1990 ◽  
Vol 49 (4) ◽  
pp. 371-382 ◽  
Author(s):  
H P H Kremer ◽  
R A C Roos ◽  
G Dingjan ◽  
G Th A.M. Bots ◽  
E Maran
Keyword(s):  

1991 ◽  
Vol 29 (3) ◽  
pp. 279-284 ◽  
Author(s):  
Berry Kremer ◽  
Dick Swaab ◽  
Gerard Bots ◽  
Bart Fisser ◽  
Rivka Ravid ◽  
...  

Endocrinology ◽  
2003 ◽  
Vol 144 (10) ◽  
pp. 4552-4561 ◽  
Author(s):  
José Miguel Cerdá-Reverter ◽  
Richard Ector Peter

Agouti-related protein (AGRP) is a naturally occurring antagonist of melanocortin. In mammals, central AGRP expression is restricted to the arcuate nucleus in which it plays a key role in the control of energy balance by antagonizing melanocortin effects at melanocortin 4 receptors. In goldfish, melanocortin 4 receptor is profusely expressed within the main brain areas for the control of energy balance, and central administration of agonist or antagonist analogs inhibits or stimulates food intake, respectively. Here we demonstrate that the goldfish genome has a homologous gene to mammalian AGRP. Detailed brain mapping by in situ hybridization shows that AGRP is exclusively expressed in the ventrobasal hypothalamic lateral tuberal nucleus, the teleostean homolog of the arcuate nucleus. Fasting up-regulates its mRNA levels in the lateral tuberal nucleus. In the periphery, AGRP is expressed in several tissues including ovary, muscle, and ventral skin, suggesting that AGRP might regulate peripheral actions of melanocortin peptides. The results provide the first evidence for an endogenous melanocortin antagonist in nontetrapod species and suggest that hypothalamic overexpression during fasting might regulate the inhibitory effects of melanocortin peptides on food intake in goldfish.


2019 ◽  
Vol 3 (Supplement_1) ◽  
Author(s):  
Shannon Stephens ◽  
Reanna Liaw ◽  
Noelia Di Giorgio ◽  
Victoria Lux-Lantos ◽  
Alexander Kauffman
Keyword(s):  

Science ◽  
2018 ◽  
Vol 361 (6397) ◽  
pp. 76-81 ◽  
Author(s):  
Sarah Xinwei Luo ◽  
Ju Huang ◽  
Qin Li ◽  
Hasan Mohammad ◽  
Chun-Yao Lee ◽  
...  

The tuberal nucleus (TN) is a surprisingly understudied brain region. We found that somatostatin (SST) neurons in the TN, which is known to exhibit pathological or cytological changes in human neurodegenerative diseases, play a crucial role in regulating feeding in mice. GABAergic tuberal SST (TNSST) neurons were activated by hunger and by the hunger hormone, ghrelin. Activation of TNSST neurons promoted feeding, whereas inhibition reduced it via projections to the paraventricular nucleus and bed nucleus of the stria terminalis. Ablation of TNSST neurons reduced body weight gain and food intake. These findings reveal a previously unknown mechanism of feeding regulation that operates through orexigenic TNSST neurons, providing a new perspective for understanding appetite changes.


1995 ◽  
Vol 54 (3) ◽  
pp. 430
Author(s):  
E. Braak ◽  
H. Braak ◽  
C. Schultz ◽  
D. Yilmazer ◽  
J. W. Goethe
Keyword(s):  

Sign in / Sign up

Export Citation Format

Share Document