Abstract

Accumulation of alpha‐synuclein protein aggregates is the hallmark neuropathologic feature of synucleinopathies such as Parkinson’s disease. Rare point mutations and multiplications in SNCA, the gene encoding alpha‐synuclein, as well as other genetic alterations are linked to familial Parkinson’s disease cases with high penetrance and hence constitute major genetic risk factors for Parkinson’s disease. However, the preponderance of cases seems sporadic, most likely based on a complex interplay between genetic predispositions, aging processes and environmental influences. Deciphering the impact of these environmental factors and their interactions with the individual genetic background in humans is challenging and often requires large cohorts, complicated study designs, and longitudinal set‐ups. In contrast, rodent models offer an ideal system to study the influence of individual environmental aspects under controlled genetic background and standardized conditions. In this review, we highlight findings from studies examining effects of environmental enrichment mimicking stimulation of the brain by its physical and social surroundings as well as of environmental stressors on brain health in the context of Parkinson’s disease. We discuss possible internal molecular transducers of such environmental cues in Parkinson’s disease rodent models and emphasize their potential in developing novel avenues to much‐needed therapies for this still incurable disease. This article is part of the Special Issue “Synuclein”

Highlights

  • Alpha-synuclein (a-syn) is a key presynaptic protein in Parkinson’s disease (PD) and other synucleinopathies

  • Misfolding and aggregation of a-syn is a central event in synucleinopathies, and the presence of eosinophilic intracellular inclusions that contain abundant levels of a-syn reflects the main neuropathological hallmark of these diseases, known as Lewy pathology (Spillantini et al, 1997; Spillantini et al, 1998; Shults, 2006)

  • Given the central role for a-syn in PD pathogenesis, a-syn transgenic models have emerged as valuable models in PD research and are well suited to study the role of environmental factors in disease unfolding

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Summary

Using animal models to study environmental impacts

Studying the role of environmental exposures and their interaction with the individual’s genetic background in humans is challenging and often requires large cohorts, complicated study designs, and long follow-ups (years or even decades). As an alternative strategy, studying the impact of environmental modulation in disease models offers advantages with respect to I. Trace the interaction between specific genetic features and environmental exposures. Rodent models are suitable to decipher the impact of environmental factors in PD as toxin-induced as well as genetic models mimic the disease. Given the central role for a-syn in PD pathogenesis, a-syn transgenic models have emerged as valuable models in PD research and are well suited to study the role of environmental factors in disease unfolding. We will focus on environmental enrichment, as a factor with protective impact on PD, and environmental stress, as a factor proposed to increase the risk of PD, and discuss the possible internal molecular transducers of such environmental influences in PD

Physical activity and environmental enrichment
Increased brain neurotrophins
Environmental enrichment and brain degeneration
Environmental enrichment in PD models
Environmental stress and brain health
Environmental stress and neurodegeneration
Environmental stress in PD models
Conclusion and outlook
Acknowledgments and conflict of interest disclosure
Full Text
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