484 related articles for article (PubMed ID: 20236223)
21. Orexin-induced feeding requires NMDA receptor activation in the perifornical region of the lateral hypothalamus.
Doane DF; Lawson MA; Meade JR; Kotz CM; Beverly JL
Am J Physiol Regul Integr Comp Physiol; 2007 Sep; 293(3):R1022-6. PubMed ID: 17537834
[TBL] [Abstract][Full Text] [Related]
22. Lateral hypothalamic orexin/hypocretin neurons: A role in reward-seeking and addiction.
Aston-Jones G; Smith RJ; Sartor GC; Moorman DE; Massi L; Tahsili-Fahadan P; Richardson KA
Brain Res; 2010 Feb; 1314():74-90. PubMed ID: 19815001
[TBL] [Abstract][Full Text] [Related]
23. Lack of hypocretin attenuates behavioral changes produced by glutamatergic activation of the perifornical-lateral hypothalamic area.
Kostin A; Siegel JM; Alam MN
Sleep; 2014 May; 37(5):1011-20. PubMed ID: 24790280
[TBL] [Abstract][Full Text] [Related]
24. Hypocretin/orexin antagonism enhances sleep-related adenosine and GABA neurotransmission in rat basal forebrain.
Vazquez-DeRose J; Schwartz MD; Nguyen AT; Warrier DR; Gulati S; Mathew TK; Neylan TC; Kilduff TS
Brain Struct Funct; 2016 Mar; 221(2):923-40. PubMed ID: 25431268
[TBL] [Abstract][Full Text] [Related]
25. Activation of orexin neurons by acute nicotine.
Pasumarthi RK; Reznikov LR; Fadel J
Eur J Pharmacol; 2006 Mar; 535(1-3):172-6. PubMed ID: 16545369
[TBL] [Abstract][Full Text] [Related]
26. Activation of a subpopulation of orexin/hypocretin-containing hypothalamic neurons by GABAA receptor-mediated inhibition of the nucleus accumbens shell, but not by exposure to a novel environment.
Baldo BA; Gual-Bonilla L; Sijapati K; Daniel RA; Landry CF; Kelley AE
Eur J Neurosci; 2004 Jan; 19(2):376-86. PubMed ID: 14725632
[TBL] [Abstract][Full Text] [Related]
27. Vesicular glutamate (VGlut), GABA (VGAT), and acetylcholine (VACht) transporters in basal forebrain axon terminals innervating the lateral hypothalamus.
Henny P; Jones BE
J Comp Neurol; 2006 Jun; 496(4):453-67. PubMed ID: 16572456
[TBL] [Abstract][Full Text] [Related]
28. Nicotine self-administration differentially modulates glutamate and GABA transmission in hypothalamic paraventricular nucleus to enhance the hypothalamic-pituitary-adrenal response to stress.
Yu G; Chen H; Wu X; Matta SG; Sharp BM
J Neurochem; 2010 May; 113(4):919-29. PubMed ID: 20202080
[TBL] [Abstract][Full Text] [Related]
29. Activation of the basal forebrain by the orexin/hypocretin neurones.
Arrigoni E; Mochizuki T; Scammell TE
Acta Physiol (Oxf); 2010 Mar; 198(3):223-35. PubMed ID: 19723027
[TBL] [Abstract][Full Text] [Related]
30. Aging-related alterations in orexin/hypocretin modulation of septo-hippocampal amino acid neurotransmission.
Stanley EM; Fadel JR
Neuroscience; 2011 Nov; 195():70-9. PubMed ID: 21884758
[TBL] [Abstract][Full Text] [Related]
31. Effects of cocaine place conditioning, chronic escalating-dose "binge" pattern cocaine administration and acute withdrawal on orexin/hypocretin and preprodynorphin gene expressions in lateral hypothalamus of Fischer and Sprague-Dawley rats.
Zhou Y; Cui CL; Schlussman SD; Choi JC; Ho A; Han JS; Kreek MJ
Neuroscience; 2008 Jun; 153(4):1225-34. PubMed ID: 18436386
[TBL] [Abstract][Full Text] [Related]
32. Lateral hypothalamic orexin neurons are critically involved in learning to associate an environment with morphine reward.
Harris GC; Wimmer M; Randall-Thompson JF; Aston-Jones G
Behav Brain Res; 2007 Oct; 183(1):43-51. PubMed ID: 17599478
[TBL] [Abstract][Full Text] [Related]
33. Upregulation of orexin/hypocretin expression in aged rats: Effects on feeding latency and neurotransmission in the insular cortex.
Hagar JM; Macht VA; Wilson SP; Fadel JR
Neuroscience; 2017 May; 350():124-132. PubMed ID: 28344067
[TBL] [Abstract][Full Text] [Related]
34. Orexins/hypocretins cause sharp wave- and theta-related synaptic plasticity in the hippocampus via glutamatergic, gabaergic, noradrenergic, and cholinergic signaling.
Selbach O; Doreulee N; Bohla C; Eriksson KS; Sergeeva OA; Poelchen W; Brown RE; Haas HL
Neuroscience; 2004; 127(2):519-28. PubMed ID: 15262340
[TBL] [Abstract][Full Text] [Related]
35. Orexin peptides enhance median preoptic nucleus neuronal excitability via postsynaptic membrane depolarization and enhancement of glutamatergic afferents.
Kolaj M; Coderre E; Renaud LP
Neuroscience; 2008 Sep; 155(4):1212-20. PubMed ID: 18674591
[TBL] [Abstract][Full Text] [Related]
36. Cocaine and nicotine research illustrates a range of hypocretin mechanisms in addiction.
Baimel C; Borgland SL; Corrigall W
Vitam Horm; 2012; 89():291-313. PubMed ID: 22640620
[TBL] [Abstract][Full Text] [Related]
37. Prolonged nicotine administration results in biphasic, brain-specific changes in kynurenate levels in the rat.
Rassoulpour A; Wu HQ; Albuquerque EX; Schwarcz R
Neuropsychopharmacology; 2005 Apr; 30(4):697-704. PubMed ID: 15496939
[TBL] [Abstract][Full Text] [Related]
38. Age-related loss of orexin/hypocretin neurons.
Kessler BA; Stanley EM; Frederick-Duus D; Fadel J
Neuroscience; 2011 Mar; 178():82-8. PubMed ID: 21262323
[TBL] [Abstract][Full Text] [Related]
39. Intravenous prenatal nicotine exposure increases orexin expression in the lateral hypothalamus and orexin innervation of the ventral tegmental area in adult male rats.
Morgan AJ; Harrod SB; Lacy RT; Stanley EM; Fadel JR
Drug Alcohol Depend; 2013 Oct; 132(3):562-70. PubMed ID: 23664126
[TBL] [Abstract][Full Text] [Related]
40. Chronic treatment with a dopamine uptake blocker changes dopamine and acetylcholine but not glutamate and GABA concentrations in prefrontal cortex, striatum and nucleus accumbens of the awake rat.
Hernández LF; Segovia G; Mora F
Neurochem Int; 2008 Feb; 52(3):457-69. PubMed ID: 17881090
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]