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Vol. 286, Issue 1, 191-200, July 1998
Department of Pharmaceutics, State University of New York at
Buffalo, Buffalo, New York
Cyclosporin A (CyA), prednisolone (Pred) and sirolimus (Sir) inhibit
lymphocyte proliferation at the cytokine transcription (CyA and Pred)
or signal transduction (Sir) levels. Their double and triple
interactions were studied on lectin-induced proliferation of whole
blood lymphocytes (WBLP) from male and female humans, rabbits and rats.
Isobols along with the Universal Response Surface Approach were used to
describe and quantify the nature and intensity of drug interactions by
determining
values. CyA was always less potent than Pred and Sir
while these two compounds were relatively equipotent. Species-related
differences were observed with single drugs. Rabbit WBLP were resistant
to Pred action (Imax = 67%) and rats were
more sensitive to Pred (IC50 = 9.1 nM in females) and Sir
(2.8 nM) actions than humans (32 and 55 nM). Gender differences were
observed but were not consistent across species. All double-drug combinations were synergistic, and combinations containing Pred were 10 to 100 times more synergistic in rabbits (
Pred/Sir = 213 and
CyA/Pred = 147 in males) than in rats (12 and 2.1)
or humans (3.7 and 5.7) in relation to the lower efficacy of Pred. Double-combination
values were able to describe CyA/Pred/Sir triple
combination effects. These studies indicate that CyA, Pred and Sir act
and synergistically interact in vitro in species- and
gender-dependent fashions. Adrenalectomized rats better resemble humans
in these responses. WBLP are useful in various species in determining
immunosuppressive drug action and interactions.
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