We have recently demonstrated that the antibody response to the T-cell-depe
ndent antigen, sheep red blood cells (SRBCs), was suppressed by ethyl carba
mate in female BALB/c mice. At the same doses, ethyl carbamate decreased in
the numbers of splenic macrophages, B cells, total T cells, CD4(+) T cells
and CD8(+) T cells. In addition, the serum level of corticosterone was inc
reased dose-dependently. To investigate the possible role of corticosterone
in ethyl carbamate-induced immunosuppression, the antibody response to SRB
Cs and the subpopulation changes of splenocytes and thymocytes were determi
ned in naive, sham-operated and adrenalectomized (ADX) female BALB/c mice.
When the mice were treated intraperitoneally with 400 mg/kg ethyl carbamate
, the antibody response was significantly suppressed by ethyl carbamate in
naive and sham-operated mice in accompanying the decrease in spleen and thy
mus weights and/or the increase in the level of serum corticosterone. Meanw
hile, the antibody response was not suppressed by ethyl carbamate in the AD
X mice. The splenic numbers of total cells, macrophages, B and T cells, and
CD4(+) cells were decreased by ethyl carbamate in naive and sham-operated
mice. Meanwhile, each cell number was comparable with control in the ADX mi
ce. The flow cytometric analyses on thymocytes did not show obvious differe
nces as seen in the spleen. Finally, when the ADX mice were treated intrape
ritoneally with 25 mg/kg corticosterone, the antibody response was signific
antly suppressed. Taken together, our present results suggested that cortic
osterone might be, at least partially, responsible for ethyl carbamate-indu
ced immunosuppression in female BALB/c mice. (C) 2001 Elsevier Science Irel
and Ltd. All rights reserved.