scholarly journals Effects of stimulation of frontal cortex on neuronal activity in association and sensory areas of the cortex

1968 ◽  
Vol 12 (5) ◽  
pp. 167-168 ◽  
Author(s):  
Lewis A. Bettinger ◽  
Herman Birch ◽  
Philip M. Groves ◽  
Kathleen S. Mayers ◽  
Richard F. Thompson
Cell Calcium ◽  
2021 ◽  
pp. 102388
Author(s):  
Alex L. Keyes ◽  
Young-cho Kim ◽  
Peter J. Bosch ◽  
Yuriy M. Usachev ◽  
Georgina M. Aldridge

Neuroscience ◽  
1980 ◽  
Vol 5 (12) ◽  
pp. 2151-2154 ◽  
Author(s):  
O.V. Godukhin ◽  
A.D. Zharikova ◽  
V.I. Novoselov

2002 ◽  
Vol 57 (1-2) ◽  
pp. 182-188 ◽  
Author(s):  
Artemis Doulgeraki ◽  
Zetta Papadopoulou-Daifoti ◽  
Stylianos Tsakiris

The effect of different ʟ-phenylalanine (Phe) concentrations (0.12D12.1 mᴍ) on acetylcholinesterase (AChE), (Na+,K+)-ATPase and Mg2+-ATPase activities was evaluated in homogenates of suckling rat frontal cortex, hippocampus and hypothalamus. Phe, at high concentrations, reduced AChE activity in frontal cortex and hippocampus by 18%-20%. On the contrary, the enzyme activity was unaltered in the hypothalamus. Na+,K+-ATPase was stimulated by high levels of the amino acid, both in the frontal cortex and the hypothalamus by 60%, whereas it was inhibited in the hippocampus by 40%. Mg2+-ATPase was not influenced by Phe. It is suggested that: a) In the frontal cortex, the improper acetylcholine (ACh) release, due to AChE inhibition by Phe, combined with the stimulation of Na+,K+-ATPase, possibly explain tremor and the hyperkinetic behaviour in patients with classical phenylketonuria (PKU). b) In the hippocampus, inhibition of AChE by Phe could lead to problems in memory, while Na+,K+-ATPase inhibition by Phe may induce metabolic disorders and electrical instability of the synaptosomal membrane. c) In the hypothalamus, the behavioral problems in PKU “off diet” may be related to noradrenaline (NA) levels, which are probably correlated with the modulated Na+,K+-ATPase by Phe.


2000 ◽  
Vol 279 (6) ◽  
pp. R2079-R2088 ◽  
Author(s):  
Hui Gong ◽  
Ronald Szymusiak ◽  
Janice King ◽  
Teresa Steininger ◽  
Dennis McGinty

Preoptic area (POA) neuronal activity promotes sleep, but the localization of critical sleep-active neurons is not completely known. Thermal stimulation of the POA also facilitates sleep. This study used the c-Fos protein immunostaining method to localize POA sleep-active neurons at control (22°C) and mildly elevated (31.5°C) ambient temperatures. At 22°C, after sleep, but not after waking, we found increased numbers of c-Fos immunoreactive neurons (IRNs) in both rostral and caudal parts of the median preoptic nucleus (MnPN) and in the ventrolateral preoptic area (VLPO). In animals sleeping at 31.5°C, significantly more Fos IRNs were found in the rostral MnPN compared with animals sleeping at 22°C. In VLPO, Fos IRN counts were no longer increased over waking levels after sleep at the elevated ambient temperature. Sleep-associated Fos IRNs were also found diffusely in the POA, but counts were lower than those made after waking. This study supports a hypothesis that the MnPN, as well as the VLPO, is part of the POA sleep-facilitating system and that the rostral MnPN may facilitate sleep, particularly at elevated ambient temperatures.


1999 ◽  
Vol 55 (2) ◽  
pp. 202-209 ◽  
Author(s):  
Jow Y. Lew ◽  
Antonio Garcia-Espana ◽  
Kwan Y. Lee ◽  
Kenneth D. Carr ◽  
Menek Goldstein ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document