Abstract
We demonstrated involvement of the ventral tegmental area (VTA) dopaminergic system in orexin-induced hyperlocomotion and stereotypy in rats. In double-label immunohistochemical study of rat brain, we found that tyrosine hydroxylase (TH)-immunoreactive cells in the VTA received innervation from orexin immunoreactive-fibers. Orexin-A induced an increase in [Ca(2+)](i) in isolated A10 dopamine neurons in a dose-dependent manner. In behavioral studies, we found that orexin-A induced hyperlocomotion, stereotypy and grooming behavior when administered centrally in rats, and these effects were abolished by dopamine D(2) (haloperidol and sulpiride) or D(1) (SCH23390) antagonists. These results suggest that the orexin-induced hyperlocomotion, stereotypy and grooming behavior are mediated by the dopaminergic system and this pathway might be involved in orexin-induced emotional responses.
MeSH terms
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Animals
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Axons / physiology
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Behavior, Animal / drug effects*
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Behavior, Animal / physiology
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Benzazepines / pharmacology
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Carrier Proteins / pharmacokinetics
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Carrier Proteins / pharmacology*
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Dopamine / physiology*
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Dopamine Antagonists / pharmacology
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Haloperidol / pharmacology
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Intracellular Signaling Peptides and Proteins*
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Male
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Motor Activity / drug effects*
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Motor Activity / physiology*
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Nerve Endings / physiology
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Neurons / drug effects
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Neurons / physiology
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Neuropeptides / pharmacokinetics
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Neuropeptides / pharmacology*
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Orexins
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Rats
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Rats, Wistar
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Stereotyped Behavior / drug effects
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Stereotyped Behavior / physiology*
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Sulpiride / pharmacology
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Tegmentum Mesencephali / cytology
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Tegmentum Mesencephali / physiology
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Tyrosine 3-Monooxygenase / metabolism
Substances
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Benzazepines
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Carrier Proteins
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Dopamine Antagonists
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Intracellular Signaling Peptides and Proteins
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Neuropeptides
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Orexins
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Sulpiride
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Tyrosine 3-Monooxygenase
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Haloperidol
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Dopamine