The objective of this research is to establish in detail the physiological properties of inputs from the basal forebrain to the limbic system in adult rats. Three specific pathways will be studies: (1) projections from the nucleus of the diagonal band of Broca to the posterior cingulate cortex, (2) projections from the diagonal band to the entorhinal cortex, and (3) projections from the ventral pallidum/nucleus basalis to the basolateral nucleus of the amgydala. The pathways will be studied by the neurophysiological techniques of in vivo intracellular recording and labeling. The basal forebrain will be activated by electrical stimulation, and neuronal responses will be recorded intracellularly in the target areas. Target neurons in the cingulate and entorhinal cortices and the amygdala will be morphologically identified by labeling them with intracellular injections of horseradish peroxidase (HRP). The basal forebrain modulation of synaptic transmission in thalamo-cingulate projections will be studied. A final goal is to inject basal forebrain neurons intracellularly with HRP in order to characterize in detail their pattern of axonal projections and coilateralization. The studies will establish the in vivo physiological and morphological relationship between the extensive projection system of the basal forebrain, and three important components of the limbic system, the cingulate cortex (one of the important cortical targets of the hippocampal formation), the entorhinal cortex (a principal source of input to the dentate gyrus and hippocampus), and the amygdala. These intracellular studies will thus fill significant gaps in our knowledge about the synaptic organization and physiology of these systems.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS023074-03
Application #
3406131
Study Section
Neurology B Subcommittee 1 (NEUB)
Project Start
1985-12-01
Project End
1988-11-30
Budget Start
1987-12-01
Budget End
1988-11-30
Support Year
3
Fiscal Year
1988
Total Cost
Indirect Cost
Name
University of California Los Angeles
Department
Type
Schools of Medicine
DUNS #
119132785
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
Mello, L E; Tan, A M; Finch, D M et al. (1996) Fos-like immunoreactivity after status epilepticus and spontaneous seizures in rats. Epilepsy Res Suppl 12:205-13
Mello, L E; Kohman, C M; Tan, A M et al. (1996) Lack of Fos-like immunoreactivity after spontaneous seizures or reinduction of status epilepticus by pilocarpine in rats. Neurosci Lett 208:133-7
Mello, L E; Cavalheiro, E A; Tan, A M et al. (1993) Circuit mechanisms of seizures in the pilocarpine model of chronic epilepsy: cell loss and mossy fiber sprouting. Epilepsia 34:985-95
Mello, L E; Cavalheiro, E A; Tan, A M et al. (1992) Granule cell dispersion in relation to mossy fiber sprouting, hippocampal cell loss, silent period and seizure frequency in the pilocarpine model of epilepsy. Epilepsy Res Suppl 9:51-9;discussion 59-60
Mello, L E; Tan, A M; Finch, D M (1992) Convergence of projections from the rat hippocampal formation, medial geniculate and basal forebrain onto single amygdaloid neurons: an in vivo extra- and intracellular electrophysiological study. Brain Res 587:24-40
Mello, L E; Tan, A M; Finch, D M (1992) GABAergic synaptic transmission in projections from the basal forebrain and hippocampal formation to the amygdala: an in vivo iontophoretic study. Brain Res 587:41-8
White, T D; Tan, A M; Finch, D M (1991) Functional connections of the rat medial cortex and basal forebrain: an in vivo intracellular study. Neuroscience 44:571-83
Finch, D M; Tan, A M; Isokawa-Akesson, M (1988) Feedforward inhibition of the rat entorhinal cortex and subicular complex. J Neurosci 8:2213-26