Amphetamine-induced dopamine (DA) release in the caudate-putamen of adult rats was compared with that in the 35-36-day-old and 21-22-day-old rat pup, using in vivo voltammetry. In the adult and 35-36-day groups, 1.0 mg/kg amphetamine (AMP) produced a significant increase in DA release, while 0.1 mg/kg produced no significant change in DA release. In the 21-22-day group, 1.0 mg/kg AMP produced a slight increase, followed immediately by a significant decrease in DA release. Similarly, at a dose of 0.1 mg/kg, AMP produced a significant decrease in DA release. This decrease was greater than that seen after the 1.0 mg/kg dose of AMP. Tyramine produced no significant change in DA release, however, it served as a control for peripheral cardiovascular effects. These data suggest that AMP-induced DA release in the caudate-putamen is mature by postnatal day 35. The AMP-induced decrease in DA release found in the 21-22-day group is not due to either the cardiovascular effects of AMP or to a depletion of DA content. This decrease in neostriatal DA release may be due to a decrease in the neuronal firing of nigrostriatal DA neurons that is caused by an AMP-induced increase in dendritic DA release in the substantia nigra, exerting an inhibitory effect through DA autoreceptors.
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Synapse
January 2025
Department of Science, De La Salle College, Institute of the Brothers of the Christian Schools, Toronto, Ontario, Canada.
Alcohol consumption is known to affect dopamine (DA) release in the brain, with significant implications for understanding addiction and its neurobiological underpinnings. This meta-analysis examined the effects of acute alcohol administration on striatal DA release in healthy humans as measured with [C]-raclopride positron emission tomography (PET). Oral alcohol administration was associated with a significant reduction in [C]-raclopride binding potential (BP) in the ventral striatum (Cohen's d = -0.
View Article and Find Full Text PDFInt J Neuropsychopharmacol
December 2024
Department of Neuroscience, Georgetown University Medical Center, Washington, District of Columbia, USA.
Eur J Neurosci
December 2024
University of Iowa, USA.
17β-Estradiol (E2) is a sex hormone that acts on many brain regions to produce changes in neuronal activity and learning. A key brain region sensitive to E2 is the dorsal striatum (also called caudate-putamen), which controls motor behaviour, goal-directed learning and habit learning. In adult rodents, oestrogen receptors (ERs) in the dorsal striatum are localized to the plasma membrane and include ERα, ERβ and G protein-coupled ER (GPER).
View Article and Find Full Text PDFJ Control Release
January 2025
HM CINAC (Centro Integral de Neurociencias Abarca Campal), Hospital Universitario HM Puerta del Sur, HM Hospitales, Madrid, Spain; Instituto de Investigación Sanitaria HM Hospitales; CIBERNED (Center for Networked Biomedical Research on Neurodegenerative Diseases), Instituto Carlos III, Madrid, Spain; Facultad HM de Ciencias de la Salud de la Universidad Camilo José Cela, Madrid, Spain. Electronic address:
Low-intensity focused ultrasound (LIFU) combined with intravenously circulating microbubbles has recently emerged as a novel approach for increasing delivery through the blood-brain barrier (BBB). This technique safely and transiently enables therapeutic agents to overcome the BBB, which typically poses a significant obstacle for treatment of brain disorders. However, the full impact of LIFU on the entire neurovascular unit (NVU), as well as the mechanisms and factors involved in restoring BBB integrity still require further elucidation.
View Article and Find Full Text PDFBiol Psychiatry
March 2025
Department of Psychiatry, Yale University School of Medicine, New Haven, Connecticut; The Clinical Neuroscience Research Unit, Connecticut Mental Health Center, New Haven, Connecticut. Electronic address:
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