SR 48692 inhibits neurotensin-induced [3H]dopamine release in rat striatal slices and mesencephalic cultures

scientific article

SR 48692 inhibits neurotensin-induced [3H]dopamine release in rat striatal slices and mesencephalic cultures is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1016/0014-2999(94)90204-6
P698PubMed publication ID8200423

P2093author name stringKitabgi P
Heaulme M
Rostene W
Le Fur G
Gully D
Brouard A
Leyris R
Pelaprat D
P433issue3
P407language of work or nameEnglishQ1860
P921main subjectdopamineQ170304
striatumQ1319792
P304page(s)289-291
P577publication date1994-03-01
P1433published inEuropean Journal of PharmacologyQ1376712
P1476titleSR 48692 inhibits neurotensin-induced [3H]dopamine release in rat striatal slices and mesencephalic cultures
P478volume253

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cites work (P2860)
Q28379094Agonist and antagonist modulation of [35S]-GTP gamma S binding in transfected CHO cells expressing the neurotensin receptor
Q40444515Anatomy and Mechanisms of Neurotensin‐Dopamine Interactions in the Central Nervous System
Q36783168Characterization and distribution of binding sites for a new neurotensin receptor antagonist ligand, [3H]SR 48692, in the guinea pig brain
Q73964518Evidence for a role of endogenous neurotensin in the initiation of amphetamine sensitization
Q48839378In vivo regulation of neurotensin receptors following long-term pharmacological blockade with a specific receptor antagonist
Q43169813Negative modulation of nitric oxide production by neurotensin as a putative mechanism of the diuretic action of SR 48692 in rats
Q28579384Neurotensin regulates intracellular calcium in ventral tegmental area astrocytes: evidence for the involvement of multiple receptors
Q46638594Neurotensin, N-acetyl-aspartylglutamate and beta-endorphin modulate [3H]dopamine release from guinea pig nucleus accumbens, prefrontal cortex and caudate-putamen
Q34668388To ingest or rest? Specialized roles of lateral hypothalamic area neurons in coordinating energy balance
Q34426946Use of nonpeptide antagonists to explore the physiological roles of neurotensin. Focus on brain neurotensin/dopamine interactions.

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