OPIOID AND ANTI-OPIOID PEPTIDES

被引:126
作者
CESSELIN, F [1 ]
机构
[1] FAC MED PARIS, SERV BIOCHIM MED, F-75634 PARIS 13, FRANCE
关键词
OPIOID PEPTIDES; MORPHINE; ANTI-OPIOID PEPTIDES; CHOLECYSTOKININ; NEUROPEPTIDE FF; MIF; ANALGESIA; OPIOID TOLERANCE; OPIOID DEPENDENCE;
D O I
10.1111/j.1472-8206.1995.tb00517.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The numerous endogenous opioid peptides (beta-endorphin, enkephalins, dynorphins...) and the exogenous opioids (such as morphine) exert their effects through the activation of receptors belonging to four main types: mu, delta, kappa and epsilon. Opioidergic neurones and opioid receptors are largely distributed centrally and peripherally. It is thus not surprising that opioids have numerous pharmacological effects and that endogenous opioids are thought to be involved in the physiological control of various functions, among which nociception is particularly emphasized. Some opioid targets may be components of homeostatic systems tending to reduce the effects of opioids. ''Anti-opioid'' properties have been attributed to various peptides, especially cholecystokinin (CCK), neuropeptide FF (NPFF) and melanocyte inhibiting factor (MIF)-related peptides. In addition, a particular place should be attributed, paradoxically, to opioid peptides themselves among the anti-opioid peptides. These peptides can oppose some of the acute effects of opioids, and a hyperactivation of anti-opioid peptidergic neurones due to the chronic administration of opioids may be involved in the development of opioid tolerance and/or dependence. In fact, CCK, NPFF and the MIF family of peptides have complex properties and can act as opioid-like as well as anti-opioid peptides. Thus, ''opioid modulating peptides'' would be a better term to designate these peptides, which probably participate, together with the opioid systems, in multiple feed-back loops for the maintenance of homeostasis. ''Opioid modulating peptides'' have generally been shown to act through the activation of their own receptors. For example, CCK appears to exert its anti-opioid actions mainly through the activation of CCK-B receptors, whereas its opioid-like effects seem to result from the stimulation of CCK-A receptors. However, the partial agonistic properties at opioid receptors of some MLF-related peptides very likely contribute to their ability to modulate the effects of opioids. CCK- and NPFF-related drugs have potential therapeutic interest as adjuncts to opioids for alleviating pain and/or for the treatment of opioid abuse.
引用
收藏
页码:409 / 433
页数:25
相关论文
共 310 条
[91]   THE CCK(A) RECEPTOR ANTAGONIST DEVAZEPIDE DOES NOT MODIFY OPIOID SELF-ADMINISTRATION OR DRUG DISCRIMINATION - COMPARISON WITH THE DOPAMINE ANTAGONIST HALOPERIDOL [J].
HIGGINS, GA ;
JOHARCHI, N ;
WANG, Y ;
CORRIGALL, WA ;
SELLERS, EM .
BRAIN RESEARCH, 1994, 640 (1-2) :246-254
[92]   BINDING-SITES FOR I-125 CHOLECYSTOKININ IN PRIMATE SPINAL-CORD ARE OF THE CCK-A SUBCLASS [J].
HILL, DR ;
SHAW, TM ;
WOODRUFF, GN .
NEUROSCIENCE LETTERS, 1988, 89 (02) :133-139
[93]   ANTINOCICEPTIVE ACTION OF CHOLECYSTOKININ OCTAPEPTIDE (CCK-8) AND RELATED PEPTIDES IN RATS AND MICE - EFFECTS OF NALOXONE AND PEPTIDASE INHIBITORS [J].
HILL, RG ;
HUGHES, J ;
PITTAWAY, KM .
NEUROPHARMACOLOGY, 1987, 26 (04) :289-300
[94]   THE CCK-B RECEPTOR ANTAGONIST CI-988 REVERSES TOLERANCE TO MORPHINE IN RATS [J].
HOFFMANN, O ;
WIESENFELDHALLIN, Z .
NEUROREPORT, 1994, 5 (18) :2565-2568
[95]  
HOLADAY JW, 1991, OPIOIDS IN ANESTHESIA II, P50
[96]   THYROTROPIN RELEASING HORMONE ANTAGONIZES BETA-ENDORPHIN HYPOTHERMIA AND CATALEPSY [J].
HOLADAY, JW ;
TSENG, LF ;
LOH, HH ;
LI, CH .
LIFE SCIENCES, 1978, 22 (17) :1537-1544
[97]   IDENTIFICATION BY RADIOIMMUNOASSAY AND HPLC OF MORPHINE MODULATORY PEPTIDE-IMMUNOREACTIVITY IN RAT SPINAL-CORD AND BRAIN [J].
HOLMES, S ;
DOCKRAY, GJ .
NEUROCHEMISTRY INTERNATIONAL, 1989, 14 (04) :477-482
[98]  
HONG EK, 1989, J PHARMACOL EXP THER, V251, P594
[99]   MODULATION OF MORPHINE-INDUCED EEG AND BEHAVIORAL-EFFECTS BY DYNORPHIN A-(1-13) IN NON-TOLERANT AND MORPHINE-TOLERANT RATS [J].
HONG, O ;
YOUNG, GA ;
KHAZAN, N .
NEUROPHARMACOLOGY, 1988, 27 (08) :807-812
[100]  
HORVATH A, 1990, INT J PEPT PROT RES, V36, P281