1989
DOI: 10.1007/bf00964919
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Changes with aging in the levels of amino acids in rat CNS structural elements II. Taurine and small neutral amino acids

Abstract: Taurine (Tau) and the small neutral amino acids glycine (Gly), serine (Ser), threonine (Thr), and alanine (Ala) were measured in 53 brain areas of 3- and 29-month-old male Fisher 344 rats. The ratio of highest to lowest level was 34 for Tau, 9.1 for Thr, 7.6 for Gly and Ser, and 6.5 for Ala. The heterogeneity was found in numerous areas; for example, Tau levels were more than 90 nmol/mg protein in 6 areas, and less than 20 nmol/mg protein in 10 areas. Similar heterogeneity was found with the other amino acids.… Show more

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Cited by 99 publications
(48 citation statements)
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“…The brain amino acid concentration of the control group re ceiving a 17% protein diet was in agreement with other data [I, [14][15][16], Taurine, lysine and tryptophan concentrations did not change in brain tissue by increasing the di etary protein content. Glutamic acid and glu tamine concentrations increased in all groups, particularly in the rats on the low protein diet.…”
Section: Plasma Liver and Brain Amino Acidsupporting
confidence: 80%
“…The brain amino acid concentration of the control group re ceiving a 17% protein diet was in agreement with other data [I, [14][15][16], Taurine, lysine and tryptophan concentrations did not change in brain tissue by increasing the di etary protein content. Glutamic acid and glu tamine concentrations increased in all groups, particularly in the rats on the low protein diet.…”
Section: Plasma Liver and Brain Amino Acidsupporting
confidence: 80%
“…Altered inputs onto fusiform cells from these inhibitory neurons would not be expected to significantly alter fusiform spontaneous rates. Previous DCN aging studies described decreased glycine levels, decreased strychnine binding (especially in the fusiform layer), and a loss of glycine immunoreactivity in cells at the junction between the deep and fusiform-cell layers of the cochlear nucleus (Banay-Schwartz et al, 1989;Willott et al, 1997;Milbrandt et al, 2000;Caspary et al, 2001). The subunit makeup of the glycine receptor showed age-related changes, in both the DCN and AVCN, that could account for functional changes observed in the present study (Krenning et al, 1998;Caspary et al, 2002).…”
Section: Discussionmentioning
confidence: 91%
“…Age-related loss of markers for inhibitory amino acids has also been described for the auditory midbrain. The inferior colliculus (IC) shows significant age-related changes related to GABA neurotransmission in rats (Banay-Schwartz et al, 1989;Caspary et al, 1990Caspary et al, , 1995Gutierrez et al, 1994;Milbrandt et al, 1994;Raza et al, 1994) and the loss of GABAimmunoreactive synaptic endings. Postmortem human studies of the cortex and IC are less clear.…”
Section: Discussionmentioning
confidence: 99%
“…Peripheral auditory changes include a sloping low-frequency loss of outer hair cells and a small loss of apical and basal inner hair cells (for review, see Willott et al, 1991;Saitoh et al, 1994;Gratton et al, 1996Gratton et al, , 1997Spongr et al, 1997;Ingham et al, 1999;Tang et al, 2014) accompanied by auditory nerve fiber loss (Keithley et al, 1989(Keithley et al, , 1992Dazert et al, 1996;Schmiedt et al, 1996). Parallel central aging effects include a net down-regulation of glycinergic and GABAergic inhibition in the cochlear nucleus (Banay-Schwartz et al, 1989b;Krenning et al, 1998;, inferior colliculus (Banay-Schwartz et al, 1989a,b;Caspary et al, 1990;Gutierrez et al, 1994;Milbrandt et al, 1994Milbrandt et al, , 1996, MGB (Richardson et al, 2013a), and auditory cortex Stebbings et al, 2016). This CANS loss of inhibition at least partially subserves the age-related loss of accurate temporal processing seen in older humans (Harris et al, 2012;Mattys and Scharenborg, 2014).…”
Section: Changes Of Bottom-up Processing With Agingmentioning
confidence: 99%