Scientists at the Florida campus of The Scripps Research Institute say they have shown that a specific molecule controls morphine receptor signaling in a small group of brain cells. The findings could lead to a new drug target for developing less-addictive pain medications and even offer a clue to the genetic predisposition of patients to addiction before treatment, according to the researchers who published their study (“RGS7 Regulates Reward Behavior by Controlling Opioid Signaling in the Striatum”) online ahead of print in Biological Psychiatry.

The molecule in question is known as a regulator of G protein signaling (RGS) protein, which controls the morphine receptor (mu opioid receptor). Using genetically modified animal models lacking a particular RGS protein called RGS7, a protein abundant in the brain, the study showed that eliminating the protein enhanced reward, increased pain relief, delayed tolerance, and heightened withdrawal in response to self-administered morphine doses. In other words, without the protein, the animals were predisposed to morphine addiction.

“The mu opioid receptor acts as a conductor of the drug's effects, while RGS7 acts as a brake on the signal,” said Kirill Martemyanov, Ph.D., an associate professor at the Institute. “The animals could press a lever to receive an infusion of morphine. We looked at the number of lever presses to determine how much they liked it and, judging from this test, mice lacking RGS7 craved the drug much more than their normal siblings.”

RGS7 appears to exert its effects by regulating morphine-induced changes in excitability of neurons and plasticity of synapses.

“This study reveals a unique modulatory role of RGS7 in a brain-region-specific action to morphine use and indicates RGS7 as a potential drug target,” said research associate Laurie P. Sutton, Ph.D., the first author of the study. “Pharmacological intervention at the level of RGS7 may reduce some of the detrimental side-effects associated with opiates.”

Dr. Martemyanov believes there is a strong diagnostic future for their discovery.

“If our findings hold true for human patients, you could look specifically for RGS7 levels for any disabling mutation with a simple blood test,” he said. “Mutations could indicate a strong reaction to a drug such as morphine—people carrying a deficient copy of the RGS7 gene might need much lower doses of opioids and could be cautioned to be extra careful with these substances.”

This might also shed light on why some people have such a difficult time with addiction to drugs such as morphine, while others are not so susceptible, he added. Surprisingly, in addition to drug craving, the animals lacking RGS7 also worked harder to obtain a food reward, further suggesting that RGS7 may be a more general regulator of reward behavior extending beyond drug-induced euphoria.








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