Publications by authors named "J W A Sijbesma"

Reducing proteinuria is a crucial approach in preventing kidney function loss. Previous preclinical studies indicated that caloric restriction (CR) imposed at a young age protects against age-related proteinuria. However, these studies have not explored CR in established renal disease.

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Background: The apolipoprotein E-deficient (apoE) mouse is a well-established model for studying atherosclerosis. However, its small size limits its use in longitudinal positron emission tomography (PET) imaging studies. Recently, the apoE rat has emerged as an alternative.

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Fluorine-18-fluorodeoxyglucose ([F]FDG) positron emission tomography (F-FDG-PET) is widely used for the detection of inflammatory and infectious diseases. Although this modality has proven to be a useful diagnostic tool, reliable distinction of bacterial infection from sterile inflammation or even from a malignancy remains challenging. Therefore, there is a need for bacteria-specific tracers for PET imaging that facilitate a reliable distinction of bacterial infection from other pathology.

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Article Synopsis
  • Adenosine A and dopamine D receptors in the basal ganglia work together to influence motor skills and mental health, and this study investigates how the A receptor affects D receptor binding using PET imaging in rats.
  • Researchers conducted dynamic scans of healthy male Wistar rats before and after giving an A agonist, CGS21680, to see if it changes D receptor availability.
  • The results indicated that CGS21680 possibly lowers D receptor availability in the striatum, whereas the A antagonist KW6002 did not have a significant effect.
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: Parkinson's disease (PD) is a neurodegenerative disorder characterized by motor dysfunction and a diverse range of nonmotor symptoms. Functional relationships between the dopaminergic and histaminergic systems suggest that dual-action pharmaceuticals like AG-0029 (D/D agonist/H antagonist) could ameliorate both the motor and cognitive symptoms of PD. The current study aimed to demonstrate the interaction of AG-0029 with its intended targets in the mammalian brain using positron emission tomography (PET).

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