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Single-Prolonged Stress Induce Changes of CaM/CaMKIIα in the Rats of Dorsal Raphe Nucleus

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Abstract

Ca2+/calmodulin-dependent protein kinase IIα (CaMKIIα) is identified as a Ca2+-dependent kinase in brain involved in the activation of Tryptophan hydroxylase (TPH) acting through direct phosphorylation of TPH, and playing key roles in the signaling pathways initiated by various G protein-coupled 5-HT receptors. The goal of this study is to detect whether there are changes of CaM and CaMKIIα in dorsal raphe nucleus in the rats exposed to single-prolonged stress (SPS), which is a model employed in post-traumatic stress disorder (PTSD) study extensively. A total of 90 male Wistar rats were randomly divided into a normal control group and SPS groups of 7d, 14d. The changes of CaM/CaMKIIα were detected by immunohistochemistry, reverse transcription-polymerase chain reaction and western blot. Our results demonstrate that both expressions of CaM and CaMKIIα significantly increase (P < 0.001) in the SPS 7d group than that in the control group, and then decreased dramatically (P < 0.001) 14 days after SPS. Our results confirm that SPS induce changes of CaM/CaMKIIα in the dorsal raphe nucleus. Changes of CaM/CaMKIIα may be associated with the activation of 5-HT1A receptor, and may contribute to the progress of molecular mechanism of PTSD.

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Acknowledgments

The authors are grateful to all of the staff members of the China Medical University Experiment Center for their technical support. In addition, this research was supported by a grant from the National Natural Science Foundation of China (no. 81171282) and China National Doctoral Fund (no. 20092104110016).

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The authors indicate no potential conflicts of interest.

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Correspondence to Xiuyu Shi.

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Huaju Xie and Fang Han contributed equally.

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Xie, H., Han, F. & Shi, X. Single-Prolonged Stress Induce Changes of CaM/CaMKIIα in the Rats of Dorsal Raphe Nucleus. Neurochem Res 37, 1043–1049 (2012). https://doi.org/10.1007/s11064-012-0705-5

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  • DOI: https://doi.org/10.1007/s11064-012-0705-5

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