SOME EFFECTS OF HISTAMINE AND SEX HORMONES ON HISTAMINERGIC PATHWAYS IN THE RAT AND CHICK BRAIN

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Date
1992-10
Authors
ANUKA, JOSEPH AKPOJO
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Abstract
The behavioural effect of histamine in young chicks revealed a triphasic response of initial behavioural sleep which was followed by a longer behavioural stimulation culminating in a very long behavioural depression. HI and H2 receptors are involved in these behavioural changes- The HI receptors were found to be excitatory while the H2 receptors were inhibitory. A blockade of the HI receptors eliminates the excitatory component leaving the inhibitory component (H2 receptors) unaffected for endogenous histamine to act. The resulting effect is inhibition. Likewise a blockade of the inhibitory component by H2 receptor antagonist leads to excitation. Chlorpheniramine (an HI receptor antagonist) induced a biphasic response of sedation/excitation. Both HI and H2 receptors are involved in thermoregulatory effect of histamine in young chicks. Activation of these two receptors leads to hypothermia while a blockage of H2 receptors produced insiginificant increase in temperature. On the other hand, a blockade of HI receptors leads to insignificant fall in temperature. Neither Hi nor H2 receptor antagonists counteracted histamine induced hypothermia but a concurrent administration of HI and (xi) H2 receptor antagonists. Steroid sex hormones (oestradiol 17B, testosterone and progesterone) counteracted hypothermia induced by histamine. They also counteracted hypothermia induced by HI and H2 receptor agonists, 2-thiazoly1-ethylamine and dimaprit respectively- Chicks pretreated with hormone showed fast recovery from hypothermia than the controls. Antioestrogens (clomiphene and tamoxifen) potentiated hypothermia induced by histamine and its selective agonists on H1` and H2 receptors. The role of histamine on seizure regulation was investigated in chicks. Histamine offered 85% protection against leptazol - induced seizure in young chicks. Both HI and H2 receptor agonists, 2- thiazoly1-ethylamine and dimaprit respectively also offered protection against this seizure. Cimetidine and triprolidine neither protected nor potentiated this seizure. Histamine, its agonists and antagonists were not convulsant at the dose level used in this work but potentiated electroshock seizures. Intracerebroventricular (ICV) adminstration of histamine was found to induce irregularities and at times persistent oestrous cycle with older rats (xii) exhibiting more cycling irregularities than the younger ones. Cimetidine (H2 receptor antagonist) produced a transient change in the cycle which returned to normal rhythm after a day or two. Triprolidine (HI receptor antagonist) showed no changes in the oestrous rhythm while chlorpheniramine, another HI receptor antagonist produced a non-significant degree of changes in the cycle. Sex hormones have been found to regulate body weight in rats through their influence on eating and drinking behaviours. Histamine-induced drinking behaviour was enhanced by sex hormones while their influence on histamine — induced eating behaviour was found to be variable. In this case, the eating behaviour was enhanced by testosterone and progesterone but depressed by oestradiol 17B. Sex hormones particularly oestrogens affected the affinity of histamine HI receptors labelled with mepyramine. The affinity of (3H) mepyramine for histamine HI receptors increased as the binding capacity decreased depending on the level of sex hormones. Ovariectomy decreased the affinity of the receptors in all the brain areas examined especially (xiiii) in the oestrogen concentrated regions (hypothalamus and amygdala). Oestrogen replacement in ovariectomized females showed binding affinity reminiscent of proestrus.
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SOME EFFECTS OF HISTAMINE AND SEX HORMONES ON, HISTAMINERGIC PATHWAYS IN THE RAT AND CHICK BRAIN
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