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HomeHealth & FitnessA Safer Opioid? Scientists Use Sodium To Reduce Harmful Effects of Fentanyl

A Safer Opioid? Scientists Use Sodium To Reduce Harmful Effects of Fentanyl

Fentanyl is a powerful synthetic opioid that is 50 to 100 times more potent than morphine. It is often prescribed to manage severe pain, but it also has a high potential for addiction and overdose. Long-term use of fentanyl can lead to physical dependence, tolerance, and withdrawal symptoms.

A mouse and cell study has yielded promising results, offering hope that scientists may be able to mitigate the harmful effects of <span class="glossaryLink" aria-describedby="tt" data-cmtooltip="

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&lt;div class=&quot;markdown prose w-full break-words dark:prose-invert light&quot;&gt;&lt;br /&gt;Fentanyl is a synthetic opioid drug that is similar to morphine but is 50 to 100 times more potent. It is used to treat severe pain, such as pain from cancer or surgery, and is typically administered via injection or transdermal patch. Fentanyl can also be used recreationally, and its use has been linked to a significant increase in opioid overdose deaths in recent years. Due to its high potency, fentanyl can be dangerous even in small doses, and its use should be closely monitored by a healthcare provider.&lt;br /&gt;&lt;/div&gt;

” data-gt-translate-attributes='[{“attribute”:”data-cmtooltip”, “format”:”html”}]’>fentanyl, the world’s deadliest opioid, and potentially other drugs as well.

Sodium, a commonly found element on Earth, may offer the potential for scientists to create opioids or other drugs with far reduced side effects.

Scientists from USC, Washington University in St. Louis, and Stanford University have published a study in the journal Nature, in which they showed that by chemically connecting fentanyl to the sodium pockets within nerve cell receptors, they were able to prevent the harmful side effects of the drug while still effectively reducing pain.

Further study is needed but the results hold promise – not just for drug development but for addressing the nation’s crisis of addiction and overdose. Nearly 70,000 Americans died in 2020 of an opioid overdose – most of them from the synthetic opioid, fentanyl, according to the National Institute on Drug Abuse. In the 1990s, the Food and Drug Administration approved the use of fentanyl to ease severe pain in cancer patients but it has since made its way into the streets, worsening the national crisis of opioid abuse.

“In its current form, fentanyl is like a weapon of mass destruction,” said Vsevolod Katritch, a computational scientist at the Bridge Institute at <span class="glossaryLink" aria-describedby="tt" data-cmtooltip="

&lt;span class=&quot;st&quot;&gt;Founded in 1880, the &lt;em&gt;University of Southern California&lt;/em&gt; is one of the world's leading private research universities. It is located in the heart of Los Angeles.&lt;/span&gt;

” data-gt-translate-attributes='[{“attribute”:”data-cmtooltip”, “format”:”html”}]’>USC Michelson Center for Convergent Bioscience and a corresponding author of the study. “Our new collaborative work suggests that we could redesign the drug in such a way that we convert this frequent overdose killer to a much more benign but still effective analgesic.”

Drugs of all kinds are designed to target certain receptors on nerve cells known as GPCRs, or G-protein coupled receptors, which act as signal transmitters. These receptors are like switches that mediate a drug’s intended effect on the brain and body, but also the unintended side effects. In the case of fentanyl, the most potent painkiller of all opioids, patients may suffer from addiction and may die from respiratory arrest.

Katritch noted that he and his fellow scientists Ray Stevens and Vadim Cherezov at the Bridge Institute and the USC Dornsife College of Letters, Arts, and Sciences have been looking at the potential of the sodium mechanism since they first identified it within adenosine and opioid receptors about a decade ago.

Katritch and his collaborators said that although further study is needed to prove that their less harmful version of fentanyl will work in humans, the results have opened a new door for scientists to potentially improve the safety of painkillers.

“We are desperately looking for ways to maintain the analgesic effects of opioids while avoiding dangerous side effects such as addiction and respiratory distress that too often lead to death,” said corresponding author Susruta Majumdar of Washington University in St. Louis. “Our research is still in its early stages, but we’re excited about its potential for leading to safer pain-relieving drugs.”

Beyond opioid receptors, noted Katritch, this work opens a new molecular design concept for dozens of other GPCRs where such functional conversion in existing drugs would be desirable.

Reference: “Structure-based design of bitopic ligands for the µ-opioid receptor” by Abdelfattah Faouzi, Haoqing Wang, Saheem A. Zaidi, Jeffrey F. DiBerto, Tao Che, Qianhui Qu, Michael J. Robertson, Manish K. Madasu, Amal El Daibani, Balazs R. Varga, Tiffany Zhang, Claudia Ruiz, Shan Liu, Jin Xu, Kevin Appourchaux, Samuel T. Slocum, Shainnel O. Eans, Michael D. Cameron, Ream Al-Hasani, Ying Xian Pan, Bryan L. Roth, Jay P. McLaughlin, Georgios Skiniotis, Vsevolod Katritch, Brian K. Kobilka and Susruta Majumdar, 30 November 2022, Nature.
DOI: 10.1038/s41586-022-05588-y

The study was funded by the National Institute on Drug Abuse and the National Cancer Institute. 



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