Neurokinin 1 and opioid receptors: relationships and interactions in nervous system
- PMID: 28409174
- PMCID: PMC5388438
Neurokinin 1 and opioid receptors: relationships and interactions in nervous system
Abstract
Opioid receptors and neurokinin 1 receptor (NK1R) are found highly expressed in the central nervous system. The co-localization of these two kinds of receptors suggests that they might interact with each other in both the transmission and modulation of the pain signal. In this review, we explore the relationships between opioid receptors and NK1R. Substance P (SP) plays a modulatory role in the pain transmission by activating the NK1R. Opioid receptor activation can inhibit SP release. NK1R is found participating in the mechanisms of the side effects of the opioids, including opioid analgesic tolerance, hyperalgesia, anxiety behaviors of morphine reward and opioids related respiratory depression. A series of compounds such as NK1R antagonists and ligands works on both mu/delta opioid receptor (MOR/DOR) and NK1R were synthesized as novel analgesics that enhance the clinical pain management efficacy and reduce the dosage and side effects. The current status of these novel ligands and the limitations are discussed in this review. Although the working mechanisms of these ligands remained unclear, they could be used as research tool for developing novel analgesic drugs in the future.
Keywords: Central nervous system; Neurokinin 1 receptor; Opioid receptors; Opioids; Substance P.
Conflict of interest statement
Conflict Interests Disclosure: The authors have no conflicting interests to disclose.
Similar articles
-
Discovery of Novel Multifunctional Ligands with μ/δ Opioid Agonist/Neurokinin-1 (NK1) Antagonist Activities for the Treatment of Pain.J Med Chem. 2015 Nov 12;58(21):8573-83. doi: 10.1021/acs.jmedchem.5b01170. Epub 2015 Oct 30. J Med Chem. 2015. PMID: 26465170 Free PMC article.
-
Dual Alleviation of Acute and Neuropathic Pain by Fused Opioid Agonist-Neurokinin 1 Antagonist Peptidomimetics.ACS Med Chem Lett. 2015 Oct 31;6(12):1209-14. doi: 10.1021/acsmedchemlett.5b00359. eCollection 2015 Dec 10. ACS Med Chem Lett. 2015. PMID: 26713106 Free PMC article.
-
Differential effects of aprepitant, a clinically used neurokinin-1 receptor antagonist on the expression of conditioned psychostimulant versus opioid reward.Psychopharmacology (Berl). 2017 Feb;234(4):695-705. doi: 10.1007/s00213-016-4504-6. Epub 2016 Dec 24. Psychopharmacology (Berl). 2017. PMID: 28013351 Free PMC article.
-
Mu Opioid Receptor Heterodimers Emerge as Novel Therapeutic Targets: Recent Progress and Future Perspective.Front Pharmacol. 2020 Jul 15;11:1078. doi: 10.3389/fphar.2020.01078. eCollection 2020. Front Pharmacol. 2020. PMID: 32760281 Free PMC article. Review.
-
Substance P receptor antagonists in psychiatry: rationale for development and therapeutic potential.CNS Drugs. 2005;19(4):275-93. doi: 10.2165/00023210-200519040-00001. CNS Drugs. 2005. PMID: 15813642 Review.
Cited by
-
Synthesis and Pharmacological Evaluation of Hybrids Targeting Opioid and Neurokinin Receptors.Molecules. 2019 Dec 5;24(24):4460. doi: 10.3390/molecules24244460. Molecules. 2019. PMID: 31817441 Free PMC article.
-
Advances in Understanding the Initial Steps of Pruritoceptive Itch: How the Itch Hits the Switch.Int J Mol Sci. 2020 Jul 10;21(14):4883. doi: 10.3390/ijms21144883. Int J Mol Sci. 2020. PMID: 32664385 Free PMC article. Review.
-
Antinociceptive and analgesic effect of continuous intravenous infusion of maropitant, lidocaine and ketamine alone or in combination in cats undergoing ovariohysterectomy.Acta Vet Scand. 2021 Nov 27;63(1):49. doi: 10.1186/s13028-021-00615-w. Acta Vet Scand. 2021. PMID: 34838084 Free PMC article.
-
Structural insights into GPCR signaling activated by peptide ligands: from molecular mechanism to therapeutic application.Exp Mol Med. 2025 Jul;57(7):1467-1481. doi: 10.1038/s12276-025-01497-y. Epub 2025 Jul 8. Exp Mol Med. 2025. PMID: 40629042 Free PMC article. Review.
-
In Vivo, In Vitro and In Silico Studies of the Hybrid Compound AA3266, an Opioid Agonist/NK1R Antagonist with Selective Cytotoxicity.Int J Mol Sci. 2020 Oct 19;21(20):7738. doi: 10.3390/ijms21207738. Int J Mol Sci. 2020. PMID: 33086743 Free PMC article.
References
-
- Breivik H, Borchgrevink PC, Allen SM, et al. Assessment of pain. Br J Anaesth. 2008;101:17–24. - PubMed
-
- Debono DJ, Hoeksema LJ, Hobbs RD. Caring for patients with chronic pain: pearls and pitfalls. J Am Osteopath Assoc. 2013;113:620–7. - PubMed
-
- Besson JM. The neurobiology of pain. Lancet. 1999;353:1610–5. - PubMed
-
- Millan MJ. Descending control of pain. Prog Neurobiol. 2002;66:355–474. - PubMed
-
- Pinto M, Sousa M, Lima D, Tavares I. Participation of mu-opioid, GABA(B), and NK1 receptors of major pain control medullary areas in pathways targeting the rat spinal cord: implications for descending modulation of nociceptive transmission. The Journal of comparative neurology. 2008;510:175–87. - PubMed
Grants and funding
LinkOut - more resources
Full Text Sources
Research Materials