Publications by authors named "J Mattison"

Article Synopsis
  • Oxytocin is being studied as a potential treatment for psychostimulant use disorders, particularly its effects on dopamine signaling in the striatum, a brain region linked to natural rewards.
  • In a study involving male rhesus macaques, oxytocin was administered both intranasally and intravenously before administering methylphenidate, a stimulant similar to cocaine, and the impacts on dopamine release were monitored.
  • Results showed that oxytocin significantly decreased dopamine release in the dorsal striatum when stimulated by methylphenidate, suggesting oxytocin may be useful in treating addictions to psychostimulants.
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Aquaporin-1 (AQP1) is a highly conserved water-channel protein, found to be expressed by astrocytes in adult humans and non-human primates (NHPs). Upregulation of cortical AQP1 expression occurs with cancer, injury, and neurodegenerative disease, but minimal information is available about the effects of normative aging on AQP1 expression. This study leverages tissues from the oldest-old rhesus macaques, some greater than 40 years of age, from the National Institute on Aging longitudinal study of caloric restriction (CR).

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There is a critical need to generate age- and sex-specific survival curves to characterize chronological aging consistently across nonhuman primates (NHP) used in biomedical research. Sex-specific Kaplan-Meier survival curves were computed in 12 translational aging models: baboon, bonnet macaque, chimpanzee, common marmoset, coppery titi monkey, cotton-top tamarin, cynomolgus macaque, Japanese macaque, pigtail macaque, rhesus macaque, squirrel monkey, and vervet/African green. After employing strict inclusion criteria, primary results are based on 12,269 NHPs that survived to adulthood and died of natural/health-related causes.

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The brain of higher organisms, such as nonhuman primates, is particularly rich in lipids, with a gray to white matter ratio of approximately 40 to 60%. White matter primarily consists of lipids, and during normal aging, it undergoes significant degeneration due to myelin pathology, which includes structural abnormalities, like sheath splitting, and local inflammation. Cognitive decline in normal aging, without neurodegenerative diseases, is strongly linked to myelin pathology.

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