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Background <p>Parkinson’s disease (PD) is becoming increasingly prevalent worldwide. The pathophysiology of this condition is characterized by oxidative stress, inflammation, iron accumulation, mitochondrial dysfunction, and protein aggregation, all of which contribute to cell death and neurodegeneration. Microglia, the innate immune cells of the brain, play a significant role in the development and progression of PD by releasing inflammatory cytokines upon activation. Essential oils (EOs) are emerging as potential therapeutic agents because of their antioxidant and anti-inflammatory properties.</p> Methods <p>In our study, we investigated the antioxidant, anti-inflammatory, and anti-apoptotic effects of sweet orange [<i>Citrus sinensis</i> (L.) Osbeck (Rutaceae)] EO and its main compound (+)-limonene on monocultures of all-trans retinoic acid-differentiated and 6-hydroxydopamine-induced (6-OHDA) SH-SY5Y cells and bilaminar co-cultures containing differentiated and 6-hydroxydopamine-induced SH-SY5Y cells and BV-2 microglia.</p> Results <p>Sweet orange EO and (+)-limonene significantly decreased reactive oxygen species (ROS) production and increased oxidative stress defense by increasing the total antioxidant capacity and glutathione peroxidase and superoxide dismutase activities in human neuroblastoma (SH-SY5Y) cells. Additionally, both EO and its main compound mitigated inflammation by downregulating the secretion of pro-inflammatory cytokines. They also decreased the cytochrome c levels and caspase-3 activity. Furthermore, sweet orange EO and (+)-limonene attenuated microglia-mediated inflammation in co-cultures, suggesting their potential application as modulators of microglial activity.</p> Conclusions <p>Based on these results, sweet orange EO and its main component, (+)-limonene, can be considered as neuroprotective agents and are promising candidates for complementary therapy in Parkinson’s disease.</p>

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Sweet orange essential oil and (+)-limonene prevent oxidative stress, reduce inflammation, and apoptosis in differentiated SH-SY5Y neuroblastoma/BV-2 microglia co-culture neurodegeneration models

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年12月9日

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  • Edina Pandur,
  • Loretta Heilmann,
  • Margita Szilágyi-Utczás,
  • Tibor Rák,
  • Katalin Sipos,
  • Adrienne Csutak,
  • Györgyi Horváth

摘要

Background

Parkinson’s disease (PD) is becoming increasingly prevalent worldwide. The pathophysiology of this condition is characterized by oxidative stress, inflammation, iron accumulation, mitochondrial dysfunction, and protein aggregation, all of which contribute to cell death and neurodegeneration. Microglia, the innate immune cells of the brain, play a significant role in the development and progression of PD by releasing inflammatory cytokines upon activation. Essential oils (EOs) are emerging as potential therapeutic agents because of their antioxidant and anti-inflammatory properties.

Methods

In our study, we investigated the antioxidant, anti-inflammatory, and anti-apoptotic effects of sweet orange [Citrus sinensis (L.) Osbeck (Rutaceae)] EO and its main compound (+)-limonene on monocultures of all-trans retinoic acid-differentiated and 6-hydroxydopamine-induced (6-OHDA) SH-SY5Y cells and bilaminar co-cultures containing differentiated and 6-hydroxydopamine-induced SH-SY5Y cells and BV-2 microglia.

Results

Sweet orange EO and (+)-limonene significantly decreased reactive oxygen species (ROS) production and increased oxidative stress defense by increasing the total antioxidant capacity and glutathione peroxidase and superoxide dismutase activities in human neuroblastoma (SH-SY5Y) cells. Additionally, both EO and its main compound mitigated inflammation by downregulating the secretion of pro-inflammatory cytokines. They also decreased the cytochrome c levels and caspase-3 activity. Furthermore, sweet orange EO and (+)-limonene attenuated microglia-mediated inflammation in co-cultures, suggesting their potential application as modulators of microglial activity.

Conclusions

Based on these results, sweet orange EO and its main component, (+)-limonene, can be considered as neuroprotective agents and are promising candidates for complementary therapy in Parkinson’s disease.