Phenylketonuria: High plasma phenylalanine decreases cerebral protein synthesis

2009 ◽  
Vol 96 (4) ◽  
pp. 177-182 ◽  
Author(s):  
Marieke Hoeksma ◽  
Dirk-Jan Reijngoud ◽  
Jan Pruim ◽  
Harold W. de Valk ◽  
Anne M.J. Paans ◽  
...  
2014 ◽  
Vol 35 (2) ◽  
pp. 200-205 ◽  
Author(s):  
Martijn J de Groot ◽  
Paul E Sijens ◽  
Dirk-Jan Reijngoud ◽  
Anne M Paans ◽  
Francjan J van Spronsen

In phenylketonuria, elevated plasma phenylalanine concentrations may disturb blood-to-brain large neutral amino acid (LNAA) transport and cerebral protein synthesis (CPS). We investigated the associations between these processes, using data obtained by positron emission tomography with l-[1-11C]-tyrosine (11C-Tyr) as a tracer. Blood-to-brain transport of non-Phe LNAAs was modeled by the rate constant for 11C-Tyr transport from arterial plasma to brain tissue (K1), while CPS was modeled by the rate constant for 11C-Tyr incorporation into cerebral protein (k3). Brain phenylalanine concentrations were measured by magnetic resonance spectroscopy in three volumes of interest (VOIs): supraventricular brain tissue (VOI 1), ventricular brain tissue (VOI 2), and fluid-containing ventricular voxels (VOI 3). The associations between k3 and each predictor variable were analyzed by multiple linear regression. The rate constant k3 was inversely associated with brain phenylalanine concentrations in VOIs 2 and 3 (adjusted R2=0.826, F=19.936, P=0.021). Since brain phenylalanine concentrations in these VOIs highly correlated with each other, the specific associations of each predictor with k3 could not be determined. The associations between k3 and plasma phenylalanine concentration, K1, and brain phenylalanine concentrations in VOI 1 were nonsignificant. In conclusion, our study shows an inverse association between k3 and increased brain phenylalanine concentrations.


2008 ◽  
Vol 28 (7) ◽  
pp. 1388-1398 ◽  
Author(s):  
Carolyn B Smith ◽  
Kathleen C Schmidt ◽  
Shrinivas Bishu ◽  
Michael A Channing ◽  
Jeff Bacon ◽  
...  

We have previously shown by direct comparison with autoradiographic and biochemical measurements that the l-[1-11C]leucine positron emission tomography method provides accurate determinations of regional rates of cerebral protein synthesis (rCPS) and the fraction (Λ) of unlabeled leucine in the precursor pool for protein synthesis derived from arterial plasma. In this study, we examine sensitivity of the method to detect changes in Λ and stability of the method to measure rCPS in the face of these changes. We studied four isoflurane-anesthetized monkeys dynamically scanned with the high resolution research tomograph under control and mild hyperphenylalaninemic conditions. Hyperphenylalaninemia was produced by an infusion of phenylalanine that increased plasma phenylalanine concentrations three- to five-fold. In phenylalanine-infused monkeys, plasma leucine concentrations remained relatively constant, but values of Λ were statistically significantly decreased by 11% to 15%; rCPS was unaffected. Effects on Λ are consistent with competitive inhibition of leucine transport by increased plasma phenylalanine. The effect on Λ shows that competition for the transporter results in a reduction in the fraction of leucine in the precursor pool for protein synthesis coming from plasma. Even under these hyperphenylalaninemic conditions, rCPS remains unchanged due to the compensating increased contribution of leucine from protein degradation to the precursor pool.


Brain ◽  
1985 ◽  
Vol 108 (1) ◽  
pp. 155-170 ◽  
Author(s):  
M.C. INGVAR ◽  
P. MAEDER ◽  
L. SOKOLOFF ◽  
C. B. SMITH

1986 ◽  
pp. 463-467
Author(s):  
K. Takahashi ◽  
W. Bodsch ◽  
T. Shibata ◽  
K.-A. Hossmann

1970 ◽  
Vol 24 (4) ◽  
pp. 219-226
Author(s):  
Shosuke WATANABE ◽  
Katsusuke MITSUNOBU ◽  
Takanori SANNOMIYA ◽  
Saburo OTSUKI

1997 ◽  
Vol 9 (2) ◽  
pp. 271-279 ◽  
Author(s):  
Hajime Nakanishi ◽  
Yun Sun ◽  
Richard K. Nakamura ◽  
Kentaro Mori ◽  
Masanori Ito ◽  
...  

1991 ◽  
Vol 11 (5) ◽  
pp. 753-761 ◽  
Author(s):  
G. Mies ◽  
S. Ishimaru ◽  
Y. Xie ◽  
K. Seo ◽  
K.-A. Hossmann

The ischemic threshold of protein synthesis and energy state was determined 1, 6, and 12 h after middle cerebral artery (MCA) occlusion in rats. Local blood flow and amino acid incorporation were measured by double tracer autoradiography, and local ATP content by substrate-induced bioluminescence. The various images were evaluated at the striatal level in cerebral cortex by scanning with a microdensitometer with 75 μm resolution. Each 75 × 75 μm digitized image pixel was then converted into the appropriate units of either protein synthesis, ATP content, or blood flow. The ischemic threshold was defined as the flow rate at which 50% of pixels exhibited complete metabolic suppression. One hour after MCA occlusion, the threshold of protein synthesis was 55.3 ± 12.0 ml 100 g−1 min−1 and that of energy failure was 18.5 ± 9.8 ml 100 g−1 min−1. After 6 and 12 h of MCA occlusion, the threshold of protein synthesis did not change (52.0 ± 9.6 and 56.0 ± 6.5 ml 100 g−1 min−1, respectively) but the threshold of energy failure increased significantly at 12 h following MCA occlusion to 31.9 ± 9.7 ml 100 g−1 min−1 ( p < 0.05 compared to 1 h ATP threshold value; all values are mean ± SD). In focal cerebral ischemia, therefore, the threshold of energy failure gradually approached that of protein synthesis. Our results suggest that with increasing duration of ischemia, survival of brain tissue is determined by the high threshold of persisting inhibition of protein synthesis and not by the much lower one of acute energy failure. If the ischemic penumbra is considered to comprise the region in which cerebral protein synthesis is suppressed and energy state is preserved, it follows that the size of the penumbra decreases with the duration of ischemia.


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