Developmental and age-related changes in the D2 dopamine receptor mRNA subtypes in rat brain

1992 ◽  
Vol 20 ◽  
pp. 49-58 ◽  
Author(s):  
Benjamin Weiss ◽  
Jang Fan Chen ◽  
Suipo Zhang ◽  
Long-Wu Zhou
1989 ◽  
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J. H. Meador-Woodruff ◽  
A. Mansour ◽  
J. R. Bunzow ◽  
H. H. Van Tol ◽  
S. J. Watson ◽  
...  

1991 ◽  
Vol 88 (5) ◽  
pp. 1859-1863 ◽  
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D. M. Weiner ◽  
A. I. Levey ◽  
R. K. Sunahara ◽  
H. B. Niznik ◽  
B. F. O'Dowd ◽  
...  

2010 ◽  
Vol 168 (1) ◽  
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Masaki Nakano ◽  
Itaru Hasunuma ◽  
Reiko Okada ◽  
Kazutoshi Yamamoto ◽  
Sakae Kikuyama ◽  
...  

1990 ◽  
Vol 111 (3) ◽  
pp. 303-308 ◽  
Author(s):  
Hubert H.M. van Tol ◽  
Marco Riva ◽  
O. Civelli ◽  
Ian Creese

2006 ◽  
Vol 1090 (1) ◽  
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Paul M. Carvey ◽  
Zaodung Ling

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Tadayuki Kobayashi ◽  
Kazunori Kawamura ◽  
Kiyoshi Matsuno

1986 ◽  
Vol 237 (1) ◽  
pp. 47-51 ◽  
Author(s):  
M C McKenna ◽  
L I Bezold ◽  
S J Kimatian ◽  
J T Tildon

The rate of conversion of [1,3-14C]glycerol into 14CO2 was measured in the presence and absence of unlabelled alternative substrates in whole homogenates from the brains of young (4-6 and 18-20 days old) and adult rats. Unlabelled glucose decreased 14CO2 production from [1,3-14C]glycerol by about 40% at all ages studied. Unlabelled 3-hydroxybutyrate significantly decreased the 14CO2 production from both low (0.2 mM) and high (2.0 mM) concentrations of glycerol in 4-6- and 18-20-day-old rat pups. However, the addition of 3-hydroxybutyrate had no effect on the rate of 14CO2 production from 2.0 mM-glycerol in adult rats, suggesting that the interaction of 3-hydroxybutyrate with glycerol in adult rat brain is complex and may be related to the biphasic kinetics previously reported for glycerol oxidation. Unlabelled glutamine decreased the production of 14CO2 by brain homogenates from 18-20-day-old and adult rats, but not in 4-6-day-old rat pups. In the converse situation, the addition of unlabelled glycerol to whole brain homogenates had little effect on the rate of 14CO2 production from [6-14C]glucose, 3-hydroxy[3-14C]butyrate and [U-14C]glutamine, although some significant differences were noted. Collectively these results suggest that glycerol and these other substrates may be metabolized in separate subcellular compartments in brain such that the products of glucose, 3-hydroxybutyrate and glutamine metabolism can dilute the oxidation of glycerol, but the converse cannot occur. The data also demonstrate that there are complex age-related changes in the interaction of glycerol with 3-hydroxybutyrate and glutamine. The fact that glycerol oxidation was only partially suppressed by the addition of 1-5 mM-glucose, -3-hydroxybutyrate or -glutamine could also suggest that glycerol may be selectively utilized as an energy substrate in some discrete brain region.


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