@SFZoe014 @DrNadolsky @Nature @NatureMedicine GLP-1R agonism shown to decrease the reward value of food many yrs ago in preclinical studies. Similarly reduces reward induced by some psychoactive drugs. Human translation difficult to predict, but fascinating observations emerging and trials underway https://t.co/rVRxyM8Gq4
The glucagon-like peptide 1 analogue, exendin-4, attenuates the rewarding properties of psychostimulant drugs in mice.
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The evaluation shows that discussions reflect a general consensus supporting the findings, with references to past preclinical studies on food reward and current exploration of psychoactive drugs. The tone indicates both curiosity and caution about translating these findings to human treatments, with words like 'fascinating observations' and mentions of 'trials underway' underscoring engagement and cautious optimism.
The post acknowledges prior research on GLP-1 receptor agonists' effects on reward, aligning with the publication’s findings, showing general agreement.
The discussion indicates a moderate interest, highlighting the potential for translating animal studies into human treatments and noting ongoing trials.
The post's mention of previous studies, potential applications, and ongoing research suggests a thoughtful, engaged reflection rather than superficial acknowledgment.
While recognizing the significance of the research, the discussion remains cautious about immediate implications for humans, reflecting a measured view on potential impact.
Abstract in brief
- The study explores how the GLP1 analogue Exendin4 reduces the rewarding effects of psychostimulant drugs like amphetamine and cocaine in mice, likely by affecting the mesolimbic dopamine system which is involved in reward and addiction.
- Since GLP1 receptors are found in brain areas related to reward, such as the nucleus accumbens and ventral tegmental area, activating these receptors with Exendin4 can decrease drug-induced behaviors like increased movement, dopamine release, and conditioned place preference.
- The findings suggest that GLP1 signaling plays a role in drug reward and dependence, and since GLP1 drugs like exenatide and liraglutide are already used to treat type II diabetes, they could potentially be repurposed as treatments for drug addiction.]
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@SFZoe014 @DrNadolsky @Nature @NatureMedicine GLP-1R agonism shown to decrease the reward value of food many yrs ago in preclinical studies. Similarly reduces reward induced by some psychoactive drugs. Human translation difficult to predict, but fascinating observations emerging and trials underway https://t.co/rVRxyM8Gq4
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