Risperidone administered during adolescence induced metabolic, anatomical and inflammatory/oxidative changes in adult brain: A PET and MRI study in the maternal immune stimulation animal model Articles uri icon

authors

  • CASQUERO VEIGA, MARTA
  • GARCIA GARCIA, DAVID
  • MACDOWELL, KARINA S.
  • PEREZ CABALLERO, LAURA
  • TORRES SANCHEZ, SONIA
  • FRAGUAS, DAVID
  • BERROCOSO, ESTHER
  • LEZA, JUAN C.
  • ARANGO, CELSO
  • DESCO MENENDEZ, MANUEL
  • SOTO MONTENEGRO, Mª LUISA

publication date

  • July 2019

start page

  • 880

end page

  • 896

issue

  • 7

volume

  • 29

International Standard Serial Number (ISSN)

  • 0924-977X

Electronic International Standard Serial Number (EISSN)

  • 1873-7862

abstract

  • Inflammation and oxidative stress (IOS) are considered key pathophysiological elements in the development of mental disorders. Recent studies demonstrated that the antipsychotic risperidone elicits an antiinflammatory effect in the brain. We administered risperidone for 2-weeks at adolescence to assess its role in preventing brain-related IOS changes in the maternal immune stimulation (MIS) model at adulthood. We also investigated the development of volumetric and neurotrophic abnormalities in areas related to the HPA-axis. Poly I:C (MIS) or saline (Sal) were injected into pregnant Wistar rats on GD15. Male offspring received risperidone or vehicle daily from PND35-PND49. We studied 4 groups (8&#-15 animals/group): Sal-vehicle, MIS-vehicle, Sal-risperidone and MIS-risperidone. [18F]FDG-PET and MRI studies were performed at adulthood and analyzed using SPM12 software. IOS and neurotrophic markers were measured using WB and ELISA assays in brain tissue. Risperidone elicited a protective function of schizophrenia-related IOS deficits. In particular, risperidone elicited the following effects: reduced volume in the ventricles and the pituitary gland; reduced glucose metabolism in the cerebellum, periaqueductal gray matter, and parietal cortex; higher FDG uptake in the cingulate cortex, hippocampus, thalamus, and brainstem; reduced NFkappaB activity and iNOS expression; and increased enzymatic activity of CAT and SOD in some brain areas. Our study suggests that some schizophrenia-related IOS changes can be prevented in the MIS model. It also stresses the need to search for novel strategies based on anti-inflammatory compounds in risk populations at early stages in order to alter the course of the disease

keywords

  • dopamine antagonist; fdg-pet; inflammation/oxidonitrosative stress; poly i:c; risperidone; schizophrenia