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 Le bâillement, du réflexe à la pathologie
Le bâillement : de l'éthologie à la médecine clinique
Le bâillement : phylogenèse, éthologie, nosogénie
 Le bâillement : un comportement universel
La parakinésie brachiale oscitante
Yawning: its cycle, its role
Warum gähnen wir ?
 
Fetal yawning assessed by 3D and 4D sonography
Le bâillement foetal
Le bâillement, du réflexe à la pathologie
Le bâillement : de l'éthologie à la médecine clinique
Le bâillement : phylogenèse, éthologie, nosogénie
 Le bâillement : un comportement universel
La parakinésie brachiale oscitante
Yawning: its cycle, its role
Warum gähnen wir ?
 
Fetal yawning assessed by 3D and 4D sonography
Le bâillement foetal
http://www.baillement.com
 
  
 

 mise à jour du
8 avril 2004
 Yawning and nitric oxide (NO)
Bâillements et oxyde nitrique (NO
no

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 no
Penile erection and yawning are two different behavioural patterns that often occur concomitantly in physiological and experimental conditions. Depending on the context in which penile erection occurs, different neural and/or humoral mechanisms may participate in its regulation. Yawning alone or associated with stretching is considered an ancestral vestige, surviving through evolution, that subserves the purpose of arousal, although its role is not entirely certain.
 
Among substances that induce both these responses the best known are dopamine receptor agonists, oxytocin, adrenocorticotropin and related peptides, N methyl-D-aspartic acid and serotonin receptor agonists. Interestingly, the paraventricular nucleus of the hypothalamus (PVN) seems to play a key role in these behavioural responses when they are induced by the dopamine receptor agonists, N-methyl-D-aspartic acid and oxytocin, but not when they are induced by adrenocorticotropin or serotonin receptor agonists.
 
Dopamine agonists, NMDA and oxytocin given at doses that induce yawning, increase NO production in the PVN. Conversely, the opiate morphine, which prevents yawning induced by dopamine agonists, oxytocin and NMDA, also prevents the increase in the paraventricular NO production induced by these compounds.
 
NO donors, such as nitroglycerin, sodium nitroprusside and hydroxylamine, induce yawning when injected into the PVN apparently by activating oxytocinergic transmission. Nitric oxide (NO) acts as an intracellular rather than an intercellular modulator inside the paraventricular hypothalamic nucleus (PVN) oxytocinergic neurons in which NO is formed to facilitate the expression of this phylogenetically old stereotyped event.
 
 
Bâillements et oxyde nitrique (NO)
 
L'érection pénienne et le bâillement sont deux comportements qui apparaîssent fréquemment simultanément de façon physiologique ou expérimentalement. Suivant les circonstances au cours desquelles l'érection pénienne apparaît, différents mécanismes neuronaux et/ou humoraux interviennent dans sa régulation. Le bâillement isolé ou associé avec des étirements est considéré comme un vestige ancestral, survivant au travers de l'évolution, et qui participe à la stimulation de l'éveil, bien que cette fonction ne soit pas complètement certaine.
 
Parmi toutes les substances qui induisent érection pénienne et bâillement, les plus connues sont les agonistes dopaminergiques, l'ocytocine, l'ACTH et différents peptides, le NMDA, les agonistes sérotininergiques. Plus précisément, le noyau paraventriculaire de l'hypothalamus (PVN) semble jouer un rôle clé dans ces réponses comportementales quand elles sont induites par les agonistes dopaminergiques, le NMDA et l'ocytocine mais pas quand elles sont induites par l'ACTH ou les agonistes sérotoninergiques.
 
Les agonistes dopaminergiques, le NMDA et l'ocytocine, donnés à des doses qui déclenchent les bâillements, accroissent la production d'oxyde nitrique (NO) dans le PVN. A contrario, les opioïdes qui empêchent l'induction des bâillements par les agonistes dopaminergiques, le NMDA ou l'ocytocine préviennent également l'augmentation de la production de NO dans le PVN.
 
