Maternal and fetal 11C-cocaine uptake and kinetics measured in vivo by combined PET and MRI in pregnant nonhuman primates

Helene Benveniste, Joanna S. Fowler, William Rooney, Yu Shin Ding, Angela L. Baumann, Daryn H. Moller, Congwu Du, Walter Backus, Jean Logan, Pauline Carter, Jeremy D. Coplan, Anat Biegon, Leonard Rosenblum, Bruce Scharf, John S. Gatley, Nora D. Volkow

Research output: Contribution to journalArticle

32 Citations (Scopus)

Abstract

Cocaine use during pregnancy has been shown to be deleterious to the infant. This may reflect reduction of flow to placenta or effects on the fetal brain. Methods to assess pharmacokinetics of drugs of abuse in vivo would be useful to investigate the mechanisms underlying the fetal adverse effects. We recently reported that combined MRI and PET technology allows the measurement of radioisotope distribution in maternal and fetal organs in pregnant Macaca radiata. Here, we evaluate the utility of PET to measure the uptake and distribution of 11C-cocaine in the third-trimester fetus. Methods: Six pregnant M. radiata weighing 3.8-9.0 kg were anesthetized and MR images were acquired on a 4-T MRI instrument. In all 6 animals, dynamic PET scans were subsequently acquired using 148-259 MBq of 11C-cocaine. Time-activity curves for both maternal and fetal organs were obtained simultaneously with the pregnant animal positioned transverse in the PET scanner. Distribution volume ratios for maternal and fetal brain for 11C-cocaine were calculated. Results: Coregistration of PET and MR images allowed identification of fetal organs and brain regions and demonstrated that 11C-cocaine or its labeled metabolites readily cross the placenta and accumulate mainly in fetal liver and to a lesser extent in the brain. Time to reach peak 11C uptake in brain was shorter for the mother than for the fetus. The distribution volume ratios of the maternal striatum were higher than those of the fetus. Placenta was clearly visible on the early time frames and showed more rapid uptake and clearance than other fetal tissues. Conclusion: The pregnant M. radiata model allows the noninvasive measurement of radioisotope pharmacokinetics in maternal and fetal brain and other organs simultaneously. Although the uptake of radioactivity into the fetal brain after the injection of 11C-cocaine is lower and slower than in the maternal brain, a measurable quantity of 11C-cocaine (or its labeled metabolites) accumulates in the fetal brain at early times after injection. The highest accumulation of 11C occurs in the fetal liver. Rapid radioisotope accumulation and clearance in the placenta offer potential as an input function for kinetic modeling for future studies of binding site availability.

Original languageEnglish (US)
Pages (from-to)312-320
Number of pages9
JournalJournal of Nuclear Medicine
Volume46
Issue number2
StatePublished - 2005
Externally publishedYes

Fingerprint

Cocaine
Primates
Mothers
Brain
Macaca radiata
Placenta
Fetus
Radioisotopes
Pharmacokinetics
Injections
Liver
Third Pregnancy Trimester
Street Drugs
Positron-Emission Tomography
Radioactivity
Binding Sites
Technology
Pregnancy

Keywords

  • C-cocaine
  • Maternal-fetal exchange
  • MRI
  • PET
  • Primate

ASJC Scopus subject areas

  • Radiological and Ultrasound Technology

Cite this

Benveniste, H., Fowler, J. S., Rooney, W., Ding, Y. S., Baumann, A. L., Moller, D. H., ... Volkow, N. D. (2005). Maternal and fetal 11C-cocaine uptake and kinetics measured in vivo by combined PET and MRI in pregnant nonhuman primates. Journal of Nuclear Medicine, 46(2), 312-320.

Maternal and fetal 11C-cocaine uptake and kinetics measured in vivo by combined PET and MRI in pregnant nonhuman primates. / Benveniste, Helene; Fowler, Joanna S.; Rooney, William; Ding, Yu Shin; Baumann, Angela L.; Moller, Daryn H.; Du, Congwu; Backus, Walter; Logan, Jean; Carter, Pauline; Coplan, Jeremy D.; Biegon, Anat; Rosenblum, Leonard; Scharf, Bruce; Gatley, John S.; Volkow, Nora D.

