3H-spiroperidol binding and dopamine-stimulated adenylate cyclase: Evidence for multiple classes of receptors in primate brain regions

Life Sciences ◽  
1978 ◽  
Vol 23 (6) ◽  
pp. 629-633 ◽  
Author(s):  
L.J. Thal ◽  
M.H. Makman ◽  
H.S. Ahn ◽  
R.K. Mishra ◽  
S.G. Horowitz ◽  
...  
2004 ◽  
Vol 370 (2-3) ◽  
pp. 201-205 ◽  
Author(s):  
Thomas J.R. Beveridge ◽  
Hilary R. Smith ◽  
Michael A. Nader ◽  
Linda J. Porrino

1969 ◽  
Vol 14 (2) ◽  
pp. 447-459 ◽  
Author(s):  
Morris Goodman ◽  
Frank N. Syner ◽  
Cyrus W. Stimson ◽  
Jessie J. Rankin

1975 ◽  
Vol 96 (2) ◽  
pp. 395-399 ◽  
Author(s):  
Ram K. Mishra ◽  
C. Demirjian ◽  
R. Katzman ◽  
M.H. Makman

1992 ◽  
Vol 229 (2-3) ◽  
pp. 197-202 ◽  
Author(s):  
Menno H. Heijna ◽  
Joost M. Bakker ◽  
François Hogenboom ◽  
Arie H. Mulder ◽  
Anton N.M. Schoffelmeer

1976 ◽  
Vol 116 (3) ◽  
pp. 437-454 ◽  
Author(s):  
Ho Sam Ahn ◽  
Ram K. Mishra ◽  
Charles Demirjian ◽  
Maynard H. Makman

Author(s):  
Martin Brüne

The human brain is the most complex organ that has ever evolved. It contains more neurons and synapses than any other primate brain. In relation to body weight, it is outstandingly large and distinctly convoluted. Several parts of the brain have enlarged disproportionally over evolutionary time. Those brain regions are mainly involved in emotion processing, understanding and reflecting upon one’s own and other minds, memory, social decision-making, and action planning, suggesting that the human brain is adapted to dealing with social matters. The human brain is also conspicuous with regard to its slow maturation, which is linked to the huge amount of social information that needs to be learned until adulthood. Cross-talk among neurons is maintained by the action of neuromodulators and neurotransmitters, many of which are ancient and have served multiple purposes in plants and animals. They help regulate defensive and agonistic behaviour, social attachment, and inhibitory control.


2013 ◽  
Vol 305 (12) ◽  
pp. E1452-E1463 ◽  
Author(s):  
Jon M. Resch ◽  
Brian Maunze ◽  
Adriana K. Gerhardt ◽  
Samuel K. Magnuson ◽  
Kailynn A. Phillips ◽  
...  

Numerous studies have demonstrated that both the hypothalamic paraventricular nuclei (PVN) and ventromedial nuclei (VMN) regulate energy homeostasis through behavioral and metabolic mechanisms. Receptors for pituitary adenylate cyclase-activating polypeptide (PACAP) are abundantly expressed in these nuclei, suggesting PACAP may be critical for the regulation of feeding behavior and body weight. To characterize the unique behavioral and physiological responses attributed to select hypothalamic cell groups, PACAP was site-specifically injected into the PVN or VMN. Overall food intake was significantly reduced by PACAP at both sites; however, meal pattern analysis revealed that only injections into the PVN produced significant reductions in meal size, duration, and total time spent eating. PACAP-mediated hypophagia in both the PVN and VMN was abolished by PAC1R antagonism, whereas pretreatment with a VPACR antagonist had no effect. PACAP injections into the VMN produced unique changes in metabolic parameters, including significant increases in core body temperature and spontaneous locomotor activity that was PAC1R dependent whereas, PVN injections of PACAP had no effect. Finally, PACAP-containing afferents were identified using the neuronal tracer cholera toxin subunit B (CTB) injected unilaterally into the PVN or VMN. CTB signal from PVN injections was colocalized with PACAP mRNA in the medial anterior bed nucleus of the stria terminalis, VMN, and lateral parabrachial nucleus (LPB), whereas CTB signal from VMN injections was highly colocalized with PACAP mRNA in the medial amygdala and LPB. These brain regions are known to influence energy homeostasis perhaps, in part, through PACAP projections to the PVN and VMN.


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