The number (Bmax) and affinity (Kd) of [3H] spiroperidol binding sites in the cerebral cortex, striatum and hypothalamus of 2-, 10- and 22-month old male Wistar rats (20 rats per group) injected i. p. for 10 days with saline, L-DOPA (250 mg/kg) or haloperidol (1 mg/kg) were determined in the presence of 10(-6) M unlabelled haloperidol. The Bmax values in the three brain structures studied decreased with aging in both controls and L-DOPA- or haloperidol-treated rats. The Kd values increased with age. That specific [3H] spiroperidol binding was determined through displacement of the labelled ligand by haloperidol suggested that an age-related loss of dopamine receptors occurred in the brain structures studied. However, considering the fact that in the cerebral cortex [3H] spiroperidol labels a subclass of serotonin receptors (5-HT2) rather than DA receptors, the present results, particularly those concerning the cerebral cortex, suggest an age-related decrease also in the number of 5-HT receptors in this cerebral structure.
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Front Public Health
January 2024
Behavioral Neuropharmacology and Neuroimaging Laboratory on Addictions (BNNLA), Research Institute on Addictions, Department of Pharmacology and Toxicology, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, NY, United States.
Background: Previous research has outlined the health benefits of exercise including its therapeutic potential for substance use disorders (SUD). These data have already been utilized and it is now common to find exercise as part of SUD treatment and relapse prevention programs. However, we need to better understand different exercise regimens and determine which would be the most beneficial for SUDs.
View Article and Find Full Text PDFInhal Toxicol
January 2023
Departamento de Toxicología, Centro de Investigación y de Estudios Avanzados del IPN, Ciudad de México, Mexico.
Alterations in dopaminergic transmission are associated with neurological disorders, such as depression, autism, and Parkinson's disease. Exposure of rats to ambient fine (FP) or ultrafine (UFP) particles induces oxidative and inflammatory responses in the striatum, a neuronal nucleus with dense dopaminergic innervation and critically involved in the control of motor activity. We used an system to evaluate the effect of inhalation exposure to FP and UFP on motor activity and dopaminergic transmission.
View Article and Find Full Text PDFEur J Pharmacol
June 2022
Department of Biotechnological and Applied Clinical Sciences, University of L'Aquila, L'Aquila, 67100, Italy. Electronic address:
(+)-4-Propyl-9-hydroxynaphthoxazine ((+)PHNO) is a high affinity, preferential dopamine D versus D agonist employed in view of its high specificity and excellent signal-to-noise ratio as a radiotracer for positron emission tomography (PET) imaging. Surprisingly, its profile at other classes of monoamine receptor remains undocumented. In addition to hD and hD receptors, (+)PHNO revealed high affinity at hD but not hD or hD receptors.
View Article and Find Full Text PDFJ Chem Neuroanat
December 2021
School of Studies in Neuroscience, Jiwaji University, Gwalior 474011, India. Electronic address:
Early-life viral infections critically influence the brain development and have been variously reported to cause neuropsychiatric diseases such as Schizophrenia, Parkinson's diseases, demyelinating diseases, etc. To investigate the alterations in the dopaminergic system, myelination and associated behavioral impairments following neonatal viral infection, the viral immune activation model was created by an intraperitoneal injection of Poly I:C (5 mg/kg bw/ip) to neonatal rat pups on PND-7. The DA-D2 receptor binding was assessed in corpus striatum by using H-Spiperone at 3, 6 and 12 weeks of age.
View Article and Find Full Text PDFSci Rep
August 2018
Institute of Pharmaceutical and Medicinal Chemistry, Heinrich Heine University Düsseldorf, Duesseldorf, Germany.
The dissociation behaviours of aripiprazole and cariprazine at the human D and D receptor are evaluated. A potential correlation between kinetics and in vivo profiles, especially cariprazine's action on negative symptoms in schizophrenia, is investigated. The binding kinetics of four ligands were indirectly evaluated.
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