Characterizing the protracted neurobiological and neuroanatomical effects of paraquat in a murine model of Parkinson's disease

Neurobiol Aging. 2021 Apr:100:11-21. doi: 10.1016/j.neurobiolaging.2020.11.013. Epub 2020 Nov 26.

Abstract

The primary motor symptoms of Parkinson's disease (PD) result from the degeneration of dopamine-producing neurons of the substantia nigra pars compacta (SNc), and often, the loss is asymmetrical, resulting in unilateral tremor presentation. Notably, age is the primary risk factor for PD, and it is likely that the disease ultimately stems from the impact of environmental factors, which interact with the aging process. Recent research has focused on the role of microglia and pro-oxidative responses in dopaminergic neuronal death. In this study, we sought to examine the neurodegenerative, inflammatory, and stress effects of exposure to the etiologically relevant pesticide, paraquat, over time (up to 6 months after injections). We also were interested in whether a high-resolution, 7-Tesla animal magnetic resonance imaging would be sensitive enough to detect the degenerative impact of paraquat. We found that paraquat induced a loss of dopaminergic SNc neurons and activation of microglia that surprisingly did not change over 6 months after the last injection. A long-lasting reduction was evident for body weight, and alterations in organ (lung and heart) weight were evident, which reflect the peripheral impact of the toxicant. The microglial proinflammatory actin-remodeling factor, WAVE2, along with the inflammatory transcription factor, nuclear factor kappa B were also elevated within the brain. Remarkably, the stress hormone, corticosterone, was still significantly elevated 1 month after paraquat, whereas the inflammasome factor, caspase-1, and antigen presentation factor, MFG-E8, both displayed delayed rises after the 6-month time. Using high-resolution magnetic resonance imaging, we detected no striatal changes but modest hemispheric differences in the SNc and time-dependent volumetric enlargement of the ventricles in paraquat-treated mice. These data suggest that paraquat induces long-term nigrostriatal pathology (possibly asymmetric) and inflammatory changes and stress and trophic/apoptotic effects that appear to either increase with the passage of time or are evident for at least 1 month. In brief, paraquat may be a useful nonspecific means to model widespread stress and inflammatory changes related to PD or age-related disease in general, but not the progressive nature of such diseases.

Keywords: Environmental; MRI; Neurodegeneration; Neuroinflammatory; Parkinson's disease; Toxin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Age Factors
  • Animals
  • Antigens, Surface / metabolism
  • Brain / diagnostic imaging
  • Brain / metabolism
  • Brain / pathology
  • Caspase 1 / metabolism
  • Corticosterone / metabolism
  • Disease Models, Animal*
  • Dopaminergic Neurons / drug effects*
  • Dopaminergic Neurons / pathology
  • Inflammation
  • Magnetic Resonance Imaging
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Milk Proteins / metabolism
  • NF-kappa B / metabolism
  • Paraquat / adverse effects*
  • Parkinson Disease / diagnostic imaging
  • Parkinson Disease / etiology*
  • Pesticides / adverse effects*
  • Protozoan Proteins
  • Wiskott-Aldrich Syndrome Protein Family / metabolism

Substances

  • Antigens, Surface
  • Mfge8 protein, mouse
  • Milk Proteins
  • NF-kappa B
  • Pesticides
  • Protozoan Proteins
  • Wasf2 protein, mouse
  • Wiskott-Aldrich Syndrome Protein Family
  • aginactin protein, Dictyostelium
  • Casp1 protein, mouse
  • Caspase 1
  • Paraquat
  • Corticosterone

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