Behavioural Specificity of Neocortical Grafts of Fetal Basal Forebrain Tissue After Unilateral Lesion of the Nucleus Basalis with α -Amino-3-OH-4-Isoxozole Propionic Acid (AMPA)

1997 ◽  
Vol 42 (6) ◽  
pp. 407-414 ◽  
Author(s):  
Fuad A. Abdulla ◽  
Mariarita Calaminici ◽  
Jeffrey A. Gray ◽  
John D. Stephenson ◽  
John D. Sinden
Keyword(s):  
Propionic Acid ◽  
Basal Forebrain ◽  
Nucleus Basalis ◽  
Unilateral Lesion ◽  
Behavioural Specificity

Sleep is differently modulated by basal forebrain GABAA and GABAB receptors

2001 ◽  
Vol 281 (1) ◽  
pp. R170-R175 ◽  
Author(s):  
Alfredo Manfridi ◽  
Dario Brambilla ◽  
Mauro Mancia
Keyword(s):  
Basal Forebrain ◽  
Slow Wave Sleep ◽  
Gabab Receptors ◽  
Nucleus Basalis ◽  
Receptor Subtype ◽  
Sleep Regulation ◽  
Sleep Parameters ◽  
Polygraphic Recordings ◽  
Sleep Modulation

There is evidence that GABA plays a major role in sleep regulation. GABAA receptor agonists and different compounds interacting with the GABAA receptor complex, such as barbiturates and benzodiazepines, can interfere with the sleep/wake cycle. On the other hand, there is very little information about the possible role of GABAB receptors in sleep modulation. The nucleus basalis of Meynert (NBM), a cholinergic area in the basal forebrain, plays a pivotal role in the modulation of sleep and wakefulness, and both GABAA and GABABreceptors have been described within the NBM. This study used unilateral infusions in the NBM to determine the effects of 3-hydroxy-5-aminomethylisoxazole hydrobromide (muscimol hydrobromide, a GABAA receptor subtype agonist) and β-(aminomethyl)-4-chlorobenzenepropanoic acid (baclofen, a GABAB receptor subtype agonist) on sleep parameters in freely moving rats by means of polygraphic recordings. Muscimol (0.5 nmol) and baclofen (0.7 nmol) induced an increase in slow-wave sleep and an inhibition of wakefulness. Muscimol, but not baclofen, also caused a decrease in desynchronized sleep parameters. The results reported here indicate that 1) the NBM activation of both GABAA and GABAB receptors influences the sleep/wake cycle, and 2) GABAA but not GABAB receptors are important for desynchronized sleep modulation, suggesting that the two GABAergic receptors play different roles in sleep modulation.

scholarly journals Functional segregation of the human basal forebrain using resting state neuroimaging

2017 ◽  
Author(s):  
Ross D. Markello ◽  
R. Nathan Spreng ◽  
Wen-Ming Luh ◽  
Adam K. Anderson ◽  
Eve De Rosa
Keyword(s):  
Functional Connectivity ◽  
Resting State ◽  
Basal Forebrain ◽  
Nucleus Basalis ◽  
Functional Networks ◽  
List Type ◽  
Functional Connections ◽  
Diagonal Band ◽  
Hippocampal Complex

AbstractThe basal forebrain (BF) is poised to play an important neuromodulatory role in brain re-gions important to cognition due to its broad projections and complex neurochemistry. While significant in vivo work has been done to elaborate BF function in nonhuman rodents and primates, comparatively limited work has examined the in vivo function of the human BF. In the current study we used multi-echo resting state functional magnetic resonance imaging (rs-fMRI) from 100 young adults (18-34 years) to assess the potential segregation of human BF nuclei as well as their associated projections. Bottom-up clustering of voxel-wise functional connectivity maps yielded adjacent functional clusters within the BF that closely aligned with the distinct, hypothesized nuclei important to cognition: the nucleus basalis of Meynert (NBM) and the me-dial septum/diagonal band of Broca (MS/DB). Examining their separate functional connections, the NBM and MS/DB revealed distinct projection patterns, suggesting a conservation of nuclei-specific functional connectivity with homologous regions known to be anatomically innervated by the BF. Specifically, the NBM demonstrated coupling with a widespread cortical network as well as the amygdala, whereas the MS/DB revealed coupling with a more circumscribed net-work, including the orbitofrontal cortex and hippocampal complex. Collectively, these in vivo rs-fMRI data demonstrate that the human BF nuclei support functional networks distinct as-pects of resting-state functional networks, suggesting the human BF may be a neuromodulatory hub important for orchestrating network dynamics.HighlightsThe basal forebrain NBM and the MS/DB support two distinct functional networksFunctional networks closely overlap with known anatomical basal forebrainBasal forebrain networks are distinct from known resting-state functional networks

Sign in / Sign up

Export Citation Format

Share Document