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Vol. 305, Issue 1, 290-297, April 2003
Departments of Pharmacology (A.H.A.) and Neuroscience (C.A.M.,
B.M.B.), Georgetown University Medical Center, Washington, DC
Recent evidence suggests that withdrawal from cocaine shares
similarities to the stress response. Here, we examine whether withdrawal from chronic cocaine produces immune system alterations and
whether the hypothalamic-pituitary-adrenal axis is involved. Sprague-Dawley male rats received cocaine (10 mg/kg i.p., b.i.d.) or
saline, followed by 2 h, 1, 2, 4, 6, and 14 days of withdrawal. Proliferation responses of peripheral blood lymphocytes to concanavalin A were significantly suppressed at the 2-h, 1- and 2-day time points,
and persisted for up to 6 days during withdrawal from chronic cocaine.
Flow cytometric analysis revealed no significant differences in the
immunophenotype of blood lymphocytic populations of T cells, B cells,
or monocytes at 2 or 6 days of withdrawal from cocaine. Consistent with
the suppression in cellular immunity observed in the in vitro response,
the in vivo delayed-type hypersensitivity response was also
significantly decreased in cocaine withdrawing animals. Plasma
corticosterone levels were significantly elevated 2 and 24 h after
cessation of cocaine but returned to basal values by 2 days of
withdrawal. The suppressive effects of cocaine withdrawal were no
longer observed in either adrenalectomized animals or those treated
with the glucocorticoid receptor antagonist mifepristone (RU486), when
administered during the first 2 days of withdrawal. These data argue
that repeated exposure to cocaine followed by withdrawal leads to an
activation of the neuroendocrine stress response, which alters cellular
immunity during the initial withdrawal phase and may contribute to an
increased susceptibility to infection.
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