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Contemporary society faces significant challenges that can lead to stress-induced tunnel vision. Positive affect can counteract these effects by expanding humans’ attentional scope, potentially promoting resilience and creativity. This preregistered triple-blind study investigated the role of endogenous opioids in mediating attentional broadening following reward receipt.
Methods
Using a placebo-controlled crossover design, 40 volunteers underwent two sessions separated by at least 1 week, receiving either 50 mg of naltrexone or a placebo. Participants completed a Navon letters task designed to contrast the effects of reward receipt versus reward anticipation on attentional scope.
Results
As predicted, our results show that the attentional broadening observed after reward receipt under placebo was eliminated when opioid receptors were blocked. Naltrexone did not result in blunted reward anticipation effects on task performance or attentional narrowing.
Conclusions
This study highlights the role of endogenous opioids in attentional breadth and their potential for cognitive flexibility and resilience through natural positive experiences, with potential implications for mental health and stress management.
This chapter presents several experimental approaches performed in the Laboratory of the Biology of Addictive Diseases to characterize the relationship of gene variations with heroin addiction and pharmacogenomics. Although opioid receptors often subserve similar physiological functions, activation of the kappa-opioid receptor (KOPr) by exogenous agonists produces dysphoria in humans and aversive effects in experimental animals, in contrast to activation of mu-opioid receptor (MOPr). Opiate addiction is a chronic relapsing disorder that is treated world-wide with methadone. The genes studied are usually those which have been shown to be involved in some aspects of development of addiction. In some studies, multiple genes, all hypothesized to be potentially involved in opioid addiction, have been studied. In other cases, genome-wide association studies (GWAS) have been performed to identify regions of chromosomes which may influence vulnerability to the development of addiction. These studies usually do not identify specific genes within chromosome regions.
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