In: Journal of Nuclear Medicine, Vol. 46, No. 2, 2005, p. 312-320.

Research output: Contribution to journalArticle

Benveniste, H, Fowler, JS, Rooney, W, Ding, YS, Baumann, AL, Moller, DH, Du, C, Backus, W, Logan, J, Carter, P, Coplan, JD, Biegon, A, Rosenblum, L, Scharf, B, Gatley, JS & Volkow, ND 2005, 'Maternal and fetal 11C-cocaine uptake and kinetics measured in vivo by combined PET and MRI in pregnant nonhuman primates', Journal of Nuclear Medicine, vol. 46, no. 2, pp. 312-320.
Benveniste, Helene ; Fowler, Joanna S. ; Rooney, William ; Ding, Yu Shin ; Baumann, Angela L. ; Moller, Daryn H. ; Du, Congwu ; Backus, Walter ; Logan, Jean ; Carter, Pauline ; Coplan, Jeremy D. ; Biegon, Anat ; Rosenblum, Leonard ; Scharf, Bruce ; Gatley, John S. ; Volkow, Nora D. / Maternal and fetal 11C-cocaine uptake and kinetics measured in vivo by combined PET and MRI in pregnant nonhuman primates. In: Journal of Nuclear Medicine. 2005 ; Vol. 46, No. 2. pp. 312-320.
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abstract = "Cocaine use during pregnancy has been shown to be deleterious to the infant. This may reflect reduction of flow to placenta or effects on the fetal brain. Methods to assess pharmacokinetics of drugs of abuse in vivo would be useful to investigate the mechanisms underlying the fetal adverse effects. We recently reported that combined MRI and PET technology allows the measurement of radioisotope distribution in maternal and fetal organs in pregnant Macaca radiata. Here, we evaluate the utility of PET to measure the uptake and distribution of 11C-cocaine in the third-trimester fetus. Methods: Six pregnant M. radiata weighing 3.8-9.0 kg were anesthetized and MR images were acquired on a 4-T MRI instrument. In all 6 animals, dynamic PET scans were subsequently acquired using 148-259 MBq of 11C-cocaine. Time-activity curves for both maternal and fetal organs were obtained simultaneously with the pregnant animal positioned transverse in the PET scanner. Distribution volume ratios for maternal and fetal brain for 11C-cocaine were calculated. Results: Coregistration of PET and MR images allowed identification of fetal organs and brain regions and demonstrated that 11C-cocaine or its labeled metabolites readily cross the placenta and accumulate mainly in fetal liver and to a lesser extent in the brain. Time to reach peak 11C uptake in brain was shorter for the mother than for the fetus. The distribution volume ratios of the maternal striatum were higher than those of the fetus. Placenta was clearly visible on the early time frames and showed more rapid uptake and clearance than other fetal tissues. Conclusion: The pregnant M. radiata model allows the noninvasive measurement of radioisotope pharmacokinetics in maternal and fetal brain and other organs simultaneously. Although the uptake of radioactivity into the fetal brain after the injection of 11C-cocaine is lower and slower than in the maternal brain, a measurable quantity of 11C-cocaine (or its labeled metabolites) accumulates in the fetal brain at early times after injection. The highest accumulation of 11C occurs in the fetal liver. Rapid radioisotope accumulation and clearance in the placenta offer potential as an input function for kinetic modeling for future studies of binding site availability.",
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T1 - Maternal and fetal 11C-cocaine uptake and kinetics measured in vivo by combined PET and MRI in pregnant nonhuman primates

AU - Benveniste, Helene

AU - Fowler, Joanna S.

AU - Rooney, William

AU - Ding, Yu Shin

AU - Baumann, Angela L.

AU - Moller, Daryn H.

AU - Du, Congwu

AU - Backus, Walter

AU - Logan, Jean

AU - Carter, Pauline

AU - Coplan, Jeremy D.

AU - Biegon, Anat

AU - Rosenblum, Leonard

AU - Scharf, Bruce

AU - Gatley, John S.

AU - Volkow, Nora D.

