The present study demonstrates the following: 1. Transplantation of ca
rdiac tissue induces an inflammatory response that ultimately leads to
the rejection of the tissue by the host within 9 days; 2. Treatment w
ith the opiate antagonist, naltrexone, significantly increased the sur
vival of the transplanted cardiac tissue to 13 days, suggesting the in
volvement of opioid signaling molecules in tissue rejection; 3. In fur
ther experiments it was demonstrated that in mixed lymphocyte populati
ons from different mice, the DNA synthesis inhibitor, mitomycin C, red
uced the lymphocyte proliferative response as did naltrexone; 4. Mice
injected with naltrexone for 10 days and given concanavalin A exhibite
d a suppressed spleen lymphocyte proliferative response compared to co
ntrols. Taken together, these data suggest that endogenous opioid sign
als not only activate immunocytes, but also stimulate DNA synthesis. (
C) 1998 Elsevier Science Ireland Ltd.