ArticleGenomic psychiatry : advancing science from genes to society2025
Translating stress systems: corticotropin releasing factor, its receptors, and the dopamine system in nonhuman primate models.
Article in Genomic psychiatry : advancing science from genes to society, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
1 citing paper in PubMed.
- Corticotropin-releasing factor (CRF) in brain aging: from mitochondrial dysfunction to inflammaging.Frontiers in aging neuroscience · 2026Review
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Authors and funding
3 authors.
Funding
Abstract
Stress is a fact of life, affecting organisms from the smallest invertebrates to humans. Mediating the stress system is the ancient neuropeptide, corticotropin releasing factor (CRF), which works as a neuromodulator to alter brain systems and homeostatic responses to stress. In humans, many stress-related psychiatric illnesses are linked to dysregulation of monoamine systems, which have cross-talk with CRF-enriched circuits. In this review, we focus on the CRF and the midbrain dopamine (DA) system, particularly as it relates to the nonhuman primate. While tremendous knowledge of CRF-DA mechanisms has been gleaned from rodent models, treatments for stress-related diseases have been elusive, raising the question of whether higher animal models might be required. Subtle shifts in CRF peptide or CRF receptor localization, and the expansion and complexity of DA neuron populations, may hold some of the keys to understanding long-standing stress effects on the DA system in humans. Our laboratory has especially been interested in laying out the neural architecture of the CRF-DA system interface in the nonhuman primate, as a close anatomic model for human. Using rodent models as a starting point, we describe aspects of this complex system that inform our understanding of CRF-DA interactions, and focus on results that have been, and those that still need to be, translated to nonhuman primate models.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.