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Noradrenaline attentiveness

Modulation of second-messenger pathways is also an attractive target upon which to base novel antidepressants. Rolipram [61413-54-5] an antidepressant in the preregistration phase, enhances the effects of noradrenaline though selective inhibition of central phosphodiesterase, an enzyme which degrades cycHc adenosiae monophosphate (cAMP). Modulation of the phosphatidyl iaositol second-messenger system coupled to, for example, 5-HT,, 5-HT,3, or 5-HT2( receptors might also lead to novel antidepressants, as well as to alternatives to lithium for treatment of mania. Novel compounds such as inhibitors of A-adenosyl-methionine or central catechol-0-methyltransferase also warrant attention. [Pg.234]

After an overview of neurotransmitter systems and function and a consideration of which substances can be classified as neurotransmitters, section A deals with their release, effects on neuronal excitability and receptor interaction. The synaptic physiology and pharmacology and possible brain function of each neurotransmitter is then covered in some detail (section B). Special attention is given to acetylcholine, glutamate, GABA, noradrenaline, dopamine, 5-hydroxytryptamine and the peptides but the purines, histamine, steroids and nitric oxide are not forgotten and there is a brief overview of appropriate basic pharmacology. [Pg.1]

Much attention has been paid to the catecholamines noradrenaline and dopamine following the discovery that their depletion in the brain leads to profound mood changes and locomotor deficits. Thus noradrenaline has been implicated in the mood changes associated with mania and depression, while an excess of dopamine has been implicated in schizophrenia and a deficit in Parkinson s disease. [Pg.65]

The mechanism of deprenyl s action is unclear. In addition to enhancing dopaminergic activity in the brain by inhibiting dopamine degradation, deprenyl is metabolized into various stimulant metabolites. In spontaneously hyperactive rats used in an animal model of ADHD, chronic deprenyl administration improved im-pulsivity (but not hyperactivity or attention) along with altering levels of noradrenaline, dopamine, and serotonin and their metabolites (Boix et ah, 1998). [Pg.537]

There is a lot of evidence that the major neurotransmitter system affected by benzodiazepines is the one that controls the release of the neurotransmitter norepinephrine (also known as noradrenaline). Studies suggest that people with anxiety illnesses have increased release of norepinephrine and that this continued release causes a depletion of this neurotransmitter and a shutdown of the neurons that are releasing it. This is important because norepinephrine is involved in making an animal or person focused or attentive to what is going on in the environment. When this neurotransmitter is overreleased, it causes anxiety. When no more norepinephrine is available for release, it causes a feeling of exhaustion. [Pg.73]

Norepinephrine (also called noradrenaline)—Controls emotional arousal and increases attention. [Pg.112]

In this chapter, we have looked at two topics in cognitive enhancement attention and memory. We have first reviewed the role of dopamine and norepinephrine/ noradrenaline in the neuropharmacology of attention, and then the syndrome of attention deficit disorder as a common problem associated with a disorder of attention. We then discussed the use of stimulants for improving attention, primarily in attention deficit disorder, and reviewed the pharmacological mechanisms of action of methylphenidate, d and 1 amphetamine, pemoline, and secondary therapies such as clonidine and guanfacine. [Pg.497]

Riekkinen M, Kejonen K, Jakala P, Soininen H, Riekkinen P, Jr. (1998) Reduction of noradrenaline impairs attention and dopamine depletion slows responses in Parkinson s disease. Eur. J. Neurosci. 10 1429-1435. [Pg.41]

Subsequently attention switched to neurotransmitter receptors in the 1970s and the monoamine hypothesis was reformulated in terms of monoamine receptors. It was found in animal experiments that several antidepressants reduced the density of beta-adrenoceptors (a type of noradrenalin receptor) in the brain after about two weeks of treatment. [Pg.132]

Now we must recall that regional brain analysis of diminished psychological function in dreaming shows an association with the lack of noradrenaline and serotonin in the REM sleep-activated brain - these two chemicals are known to be necessary for attention, learning, and memory (and by implication for orientation and... [Pg.101]

Kratochvil CJ, Vaughan BS, Harrington MJ, Burke WJ. Atomoxetine a selective noradrenaline reuptake inhibitor for the treatment of attention-deficit/hyperactivity disorder. Expert Opin Pharmacother 2003 4(7) 1165-74. [Pg.35]

It was named Dopamine because it was a monoamine, and its synthetic precursor was 3,4-dihydroxyphenylalanine (L-DOPA). He was awarded Nobel Prize in 2000 along with Eric Kandel and Paul Greengard in Medicine for showing that dopamine is not just a precursor of noradrenaline and adrenaline, but also neurotransmitter as well. DO is a type of neurotransmitter naturally produced in by the human body. It is also a neurohormone released by the hypothalamus. It is a chemical messenger that is similar to adrenaline and affects the brain processes that control movement, emotional response, and the capacity to feel pleasure and pain. It is vital for performing balanced and controlled movements [172,173], In the extra-cellular fluid of the central nervous system, the basal DO concentration is very low (0.01-1 pM). Abnormal levels of DO have been linked with Parkinson s disease, Tourette s syndrome, Schizophrenia, attention deficit hyperactive disorder and generation of pituitary tumours [174-176],... [Pg.120]

S-methylhomocy teine methionine, methylisogenistin genistein. /V-methylmescaline mescaline, methylmorphine codeine, a-methy I noradrenaline levonordefrin. methyl pentynol (ban. inn] is an acetylenic carbinol. with HYPNOTIC and SEDATIVE properties. It has been used in the treatment of insomnia and as an anxiolytic. methyl-PGEj arbaprostil. methylphenidate [ban, inn] (methylphenidate hydrochloride [jan, usan] Ritalin ) is a CNS STIMULANT and dopamine (re) UPTAKE INHIBITOR. It is used in the treatment of attention-deficit hyperactivity disorder in children, methylphenidate hydrochloride methylphenidate. [Pg.179]


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