TY - JOUR
T1 - Food-deprived activity stress decreased the activity of the histaminergic neuron system in rats
AU - Endou, Masatoshi
AU - Yanai, Kazuhiko
AU - Sakurai, Eiko
AU - Fukudo, Shin
AU - Hongo, Michio
AU - Watanabe, Takehiko
N1 - Funding Information:
This work was supported by grants-in-aid from the Ministry of Education, Science and Culture and Ministry of Health. We also thank Dr. A. Yamatodani (Osaka University, Faculty of Medicine) and Dr. Z.B. Yang (Research Center, Suntory) for their helpful comments on this manuscript.
PY - 2001/2/9
Y1 - 2001/2/9
N2 - The hypothalamus, which is rich in histaminergic neurons, is highly sensitive to aversive stimuli such as stress. Histamine H3 receptors, which regulate histamine release from the presynaptic site, are associated with stress-induced brain activity. In this study, we investigated the changes of histamine content and histamine H1 and H3 receptors in the brains of rats subjected to stress induced through food deprivation and physical activity on a running wheel (food-deprived activity stress). For purposes of comparison, we also examined the stressful effects of forced swimming on the histaminergic neuron system of rats. The H3 receptor density rapidly declined in the acute phase of stress but gradually returned to the control level in the chronic phase. On the other hand, the H1 receptor slowly decreased and remained at a low level during the chronic phase. These results reveal that there is a discrepancy between the levels of H1 and H3 receptors in the acute and chronic phases of stress. Brain histamine content gradually increased during the late phase of both food-deprived activity stress and forced swimming stress. These changes presumably resulted in the inhibition of histaminergic neuronal activity in the chronic stress condition. In accordance with this hypothesis, the intraventricular administration of histamine significantly reduced the hyperactivity caused by food-deprived activity stress. Since extensive exercise and restricted feeding are thought to be associated with anorexia nervosa, the abnormalities in the histaminergic neuron system might contribute to trait status in anorexia nervosa.
AB - The hypothalamus, which is rich in histaminergic neurons, is highly sensitive to aversive stimuli such as stress. Histamine H3 receptors, which regulate histamine release from the presynaptic site, are associated with stress-induced brain activity. In this study, we investigated the changes of histamine content and histamine H1 and H3 receptors in the brains of rats subjected to stress induced through food deprivation and physical activity on a running wheel (food-deprived activity stress). For purposes of comparison, we also examined the stressful effects of forced swimming on the histaminergic neuron system of rats. The H3 receptor density rapidly declined in the acute phase of stress but gradually returned to the control level in the chronic phase. On the other hand, the H1 receptor slowly decreased and remained at a low level during the chronic phase. These results reveal that there is a discrepancy between the levels of H1 and H3 receptors in the acute and chronic phases of stress. Brain histamine content gradually increased during the late phase of both food-deprived activity stress and forced swimming stress. These changes presumably resulted in the inhibition of histaminergic neuronal activity in the chronic stress condition. In accordance with this hypothesis, the intraventricular administration of histamine significantly reduced the hyperactivity caused by food-deprived activity stress. Since extensive exercise and restricted feeding are thought to be associated with anorexia nervosa, the abnormalities in the histaminergic neuron system might contribute to trait status in anorexia nervosa.
KW - Anorexia nervosa
KW - Food-deprived activity stress
KW - Forced swimming
KW - H Receptor
KW - H Receptor
KW - Histamine
KW - Histidine decarboxylase activity
KW - Hypothalamus
KW - Microdialysis
KW - Reward
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U2 - 10.1016/S0006-8993(00)03226-1
DO - 10.1016/S0006-8993(00)03226-1
M3 - Article
C2 - 11164807
AN - SCOPUS:0035830771
SN - 0006-8993
VL - 891
SP - 32
EP - 41
JO - Molecular Brain Research
JF - Molecular Brain Research
IS - 1-2
ER -