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Cited by 370

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Morphine-activated opioid receptors elude desensitization by β-arrestin

Open access
Whistler, Jennifer L., von Zastrow, Mark·1998·Proceedings of the National Academy of Sciences

Abstract

μ opioid receptors are targets of native opioid peptides and addictive analgesic drugs. A major clinical liability of opiate drugs is their ability to cause physiological tolerance. Individual opiates, such as morphine and etorphine, differ both in their ability to promote physiological tolerance and in their effects on receptor regulation by endocytosis. Here, we demonstrate that arrestins play a fundamental role in mediating this agonist-selective regulation and that morphine-activated μ receptors fail to undergo arrestin-dependent uncoupling from cognate G proteins. Thus, highly addictive opiate drugs elude a fundamental mode of physiological regulation that is mediated by agonist-specific interaction of opioid receptors with arrestins.

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Crossref · 10.1073/pnas.95.17.9914

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Metadata

Authors
Whistler, J. L., & von Zastrow, M.
Venue
Proceedings of the National Academy of Sciences
Published
1998-08-18
Volume
95
Issue
17
Pages
9914-9919
ISSN
  • 0027-8424 (ISSN-L)
  • 1091-6490
OpenAlex
W2004120139
Cited by
370
References
1
FWCI
6.53
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Morphine-activated opioid receptors elude desensitization by β-arrestin. https://app.cochat.ai/papers/10.1073/pnas.95.17.9914
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Whistler, J. L., & von Zastrow, M. (1998). Morphine-activated opioid receptors elude desensitization by β-arrestin. Proceedings of the National Academy of Sciences. https://doi.org/10.1073/pnas.95.17.9914

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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.