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Vol. 290, Issue 3, 1427-1435, September 1999
Department of Pharmacology and Experimental Therapeutics, Tufts
University School of Medicine, Boston, Massachusetts
The activation of presynaptic histamine 3 (H3) receptors
inhibits the release of histamine and other neurotransmitters from central nervous system neurons. Rat brain mast cells (MCs) release histamine and 5-hydroxytryptamine (5-HT) in response to neuropeptides and neurotransmitters secreted from adjacent neurons. Dura MCs also
degranulate in response to antidromic trigeminal nerve stimulation and
with acute psychological stress. Such findings have implicated brain
MCs in certain neuroinflammatory disorders, such as migraines. We
investigated the ultrastructural appearance of control and stimulated
thalamic/hypothalamic (brain) MCs before and after treatment with the
H3 receptor agonist
N
-methylhistamine (N
-mH)
and the H3 receptor antagonist thioperamide (Th).
Ultrastructural investigation of brain MCs stimulated with compound
48/80 revealed extensive intragranular changes that paralleled 5-HT
secretion but without degranulation by exocytosis typical of connective tissue MCs. N
-mH significantly reduced these
morphological changes, as well as 5-HT release from brain MCs and
neurons stimulated with KCl; conversely, Th augmented both histamine
and 5-HT release from brain neurons and MCs. Neither
N
-mH nor Th had any effect on peritoneal MCs.
Simultaneous addition of both drugs largely antagonized each other's
effects on brain MC activation and 5-HT secretion. Ultrastructural
observations and lack of lactic dehydrogenase release in the perfusate
excluded any cytotoxic effect. The ability of H3 agonists
to inhibit brain MC activation, as well as secretion of 5-HT from both
brain MCs and neurons, may be useful in the management of migraines.