Abstract

Introduction: The neuropeptide Y (NPY) in the neural circuits of the hypothalamus has a stimulating effect on reproductive activities in mammals. Kisspeptin (KiSS1) is a quintessential neurotransmitter in the reproductive axis which directly stimulates gonadotropin-releasing hormone neurons in the hypothalamus. The distribution of KiSS1 expressing cells in the pituitary was described previously. Despite earlier reports showing the KiSS1 receptor, G-protein coupled receptor 54 (GPR54) expression in the pituitary, the potential physiological roles of kisspeptin at this gland have remained obscure. Accordingly, this study investigated the role of NPY on the relative expression of Kiss1 and Gpr54 genes in the pituitary gland in male Wistar rats. Methods: In general, 20 male Wistar rats weighing 200-250 g in 4 groups (5 in each group) received saline, NPY (2.3 nM), BIBP3226 (NPY receptor antagonist, 7.8 nM), and NPY+ BIBP3226. Then, they received the simultaneous injection of these molecules through the third ventricle of the brain. Finally, the relative mean expressions of Kiss1 and Gpr54 genes in the anterior pituitary were quantitatively analyzed by the real-time polymerase chain reaction. Results: The central injection of NPY increased the relative mean expressions of Kiss1 and Gpr54 genes in the pituitary gland compared to the control group although the injection of BIBP3226 eradicated these effects. However, the gene expression of Gpr54 in the rats receiving NPY coupled with BIBP3226 in hypophysis in comparison to the group receiving only NPY demonstrated a significant reduction (P<0.05). Conclusion: Overall, the central injection of NPY stimulated the gene expression of Kiss1 and Gpr54 in the pituitary gland.

Highlights

  • The neuropeptide Y (NPY) in the neural circuits of the hypothalamus has a stimulating effect on reproductive activities in mammals

  • This study examined the effects of NPY and BIBP3226 and their concomitant injections on the relative expression of Kiss1 and Gpr54 genes in the pituitary in order to determine the molecular interaction of NPY and KiSS1 in regulating pituitary-gonadal axis activity

  • The Effects of Intracerebroventricular Injection of NPY and BIBP3226 on Kiss1 Gene Expression The analyses of the obtained results from Quantitative Real-time Polymerase Chain Reaction (qPCR) showed that the central injection of NPY increased the relative gene expression of Kiss1 (P< 0.001)

Read more

Summary

Introduction

The neuropeptide Y (NPY) in the neural circuits of the hypothalamus has a stimulating effect on reproductive activities in mammals. Despite earlier reports showing the KiSS1 receptor, G-protein coupled receptor 54 (GPR54) expression in the pituitary, the potential physiological roles of kisspeptin at this gland have remained obscure. This study investigated the role of NPY on the relative expression of Kiss and Gpr genes in the pituitary gland in male Wistar rats. Results: The central injection of NPY increased the relative mean expressions of Kiss and Gpr genes in the pituitary gland compared to the control group the injection of BIBP3226 eradicated these effects. Conclusion: Overall, the central injection of NPY stimulated the gene expression of Kiss and Gpr in the pituitary gland. Most research has focused on the hypothalamic-pituitary-gonadal axis function in kisspeptin (KiSS1) and G-protein coupled receptor 54 (GPR54). The symptoms of hypogonadism resulted from a decrease in the pituitary gonadotropins are observable.

Objectives
Methods
Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.