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Submitted on September 17, 2007
Accepted on November 20, 2007
Division of Integrative Physiology, Department of Physiology, Jichi Medical University School of Medicine, Tochigi 329-0498, Japan; Department of Medicine and Molecular Science, Gunma University Graduate School of Medicine, Gunma 371-8511, Japan; Division of Brain and Neurophysiology, Department of Physiology, Jichi Medical University School of Medicine, Tochigi 329-0498, Japan
* To whom correspondence should be addressed. E-mail: tyada{at}jichi.ac.jp.
Nesfatin-1, a newly discovered satiety molecule, is located in the hypothalamic nuclei, including the paraventricular nucleus (PVN) and supraoptic nucleus (SON). In this study, fine localization and regulation of nesfatin-1 neurons in the PVN and SON were investigated by immunohistochemistry of neuropeptides and c-Fos. In the PVN, 24% of nesfatin-1 neurons overlapped with oxytocin, 18% with vasopressin, 13% with CRH, and 12% with TRH neurons. In the SON, 35% of nesfatin-1 neurons overlapped with oxytocin, and 28% with vasopressin. Following a 48 hour fast, refeeding for 2 hours dramatically increased the number of nesfatin-1 neurons expressing c-Fos immunoreactivity in the PVN approximately by 10 times and in the SON by 30 times compared to the fasting controls. In the SON, refeeding also significantly increased the number of nesfatin-1-immunoreactive neurons and NUCB2 mRNA expression, as compared to fasting. These results indicate that nesfatin-1 neurons in the PVN and SON highly overlap with oxytocin and vasopressin neurons, and that they are activated markedly by refeeding. Feeding-activated nesfatin-1 neurons in the PVN and SON could play a role in the postprandial regulation of feeding behavior and energy homeostasis.
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