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ID 32870
JaLCDOI
フルテキストURL
著者
Amano, Manabu Okayama University
Suemaru, Katsuya Ehime University
Cui, Ranji Ehime University
Umeda, Yuichi Ehime University
Li, Bingjin Ehime University
Gomita, Yutaka Okayama University
Kawasaki, Hiromu Okayama University Kaken ID publons
Araki, Hiroaki Ehime University
抄録
Several epidemiological and clinical studies have indicated that the prevalence of psychiatric disorders is higher in diabetic patients than in the general population. In the present studies, we examined the behavioral changes in streptozotocin-induced diabetic rats, and investigated the effects of physical and psychological stress on the hippocampal BDNF levels and on the serotonin 2A (5-HT2A) receptor-mediated wet-dog shake responses. The streptozotocin (60 mg/kg, i.p.)-induced diabetes had no significant effects on the immobility time in the forced swim test or on locomotor activity in the open-field test. Moreover, there was no significant difference in the wet-dog shake responses induced by DOI, a 5-HT2A receptor agonist, between nondiabetic and diabetic rats. Five-day exposure to physical (electric footshock) and psychological (non-footshock) stress had no signifi cant effect on the hippocampal BDNF level in diabetic or nondiabetic rats. The 2 types of stress had no significant effect on the DOI-induced wet-dog shake responses in nondiabetic rats. In diabetic rats, the repeated exposure to physical stress markedly increased the DOI-induced wet-dog shake responses, but the repeated exposure to psychological stress had no effect. These results suggest that exposure to physical stress augmented the susceptibility to the wet-dog shake responses to 5-HT2A receptor stimulation in streptozotocin-induced diabetic rats.
キーワード
streptozotocin
physical stress
psychological stress
5-HT2A receptor
wet-dog shake
Amo Type
Original Article
出版物タイトル
Acta Medica Okayama
発行日
2007-08
61巻
4号
出版者
Okayama University Medical School
開始ページ
205
終了ページ
212
ISSN
0386-300X
NCID
AA00508441
資料タイプ
学術雑誌論文
言語
英語
論文のバージョン
publisher
査読
有り
PubMed ID
Web of Science KeyUT