Prolonged glucocorticoid treatment decreases cannabinoid CB, receptor density in the hippocampus

被引:76
作者
Hill, Matthew N. [2 ]
Carrier, Erica J. [1 ]
Ho, W. -S. Vanessa [1 ]
Shi, Leyu [1 ]
Patel, Sachin [1 ]
Gorzalka, Boris B. [2 ]
Hillard, Cecilia J. [1 ]
机构
[1] Med Coll Wisconsin, Dept Pharmacol & Toxicol, Milwaukee, WI 53226 USA
[2] Univ British Columbia, Dept Psychol, Vancouver, BC V6T 1Z4, Canada
关键词
endocannabinoid; depression; corticosterone; anandamide; 2-arachidonylglycerol;
D O I
10.1002/hipo.20386
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Experimental studies indicate a bidirectional, functional relationship between glucocorticoids and the endocannabinoid system; however, the effects of repeated glucocorticoid treatment on the endocannabinoid system have not been examined. In this study, we treated male rats with either a single dose or a 21-day course of treatment with corticosterone (20 mg/kg) and measured hippocampal cannabinoid CB, receptor expression and endocannabinoid content. The 21-day, but not the single, administration of corticosterone significantly reduced both the binding site density and amount of protein of the hippocampal cannabinoid CB, receptor without affecting affinity for the CB, receptor agonist, [H-3]CP55940. With regard to hippocampal endocannabinoid content, acute corticosterone treatment resulted in a significant reduction in anandamide but did not affect 2-arachidonylglycerol, while repeated corticosterone treatment did not alter content of either anandamide or 2-arachidonylglycerol. These data support the hypothesis that the cannabinoid CB, receptor is under negative regulation by glucocorticoids in the hippocampus, and suggest that hippocampal cannabinoid CRI receptor signaling could be reduced under conditions associated with hypersecretion of glucocorticoids, such as chronic stress. (c) 2007 Wiley-Liss, Inc.
引用
收藏
页码:221 / 226
页数:6
相关论文
共 35 条
[1]
The endocannabinoid system drives neural progenitor proliferation [J].
Aguado, T ;
Monory, K ;
Palazuelos, J ;
Stella, N ;
Cravatt, B ;
Lutz, B ;
Marsicano, G ;
Kokaia, Z ;
Guzmán, M ;
Galve-Roperh, I .
FASEB JOURNAL, 2005, 19 (09) :1704-+
[2]
BODNOFF SR, 1995, J NEUROSCI, V15, P61
[3]
Hippocampal remodeling and damage by corticosteroids: Implications for mood disorders [J].
Brown, ES ;
Rush, AJ ;
McEwen, BS .
NEUROPSYCHOPHARMACOLOGY, 1999, 21 (04) :474-484
[4]
Campbell S, 2004, J PSYCHIATR NEUROSCI, V29, P417
[5]
Endocannabinoids facilitate the induction of LTP in the hippocampus [J].
Carlson, G ;
Wang, Y ;
Alger, BE .
NATURE NEUROSCIENCE, 2002, 5 (08) :723-724
[6]
Endocannabinoid-mediated metaplasticity in the hippocampus [J].
Chevaleyre, V ;
Castillo, PE .
NEURON, 2004, 43 (06) :871-881
[7]
Requirement of cannabinoid receptor type 1 for the basal modulation of hypothalamic-pituitary-adrenal axis function [J].
Cota, Daniela ;
Steiner, Michel-Alexander ;
Marsicano, Giovanni ;
Cervino, Cristina ;
Herman, James P. ;
Gruebler, Yvonne ;
Stalla, Johanna ;
Pasquali, Renato ;
Lutz, Beat ;
Stalla, Guenter K. ;
Pagotto, Uberto .
ENDOCRINOLOGY, 2007, 148 (04) :1574-1581
[8]
Brain corticosteroid receptor balance in health and disease [J].
De Kloet, ER ;
Vreugdenhil, E ;
Oitzl, MS ;
Joëls, M .
ENDOCRINE REVIEWS, 1998, 19 (03) :269-301
[9]
Endocannabinoids: endogenous cannabinoid receptor ligands with neuromodulatory action [J].
Di Marzo, V ;
Melck, D ;
Bisogno, T ;
De Petrocellis, L .
TRENDS IN NEUROSCIENCES, 1998, 21 (12) :521-528
[10]
Rapid glucocorticoid-mediated endocannabinoid release and opposing regulation of glutamate and γ-aminobutyric acid inputs to hypothalamic magnocellular neurons [J].
Di, S ;
Malcher-Lopes, R ;
Marcheselli, VL ;
Bazan, NG ;
Tasker, JG .
ENDOCRINOLOGY, 2005, 146 (10) :4292-4301