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Vol. 299, Issue 2, 536-541, November 2001
Impairs Memory Processing in
Mice: Dependence on Blood-Brain Barrier Transport into Posterior
Division of the Septum
Geriatric Research, Education, Clinical Center, Veterans Affairs
Medical Center, St. Louis, Missouri; and Department of Internal
Medicine, Division of Geriatrics, St. Louis University School of
Medicine, St. Louis, Missouri
Peripherally administered cytokines profoundly affect the central
nervous system (CNS). One mechanism by which they could affect the CNS
is by crossing the blood-brain barrier (BBB) to interact directly with
brain receptors. Human and murine IL-1
(hIL-1
; mIL-1
) are
transported across the murine BBB with a high rate of transport into
the posterior division of the septum (PDS), but it is unknown whether
BBB transport is relevant to their actions. Here, we injected
species-specific blocking antibodies into the PDS to determine whether
transport across the BBB is required for blood-borne hIL-1
to affect
memory. Retention was impaired in a dose-dependent manner when hIL-1
was injected either by tail vein (i.v.) or into the PDS, with the PDS
route being 1000 times more potent. About 70% of the memory impairment
induced by i.v. hIL-1
was reversed by injecting a blocking antibody
(Ab) specific for hIL-1
into the PDS. This shows that much of the memory impairment induced by hIL-1
depends on its ability to cross
the BBB. Ab specific for mIL-1
was also effective in reversing memory impairment, showing that hIL-1
releases mIL-1
from
endogenous stores. Whether the mIL-1
was released from peripheral
stores, which would require it to cross the BBB, or from brain stores is unknown. In conclusion, these results show that exogenous, blood-borne hIL-1
affects memory by releasing mIL-1
from
endogenous stores and by crossing the BBB to act at sites within the
PDS.
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