Opiate, cannabinoid, and eicosanoid signaling converges on common intracellular pathways Nitric oxide coupling

被引:42
作者
Fimiani, C [1 ]
Liberty, T [1 ]
Aquirre, AJ [1 ]
Amin, I [1 ]
Ali, N [1 ]
Stefano, GB [1 ]
机构
[1] SUNY Coll Old Westbury, Neurosci Res Inst, Old Westbury, NY 11568 USA
关键词
morphine; cannabinoid; nitric oxide; eicosanoid; aspirin;
D O I
10.1016/S0090-6980(98)00068-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Scientific fields as they emerge initially appear to be unrelated to other projects even if they are in a similar area of interest. This is especially true in the case of opiate, cannabinoid, and eicosanoid signaling processes. In this limited speculative review, we attempt to examine aspects of their intracellular cascading signaling systems for their commonalties. We find intracellular calcium mobilization, nuclear factor kappa B involvement, adenylate cyclase activity, and, finally, constitutive nitric oxide release to be converging points for these signaling processes, occurring by separate and distinct receptor-mediated effector systems. Phosphokinase C, mitogen activated protein kinase, and cytosolic phospholipase A(2) also represent points of common impact. In this regard, aspirin also appears to be involved in an aspect of this signaling convergence. We conclude that many of the physiological observations regarding the actions of these signaling molecules, for example, immunosuppression, neurotransmission, vasodilation, cellular adherence, and cytotoxicity, can now be understood by considering their converging biochemical cascades. (C) 1999 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:23 / 34
页数:12
相关论文
共 86 条
[41]  
NADLER JL, 1993, HYPERTENSION PRIMER, P25
[42]  
NASJLETTI A, 1993, HYPERTENSION PRIMER, P23
[43]   Activation of NF-kappa B by ER stress requires both Ca2+ and reactive oxygen intermediates as messengers [J].
Pahl, HL ;
Baeuerle, PA .
FEBS LETTERS, 1996, 392 (02) :129-136
[44]  
Pasotti D, 1993, Riv Eur Sci Med Farmacol, V15, P71
[45]  
QIU ZH, 1994, J BIOL CHEM, V269, P19480
[46]   GLUCOCORTICOIDS INHIBIT THE EXPRESSION OF AN INDUCIBLE, BUT NOT THE CONSTITUTIVE, NITRIC-OXIDE SYNTHASE IN VASCULAR ENDOTHELIAL-CELLS [J].
RADOMSKI, MW ;
PALMER, RMJ ;
MONCADA, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (24) :10043-10047
[47]   Endocannabinoids: a new class of vasoactive substances [J].
Randall, MD ;
Kendall, DA .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1998, 19 (02) :55-58
[48]   INVITRO EFFECT OF DELTA-9-TETRAHYDROCANNABINOL TO STIMULATE SOMATOSTATIN RELEASE AND BLOCK THAT OF LUTEINIZING-HORMONE-RELEASING HORMONE BY SUPPRESSION OF THE RELEASE OF PROSTAGLANDIN-E2 [J].
RETTORI, V ;
AGUILA, MC ;
GIMENO, MF ;
FRANCHI, AM ;
MCCANN, SM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (24) :10063-10066
[49]   Down-regulation of cytokine-induced cyclo-oxygenase-2 transcript isoforms by dexamethasone: Evidence for post-transcriptional regulation [J].
Ristimaki, A ;
Narko, K ;
Hla, T .
BIOCHEMICAL JOURNAL, 1996, 318 :325-331
[50]   Morphine modulates NFκB activation in macrophages [J].
Roy, S ;
Cain, KJ ;
Chapin, RB ;
Charboneau, RG ;
Barke, RA .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 245 (02) :392-396