The Angiotensin Antagonist Losartan Modulates Social Reward Motivation and Punishment Sensitivity via Modulating Midbrain-Striato-Frontal Circuits

التفاصيل البيبلوغرافية
العنوان: The Angiotensin Antagonist Losartan Modulates Social Reward Motivation and Punishment Sensitivity via Modulating Midbrain-Striato-Frontal Circuits
المؤلفون: Ting Xu, Benjamin Becker, Keith M. Kendrick, Ziyu Qi, Ran Zhang, Weihua Zhao, Xinqi Zhou, Yixu Zeng
المصدر: The Journal of Neuroscience. 43:472-483
بيانات النشر: Society for Neuroscience, 2022.
سنة النشر: 2022
مصطلحات موضوعية: Punishment (psychology), General Neuroscience, Dopaminergic, Striatum, Anticipation, Arousal, Ventral tegmental area, medicine.anatomical_structure, Dopamine, medicine, Psychology, Insula, Neuroscience, psychological phenomena and processes, medicine.drug
الوصف: Social deficits and dysregulations in dopaminergic midbrain-striato-frontal circuits represent transdiagnostic symptoms across psychiatric disorders. Animal models suggest that interactions between the dopamine (DA) and renin-angiotensin system (RAS) may modulate learning and reward-related processes. The present study therefore examined the behavioral and neural effects of the Angiotensin II type 1 receptor (AT1R) antagonist losartan on social reward and punishment processing in humans. A preregistered randomized double-blind placebo-controlled between-subject pharmacological design was combined with a social incentive delay (SID) functional MRI (fMRI) paradigm during which subjects could avoid social punishment or gain social reward. Healthy volunteers received a single-dose of losartan (50 mg,n= 43, female = 17) or placebo (n= 44, female = 20). We evaluated reaction times (RTs) and emotional ratings as behavioral and activation and functional connectivity as neural outcomes. Relative to placebo, losartan modulated the reaction time and arousal differences between social punishment and social reward. On the neural level the losartan-enhanced motivational salience of social rewards was accompanied by stronger ventral striatum-prefrontal connectivity during reward anticipation. Losartan increased the reward-neutral difference in the ventral tegmental area (VTA) and attenuated VTA associated connectivity with the bilateral insula in response to punishment during the outcome phase. Thus, losartan modulated approach-avoidance motivation and emotional salience during social punishment versus social reward via modulating distinct core nodes of the midbrain-striato-frontal circuits. The findings document a modulatory role of the renin-angiotensin system in these circuits and associated social processes, suggesting a promising treatment target to alleviate social dysregulations.SIGNIFICANCE STATEMENTSocial deficits and anhedonia characterize several mental disorders and have been linked to the midbrain-striato-frontal circuits of the brain. Based on initial findings from animal models we here combine the pharmacological blockade of the Angiotensin II type 1 receptor (AT1R) via losartan with functional MRI (fMRI) to demonstrate that AT1R blockade enhances the motivational salience of social rewards and attenuates the negative impact of social punishment via modulating the communication in the midbrain-striato-frontal circuits in humans. The findings demonstrate for the first time an important role of the AT1R in social reward processing in humans and render the AT1R as promising novel treatment target for social and motivational deficits in mental disorders.
تدمد: 1529-2401
0270-6474
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1389b6d49d2f7254c55245fbba991ef0
https://doi.org/10.1523/jneurosci.1114-22.2022
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....1389b6d49d2f7254c55245fbba991ef0
قاعدة البيانات: OpenAIRE