We describe the presence of functional GABA(A) receptors on T cells. GABA i
nhibited anti-CDS and antigen-specific T cell proliferation in vitro in a d
ose-dependent manner that was 1) mimicked by the GABA(A), receptor agonist
muscimol (but not the GABA(B) receptor agonist baclofen), 2) blocked by GAB
A(A) receptor antagonists and a GABA, receptor Cl- channel blocker (picroto
xin) and 3) enhanced by pentobarbital. These data suggest that GABA(A) rece
ptors mediate this immune inhibition and that these receptors can be modula
ted in a similar fashion to their neuronal counterparts. Finally, GABA inhi
bited DTH responses in vivo. Thus, pharmacological modulation of GABA(A) re
ceptors may provide new approaches to modulate T cell responses in inflamma
tion and autoimmune disease. (C) 1999 Elsevier Science B.V. All nights rese
rved.