Abstract
The effects of systemic administration of rolipram, a selective phosphodiesterase type 4 inhibitor, on [{sup 3}H]2-deoxyglucose (DG) uptake in brain and peripheral tissues were examined. Rolipram significantly and dose-dependently decreased [{sup 3}H]DG uptake in brain, heart and skeletal muscle. In contrast, the radioactivity concentrations in the plasma of rolipram-treated mice were significantly higher than those of control mice at all times after injection of the tracer. In the kinetic study, the initial uptake of [{sup 3}H]DG in brain was decreased by rolipram, whereas no significant differences were observed in the uptake in heart and skeletal muscle. However, radioactivity concentrations in the brain, heart and skeletal muscle 30 min after the injection of [{sup 3}H]DG were significantly lowered by rolipram to about 60%, 10% and 10% of control values, respectively. The uptake of [{sup 13}N]ammonia in brain and heart of rolipram-treated mice was slightly decreased, which indicated that rolipram diminished both cerebral and cardiac blood flow. These results indicate that the phosphorylation process via hexokinase rather than the transport of [{sup 3}H]DG might be depressed by rolipram. Together with the previous observations that inhibition of protein kinase A (PKA) markedly enhanced [{sup 14}C]DG uptake in rat brain, these results indicate an
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Ishikawa, Megumi;
Hosoi, Rie;
Kobayashi, Kaoru;
Inoue, Osamu;
[1]
Nishimura, Tsunehiko
[2]
- Department of Medical Physics, School of Allied Health Sciences, Faculty of Medicine, Osaka University, 1-7 Yamadaoka, Suita-shi, Osaka (Japan)
- Department of Radiology, Kyoto Prefectural University of Medicine, Kyoto (Japan)
Citation Formats
Ishikawa, Megumi, Hosoi, Rie, Kobayashi, Kaoru, Inoue, Osamu, and Nishimura, Tsunehiko.
Rolipram depresses [{sup 3}H]2-deoxyglucose uptake in mouse brain and heart in vivo.
Germany: N. p.,
2002.
Web.
doi:10.1007/s00259-002-0870-x.
Ishikawa, Megumi, Hosoi, Rie, Kobayashi, Kaoru, Inoue, Osamu, & Nishimura, Tsunehiko.
Rolipram depresses [{sup 3}H]2-deoxyglucose uptake in mouse brain and heart in vivo.
Germany.
https://doi.org/10.1007/s00259-002-0870-x
Ishikawa, Megumi, Hosoi, Rie, Kobayashi, Kaoru, Inoue, Osamu, and Nishimura, Tsunehiko.
2002.
"Rolipram depresses [{sup 3}H]2-deoxyglucose uptake in mouse brain and heart in vivo."
Germany.
https://doi.org/10.1007/s00259-002-0870-x.
@misc{etde_20304016,
title = {Rolipram depresses [{sup 3}H]2-deoxyglucose uptake in mouse brain and heart in vivo}
author = {Ishikawa, Megumi, Hosoi, Rie, Kobayashi, Kaoru, Inoue, Osamu, and Nishimura, Tsunehiko}
abstractNote = {The effects of systemic administration of rolipram, a selective phosphodiesterase type 4 inhibitor, on [{sup 3}H]2-deoxyglucose (DG) uptake in brain and peripheral tissues were examined. Rolipram significantly and dose-dependently decreased [{sup 3}H]DG uptake in brain, heart and skeletal muscle. In contrast, the radioactivity concentrations in the plasma of rolipram-treated mice were significantly higher than those of control mice at all times after injection of the tracer. In the kinetic study, the initial uptake of [{sup 3}H]DG in brain was decreased by rolipram, whereas no significant differences were observed in the uptake in heart and skeletal muscle. However, radioactivity concentrations in the brain, heart and skeletal muscle 30 min after the injection of [{sup 3}H]DG were significantly lowered by rolipram to about 60%, 10% and 10% of control values, respectively. The uptake of [{sup 13}N]ammonia in brain and heart of rolipram-treated mice was slightly decreased, which indicated that rolipram diminished both cerebral and cardiac blood flow. These results indicate that the phosphorylation process via hexokinase rather than the transport of [{sup 3}H]DG might be depressed by rolipram. Together with the previous observations that inhibition of protein kinase A (PKA) markedly enhanced [{sup 14}C]DG uptake in rat brain, these results indicate an important role of the cAMP/PKA systems in the regulation of glucose metabolism in the living brain as well as in peripheral tissues such as the heart and skeletal muscle. (orig.)}
doi = {10.1007/s00259-002-0870-x}
journal = []
issue = {9}
volume = {29}
journal type = {AC}
place = {Germany}
year = {2002}
month = {Sep}
}
title = {Rolipram depresses [{sup 3}H]2-deoxyglucose uptake in mouse brain and heart in vivo}
author = {Ishikawa, Megumi, Hosoi, Rie, Kobayashi, Kaoru, Inoue, Osamu, and Nishimura, Tsunehiko}
abstractNote = {The effects of systemic administration of rolipram, a selective phosphodiesterase type 4 inhibitor, on [{sup 3}H]2-deoxyglucose (DG) uptake in brain and peripheral tissues were examined. Rolipram significantly and dose-dependently decreased [{sup 3}H]DG uptake in brain, heart and skeletal muscle. In contrast, the radioactivity concentrations in the plasma of rolipram-treated mice were significantly higher than those of control mice at all times after injection of the tracer. In the kinetic study, the initial uptake of [{sup 3}H]DG in brain was decreased by rolipram, whereas no significant differences were observed in the uptake in heart and skeletal muscle. However, radioactivity concentrations in the brain, heart and skeletal muscle 30 min after the injection of [{sup 3}H]DG were significantly lowered by rolipram to about 60%, 10% and 10% of control values, respectively. The uptake of [{sup 13}N]ammonia in brain and heart of rolipram-treated mice was slightly decreased, which indicated that rolipram diminished both cerebral and cardiac blood flow. These results indicate that the phosphorylation process via hexokinase rather than the transport of [{sup 3}H]DG might be depressed by rolipram. Together with the previous observations that inhibition of protein kinase A (PKA) markedly enhanced [{sup 14}C]DG uptake in rat brain, these results indicate an important role of the cAMP/PKA systems in the regulation of glucose metabolism in the living brain as well as in peripheral tissues such as the heart and skeletal muscle. (orig.)}
doi = {10.1007/s00259-002-0870-x}
journal = []
issue = {9}
volume = {29}
journal type = {AC}
place = {Germany}
year = {2002}
month = {Sep}
}