PHARMACOLOGY OF NGF FOR FOREBRAIN CHOLINERGIC NEURONS
PHARMACOLOGY OF NGF FOR FOREBRAIN CHOLINERGIC NEURONS
批准号:
3405768
负责人:
FRANZ F HEFTI
金额:
$19.27万
依托单位国家:
美国
项目类别:
财政年份:
1987
资助国家:
美国
项目状态:
已结题
起止时间:
1987-09-01 至 1995-08-31
关键词:
carbachol cell death choline acetyltransferase embryo /fetus hippocampus immunochemistry immunocytochemistry insulinlike growth factor laboratory rat mature animal messenger RNA neurochemistry neurogenesis neuropharmacology neurotrophic factors parasympathetic nervous system phosphatidylinositols prosencephalon synapses tissue /cell culture
中文摘要
提出的研究旨在功能表征
英文摘要
The proposed studies are aimed at the characterization of functionally
important responses of basal forebrain cholinergic neurons to NGF. During
the previous funding period it was established that NGF promotes survival,
neurite growth, and biochemical differentiation of cholinergic neurons
developing in vitro. In adult rats with partial fimbrial transections, it
was shown that intraventricular administration of NGF prevents the
lesion-induced disappearance of cholinergic cell bodies in the septal area,
that single injections or administration for up to five months does not
result in permanent rescue of the cells, and that NGF is equally effective
in middle-aged as in young adult rats. The first part of this proposal
addresses specific remaining questions regarding the response of cell
bodies to NGF in our lesion paradigm (death or shrinkage of neurons,
penetration of NGF in the brain). The second part deals with the functional
response of adult cholinergic neurons to NGF. At the presynaptic level the
actions of NGF on choline acetyltransferase (ChAT) expression, high
affinity choline uptake, acetylcholine synthesis and release will be
explored. To assess whether presynaptic changes have consequences at the
postsynaptic level, carbachol-stimulated breakdown of phosphatidylinositol
will be monitored. The third part addresses the question whether bFGF and
insulin (which, similar to NGF, stimulate ChAT activity of cultured
cholinergic neurons) produce similar or different actions on cholinergic
neurons. Studies will be carried out on cholinergic neurons in culture and
on adult rats with partial fimbrial transection. The findings will help to
understand the physiological role of NGF in development and adult function
of basal forebrain cholinergic neurons. The major goal of the study is to
understand the consequences of pharmacological administration of NGF
administration. The findings have direct relevance for the potential use of
NGF in Alzheimer's disease and will help to develop neuropharmacological
applications of neurotrophic factors.
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