Les donneurs de NO comme la nitroglycérine, le nitroprussiate de Na, ou l'hydroxylamine induisent des bâillements quand ils sont injectés dans le PVN, apparemment en activant la transmission ocytocinergique. NO agit plutôt comme modulateur intracellulaire que comme médiateur intercellulaire, en particulier au sein des neurones ocytocinergiques du PVN où le NO est formé pour faciliter l'expression de ce comportement stéréotypé ancien.
Nitric oxide synthase inhibitors prevent apomorphine and oxytocin-induced penile erection and yawning in male rats Melis MR, Argiolas A Brain Res Bull1993; 32; 1; 71-74
Prevention by ng-nitro-l-arginine methyl ester of apomorphine- and oxytocin-induced penile erection and yawning: site of action in the brain Melis MR, R Stancampiano, A Argiolas Phamcol Biochem Behav 1994; 48; 3; 799-804
Nitric oxide synthase inhibitors prevent N-methyl-D-aspartic acid induced penile erection and ya wning in male rats Melis MR et al Neuroscience letters1994; 179; 9-12
Role of nitric oxide in penile erection and yawning induced by 5-HT1c receptor agonists in male rats Melis MR, Argiolas A Naunyn-Schmiedeberg's arch Pharmacol1995; 351; 439-445
Nitric oxide donors induce penile erection and yawning when injected in the central nervous system of male rats Melis MR et Argiolas A Europ J Pharmacol 1995; 294; 1-9
Nitric oxide is involved in the ACTH-induced behavioral syndrome R Poggioli Peptides 1995; 16; 7; 1263-1268
Nitroglycerin-induced penile erection and yawning in male rats: mechanisrn of action in the brain Melis MR, et al Brain Res Bull 1995; 36; 6; 527-531
Dopamine agonists increase nitric oxide production in the paraventricular nucleus of the hypothalamus: correlation with penile erection and yawning MR Melis et al Europ J Neurosci 1996; 8; 2056-2063
Nitric oxide (NO) and central dopamine (DA) D3 receptor reactivity to quinpirole in rats Brus R et al Act Neurobiol Exp 1996; 56; 15-19
Role of central nitric oxide in the control of penile erection and yawning Melis MR, Argiolas A Prog Neuropsycho pharmacol Biol Psychiatry 1997; 21; 6; 899-922
Prevention by morphine of apomorphine- and oxytocin-induced penile erection and yawning: involvement of nitric oxide Melis MR et al Naunyn-Schmiedeberg's arch Pharmacol1997; 600; 355-595
Prevention by morphine of N-Methyl-D-Aspartic Acid induced penile erection and yawning: involvement of Nitric Oxide MR Melis et al Brain Research Bull1997; 44; 6; 689-694
Oxytocin increases nitric oxide production in the paraventricular nucleus of the hypothalamus of male rats: correlation with penile erection and yawning Melis MR et al Regulatory Peptides 1997; 69; 105-11
Sereotyped yawning responses induced by electrical and chemical stimulation of paraventricular nucleus of the rat Sato-Suzuki I, Kita I, et al J Neurophysiol 1998; 80, 5; 2765-2775
Yawning role of hypothalamic paraventricular nitric oxide Melis MR, Argiolas A Acta Pharmacologica Sinica 1999; 20; 9; 778-788
Yawning responses induced by local hypoxia in the paraventricular nucleus of the rat Kita I, Sato-Suzuki et al. Behavioural Brain Research 2000; 117; 1-2; 119 - 126
Substance P and its transglutaminase-synthesized spermine derivative elicit yawning behavior via nitric oxide in rat Mancuso F, Porta R et al Peptides 2001; 22; 9; 1453-1457
Reduction of drug-induced yawning and penile erection and of noncontact erections in male rats by the activation of GABAA receptors in the paraventricular nucleus: involvement of nitric oxide Melis MR , A.Argiolas Eur J Neurosci 2002; 15; 5; 852-860

 
NO as a signalling molecule
in the nervous system
Esplugues Juan V
British Journal of Pharmacology
2002; 135; 1079-1095
 
«The discovery that nitric oxide (NO) functions as a signalling molecule in the nervous system has radically changed the concept of neural communication. Indeed, the adoption of the term nitrergic for nerves whose transmitter function depends on the release of NO or for transmission mechanisms brought about by NO emphasizes the specific characteristics of this mediator. The physical properties of NO prevent its storage in lipid-lined vesicles and metabolism by hydrolytic degradatory enzymes. Therefore, unlike established neurotransmitters, NO is synthesized on demand and is neither stored in synaptic vesicles nor released by exocytosis, but simply diffuses from nerve terminals. The distance of this NO diffusion (40 Ð 300 µm in diameter) implies that structures in the vicinity of the producing cell, both neuronal and non-neuronal, are influenced following its release. This suggests that, as well as acting as a neurotransmitter, NO has a neuromodulatory role. In addition, it diffuses into rather than binds with protein receptors on adjacent cells, and most of its known actions are the consequence of interplay with intracellular targets that would usually be regarded as secondary messengers. The activity of conventional neurotransmitters is terminated either by re-uptake mechanisms or enzymatic degradation while inactivation of NO follows reaction with a substrate. There are multiple points at which biological control can be exerted over the production and activity of conventional neurotransmitters. However, control of the synthesis of NO is the key to regulating its activity.»
NO
Activation of nNOS in the CNS. Release of glutamate activates NMDA receptors (NMDAr), and the consequent flux of Ca2+ entering the ion channel activates nNOS, which is linked to the receptor via the postsynaptic density protein PSD-95. It is possible that NO bioactivity feeds back to control the presynaptic neuron and the activity of the channel. The protein CAPON is thought to be selectively associated with nNOS and regulates NO formation in neurones.
 

pour la science
 
Pour La Science
A lire, page 66, dans le numéro 312, d'octobre 2003