Abstract |
To understand the mechanism of interaction of the dopamine D2L receptors with NMDA receptors, we have developed a model by transfecting human neuroblastoma SH-SY5Y cells with the human dopamine D2L receptor gene. In vitro blockade of NMDA receptors by the specific antagonists MK-801 and (+/-)-3-(2-carboxypiperazin-4-yl)-propyl-1- phosphonic acid ( CPP) on human neuroblastoma SH-SY5Y cells expressing human dopamine D2L receptors resulted in a significant increase in the density of D2L receptors without a significant change in receptor affinity. Moreover, the dopamine receptor mRNA level increased by approximately 50% by the blockade of NMDA with MK-801. These results suggest a possible interaction of NMDA and dopamine D2L receptors in neuroblastoma SH-SY5Y cells. This system would serve as an excellent model to study the molecular mechanisms involved in the interaction of these two receptors.
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Authors | V D Nair, H B Niznik, R K Mishra |
Journal | Journal of neurochemistry
(J Neurochem)
Vol. 66
Issue 6
Pg. 2390-3
(Jun 1996)
ISSN: 0022-3042 [Print] England |
PMID | 8632161
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- Excitatory Amino Acid Antagonists
- Piperazines
- RNA, Messenger
- Receptors, Dopamine D2
- Receptors, N-Methyl-D-Aspartate
- Dizocilpine Maleate
- 3-(2-carboxypiperazin-4-yl)propyl-1-phosphonic acid
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Topics |
- Base Sequence
- Dizocilpine Maleate
(pharmacology)
- Excitatory Amino Acid Antagonists
(pharmacology)
- Humans
- Molecular Sequence Data
- Neuroblastoma
- Piperazines
(pharmacology)
- Polymerase Chain Reaction
- RNA, Messenger
(analysis)
- Receptors, Dopamine D2
(genetics, physiology)
- Receptors, N-Methyl-D-Aspartate
(antagonists & inhibitors, physiology)
- Transfection
- Tumor Cells, Cultured
(chemistry)
- Up-Regulation
(physiology)
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