Comparison of radiolabeled isatin analogs for imaging apoptosis with positron emission tomography

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• 作者：Delphine L. Chen ; Dong Zhou ; Wenhua Chu ; Phillip E. Herrbrich ; Lynne A. Jones ; Justin M. Rothfuss ; Jacquelyn T. Engle ; Marco Geraci ; Michael J. Welch ; Robert H. Mach
• 关键词：Apoptosis ; Caspase-3 ; Positron emission tomography ; Radiolabeled isatins ; Liver injury
• 刊名：Nuclear Medicine and Biology
• 出版年：2009
• 出版时间：August 2009
• 年：2009
• 卷：36
• 期：6
• 页码：651-658
• 全文大小：423 K

文摘

Introduction

Caspase-3 is one of the executioner caspases activated as a result of apoptosis. Radiolabeled isatins bind to caspase-3 with high affinity and are potential tracers for use with positron emission tomography to image apoptosis. We compared the ability of two novel radiolabeled isatins, [¹⁸F]WC-IV-3 and [¹¹C]WC-98, to detect caspase-3 activation in a rat model of cycloheximide-induced liver injury.

Methods

Male Sprague-Dawley rats were treated with cycloheximide and then imaged with microPET 3 h later with [¹⁸F]WC-IV-3 and [¹¹C]WC-98. Biodistribution studies were also performed simultaneously, with caspase-3 activation verified by fluorometric enzyme assay and Western blots.

Results

MicroPET imaging studies demonstrated similar behavior of both tracers but with a lower maximum peak with [¹¹C]WC-98 than with [¹⁸F]WC-IV-3. Biodistribution studies demonstrated increased uptake of both tracers in the liver and spleen, but this was statistically significant only in the liver with both compounds. The level of [¹⁸F]WC-IV-3 uptake appeared to correlate roughly with rates of caspase-3 activation by the enzyme assay, but the magnitude of difference between treated and control groups was lower than that observed in previously published data with [¹⁸F]WC-II-89, another radiolabeled isatin analog. Activation was also confirmed in the liver and spleen but not in fat by Western blot.

Conclusion

[¹⁸F]WC-IV-3 uptake appears to correlate with increased caspase-3 enzyme activity, but the dynamic range of uptake of these two tracers appears to be less than that seen with [¹⁸F]WC-II-89. Studies are ongoing to verify these results in other animal models of apoptosis.