AMANTADINA MECANISMO DE ACCION PDF

Sus mecanismos de acción están mediados por la interacción con receptores . La administración intravenosa de la amantadina disminuye el dolor de la. Aunque por su mecanismo de acción todos los análogos pueden producir toxicidad bisoprolol, ranitidina, dolutegravir, rilpivirina, Amantadina, metformina. MECANISMO DE ACCIÓN. Inhibidores . Con: Amantadina: posible potenciación de la toxicidad de la Amantadina, por disminución de su secreción tubular.

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Neira F, Ortega JL. Trends Neurosci ; Prolonged analgesic effect of ketamina, an N-Methyl-D-Aspartate receptor inhibitor, in patients with chronic pain. The clinical effectiveness of NMDA receptor antagonists ketamine, memantine, amantadine, dextromethorphan, methadone is analyzed.

Current Op Anaesth ; 9: Figiel I, Kaczmarek L.

The Pain Clinic ; 11 1: Sin embargo, a una dosis de 30 mg. Secretos del tratamiento de dolor. N-methyl-D-aspartate receptors and pain. La glicina tiene amantadlna efecto facilitador sobre los receptores NMDA Realidad hoy reto para el futuro.

Interactions between substance P, calcitonin gene-related peptide, taurine and excitatory amino acids in the spinal cord.

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These drugs are frequently combined with other analgesics, generally acting as coadjuvants. In vivo antinociceptive activity of anti-rat mGluR1 and mGluR5 antibodies in rats. Spinal neurokinin NK1 receptor down-regulation and antinociception: Mecanisml la replicacion del CMV humano.

Tiene accion sobre los herpesvirus. J Pain Symptom Manage zccion 20,4: Acta Neurol Scand ; ,3: It reduces the intracortical activation and increases the intracortical inhibition. The contribution of metabotropic glutamate receptors mGluRs to formalin-induced nociception.

Antidepresivos, relajantes musculares y antagonistas del receptor de N-metil-D-aspartato. Their potential indications include: Eur J Pain ; 2,4: Amin P, Sturrock ND.

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. Spinal antinociceptive effects of excitatory amino acid antagonists: A pilot study of the beneficial effects of amantadine in the treatment of painful diabetic peripheral neuropathy.

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Dextromethorphan mitigates phantom pain in cancer amputees. Gabapentin and neuropathic pain.

Glutamate is the main amino acid that stimulates the CNS, can be involved in nociceptive transmission processes at the spine level and is the main responsible for the fast synaptic transmission. Requirement of metabotropic glutamate receptors for the generation of inflammation-evoked hyperexcitability in rat spinal cord neurons.

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Pain ; 66, The disparate results obtained with different antagonists used for the same indication confirm the complexity of their mechanism of action, which is not limited to antagonism of NMDA receptors, but it goes much more beyond that.

Entre sus indicaciones se han propuesto: Ketamine in chronic pain management: Se debe tener en cuenta su efecto de primer paso. Phencyclidine selectively blocks a spinal action of N-methyl-D- aspartate in mice.

The pharmacology of excitatory and inhibitory amino acid-mediated events in the transmission and modulation of pain in the spinal cord. Memantina Es un derivado de la amantadina, que se utiliza habitualmente en el tratamiento de la enfermedad de Parkinson y el Alzheimer desde