Glucocorticoid binding to receptor-like proteins in rat brain and pituitary: Ontogenetic and experimentally induced changes

1976 ◽  
Vol 105 (1) ◽  
pp. 121-128 ◽  
Author(s):  
Hans-Rudolf Olpe ◽  
Bruce S. McEwen
1948 ◽  
Vol 175 (2) ◽  
pp. 945-952
Author(s):  
Armand J. Quick ◽  
Mario. Stefanini

1990 ◽  
Vol 167 (3) ◽  
pp. 1294-1301 ◽  
Author(s):  
Teng-Nan Lin ◽  
Grace Y. Sun ◽  
Noel Premkumar ◽  
Ronald A. MacQuarrie ◽  
Steven R. Carter

1992 ◽  
Vol 15 ◽  
pp. 454B
Author(s):  
T Chishima ◽  
S. M. Babb ◽  
D. J. Ennulat ◽  
B. M. Cohen
Keyword(s):  

1987 ◽  
Vol 45 (2) ◽  
pp. 243-248
Author(s):  
Koji OKAMURA ◽  
Futoshi MATSUBARA ◽  
Yasuyuki YOSHIOKA ◽  
Noriaki KIKUCHI ◽  
Yuko KIKUCHI ◽  
...  

1973 ◽  
Vol 132 (1) ◽  
pp. 95-100 ◽  
Author(s):  
David J. Edwards ◽  
Karl Blau

1. Phenethylamines were extracted from brain and liver of rats with phenylketonuria-like characteristics produced in vivo by inhibition of phenylalanine hydroxylase (EC 1.14.3.1) with p-chlorophenylalanine, with or without phenylalanine administration. To protect amines against oxidation by monoamine oxidase, pargyline was also administered. 2. β-Phenethylamine was the major compound found in brain and liver. β-Phenethanolamine and octopamine were also present, in lesser amounts, and the concentrations of these three amines paralleled blood phenylalanine concentrations. By comparison, tissues from control animals had only very low concentrations of these amines. 3. Small amounts of normetadrenaline, m-tyramine and 3-methoxytyramine were also found. 4. The inhibitors used, p-chlorophenylalanine and pargyline, gave rise to p-chlorophenethylamine and benzylamine respectively, the first via decarboxylation, the second probably by breakdown during extraction. 5. Distribution of phenethylamines in different brain regions and in subcellular fractions of rat brain cells was also investigated. The content of phenethylamine was highest in the striatum. 6. These findings are discussed in the light of changes occurring in human patients with uncontrolled phenylketonuria.


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