Specialized compound could lead to chronic pain relief without the use of opioids
Purdue University Research news Mar 23, 2017
Purdue researchers have discovered a compound that could lead to the treatment of chronic pain without the need for patients to rely on opioids.
A team led by Val Watts, associate head and professor of medicinal chemistry and molecular pharmacology in PurdueÂs College of Pharmacy, said the compound shows unparalleled selectivity in inhibiting the adenylyl cyclase 1 (AC1).
Adenylyl cyclases are enzymes that organize the production of cyclic adenosine monophosphate, an important biological messenger in numerous organisms. There are 10 isoforms of adenylyl cyclases found in humans. Numerous studies have suggested that AC1 could be used as a drug target for chronic pain.
The compound identified at Purdue has shown selectivity for inhibiting AC1 versus the other nine isoforms.
ÂWith the AC1 technology, thereÂs a chance to treat chronic pain directly or through reducing the side effects of the opioids, said team member Richard van Rijn, assistant professor of medicinal chemistry and molecular pharmacology in PurdueÂs College of Pharmacy. ÂThereÂs an issue with misuse of opioids used to treat chronic pain. They are good as a short–term analgesic for acute pain, but don't address the underlying issues of chronic pain.Â
Opioids are a class of drugs that include the illicit drug heroin as well as prescription pain relievers oxycodone, hydrocodone, codeine, morphine, fentanyl and others. They interact with opioid receptors on nerve cells in the brain and nervous system to produce pleasurable effects and relieve pain.
The Watts group is the first to identify a compound that is selective for AC1 only.
Findings from the study were published in a research paper by Watts group that recently appeared in the journal Science Signaling. There is also a recent news feature about the research in the journal Science.
While the research is still in its early stages, another potential application for the compound is the possibility of reducing opioid dependence. Separate research has shown that completely deleting the AC1 enzyme reduces the signs of dependence.
ÂIf you decrease the physical symptoms of withdrawal, that could help reduce psychological dependence, Watts said. ÂYou might also be able to stop relapse.Â
The Purdue Office of Technology Commercialization has filed a provisional patent for the technology.
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A team led by Val Watts, associate head and professor of medicinal chemistry and molecular pharmacology in PurdueÂs College of Pharmacy, said the compound shows unparalleled selectivity in inhibiting the adenylyl cyclase 1 (AC1).
Adenylyl cyclases are enzymes that organize the production of cyclic adenosine monophosphate, an important biological messenger in numerous organisms. There are 10 isoforms of adenylyl cyclases found in humans. Numerous studies have suggested that AC1 could be used as a drug target for chronic pain.
The compound identified at Purdue has shown selectivity for inhibiting AC1 versus the other nine isoforms.
ÂWith the AC1 technology, thereÂs a chance to treat chronic pain directly or through reducing the side effects of the opioids, said team member Richard van Rijn, assistant professor of medicinal chemistry and molecular pharmacology in PurdueÂs College of Pharmacy. ÂThereÂs an issue with misuse of opioids used to treat chronic pain. They are good as a short–term analgesic for acute pain, but don't address the underlying issues of chronic pain.Â
Opioids are a class of drugs that include the illicit drug heroin as well as prescription pain relievers oxycodone, hydrocodone, codeine, morphine, fentanyl and others. They interact with opioid receptors on nerve cells in the brain and nervous system to produce pleasurable effects and relieve pain.
The Watts group is the first to identify a compound that is selective for AC1 only.
Findings from the study were published in a research paper by Watts group that recently appeared in the journal Science Signaling. There is also a recent news feature about the research in the journal Science.
While the research is still in its early stages, another potential application for the compound is the possibility of reducing opioid dependence. Separate research has shown that completely deleting the AC1 enzyme reduces the signs of dependence.
ÂIf you decrease the physical symptoms of withdrawal, that could help reduce psychological dependence, Watts said. ÂYou might also be able to stop relapse.Â
The Purdue Office of Technology Commercialization has filed a provisional patent for the technology.
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