Silva Eduardo Simão da, Flores Rafael Appel, Ribas Anderson Savaris, Taschetto Ana Paula, Faria Moacir Serralvo, Lima Leandro Bueno, Metzger Martin, Donato José, Paschoalini Marta Aparecida
Department of Natural Sciences, Center of Exact and Natural Sciences - CCEN, Regional University of Blumenau (FURB), 89030-903, Blumenau, SC, Brazil.
Department of Physiological Sciences, Center of Biological Sciences - CCB, Federal University of Santa Catarina (UFSC), 88040-970, Florianópolis, SC, Brazil.
Behav Brain Res. 2017 May 1;324:87-95. doi: 10.1016/j.bbr.2017.02.021. Epub 2017 Feb 14.
Previously, we showed that the blockade of α1-adrenoreceptors in the median raphe nucleus (MnR) increased food intake in free-feeding rats, indicating that adrenergic mechanisms in the MnR participate in the regulation of food intake. However, the impact of such a pharmacological manipulation on other neural circuits related to food intake remains unknown. In the current study, we sought to identify forebrain regions which are responsive to α1-adrenergic receptor blockade and presumably involved in the modulation of the feeding response. For this purpose, we examined the induction of c-Fos immunoreactivity in forebrain structures following injections of the α1-adrenoceptor antagonist prazosin into the MnR of free-feeding rats. To determine the chemical identity of hypothalamic c-Fos-positive cells, we then conducted double-label immunohistochemistry for Fos/orexin (OX) or Fos/melanin-concentrating hormone (MCH). Finally, we combined anterograde tracing from the MnR with immunohistochemical detection of orexin. Prazosin injections into the MnR significantly increased food intake. The ingestive response was accompanied by an increase in Fos expression in the basolateral amygdala (BLA) and lateral hypothalamic area (LHA). In the LHA, Fos expression occurred in neurons expressing OX, but not MCH. Combined anterograde tracing experiments revealed that LHA OX neurons are prominently targeted by MnR axons. These findings suggest that intra-MnR injection of prazosin, via activation of orexinergic neurons in the LHA and non-orexinergic neurons in the BLA, evoked a motivational response toward food intake.
此前,我们发现,阻断中缝正中核(MnR)中的α1 - 肾上腺素能受体可增加自由进食大鼠的食物摄入量,这表明MnR中的肾上腺素能机制参与了食物摄入的调节。然而,这种药理学操作对与食物摄入相关的其他神经回路的影响仍不清楚。在当前研究中,我们试图确定对α1 - 肾上腺素能受体阻断有反应且可能参与调节进食反应的前脑区域。为此,我们检测了向自由进食大鼠MnR注射α1 - 肾上腺素能受体拮抗剂哌唑嗪后前脑结构中c - Fos免疫反应性的诱导情况。为了确定下丘脑c - Fos阳性细胞的化学特性,我们随后进行了Fos/食欲素(OX)或Fos/促黑素细胞激素(MCH)的双重免疫组织化学检测。最后,我们将从MnR的顺行示踪与食欲素的免疫组织化学检测相结合。向MnR注射哌唑嗪显著增加了食物摄入量。摄食反应伴随着基底外侧杏仁核(BLA)和下丘脑外侧区(LHA)中Fos表达的增加。在LHA中,Fos表达出现在表达OX的神经元中,而非表达MCH的神经元中。联合顺行示踪实验表明,LHA的OX神经元是MnR轴突的主要靶点。这些发现表明,向MnR内注射哌唑嗪,通过激活LHA中的食欲素能神经元和BLA中的非食欲素能神经元,引发了对食物摄入的动机反应。