Cd38 Gene Knockout Juvenile Mice: A Model of Oxytocin Signal Defects in Autism
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- Higashida Haruhiro
- Department of Biophysical Genetics, Graduate School of Medicine, Kanazawa University
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- Yokoyama Shigeru
- Department of Biophysical Genetics, Graduate School of Medicine, Kanazawa University
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- Munesue Toshio
- Department of Biophysical Genetics, Graduate School of Medicine, Kanazawa University
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- Kikuchi Mitsuru
- Department of Biophysical Genetics, Graduate School of Medicine, Kanazawa University
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- Minabe Yoshio
- Department of Biophysical Genetics, Graduate School of Medicine, Kanazawa University
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- Lopatina Olga
- Department of Biophysical Genetics, Graduate School of Medicine, Kanazawa University
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Oxytocin (OXT) in the hypothalamus is the biological basis of social recognition, trust, and bonding. We showed that CD38, a leukaemia cell marker, plays an important role in the hypothalamus in the process of OXT release in adult mice. Disruption of Cd38 (Cd38−/−) produced impairment of maternal behavior and male social recognition in mice, similar to the behavior observed in Oxt and OXT receptor (Oxtr) gene knockout (Oxt−/− and Oxtr−/−, respectively) mice. Locomotor activity induced by separation from the dam was higher and the number of ultrasonic vocalization (USV) calls was lower in Cd38−/− than Cd38+/+ pups. These phenotypes seemed to be caused by the high plasma OXT levels during development from neonates to 3-week-old juvenile mice. ADP-ribosyl cyclase activity was markedly lower in the knockout mice from birth, suggesting that weaning for mice is a critical time window of differentiating plasma OXT. Contribution by breastfeeding was an important exogenous source for regulating plasma OXT before weaning by the presence of OXT in milk and the dam's mammary glands. The dissimilarity of Cd38−/− infant behaviour to Oxt−/− or Oxtr−/− mice can be explained partly by this exogenous source of OXT. These results suggest that secretion of OXT into the brain in a CD38-dependent manner may play an important role in the development of social behavior, and mice with OXT signalling deficiency, including Cd38−/−, Oxt−/− and Oxtr−/− mice are good animal models for developmental disorders, such as autism.
収録刊行物
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- Biological & Pharmaceutical Bulletin
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Biological & Pharmaceutical Bulletin 34 (9), 1369-1372, 2011
公益社団法人 日本薬学会
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詳細情報 詳細情報について
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- CRID
- 1390282679608141056
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- NII論文ID
- 130001872426
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- NII書誌ID
- AA10885497
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- ISSN
- 13475215
- 09186158
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- NDL書誌ID
- 11217172
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- PubMed
- 21881219
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- IRDB
- NDL
- Crossref
- PubMed
- CiNii Articles
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