Absence of SHATI/Nat8l reduces social interaction in mice |
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Authors: | Yoko Furukawa-Hibi Atsumi Nitta Hidefumi Fukumitsu Hitomi Somiya Kazuya Toriumi Shoei Furukawa Toshitaka Nabeshima Kiyofumi Yamada |
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Affiliation: | 1. Department of Neuropsychopharmacology and Hospital Pharmacy, Nagoya University Graduate School of Medicine, Nagoya 466-8560, Japan;2. Department of Pharmaceutical Therapy & Neuropharmacology, Faculty of Pharmaceutical Sciences, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Toyama 930-0194, Japan;3. Laboratory of Molecular Pharmacology, Gifu Pharmaceutical University, Gifu 502-8585, Japan;4. Department of Chemical Pharmacology, Graduate School of Pharmaceutical Science, Meijo University, Nagoya 466-8503, Japan;5. Academic Frontier Project for Private Universities, Comparative Cognitive Science Institute, Meijo University, Nagoya 466-8503, Japan |
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Abstract: | We previously identified a novel molecule “Shati/Nat8l” from the nucleus accumbens of mice. However, the physiological roles of the SHATI protein are not clear. To investigate the effect of SHATI on the central nervous system and behavior, we studied knockout mice of this protein. We carried out various behavior tests using Shati-knockout mice. Shati-knockout mice did not differ from wild type mice in learning and memory. In the open field test, Shati-knockout mice did not differ from wild-type mice in time of stay in the outer, middle and center areas. On the other hand, Shati-knockout mice showed increases in rearing and grooming time in the open field test, and exploration time of novel objects. These results suggested that knockout of the Shati gene may increase exploration in specific circumstances. Interestingly, the Shati-knockout mice avoided social interaction with unfamiliar mice out of their home cage, although there was no difference in social interaction in their home cage compared with wild type mice. Lack of the Shati gene increased brain-derived neurotrophic factor (BDNF) mRNA in the prefrontal cortex and hippocampus, and decreased glial cell line-derived neurotrophic factor (GDNF) mRNA in the striatum and hippocampus, and lipopolysaccharides-induced TNF-α factor (LITAF) mRNA in the striatum. Since these factors play important roles in behavior, alteration of expression of these factors may be related to the induction of exploration and reduction of social interaction in Shati-knockout mice. |
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Keywords: | ANOVA, analysis of variance BDNF, brain-derived neurotrophic factor GDNF, glial cell line-derived neurotrophic factor LITAF, lipopolysaccharides-induced tumor necrosis factor-α factor RT-PCR, reverse transcription polymerase chain reaction TNF-α, tumor necrosis factor-α |
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