• Ning Li, Chun-Yan Fang, Zun-Zhe Wang, Yü-Liang Wang, Feng-Bin Wang, Er Gao, and Guang-Xüe Zhang.
• Department of Physiology, Weifang Medical College, Weifang 261042, Shandong Province, People's Republic of China. liningmk@yahoo.com.cn
• Neurosci. Lett. 2004 May 20; 362 (2): 146-9.

AbstractThe calcitonin receptor-like receptor (CRLR) and the orphan receptor RDC-1 have been proposed to be calcitonin gene-related peptide type 1 (CGRP1) receptors, and receptor activity-modifying proteins (RAMPs) determine the ligand specificity of CRLR. Coexpression of RAMP1 and CRLR resulted in functional CGRP1 receptors; the complex of RAMP2 or RAMP3 and CRLR created functional adrenomedullin receptor. Although high levels of CGRP binding sites in the nucleus accumbens have been reported, little is known about the expression of these novel CGRP receptors. In the present study, we used real-time quantitative RT-PCR to detect and quantitate the relative expression of CGRP, CRLR, RAMP1-3 and RDC-1 in the nucleus accumbens of intact rats and rats with inflammation. Our results demonstrate that CGRP, CRLR, RAMP1 and RAMP2 exist in the nucleus accumbens of intact rats, and that they were significantly upregulated in rats with inflammation. In contrast, no expression was detected for RDC-1 and RAMP3. These findings indicated a functional role for CGRP and its receptors in inflammation and pain modulation.Copyright 2004 Elsevier Ireland Ltd.

30 keywords...

hide…