temperature by about 19°C without affecting the energies of activation of the enzyme. Mitochondrial total phospholipid content increased significantly with a reciprocal decrease in the cholesterol content. The total phopholipid/cholesterol molar ratio increased by 50% after paracetamol treatment. However, phospholipid composition (as % of total) of the mitochondria was unaltered.</p></div>","PeriodicalId":100501,"journal":{"name":"European Journal of Pharmacology: Environmental Toxicology and Pharmacology","volume":"293 3","pages":"Pages 225-229"},"PeriodicalIF":0.0000,"publicationDate":"1995-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0926-6917(95)00021-6","citationCount":"60","resultStr":"{\"title\":\"Mitochondrial ATPase: a target for paracetamol-induced hepatotoxicity\",\"authors\":\"Dipak V. parmar, Gazala Ahmed, Milind A. Khandkar, Surendra S. Katyare\",\"doi\":\"10.1016/0926-6917(95)00021-6\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>We examined the effect of paracetamol treatment (650 mg/kg) on the function of the ATPase from rat hepatic mitochondria. The drug treatment caused an overall 35% decrease in ATPase activity, with a complete loss of the high affinity component as determined by substrate kinetic studies. The <em>K</em><sub>m</sub> for the intermediate and low affinity components decreased by about 30% without change in <em>V</em><sub>max</sub>, which may represent a compensatory mechanism. The drug treatment also resulted in a dramatic decrease in the phase transition temperature by about 19°C without affecting the energies of activation of the enzyme. Mitochondrial total phospholipid content increased significantly with a reciprocal decrease in the cholesterol content. The total phopholipid/cholesterol molar ratio increased by 50% after paracetamol treatment. However, phospholipid composition (as % of total) of the mitochondria was unaltered.</p></div>\",\"PeriodicalId\":100501,\"journal\":{\"name\":\"European Journal of Pharmacology: Environmental Toxicology and Pharmacology\",\"volume\":\"293 3\",\"pages\":\"Pages 225-229\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1995-10-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/0926-6917(95)00021-6\",\"citationCount\":\"60\",\"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/0926691795000216\",\"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/0926691795000216","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Mitochondrial ATPase: a target for paracetamol-induced hepatotoxicity
We examined the effect of paracetamol treatment (650 mg/kg) on the function of the ATPase from rat hepatic mitochondria. The drug treatment caused an overall 35% decrease in ATPase activity, with a complete loss of the high affinity component as determined by substrate kinetic studies. The Km for the intermediate and low affinity components decreased by about 30% without change in Vmax, which may represent a compensatory mechanism. The drug treatment also resulted in a dramatic decrease in the phase transition temperature by about 19°C without affecting the energies of activation of the enzyme. Mitochondrial total phospholipid content increased significantly with a reciprocal decrease in the cholesterol content. The total phopholipid/cholesterol molar ratio increased by 50% after paracetamol treatment. However, phospholipid composition (as % of total) of the mitochondria was unaltered.