Literature DB >> 7310700

Monoamine release from cat spinal cord by somatic stimuli: an intrinsic modulatory system.

G M Tyce, T L Yaksh.   

Abstract

1. Superfusates taken from spinal cords of cats anaesthetized with chloralose and urethane were assayed for endogenous serotonin and noradrenaline by high-pressure liquid chromatography with electrochemical detection. 2. Stimulating the dorsolateral funiculus, caudal to a spinal transection, enhanced in a frequency-dependent manner the levels of monoamines in the spinal superfusate. 3. Tyramine added to the superfusate enhanced the release of noradrenaline and serotonin. 4. In cats with intact neuraxes, stimulation of the sciatic nerve at high, but not low intensities produced a 2- to 3-fold increase in the levels of monoamines in the spinal superfusate. This evoked monoamine efflux was attenuated by cold block of the cervical spinal cord. 5. Stimulation of the infraorbital branch of the trigeminal nerve evoked the release of noradrenaline and serotonin from the lumbar cord in animals with intact neuraxes. Cold block of the cervical cord blocked trigeminal-evoked release of lumbar serotonin and noradrenaline. 6. That the monoamine efflux was not due to elevations in blood pressure was indicated by the failure of vasoxyl, an alpha-agonist producing hypertension, to evoke any changes in spinal monoamine levels. 7. The monoamine release was not dependent upon either an opiate-sensitive link or upon the activation of the sympathetic ganglia, because systemic administration of naloxone (an opiate antagonist) and chlorisondamine (a ganglionic blocking agent) failed to antagonize the evoked release of amines. 8. These results suggest the existence of a spinopetal monoamine system which is activated by peripheral stimuli. The modulatory influence associated with increasing monoamine tone in the spinal cord clearly indicated that somatic stimuli may activate a descending monoamine pathway which serves to modulate the magnitude of the ascending sensory message.

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Year:  1981        PMID: 7310700      PMCID: PMC1249448          DOI: 10.1113/jphysiol.1981.sp013722

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  45 in total

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2.  Modifications of the firing rate of bulbar reticular units (nucleus gigantocellularis) after intra-arterial injection of bradykinin into the limbs.

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4.  Bulbospinal serotonin-containing neurons and motor control.

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5.  Projections of the nuclei of the periaqueductal gray matter in the cat.

Authors:  B L Hamilton
Journal:  J Comp Neurol       Date:  1973-11-01       Impact factor: 3.215

6.  Ultrastructural observations on the degeneration of spinal afferents to the nucleus medullae oblongatae centralis (pars caudalis) of the cat.

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Journal:  Brain Res       Date:  1971-03-05       Impact factor: 3.252

7.  Suppression of a spinal and a cranial nerve reflex by vaginal or rectal probing in rats.

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Review 8.  Pain mechanisms: a new theory.

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9.  Single neurons in the rat medulla responsive to nociceptive stimulation.

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Journal:  Brain Res       Date:  1970-12-18       Impact factor: 3.252

10.  Projection of dorsal column nuclei and spinal cord to brainstem and thalamus in the tree shrew, Tupaia glis.

Authors:  D M Schroeder; J A Jane
Journal:  J Comp Neurol       Date:  1971-07       Impact factor: 3.215

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2.  Theoretical studies of impulse propagation in serotonergic axons.

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3.  5-HT agonist induced analgesia modulated by central but not peripheral noradrenaline depletion in rats.

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4.  Effect of chrysin on nociception in formalin test and serum levels of noradrenalin and corticosterone in rats.

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5.  Effect of treadmill exercise on serotonin immunoreactivity in medullary raphe nuclei and spinal cord following sciatic nerve transection in rats.

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6.  Descending control of spinal nociceptive transmission. Actions produced on spinal multireceptive neurones from the nuclei locus coeruleus (LC) and raphe magnus (NRM).

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8.  Depletion of endogenous noradrenaline does not prevent spinal cord plasticity following peripheral nerve injury.

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9.  DNIC-mediated analgesia produced by a supramaximal electrical or a high-dose formalin conditioning stimulus: roles of opioid and alpha2-adrenergic receptors.

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Review 10.  Transcutaneous electrical nerve stimulation (TENS) for dementia.

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