SYNAPTICALLY RELEASED HISTAMINE INCREASES DYE-COUPLING AMONG VASOPRESSINERGIC NEURONS OF THE SUPRAOPTIC NUCLEUS - MEDIATION BY H-1 RECEPTORS AND CYCLIC-NUCLEOTIDES
Gi. Hatton et Qz. Yang, SYNAPTICALLY RELEASED HISTAMINE INCREASES DYE-COUPLING AMONG VASOPRESSINERGIC NEURONS OF THE SUPRAOPTIC NUCLEUS - MEDIATION BY H-1 RECEPTORS AND CYCLIC-NUCLEOTIDES, The Journal of neuroscience, 16(1), 1996, pp. 123-129
Activating direct olfactory (glutamatergic) inputs to supraoptic nucle
us (SON) neurons increases interneuronal coupling in slices from lacta
ting but from not virgin or male rats. Studied here were influences on
coupling of another monosynaptic input to SON, the histaminergic tube
romammillary nucleus (TM) projection, activation of which selectively
excites phasically firing (putative vasopressin) cells. Effects of TM
stimulation and its possible downstream consequences on Lucifer yellow
(LY) dye coupling among putative vasopressin cells were determined in
male rat SONs. in unstimulated slices, 12 LY injections (1 cell/SON)
yielded eight single and four pairs of coupled neurons. In slices in w
hich TM was stimulated for 10 min at 10 Hz, 13 injections yielded 4 si
ngle and 28 coupled cells, with groups of 2 to 4 cells coupled to the
injected neuron, a threefold increase in the number of coupled cells p
er injection (p < 0.02). Bathing slices in medium containing 10 mu M p
yrilamine (H-1 antagonist) blocked this stimulation-induced coupling i
ncrease, suggesting mediation by activation of guanylate cyclase-cGMP
to which H-1 receptors often are linked. Bathing slices in medium cont
aining 0.5-1 mM 8-bromo-cGMP yielded results similar to those of TM st
imulation, a 2.5-fold increase over control in the number of coupled c
ells per injection. Effects of TM stimulation on coupling also were bl
ocked by bathing slices in a guanylate cyclase inhibitor (10 mu M LY83
583). in contrast to cGMP, 1 mM 8-bromo-cAMP significantly reduced cou
pling. We conclude that synaptically released histamine increases coup
ling via cGMP-dependent mechanisms.