Chronic Self-Administration of Nicotine in Rats Impairs T Cell Responsiveness

Abstract

Chronic exposure of rodents to nicotine via subcutaneously or intracerebroventricularly implanted miniosmotic pumps affects T cell function. However, this method of continuous nicotine administration does not replicate the self-motivated administration of nicotine in human smokers. To determine whether nicotine impairs the immune system under conditions pertinent to human smokers, we investigated the T cell responsiveness of male Lewis rats self-administering (SA) nicotine (0.03 mg/kg of body weight per injection) 40 to 50 times/day for 5 weeks, using a model of virtually unlimited access to nicotine. Compared with sham control animals, the concanavalin A-induced proliferation of spleen cells from SA rats was significantly decreased. Moreover, the ability of spleen cells to mobilize intracellular Ca²⁺ after ligation of the T cell antigen receptor (TCR) with an anti-αβ TCR antibody was significantly less in SA than in control rats. In addition, inositol 1,4,5-trisphosphate (IP₃)-sensitive intracellular Ca²⁺ stores were markedly depleted in spleen cells from SA animals. These results suggest that chronic nicotine self-administration suppresses T cell responsiveness, and this suppression may result from an impaired TCR-mediated signaling that stems from the depletion of IP₃-sensitive intracellular Ca²⁺ stores.