TY - JOUR
T1 - Elevated anxiety-like and depressive behavior in Desert hedgehog knockout male mice
AU - Umehara, Fujio
AU - Mishima, Kenichi
AU - Egashira, Nobuaki
AU - Ogata, Ayumi
AU - Iwasaki, Katsunori
AU - Fujiwara, Michihiro
N1 - Funding Information:
We thank Miss. Yuko Shirahama for technical assistance and Dr. Arlene Rosales Ng for critical reading of the manuscript. This work was supported by a grant from the Ministry of Education, Culture, Sports, Science and Technology of Japan.
PY - 2006/11/1
Y1 - 2006/11/1
N2 - To investigate the functional role of Desert hedgehog (Dhh) gene in the nervous system, we examined motor, sensory, learning and memory functions as well as mood in Dhh knockout (KO) mice. Dhh KO male mice exhibited prolonged immobility time compared with wild-type male mice in the forced swimming test, and showed enhanced inhibition in the Vogel's conflict model. These findings suggest that Dhh KO male mice exhibited enhanced anxiety and depressive behavior compared with wild-type male mice. In contrast, Dhh KO female mice did not show any significant difference compared to wild-type female mice. These behavioral abnormalities of Dhh KO male mice may be due to lower testosterone levels with abnormal development of the testes caused by Dhh-null mutation.
AB - To investigate the functional role of Desert hedgehog (Dhh) gene in the nervous system, we examined motor, sensory, learning and memory functions as well as mood in Dhh knockout (KO) mice. Dhh KO male mice exhibited prolonged immobility time compared with wild-type male mice in the forced swimming test, and showed enhanced inhibition in the Vogel's conflict model. These findings suggest that Dhh KO male mice exhibited enhanced anxiety and depressive behavior compared with wild-type male mice. In contrast, Dhh KO female mice did not show any significant difference compared to wild-type female mice. These behavioral abnormalities of Dhh KO male mice may be due to lower testosterone levels with abnormal development of the testes caused by Dhh-null mutation.
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U2 - 10.1016/j.bbr.2006.07.022
DO - 10.1016/j.bbr.2006.07.022
M3 - Article
C2 - 16952407
AN - SCOPUS:33748687973
SN - 0166-4328
VL - 174
SP - 167
EP - 173
JO - Behavioural Brain Research
JF - Behavioural Brain Research
IS - 1
ER -