V.W Pike , M.P Law , S Osman , R.J Davenport , O Rimoldi , D Giardinà , P.G Camici
{"title":"用于心脏肾上腺素受体PET研究的新型放射配体的选择、设计和评价","authors":"V.W Pike , M.P Law , S Osman , R.J Davenport , O Rimoldi , D Giardinà , P.G Camici","doi":"10.1016/S0031-6865(99)00032-1","DOIUrl":null,"url":null,"abstract":"<div><p><span>Changes in the numbers of human cardiac adrenoceptors<span><span> (ARs) are associated with various diseases, such as myocardial ischemia, </span>congestive heart failure<span>, cardiomyopathy<span> and hypertension. There is a clear need for capability to assess human cardiac ARs directly in vivo. Positron emission tomography (PET) is an imaging technique that provides this possibility, if effective radioligands can be developed for the targeted ARs. Here, the status of myocardial AR radioligand development for PET is described. Currently, there exist effective radioligands for imaging β-ARs in human myocardium. One of these, [</span></span></span></span><span><math><msup><mi></mi><mn>11</mn></msup><mtext>C</mtext></math></span>](<em>S</em><span>)-CGP 12177, is applied extensively to clinical research with PET, sometimes with other tracers of other aspects of the noradrenalin system. Alternative radioligands are in development for β-ARs, including β</span><sub>1</sub>-selective radioligands. A promising radioligand for imaging myocardial α<sub>1</sub>-ARs, [<span><math><msup><mi></mi><mn>11</mn></msup><mtext>C</mtext></math></span>]GB67, is now being evaluated in human PET experiments.</p></div>","PeriodicalId":19830,"journal":{"name":"Pharmaceutica acta Helvetiae","volume":"74 2","pages":"Pages 191-200"},"PeriodicalIF":0.0000,"publicationDate":"2000-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0031-6865(99)00032-1","citationCount":"27","resultStr":"{\"title\":\"Selection, design and evaluation of new radioligands for PET studies of cardiac adrenoceptors\",\"authors\":\"V.W Pike , M.P Law , S Osman , R.J Davenport , O Rimoldi , D Giardinà , P.G Camici\",\"doi\":\"10.1016/S0031-6865(99)00032-1\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><span>Changes in the numbers of human cardiac adrenoceptors<span><span> (ARs) are associated with various diseases, such as myocardial ischemia, </span>congestive heart failure<span>, cardiomyopathy<span> and hypertension. There is a clear need for capability to assess human cardiac ARs directly in vivo. Positron emission tomography (PET) is an imaging technique that provides this possibility, if effective radioligands can be developed for the targeted ARs. Here, the status of myocardial AR radioligand development for PET is described. Currently, there exist effective radioligands for imaging β-ARs in human myocardium. One of these, [</span></span></span></span><span><math><msup><mi></mi><mn>11</mn></msup><mtext>C</mtext></math></span>](<em>S</em><span>)-CGP 12177, is applied extensively to clinical research with PET, sometimes with other tracers of other aspects of the noradrenalin system. Alternative radioligands are in development for β-ARs, including β</span><sub>1</sub>-selective radioligands. A promising radioligand for imaging myocardial α<sub>1</sub>-ARs, [<span><math><msup><mi></mi><mn>11</mn></msup><mtext>C</mtext></math></span>]GB67, is now being evaluated in human PET experiments.</p></div>\",\"PeriodicalId\":19830,\"journal\":{\"name\":\"Pharmaceutica acta Helvetiae\",\"volume\":\"74 2\",\"pages\":\"Pages 191-200\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2000-03-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/S0031-6865(99)00032-1\",\"citationCount\":\"27\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Pharmaceutica acta Helvetiae\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0031686599000321\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pharmaceutica acta Helvetiae","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0031686599000321","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Selection, design and evaluation of new radioligands for PET studies of cardiac adrenoceptors
Changes in the numbers of human cardiac adrenoceptors (ARs) are associated with various diseases, such as myocardial ischemia, congestive heart failure, cardiomyopathy and hypertension. There is a clear need for capability to assess human cardiac ARs directly in vivo. Positron emission tomography (PET) is an imaging technique that provides this possibility, if effective radioligands can be developed for the targeted ARs. Here, the status of myocardial AR radioligand development for PET is described. Currently, there exist effective radioligands for imaging β-ARs in human myocardium. One of these, [](S)-CGP 12177, is applied extensively to clinical research with PET, sometimes with other tracers of other aspects of the noradrenalin system. Alternative radioligands are in development for β-ARs, including β1-selective radioligands. A promising radioligand for imaging myocardial α1-ARs, []GB67, is now being evaluated in human PET experiments.