“…Effectively, the voltage dependence of the Ca 2 + channels and thus of the triggering of transmitter release, is shifted to more depolarized potentials. Many other presynaptic receptors have been described to mediate inhibition of the presynaptic stimulus-secretion coupling (see Chesselet, 1984), such as ~2-adrenergic receptors (see for instance, Starke, 1977;Maura et al, 1982), adenosine A,-receptors (Prince and Stevens, 1992;Barrie and Nicholls, 1993), opioid receptors (see for instance, Hagan and Hughes, 1984;McWilliam and Campbell, 1987). For these receptors the most likely targets are presynaptic K + channels and Ca 2 + channels, either via G proteins or through intracellular messengers.…”