Effects of orexin (hypocretin) on GIRK channels

Q. V. Hoang, D. Bajic, Masashi Yanagisawa, S. Nakajima, Y. Nakajima

Research output: Contribution to journalArticle

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Abstract

Orexins (hypocretins) are recently discovered excitatory transmitters implicated in arousal and sleep. Yet, their ionic and signal transduction mechanisms have not been fully clarified. Here we show that orexins suppress G-protein-coupled inward rectifier (GIRK) channel activity, and this suppression is likely to lead to neuronal excitation. Cultured neurons from the locus coeruleus (LC) and the nucleus tuberomammillaris (TM) were used, as well as HEK293A cells transfected with GIRK1 and 2, either human orexin receptor type 1 (OX1R) or type 2 (OX2R), mu opioid receptor and GFP cDNAs. In GTPγS-loaded cells, orexin A (OXA, 3 μM) inhibited GIRK currents that had previously been activated by somatostatin (in LC cells), nociceptin (TM cells), or the mu opioid agonist DAMGO (HEK cells). In guanosine triphosphate (GTP)-loaded HEK cells, in which GIRK currents were not preactivated, OXA induced a biphasic response through both types of orexin receptors: an initial current increase and a subsequent decrease to below resting levels. Current-voltage (I-V) relationships revealed that both the OXA-induced and suppressed currents are inwardly rectifying with reversal potentials around Eκ. The OXA-induced initial current was partially pertussis toxin (PTX) sensitive and partially PTX insensitive, whereas the OXA-suppressed current was PTX insensitive. These data suggest that orexin receptors couple with more than one type of G-protein, including PTX-sensitive (such as Gi/o) and PTX-insensitive (such as G q/11) G-proteins. The modulation of GIRK channels by orexins may be one of the cellular mechanisms for the regulation of brain nuclei (e.g., LC and TM) that are crucial for arousal, sleep, and appetite.

Original languageEnglish (US)
Pages (from-to)693-702
Number of pages10
JournalJournal of Neurophysiology
Volume90
Issue number2
DOIs
StatePublished - Aug 1 2003

Fingerprint

Pertussis Toxin
Orexin Receptors
Locus Coeruleus
GTP-Binding Proteins
Arousal
Sleep
Ala(2)-MePhe(4)-Gly(5)-enkephalin
mu Opioid Receptor
Appetite
Guanosine Triphosphate
Somatostatin
Opioid Analgesics
Orexins
Signal Transduction
Complementary DNA
Asp(5)-oxytocin
Neurons
Brain

ASJC Scopus subject areas

  • Physiology
  • Neuroscience(all)

Cite this

Effects of orexin (hypocretin) on GIRK channels. / Hoang, Q. V.; Bajic, D.; Yanagisawa, Masashi; Nakajima, S.; Nakajima, Y.

In: Journal of Neurophysiology, Vol. 90, No. 2, 01.08.2003, p. 693-702.

Research output: Contribution to journalArticle

Hoang, QV, Bajic, D, Yanagisawa, M, Nakajima, S & Nakajima, Y 2003, 'Effects of orexin (hypocretin) on GIRK channels', Journal of Neurophysiology, vol. 90, no. 2, pp. 693-702. https://doi.org/10.1152/jn.00001.2003
Hoang, Q. V. ; Bajic, D. ; Yanagisawa, Masashi ; Nakajima, S. ; Nakajima, Y. / Effects of orexin (hypocretin) on GIRK channels. In: Journal of Neurophysiology. 2003 ; Vol. 90, No. 2. pp. 693-702.
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