On Mar 25, 7:21 am, "ironjust...@aol.com" <ironjust...@aol.com> wrote:
tyrosine <<
"Here, take a cookie. I promise, by the time you're done eating it,
you'll feel right as rain."
"Baseline mesocortical DA synthesis is dependent on tyrosine
availability"
Brain Res. 2008 Jan 23;1190:39-48. Epub 2007 Nov 4.Related Articles,
Links
Tyrosine depletion lowers dopamine synthesis and desipramine-induced
prefrontal cortex catecholamine levels.
Bongiovanni R, Newbould E, Jaskiw GE.
Psychiatry Service, Louis Stokes Cleveland Veterans Affairs Medical
Center, Brecksville, OH 44141, USA.
The relationship between limited tyrosine availability, DA (dopamine)
synthesis and DA levels in the medial prefrontal cortex (MPFC) of the
rat was examined by in vivo microdialysis.
We administered a tyrosine- and phenylalanine-free mixture of large
neutral amino acids (LNAA-) IP to lower brain tyrosine, and the
norepinephrine transporter inhibitor desipramine (DMI) 10 mg/kg IP to
raise MPFC DA levels without affecting DA synthesis.
For examination of DOPA levels, NSD-1015 20 microM was included in
perfusate.
Neither NSD-1015 nor DMI affected tyrosine levels. LNAA- lowered
tyrosine levels by 45%, and lowered DOPA levels as well; this was not
additionally affected by concurrent DMI 10 mg/kg IP. In parallel
studies DMI markedly increased extracellular levels of DA (420%
baseline) and norepinephrine (NE) (864% baseline). LNAA- had no effect
on baseline levels of DA or NE but robustly lowered DMI-induced DA
(176% baseline) as well as NE (237% baseline) levels.
Even when DMI (20 microM) was administered in perfusate, LNAA- still
lowered DMI-induced DA and NE levels.
We conclude that while baseline mesocortical DA synthesis is indeed
dependent on tyrosine availability, the MPFC maintains normal
extracellular DA and NA levels in the face of moderately lower DA
synthesis.
During other than baseline conditions, however, tyrosine depletion can
lower ECF DA and NE levels in MPFC.
These data offer a potential mechanism linking dysregulation of
tyrosine transport and cognitive deficits in schizophrenia.
Publication Types:
Research Support, U.S. Gov't, Non-P.H.S.
PMID: 18082673 [PubMed - in process]
--------------------------------------------------------------------------------
Who loves ya.
Tom
Jesus Was A Vegetarian!
http://tinyurl.com/2r2nkh
Man Is A Herbivore!
http://tinyurl.com/a3cc3
DEAD PEOPLE WALKING
http://tinyurl.com/zk9fk
> On Mar 23, 9:57 am, ironjustice <teamtan...@hotmail.com> wrote:tyrosine<<
>
[quoted text clipped - 64 lines]
>
> - Show quoted text -
ironjustice - 26 Mar 2008 05:37 GMT
On Mar 25, 9:13 pm, ironjustice <teamtan...@hotmail.com>
wrote:tyrosine <<
The effects of tyrosine depletion in normal healthy volunteers:
implications for unipolar depression
by
McLean A, Rubinsztein JS, Robbins TW, Sahakian BJ.
Department of Psychiatry,
University of Cambridge,
School of Clinical Medicine,
Addenbrooke's Hospital,
Hills Road, CB2 2QQ,
Cambridge, UK
Psychopharmacology (Berl). 2003 Sep 4.
ABSTRACT
RATIONALE.
In recent years, there has been a growing interest in the role of
dopamine (DA) both in the pathogenesis of unipolar depression and in
motivated behaviour.
The innovative technique of acute tyrosine depletion presents an
opportunity to characterise further its function in these domains.
OBJECTIVE.
The present study examined the physiological, subjective and cognitive
effects of acute tyrosine depletion in healthy volunteers.
METHODS.
A double-blind, placebo-controlled, parallel group design was
employed.
Half of the participants ingested a balanced amino-acid mixture (BAL)
and the other half received an identical mixture except that tyrosine
and phenylalanine were absent (TYR-free).
Plasma amino acid concentrations and subjective ratings were monitored
at both baseline (T(0)) and 5 h following consumption (T(5)) of the
mixtures.
A comprehensive neuropsychological test battery was also administered
at T(5). RESULTS.
Relative to the BAL group, the reduction in TYR availability to the
brain was more marked in the TYR-free group.
Employment of psychological rating scales revealed that, compared with
the BAL group, the TYR-free group became less content and more
apathetic.
For the affective go/no-go task, whilst the BAL group exhibited a
happy latency bias, the TYR-free group demonstrated a sad latency
bias.
Furthermore, in the decision-making task, the rate at which the TYR-
free group increased their bets in response to more likely outcomes
was lower than that of the BAL group.
Taken together, these neuropsychological findings strikingly
paralleled those reported in previous investigations of unipolar
depression.
The experimental groups could not be differentiated on any of the
other neuropsychological measures, including more classical
assessments of fronto-executive function.
CONCLUSION.
These findings are consistent with the hypothesis that dopaminergic
factors are particularly involved in disrupted affect/reward-based
processing characteristic of clinical depression.
Who loves ya.
Tom
Jesus Was A Vegetarian!
http://tinyurl.com/2r2nkh
Man Is A Herbivore!
http://tinyurl.com/a3cc3
DEAD PEOPLE WALKING
http://tinyurl.com/zk9fk
> On Mar 25, 7:21 am, "ironjust...@aol.com" <ironjust...@aol.com> wrote:
> tyrosine <<
[quoted text clipped - 128 lines]
>
> - Show quoted text -