1. Academic Validation
  2. The Circadian Hormone Melatonin Inhibits Morphine-Induced Tolerance and Inflammation via the Activation of Antioxidative Enzymes

The Circadian Hormone Melatonin Inhibits Morphine-Induced Tolerance and Inflammation via the Activation of Antioxidative Enzymes

  • Antioxidants (Basel). 2020 Aug 22;9(9):780. doi: 10.3390/antiox9090780.
Ing-Jung Chen 1 2 Chih-Ping Yang 3 4 Sheng-Hsiung Lin 5 Chang-Mei Lai 6 Chih-Shung Wong 1 6
Affiliations

Affiliations

  • 1 Department of Anesthesiology, Cathay General Hospital, Taipei 10630, Taiwan.
  • 2 Department of Medical Research, Cathay General Hospital, Taipei 10630, Taiwan.
  • 3 Department of Anesthesiology, Chi-Mei Medical Center, Tainan 71004, Taiwan.
  • 4 Department of Anesthesiology, School of Medicine, National Defense Medical Center, Taipei 11490, Taiwan.
  • 5 Planning & Management Office, Tri-Service General Hospital, Taipei 11490, Taiwan.
  • 6 Graduate Institute of Medical Sciences, National Defense Medical Center, Taipei 11490, Taiwan.
Abstract

Opioids are commonly prescribed for clinical pain management; however, dose-escalation, tolerance, dependence, and addiction limit their usability for long-term chronic pain. The associated poor sleep pattern alters the circadian neurobiology, and further compromises the pain management. Here, we aim to determine the correlation between constant LIGHT exposure and morphine tolerance and explore the potential of melatonin as an Adjuvant of morphine for neuropathic pain treatment.

Methods: Wistar rats were preconditioned under constant LIGHT (LL) or a regular LIGHT/dark (LD) cycle before neuropathic pain induction by chronic constriction injury. An intrathecal (i.t.) osmotic pump was used for continued Drug Delivery to induce morphine tolerance. Pain assessments, including the plantar test, static weight-bearing symmetry, and tail-flick latency, were used to determine the impact of the LIGHT disruption or exogenous melatonin on the morphine tolerance progression.

Results: constant LIGHT exposure significantly aggravates morphine tolerance in neuropathic rats. Continued infusion of low-dose melatonin (3 μg/h) attenuated morphine tolerance in both neuropathic and naïve rats. This protective effect was independent of melatonin receptors, as shown by the neutral effect of melatonin receptors inhibitors. The transcriptional profiling demonstrated a significant enhancement of proinflammatory and pain-related receptor genes in morphine-tolerant rats. In contrast, this transcriptional pattern was abolished by melatonin coinfusion along with the upregulation of the Kcnip3 gene. Moreover, melatonin increased the antioxidative Enzymes SOD2, HO-1, and GPx1 in the spinal cord of morphine-tolerant rats.

Conclusion: Dysregulated circadian LIGHT exposure significantly compromises the efficacy of morphine's antinociceptive effect, while the cotreatment with melatonin attenuates morphine tolerance/hyperalgesia development. Our results suggest the potential of melatonin as an Adjuvant of morphine in clinical pain management, particularly in patients who need long-term opioid treatment.

Keywords

DREAM; Kcnip3; antioxidants; antioxidative enzyme; chronic constriction injury; circadian rhythms; melatonin; morphine tolerance; neuropathic pain.

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