A. Lecklin et al., EFFECTS OF INTRACEREBROVENTRICULARLY INFUSED HISTAMINE AND SELECTIVE H-1, H-2 AND H-3 AGONISTS ON FOOD AND WATER-INTAKE AND URINE FLOW IN WISTAR RATS, Brain research, 793(1-2), 1998, pp. 279-288
The actions of intracerebroventricularly infused histamine and selecti
ve histamine H-1, H-2 and H-3 receptor agonists on food and water inta
ke and urine flow were studied in rats. It was found that 100-800 nmol
es of histamine significantly suppressed feeding. The H-1 agonist 2-(3
-trifluoromethylphenyl)histamine (FMPH) decreased food intake, whereas
the H-2 agonist dimaprit was without effect. Histamine- and FMPH-indu
ced suppressions of feeding were attenuated by blockade of H-1 but not
by H-2 receptors. The results clearly demonstrate that activation of
brain H-1 receptors decreases food intake. In subsequent studies, we f
ound that both metoprine and thioperamide, which increase histaminergi
c activity through different mechanisms, also reduced food intake. Thi
s finding indicates that the brain histaminergic system is associated
with feeding behavior. The same is true with body water homeostasis. H
istamine caused a long-lasting diuresis. Also dimaprit and metoprine i
ncreased urine flow and the blockade of H-2 receptors abolished the di
uretic responses to histamine and dimaprit. On the other hand, the H-3
agonist (R)-alpha-methylhistamine elicited drinking and this effect c
ould be prevented by thioperamide pretreatment. The results imply that
activation of H-3 receptors predominantly provokes drinking, whereas
central H-2 receptors mediate the diuretic effect of histamine. (C) 19
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