1. Academic Validation
  2. Exoticin as a selective agonist of 6TM μ opioid receptors identifies endogenous chaperones essential for its activity

Exoticin as a selective agonist of 6TM μ opioid receptors identifies endogenous chaperones essential for its activity

  • Phytomedicine. 2024 Oct:133:155898. doi: 10.1016/j.phymed.2024.155898.
Fenfen Qin 1 Qisheng Wang 1 Yuxuan Wang 1 Zhonghao Li 1 Anlong Liu 2 Qingyang Liu 1 Weixin Lin 1 Xinru Mu 1 Xingjun Liu 3 Qian Wang 4 Zhigang Lu 5
Affiliations

Affiliations

  • 1 School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210023, China; Key Laboratory of Acupuncture and Medicine Research of Ministry of Education, Nanjing University of Chinese Medicine, Nanjing 210023, China.
  • 2 Nanjing Hospital of Traditional Chinese Medicine Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing 210008, China.
  • 3 School of Pharmacy, Nantong University, Nantong 226001, China. Electronic address: edvin201@163.com.
  • 4 International Education college, Nanjing University of Chinese Medicine, Nanjing 210023, China. Electronic address: aqqwang@126.com.
  • 5 School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210023, China; Key Laboratory of Acupuncture and Medicine Research of Ministry of Education, Nanjing University of Chinese Medicine, Nanjing 210023, China; School of Integrative Medicine, Nanjing University of Chinese Medicine, Nanjing 210023, China. Electronic address: Luzg@njucm.edu.cn.
Abstract

Background: Classical opioids are effective analgesics but carry various side effects, necessitating safer alternatives. Truncated six-transmembrane mu opioid receptors (6TM-μORs) mediate potent analgesia with fewer side effects and are a promising therapeutic target. However, few ligands known selectively target 6TM-μORs. Moreover, endogenous chaperones are believed essential for 6TM-μOR ligand binding and function.

Purpose: To identify a 6TM-μOR selective agonist and elucidate requisite endogenous chaperones.

Methods: Virtual screening was used to identify promising selective 6TM-μOR agonists from traditional Chinese medicines. The role of 6TM-μOR in Exoticin analgesia was validated in loss- and gain-of-function models. APEX2 proteomics profiled proximal proteins under Exoticin or IBNtxA. Interactions were further characterized in vivo and in vitro.

Results: Exoticin was shortlisted for its selective binding to 6TM-μOR and ability to induce 6TM-μOR-dependent signal transduction. Exoticin analgesia was sensitive to β-FNA and absent in E11 KO mice, but restored in mice infected with AAV-μOR1G. Slc3a2, Lrrc59, and Ppp1cb co-interacted with 6TM-μOR1G and were equally essential for Exoticin binding and 6TM-μOR1G activity.

Conclusion: Exoticin is a promising selective agonist of 6TM μ opioid receptors with broad-spectrum analgesic efficacy but few side effects. Slc3a2, Lrrc59, Ppp1cb are endogenous chaperones essential for 6TM-μOR ligand binding and function.

Keywords

6TM-μOR; Exoticin; Lrrc59; Ppp1cb; Slc3a2.

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