Abstract

Paraquat (PQ), a widely used herbicide, could cause neurodegenerative diseases, yet the mechanism remains incompletely understood. This study aimed to investigate the direct effect of PQ on NSC in vivo and its possible mechanism. Adult C57BL/6 mice were subcutaneously injected with 2 mg/kg PQ, 20 mg/kg PQ or vehicle control once a week for 2 weeks, and sacrificed 1 week after the last PQ injection. Furthermore, extra experiments with Tauroursodeoxycholic Acid (TUDCA) intervention were performed to observe the relationship between ER stress, neuroinflammation and the neural stem cell (NSC) impairment. The results showed that 20 mg/kg PQ caused the NSC number decrease in both subgranular zones (SGZ) and subventricular zone (SVZ). Further analysis indicated that the 20 mg/kg PQ suppressed the proliferation of NSC, without affecting the apoptosis. Moreover, 20 mg/kg PQ also induced ER stress in microglia and caused neuroinflammation in SGZ and SVZ. Interestingly, the ER stress inhibitor could simultaneously ameliorate the neuroinflammation and NSC reduction. These data suggested that increased ER stress in microglia might be a possible pathway for PQ-induced neuroinflammation and NSC impairment. That is a previously unknown mechanism for PQ neurotoxicity.

Highlights

  • Paraquat (PQ), a widely used herbicide, could cause neurodegenerative diseases, yet the mechanism remains incompletely understood

  • We especially focused on subgranular zones (SGZ) and subventricular zone (SVZ) where neural stem cell (NSC) persist and found that PQ-induced NSC impairment and neuroinflammation, could be restored by an ER stress inhibitor–Tauroursodeoxycholic Acid (TUDCA)[22,23]

  • PQ reduced the number of NSC in SGZ and SVZ

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Summary

Introduction

Paraquat (PQ), a widely used herbicide, could cause neurodegenerative diseases, yet the mechanism remains incompletely understood. The underlying mechanism may be associated with mitochondrial dysfunction, lipid peroxidation, and oxidative stress etc.[2,3,4,5] In line with these data, epidemiological studies reported that PQ could result in cognitive and behavioral impairments and increase the risk of neurodegenerative diseases, such as autism spectrum disorders and Parkinson’s ­disease[6,7,8]. In this context, experimental evidences showed that PQ exposure could cause permanent nerve damage in m­ ice[9,10]. It is necessary to study the relation between PQ-induced inflammatory and NSC in the brain

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