PY - 2005

Y1 - 2005

N2 - Cocaine use during pregnancy has been shown to be deleterious to the infant. This may reflect reduction of flow to placenta or effects on the fetal brain. Methods to assess pharmacokinetics of drugs of abuse in vivo would be useful to investigate the mechanisms underlying the fetal adverse effects. We recently reported that combined MRI and PET technology allows the measurement of radioisotope distribution in maternal and fetal organs in pregnant Macaca radiata. Here, we evaluate the utility of PET to measure the uptake and distribution of 11C-cocaine in the third-trimester fetus. Methods: Six pregnant M. radiata weighing 3.8-9.0 kg were anesthetized and MR images were acquired on a 4-T MRI instrument. In all 6 animals, dynamic PET scans were subsequently acquired using 148-259 MBq of 11C-cocaine. Time-activity curves for both maternal and fetal organs were obtained simultaneously with the pregnant animal positioned transverse in the PET scanner. Distribution volume ratios for maternal and fetal brain for 11C-cocaine were calculated. Results: Coregistration of PET and MR images allowed identification of fetal organs and brain regions and demonstrated that 11C-cocaine or its labeled metabolites readily cross the placenta and accumulate mainly in fetal liver and to a lesser extent in the brain. Time to reach peak 11C uptake in brain was shorter for the mother than for the fetus. The distribution volume ratios of the maternal striatum were higher than those of the fetus. Placenta was clearly visible on the early time frames and showed more rapid uptake and clearance than other fetal tissues. Conclusion: The pregnant M. radiata model allows the noninvasive measurement of radioisotope pharmacokinetics in maternal and fetal brain and other organs simultaneously. Although the uptake of radioactivity into the fetal brain after the injection of 11C-cocaine is lower and slower than in the maternal brain, a measurable quantity of 11C-cocaine (or its labeled metabolites) accumulates in the fetal brain at early times after injection. The highest accumulation of 11C occurs in the fetal liver. Rapid radioisotope accumulation and clearance in the placenta offer potential as an input function for kinetic modeling for future studies of binding site availability.

AB - Cocaine use during pregnancy has been shown to be deleterious to the infant. This may reflect reduction of flow to placenta or effects on the fetal brain. Methods to assess pharmacokinetics of drugs of abuse in vivo would be useful to investigate the mechanisms underlying the fetal adverse effects. We recently reported that combined MRI and PET technology allows the measurement of radioisotope distribution in maternal and fetal organs in pregnant Macaca radiata. Here, we evaluate the utility of PET to measure the uptake and distribution of 11C-cocaine in the third-trimester fetus. Methods: Six pregnant M. radiata weighing 3.8-9.0 kg were anesthetized and MR images were acquired on a 4-T MRI instrument. In all 6 animals, dynamic PET scans were subsequently acquired using 148-259 MBq of 11C-cocaine. Time-activity curves for both maternal and fetal organs were obtained simultaneously with the pregnant animal positioned transverse in the PET scanner. Distribution volume ratios for maternal and fetal brain for 11C-cocaine were calculated. Results: Coregistration of PET and MR images allowed identification of fetal organs and brain regions and demonstrated that 11C-cocaine or its labeled metabolites readily cross the placenta and accumulate mainly in fetal liver and to a lesser extent in the brain. Time to reach peak 11C uptake in brain was shorter for the mother than for the fetus. The distribution volume ratios of the maternal striatum were higher than those of the fetus. Placenta was clearly visible on the early time frames and showed more rapid uptake and clearance than other fetal tissues. Conclusion: The pregnant M. radiata model allows the noninvasive measurement of radioisotope pharmacokinetics in maternal and fetal brain and other organs simultaneously. Although the uptake of radioactivity into the fetal brain after the injection of 11C-cocaine is lower and slower than in the maternal brain, a measurable quantity of 11C-cocaine (or its labeled metabolites) accumulates in the fetal brain at early times after injection. The highest accumulation of 11C occurs in the fetal liver. Rapid radioisotope accumulation and clearance in the placenta offer potential as an input function for kinetic modeling for future studies of binding site availability.

KW - C-cocaine

KW - Maternal-fetal exchange

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KW - PET

KW - Primate

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