Shedding Light on the Pharmacological Interactions between μ-Opioid Analgesics and Angiotensin Receptor Modulators: A New Option for Treating Chronic Pain

Molecules. 2021 Oct 13;26(20):6168. doi: 10.3390/molecules26206168.

Abstract

The current protocols for neuropathic pain management include µ-opioid receptor (MOR) analgesics alongside other drugs; however, there is debate on the effectiveness of opioids. Nevertheless, dose escalation is required to maintain their analgesia, which, in turn, contributes to a further increase in opioid side effects. Finding novel approaches to effectively control chronic pain, particularly neuropathic pain, is a great challenge clinically. Literature data related to pain transmission reveal that angiotensin and its receptors (the AT1R, AT2R, and MAS receptors) could affect the nociception both in the periphery and CNS. The MOR and angiotensin receptors or drugs interacting with these receptors have been independently investigated in relation to analgesia. However, the interaction between the MOR and angiotensin receptors has not been excessively studied in chronic pain, particularly neuropathy. This review aims to shed light on existing literature information in relation to the analgesic action of AT1R and AT2R or MASR ligands in neuropathic pain conditions. Finally, based on literature data, we can hypothesize that combining MOR agonists with AT1R or AT2R antagonists might improve analgesia.

Keywords: angiotensin receptors; chronic pain; neuropathic pain; µ-opioid analgesics.

Publication types

  • Review

MeSH terms

  • Analgesics / pharmacology
  • Analgesics, Opioid / pharmacology
  • Animals
  • Chronic Pain / drug therapy*
  • Humans
  • Neuralgia / drug therapy
  • Nociception / drug effects
  • Pain Management / methods
  • Proto-Oncogene Mas
  • Receptors, Angiotensin / drug effects*
  • Receptors, Angiotensin / metabolism
  • Receptors, Opioid / agonists
  • Receptors, Opioid, mu / agonists
  • Receptors, Opioid, mu / drug effects*
  • Receptors, Opioid, mu / metabolism

Substances

  • Analgesics
  • Analgesics, Opioid
  • MAS1 protein, human
  • Proto-Oncogene Mas
  • Receptors, Angiotensin
  • Receptors, Opioid
  • Receptors, Opioid, mu