The sigma-2 receptor agonist PB28 inhibits calcium release from the endoplasmic reticulum of SK-N-SH neuroblastoma cells

被引:28
作者
Cassano, Giuseppe
Gasparre, Giuseppe
Contino, Marialessandra
Niso, Mauro
Berardi, Francesco
Perrone, Roberto
Colabufo, Nicola Antonio
机构
[1] Univ Bari, Dipartimento Fisiol Gen & Ambientale, I-70126 Bari, Italy
[2] Univ Bari, Dipartimento Farm Chim, I-70125 Bari, Italy
关键词
caffeine; carbachol; fura-2; PB28; sigma receptors;
D O I
10.1016/j.ceca.2006.03.004
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In this paper we demonstrate that PB28 abolishes the Ca2+ release through the inositol 1,4,5-trisphosphate (InSP3) receptors and ryanodine receptors in SK-N-SH cells. Sigma receptors are divided into the subtypes sigma-1 and sigma-2, which are expressed in tumor cell lines and characterized by distinct pharmacological profiles. The sigma-1 receptor has been recently cloned, whereas the sigma-2 receptor is less well characterized. The endogenous ligand(s) of both subtypes remain unclear. In isolated guinea pig ileum, PB28 inhibits the contraction induced by carbachol dose dependently and in a non-competitive manner. In SK-N-SH cells PB28 challenge does not affect the intracellular Ca2+ concentration but incubation with PB28 for 45 min abolishes the cytosolic Ca2+ increases evoked by carbachol or histamine. This effect, not sensitive to cycloheximide, is caused by direct inhibition of the InsP(3) receptors, since PB28 abolishes the response elicited by InsP(3) administration in permeabilized SK-N-SH cells. Finally, incubation for 45 min with PB28 also abolishes the cytosolic Ca2+ increase evoked by caffeine. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:23 / 28
页数:6
相关论文
共 20 条
[1]   4-(tetralin-1-yl)- and 4-(naphthalen-1-yl)alkyl derivatives of 1-cyclohexylpiperazine as σ receptor ligands with agonist σ2 activity [J].
Berardi, F ;
Ferorelli, S ;
Abate, C ;
Colabufo, NA ;
Contino, M ;
Perrone, R ;
Tortorella, V .
JOURNAL OF MEDICINAL CHEMISTRY, 2004, 47 (09) :2308-2317
[2]  
Bowen W D, 2000, Pharm Acta Helv, V74, P211
[3]   CHARACTERIZATION OF A POSTJUNCTIONAL 5-HT RECEPTOR MEDIATING RELAXATION OF GUINEA-PIG ISOLATED ILEUM [J].
CARTER, D ;
CHAMPNEY, M ;
HWANG, B ;
EGLEN, RM .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1995, 280 (03) :243-250
[4]   Antiproliferative and cytotoxic effects of some σ2 agonists and σ1 antagonists in tumour cell lines [J].
Colabufo, NA ;
Berardi, F ;
Contino, M ;
Niso, M ;
Abate, C ;
Perrone, R ;
Tortorella, V .
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 2004, 370 (02) :106-113
[5]   σ2-receptor regulation of dopamine transporter via activation of protein kinase C [J].
Derbez, AE ;
Mody, RM ;
Werling, LL .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2002, 301 (01) :306-314
[6]   Inositol 1,4,5-trisphosphate and ryanodine receptors mobilize calcium from a common functional pool in human U373 MG cells [J].
Galiano, M ;
Gasparre, G ;
Lippe, C ;
Cassano, G .
CELL CALCIUM, 2004, 36 (05) :359-365
[7]   Sigma receptors: biology and therapeutic potential [J].
Guitart, X ;
Codony, X ;
Monroy, X .
PSYCHOPHARMACOLOGY, 2004, 174 (03) :301-319
[8]   Regulating ankyrin dynamics: Roles of sigma-1 receptors [J].
Hayashi, T ;
Su, TP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (02) :491-496
[9]   Modulation of bradykinin-induced calcium changes in SH-SY5Y cells by neurosteroids and sigma receptor ligands via a shared mechanism [J].
Hong, WM ;
Nuwayhid, SJ ;
Werling, LL .
SYNAPSE, 2004, 54 (02) :102-110
[10]  
MARTIN WR, 1976, J PHARMACOL EXP THER, V197, P517