Emerging role of cyclic ADP-ribose (cADPR) in smooth muscle

被引:22
作者
Bai, N
Lee, HC
Laher, I [1 ]
机构
[1] Univ British Columbia, Dept Pharmacol & Therapeut, Vancouver, BC V6T 1Z3, Canada
[2] Univ Minnesota, Dept Pharmacol, Minneapolis, MN 55455 USA
关键词
cyclic ADP-ribose; cADPR; Ca2+; smooth muscle function;
D O I
10.1016/j.pharmthera.2004.10.005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cyclic adenosine diphosphate ribose (cADPR) is a naturally, occurring cyclic nucleotide and represents a novel class of endogenous Ca2+ messengers implicated in the regulation of the gating properties of ryanodine receptors (RvRs). This action of cADPR occurs, independantly. from the inositol-1.4.5-trisphosphate (IP3) receptor, The regulation of intracellular Ca2+ release is a fundamental element of cellular Ca-2 homeostasis since a number of smooth muscle functions (tone. proliferation. apoptosis. and gene expression) are modulated by intracellular Ca2+ concentration ([Ca2-](i)). There has been a surge in the efforts aimed at understanding the mechanisms of cADPR-mediated Ca-2 mobilization and its impact on smooth muscle function. This review summarizes the proposed roles of cADPR in the regulation of smooth muscle tone (C) 2004 Published by Elsevier Inc.
引用
收藏
页码:189 / 207
页数:19
相关论文
共 199 条
[11]   NAADP receptors are present and functional in the heart [J].
Bak, J ;
Billington, RA ;
Timar, G ;
Dutton, AC ;
Genazzani, AA .
CURRENT BIOLOGY, 2001, 11 (12) :987-990
[12]   The role of cyclic-ADP-ribose-signaling pathway in oxytocin-induced Ca2+ transients in human myometrium cells [J].
Barata, H ;
Thompson, M ;
Zielinska, W ;
Han, YS ;
Mantilla, CB ;
Prakash, YS ;
Feitoza, S ;
Sieck, G ;
Chini, EN .
ENDOCRINOLOGY, 2004, 145 (02) :881-889
[13]   A pivotal role for cADPR-mediated Ca2+ signaling:: regulation of endothelin-induced contraction in peritubular smooth muscle cells [J].
Barone, F ;
Genazzani, AA ;
Conti, A ;
Churchill, GC ;
Palombi, F ;
Ziparo, E ;
Sorrentino, V ;
Galione, A ;
Filippini, A .
FASEB JOURNAL, 2002, 16 (07) :697-705
[14]   Overview of current research in parturition [J].
Bernal, AL .
EXPERIMENTAL PHYSIOLOGY, 2001, 86 (02) :213-222
[15]   INOSITOL TRISPHOSPHATE AND CALCIUM SIGNALING [J].
BERRIDGE, MJ .
NATURE, 1993, 361 (6410) :315-325
[16]  
Berruet L, 1998, BIOCHEM MOL BIOL INT, V46, P847
[17]   NITRIC-OXIDE DECREASES [CA2+](I) IN VASCULAR SMOOTH-MUSCLE BY INHIBITION OF THE CALCIUM CURRENT [J].
BLATTER, LA ;
WIER, WG .
CELL CALCIUM, 1994, 15 (02) :122-131
[18]   Vasodilation by the calcium-mobilizing messenger cyclic ADP-ribose [J].
Boittin, FX ;
Dipp, M ;
Kinnear, NP ;
Galione, A ;
Evans, AM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (11) :9602-9608
[19]   Nicotinic acid adenine dinucleotide phosphate mediates Ca2+ signals and contraction in arterial smooth muscle via a two-pool mechanism [J].
Boittin, FX ;
Galione, A ;
Evans, AM .
CIRCULATION RESEARCH, 2002, 91 (12) :1168-1175
[20]   NITRIC-OXIDE DIRECTLY ACTIVATES CALCIUM-DEPENDENT POTASSIUM CHANNELS IN VASCULAR SMOOTH-MUSCLE [J].
BOLOTINA, VM ;
NAJIBI, S ;
PALACINO, JJ ;
PAGANO, PJ ;
COHEN, RA .
NATURE, 1994, 368 (6474) :850-853