Melanocortin-4 receptor expression in the rostral ventromedial medulla involved in modulation of nociception in transgenic mice.
10.1007/s11596-013-1096-9
- Author:
Xu-chu PAN
1
;
Yong-tang SONG
;
Cheng LIU
;
Hong-bing XIANG
;
Chuan-jian LU
Author Information
1. Medical Association of Hubei Province, Wuhan, 430060, China. panxuchu@sina.com
- Publication Type:Journal Article
- MeSH:
Animals;
Female;
Male;
Medulla Oblongata;
cytology;
metabolism;
Mice;
Mice, Transgenic;
Neural Pathways;
cytology;
metabolism;
Neurons, Afferent;
cytology;
metabolism;
Nociception;
physiology;
Receptor, Melanocortin, Type 4;
genetics;
metabolism;
Serotonergic Neurons;
metabolism;
Tyrosine 3-Monooxygenase;
metabolism
- From:
Journal of Huazhong University of Science and Technology (Medical Sciences)
2013;33(2):195-198
- CountryChina
- Language:English
-
Abstract:
The rostral ventromedial medulla (RVM) is a prominent component of the descending modulatory system involved in the control of spinal nociceptive transmission. In the current study, we investigated melanocortin-4 receptor (MC4R) expression in the RVM, where the neurons involved in modulation of nociception reside. Using a line of mice expressing green fluorescent protein (GFP) under the control of the MC4R promoter, we found a large number of GFP-positive neurons in the RVM [nucleus raphe magnus (NRM) and nucleus gigantocellularis pars α (NGCα)]. Fluorescence immunohistochemistry revealed that approximately 10% of MC4R-GFP-positive neurons coexpressed tyrosine hydroxylase, indicating that they were catecholaminergic, whereas 50%-75% of those coexpressed tryptophan hydroxylase, indicating that they were serotonergic. Our findings support the hypothesis that MC4R signaling in RVM may modulate the activity of serotonergic sympathetic outflow sensitive to nociceptive signals, and that MC4R signaling in RVM may contribute to the descending modulation of nociceptive transmission.
