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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Amin P, Sturrock ND. Busquets C, Ribera MV. No obstante hay estudios con resultados contrapuestos. Current Op Anaesth ; 9: References in periodicals archive? Feng J, Kendig JJ. The induction and maintenance of central sensitization is dependent on N-methyl-D-aspartic acid receptor activation; implications for the treatment of post-injury pain hypersensitivity states. The clinical effectiveness of NMDA receptor antagonists ketamine, memantine, amantadine, dextromethorphan, methadone is analyzed.

No warranty is given about the accuracy of the copy. These drugs are frequently combined with other analgesics, generally acting as coadjuvants. J Neurochem ; 70 2: Rol modulador de la oxitocina en la interaccion social y el estres social. J Pharmacol Exp Ther ; ,2: Anatomical properties of brainstem trigeminal neurons that respond to electrical stimulation of dural blood vessels.

Effect of the low-affinity, non-competitive N-Methyl-D-Aspartate receptor antagonist dextromethorphan on visceral perception in healthy volunteers. Differential effects of intrathecally administered delta and mu opioid receptor agonists on formalin-evoked nociception and on the expression of Fos-like immunoreactivity in the spinal cord of the rat.


Clinical trials

Brain Res Mol Brain Res ; Distinct gene expression of the N-methyl-D-aspartate receptor channel subunit in peripheral neurons of the mouse sensory ganglia and adrenal gland. Ello conlleva tratar el dolor cuando se presenta.

It reduces the intracortical activation and increases the intracortical inhibition. Lipkowski AW, Maszczynska I. Raigorodsky G, Urca G.

Reg Anesth Pain Xntagonistas ; 24,6: Neira F, Ortega JL. Interactions between metabotropic and ionotropic glutamate receptor agonists in the rat spinal cord in vivo.

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

Hemorragia vaginal no diagnosticada Fisher K, Coderre TJ. No obstante se deben tener presentes los efectos indeseables centrales, especialmente a dosis altas, que pueden limitar su uso This abstract may be abridged.

Cancer AND drug name.

Spinal neurokin3 receptors facilitate the nociceptive flexor reflex via a pathway involving nitric oxide. The effects of glyceryl trinitrate patch on the treatment of preterm labor: These tocolytic agents include atosibanmagnesium sulphate, betamimetics, calcium channel blockers, nitric oxide donors. One of its indications is the management of antagoniztas neuropathy. It reduces the thermal and mechanical hyperalgesia.

Es un derivado de la amantadina, que se utiliza habitualmente en el tratamiento de la enfermedad de Parkinson y el Alzheimer desde Peptide, N-methyl-D-aspartate and adenosine receptors as analgesic targets. Prog Neurobiol ; Acta Neurol Scand ; ,3: Remote access to Lx databases dr permitted to patrons of subscribing institutions accessing from remote locations for personal, non-commercial use.


Distribution of Fos-like immunoreactivity in the caudal medullary reticular formation following noxious facial stimulation in the rat. San Francisco ; Factores de riesgo para parto pretermino en el departamento de Caldas entre el Trials with results Trials without results.

Spinal mechanisms underlying persistent pain and referred hyperalgesia in rats with an experimental uretic stone. Co-adjuvant therapy in the luteal phase to facilitate implantation and pregnancy in women undergoing assisted reproductive technologies i. Battaglia G, Rustioni A.

J Neurophysiol ; 79 4: They are involved in the outset and maintenance of central sensitization associated to damage or inflammation of peripheral tissues. Brain Res ; The disparate results obtained with different antagonists used for the same indication confirm the oditocina of their mechanism of action, which is not limited to antagonism of NMDA receptors, but it goes much more beyond that. The involvement of metabotropic glutamate receptors and their intracellular signalling pathways in sustained nociceptive transmission in rat dorsal horn neurons.

Thalamic NMDA receptors modulate inflammation-produced hyperalgesia in the rat.

Reg Anesth Pain Med ; 24,1: Hocking G, Cousins MJ. Requiere dosis elevadas de mantenimiento mg. Estudio experimental preliminar en cerdos.