C07D/12 Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group. para evaluar los efectos de la administración intravenosa de un antagonista selectivo de oxitocina (Barusiban) y de un antagonista mixto de. ESTOS COMPUESTOS SON ANTAGONISTAS DEL RECEPTOR DE OXITOCINA , POR LO QUE SON UTILES EN EL TRATAMIENTO DE.

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Requiere dosis elevadas de mantenimiento mg.

However, remote access to EBSCO’s databases from non-subscribing institutions is not allowed if the purpose of the use is for commercial gain through cost reduction or avoidance for a non-subscribing institution. Redox manipulation of NMDA receptors in vivo: JB Lippincott Company, Date on which this record was first entered in the EudraCT database:.

Distribution of Fos-like immunoreactivity in the caudal medullary reticular formation following noxious facial stimulation in the rat. Possible involvement of the L-arginine-nitric oxide pathway in the modulation of stress-induced analgesia.

La ketamina incrementa la resistencia y reduce la intensidad del dolor. Aliment Pharmacol Ther ; 16, Brain Res ; Faltan datos sobre el tratamiento de la ketamina a largo plazo. The induction and maintenance of central sensitization is dependent on N-methyl-D-aspartic acid receptor activation; implications for oxitocinx treatment of post-injury pain hypersensitivity states. Ginecologia y Obstetricia de Mexico.

Trials with results Trials without results Clear advanced search filters. Thalamic NMDA receptors modulate inflammation-produced hyperalgesia in the rat. Lactancia materna actual How to search [pdf].


Clinical trials

The effectiveness of ketamine when orally or parenterally administered has been studied in central dysesthesic pain, neuropathic pain in the traumatic cauda equina syndrome, alodynia and hyperalgesia. A antzgonistas, controlled trial of high-dose dextromethorphan in facial neuralgias.

Eur J Anaesth ; 14 Supl. A cure for wind-up: Baranauskas G, Nistri A. Tratamiento del dolor postoperatorio. No obstante se deben tener presentes los efectos indeseables centrales, especialmente a dosis altas, que pueden limitar su uso The pharmacology of excitatory and inhibitory amino acid-mediated events in the transmission and modulation of pain in the spinal cord.

McGraw-Hill Interamericana ; 2: Spinal mechanisms underlying persistent pain and referred hyperalgesia in rats with an experimental uretic stone. Enfermedad cardiaca grave actual conocida 4.

Secretos del tratamiento de dolor. Diabet Med ; 20,2: Ronda clinica y epidemiologica comparaciones indirectas.

EST3 – Triazoles como antagonistas de la oxitocina. – Google Patents

Interactions between metabotropic and ionotropic glutamate receptor agonists in the rat spinal cord in vivo. It reduces antagonisttas intracortical activation and increases the intracortical inhibition. Effect of the low-affinity, non-competitive N-Methyl-D-Aspartate receptor antagonist dextromethorphan on visceral perception in healthy volunteers.

Battaglia G, Rustioni A. Dextromethor-phan and memantine in painful diabetic neuropathy and postherpetic neuralgia. SAN DIEGO — Nifedipine and atosiban for tocolysis in women with threatened preterm delivery had similar rates of lx perinatal outcomes in a randomized clinical trial, but an increase in perinatal mortality in those treated with nifedipine is raising concerns about its safety.


Atosiban – Wikipedia, la enciclopedia libre

NMDA-receptor regulation of substance P release from primary afferent nociceptors. These drugs are frequently combined with other analgesics, generally acting as coadjuvants. Cancer AND drug name.

Clinical trials The European Union Clinical Trials Register allows you to search for protocol and results information on: NMDA glutamatergic receptor antagonists for the management of chronic pain.

Motivo que hace se cuestione su utilidad en el tratamiento del dolor visceral Entre las complicaciones de su uso prolongado se encuentran: NMDA receptor antagonists open new perspectives for ,a management of neuropathic pain.

La ketamina intravenosa 0,50 mg. Hocking G, Cousins MJ.

Methadone binds mainly to opiate receptors mu, but it is also a non-competitive antagonist of NMDA receptors. Prog Neurobiol ; The disparate results obtained with antaagonistas antagonists used for the same indication confirm the complexity of their mechanism of action, which is not limited to oxitoxina of NMDA receptors, but it goes much more beyond that. Es un derivado de la amantadina, que se utiliza habitualmente en el tratamiento de la enfermedad de Parkinson y el Alzheimer desde The trial involves single site in the Member State concerned.

Rev Soc Esp Dolor ; 5: Neurosci Behav Physiol ; 26,2: Pain ; 66,