The Role of the Cannabinoid System in Opioid Analgesia and Tolerance

被引:12
作者
Ozdemir, Ercan [1 ]
机构
[1] Cumhuriyet Univ, Sch Med, Dept Physiol, TR-58140 Sivas, Turkey
关键词
Cannabinoids; cannabinoid receptors; cannabinoid analgesia; opioid analgesia; opioid tolerance; analgesic; MORPHINE ANTINOCICEPTIVE TOLERANCE; TYPE-2 RECEPTOR AGONIST; CYCLIC-AMP ACCUMULATION; NEUROPATHIC PAIN; LOCUS-COERULEUS; RHESUS-MONKEYS; RAT MODEL; SYNERGISTIC INTERACTIONS; ENDOGENOUS OPIOIDS; ANIMAL-MODELS;
D O I
10.2174/1389557520666200313120835
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Opioid receptor agonist drugs, such as morphine, are very effective for treating chronic and severe pain; but, tolerance can develop with long-term use. Although there is a lot of information about the pathophysiological mechanisms of opioid tolerance, it is still not fully clarified. Suggested mechanisms for opioid tolerance include opioid receptor desensitisation, reduction of sensitivity G-proteins, activation of Mitogen-Activated Protein Kinase (MAPK), altered intracellular signaling pathway including nitric oxide, and activation of mammalian Target of Rapamycin (mTOR). One way to reduce opioid tolerance and increase the analgesic potential is to use low doses. Combination of cannabinoids with opioids has been shown to manifest the reduction of the opioid dose. Experimental studies revealed an interaction of the endocannabinoid system and opioid antinociception. Cannabinoid and opioid receptor systems use common pathways in the formation of analgesic effect and demonstrate their activity via G Protein Coupled Receptors (GPCR). Cannabinoid drugs modulate opioid analgesic activity at a number of distinct levels within the cell, ranging from direct receptor associations to post-receptor interactions through shared signal transduction pathways. This review summarizes the data indicating that with combining cannabinoids and opioids drugs may be able to produce long-term analgesic effects, while preventing the opioid analgesic tolerance.
引用
收藏
页码:875 / 885
页数:11
相关论文
共 113 条
  • [1] DEPRESSION OF MESOLIMBIC DOPAMINE TRANSMISSION AND SENSITIZATION TO MORPHINE DURING OPIATE ABSTINENCE
    ACQUAS, E
    DICHIARA, G
    [J]. JOURNAL OF NEUROCHEMISTRY, 1992, 58 (05) : 1620 - 1625
  • [2] Opioid receptor desensitization: mechanisms and its link to tolerance
    Allouche, Stephane
    Noble, Florence
    Marie, Nicolas
    [J]. FRONTIERS IN PHARMACOLOGY, 2014, 5
  • [3] The effects of endocannabinoid receptor agonist anandamide and antagonist rimonabant on opioid analgesia and tolerance in rats
    Altun, Ahmet
    Ozdemir, Ercan
    Yildirim, Kemal
    Gursoy, Sinan
    Durmus, Nedim
    Bagcivan, Ihsan
    [J]. GENERAL PHYSIOLOGY AND BIOPHYSICS, 2015, 34 (04) : 433 - 440
  • [4] Attenuation of morphine antinociceptive tolerance by cannabinoid CB1 and CB2 receptor antagonists
    Altun, Ahmet
    Yildirim, Kemal
    Ozdemir, Ercan
    Bagcivan, Ihsan
    Gursoy, Sinan
    Durmus, Nedim
    [J]. JOURNAL OF PHYSIOLOGICAL SCIENCES, 2015, 65 (05) : 407 - 415
  • [5] Arends RH, 1998, J PHARMACOL EXP THER, V286, P585
  • [6] Long-lasting self-inhibition of neocortical interneurons mediated by endocannabinoids
    Bacci, A
    Huguenard, JR
    Prince, DA
    [J]. NATURE, 2004, 431 (7006) : 312 - 316
  • [7] Battista Natalia, 2006, Ital J Biochem, V55, P283
  • [8] CB2 receptor-mediated antihyperalgesia: possible direct involvement of neural mechanisms
    Beltramo, M
    Bernardini, N
    Bertorelli, R
    Campanella, M
    Nicolussi, E
    Fredduzzi, S
    Reggiani, A
    [J]. EUROPEAN JOURNAL OF NEUROSCIENCE, 2006, 23 (06) : 1530 - 1538
  • [9] Endocannabinoids inhibit transmission at granule cell to Purkinje cell synapses by modulating three types of presynaptic calcium channels
    Brown, SP
    Safo, PK
    Regehr, WG
    [J]. JOURNAL OF NEUROSCIENCE, 2004, 24 (24) : 5623 - 5631
  • [10] DIFFERENCES IN HYPOTHALAMO-PITUITARY-ADRENOCORTICAL ACTIVITY IN THE RAT AFTER ACUTE AND PROLONGED TREATMENT WITH MORPHINE
    BUCKINGHAM, JC
    COOPER, TA
    [J]. NEUROENDOCRINOLOGY, 1984, 38 (05) : 411 - 417