» Articles » PMID: 38671147

Alterations in Adolescent Brain Serotonin (5HT), 5HT, and Dopamine (D) Receptor Systems in a Nonhuman Primate Model of Early Life Adversity

Overview
Date 2024 Apr 26
PMID 38671147
Authors
Affiliations
Soon will be listed here.
Abstract

Stress affects brain serotonin (5HT) and dopamine (DA) function, and the effectiveness of 5HT and DA to regulate stress and emotional responses. However, our understanding of the long-term impact of early life adversity (ELA) on primate brain monoaminergic systems during adolescence is scarce and inconsistent. Filling this gap in the literature is critical, given that the emergence of psychopathology during adolescence has been related to deficits in these systems. Here, we use a translational nonhuman primate (NHP) model of ELA (infant maltreatment by the mother) to examine the long-term impact of ELA on adolescent 5HT, 5HT and D receptor systems. These receptor systems were chosen based on their involvement in stress/emotional control, as well as reward and reinforcement. Rates of maternal abuse, rejection, and infant's vocalizations were obtained during the first three postnatal months, and hair cortisol concentrations obtained at 6 months postnatal were examined as early predictors of binding potential (BP) values obtained during adolescence using positron emission tomography (PET) imaging. Maltreated animals demonstrated significantly lower 5HT receptor BP in prefrontal cortical areas as well as the amygdala and hippocampus, and lower 5HT receptor BP in striatal and prefrontal cortical areas. Maltreated animals also demonstrated significantly lower D BP in the amygdala. None of the behavioral and neuroendocrine measurements obtained early in life predicted any changes in BP data. Our findings suggest that early caregiving experiences regulate the development of brain 5HT and DA systems in primates, resulting in long-term effects evident during adolescence.

Citing Articles

Cannabinoids and monoaminergic system: implications for learning and memory.

Zhao S, Gu Z, Yue Y, Zhang X, Dong Y Front Neurosci. 2024; 18:1425532.

PMID: 39206116 PMC: 11349573. DOI: 10.3389/fnins.2024.1425532.

References
1.
Denys D, van der Wee N, Janssen J, de Geus F, Westenberg H . Low level of dopaminergic D2 receptor binding in obsessive-compulsive disorder. Biol Psychiatry. 2004; 55(10):1041-5. DOI: 10.1016/j.biopsych.2004.01.023. View

2.
Hoetjes N, van Velden F, Hoekstra O, Hoekstra C, Krak N, Lammertsma A . Partial volume correction strategies for quantitative FDG PET in oncology. Eur J Nucl Med Mol Imaging. 2010; 37(9):1679-87. PMC: 2918791. DOI: 10.1007/s00259-010-1472-7. View

3.
Nash J, Sargent P, Rabiner E, Hood S, Argyropoulos S, Potokar J . Serotonin 5-HT1A receptor binding in people with panic disorder: positron emission tomography study. Br J Psychiatry. 2008; 193(3):229-34. DOI: 10.1192/bjp.bp.107.041186. View

4.
Maes F, Collignon A, Vandermeulen D, Marchal G, Suetens P . Multimodality image registration by maximization of mutual information. IEEE Trans Med Imaging. 1997; 16(2):187-98. DOI: 10.1109/42.563664. View

5.
Christian B, Vandehey N, Fox A, Murali D, Oakes T, Converse A . The distribution of D2/D3 receptor binding in the adolescent rhesus monkey using small animal PET imaging. Neuroimage. 2008; 44(4):1334-44. PMC: 2649779. DOI: 10.1016/j.neuroimage.2008.10.020. View