Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
1999-4-26
pubmed:abstractText
Inflammatory processes may play a critical role in the degeneration of basal forebrain cholinergic cells that underlies some of the cognitive impairments associated with Alzheimer's disease. In the present study, the proinflammagen lipopolysaccharide, from the cell wall of Gram-negative bacteria, was used to produce inflammation within the basal forebrain of rats. The effects of acute, high-dose injections of lipopolysaccharide (2, 20 or 40 microg) upon basal forebrain chemistry and neuronal integrity were compared with the effects of chronic, low-dose lipopolysaccharide infusions (0.18, 0.25, 1.8 or 5.0 microg/h) for either 14, 37, 74 or 112 days. Acute exposure to lipopolysaccharide decreased cortical choline acetyltransferase activity and the number of immunoreactive choline acetyltransferase-positive cells within a small region of the basal forebrain. Regional levels of five different neuropeptides were unchanged by acute, high-dose lipopolysaccharide injections. Chronic lipopolysaccharide infusions produced (i) a time-dependent, but not dose-dependent, decrease in cortical choline acetyltransferase activity that paralleled a decline in the number of choline acetyltransferase- and p75-immunoreactive cells within the basal forebrain, and (ii) a dense distribution of reactive astrocytes and microglia within the basal forebrain. Chronic neuroinflammation might underlie the genesis of some neuropathological changes associated with normal ageing or Alzheimer's disease.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0306-4522
pubmed:author
pubmed:issnType
Print
pubmed:volume
88
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
193-200
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:10051200-Acute Disease, pubmed-meshheading:10051200-Animals, pubmed-meshheading:10051200-Cerebral Cortex, pubmed-meshheading:10051200-Choline O-Acetyltransferase, pubmed-meshheading:10051200-Chronic Disease, pubmed-meshheading:10051200-Escherichia coli, pubmed-meshheading:10051200-Galanin, pubmed-meshheading:10051200-Inflammation, pubmed-meshheading:10051200-Lipopolysaccharides, pubmed-meshheading:10051200-Male, pubmed-meshheading:10051200-Neurokinin B, pubmed-meshheading:10051200-Neuropeptide Y, pubmed-meshheading:10051200-Neuropeptides, pubmed-meshheading:10051200-Neurotensin, pubmed-meshheading:10051200-Prosencephalon, pubmed-meshheading:10051200-Rats, pubmed-meshheading:10051200-Rats, Inbred F344, pubmed-meshheading:10051200-Somatostatin, pubmed-meshheading:10051200-Time Factors
pubmed:year
1999
pubmed:articleTitle
Pathological and biochemical consequences of acute and chronic neuroinflammation within the basal forebrain cholinergic system of rats.
pubmed:affiliation
Division of Neural Systems, Memory & Aging, University of Arizona, Tucson 85724, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't