Repurposing Anakinra for Alzheimer's Disease: The In Vitro and In Vivo Effects of Anakinra on LPS- and AC-Induced Neuroinflammation

被引:1
作者
Retinasamy, Thaarvena [1 ]
Lee, Amber Lot Yee [2 ]
Lee, Hsien Siang [1 ]
Lee, Vanessa Lin Lin [1 ]
Shaikh, Mohd Farooq [1 ,3 ]
Yeong, Keng Yoon [2 ]
机构
[1] Monash Univ Malaysia, Jeffrey Cheah Sch Med & Hlth Sci, Neuropharmacol Res Lab, Bandar Sunway, Selangor, Malaysia
[2] Monash Univ, Sch Sci, Malaysia Campus, Bandar Sunway 47500, Selangor, Malaysia
[3] Charles Sturt Univ, Sch Dent & Med Sci, Orange, NSW 2800, Australia
来源
ACS CHEMICAL NEUROSCIENCE | 2024年 / 15卷 / 18期
关键词
Alzheimer's disease; anakinra; neuroinflammation; oxidative stress; proinflammatory cytokines; INTERLEUKIN-1 RECEPTOR ANTAGONIST; NF-KAPPA-B; NITRIC-OXIDE SYNTHASE; INFLAMMATORY RESPONSES; SIGNALING PATHWAY; ACTIVATION; ACRYLAMIDE; MICROGLIA; NEURONS; BRAIN;
D O I
10.1021/acschemneuro.4c00205
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Alzheimer's disease is a significant global health issue, and studies suggest that neuroinflammation plays a vital role in the advancement of this disease. In this study, anakinra has been shown to display a time- and concentration-dependent antineuroinflammatory effect. In the in vitro studies, it diminished the gene expressions of tumor necrosis factor-alpha (TNF-alpha) and nitric oxide (NO) synthase 2 stimulated by lipopolysaccharide (LPS). Anakinra also reduced the LPS-induced production of NO and reactive oxygen species. Thus, the hypertrophic state of LPS-activated BV2 microglial cells was reversed by anakinra. Furthermore, acrylamide (ACR)-induced activation of nuclear transcription factor-kappa B, TNF-alpha, and interleukin-1 beta was downregulated, while cAMP response element binding protein and brain-derived neurotrophic factor expression levels were markedly enhanced in ACR-treated zebrafish larvae. It was also observed that anakinra improved the uncoordinated swimming behaviors in ACR-exposed zebrafish larvae. Overall, anakinra demonstrated potential antineuroinflammatory and antioxidative effects.
引用
收藏
页码:3298 / 3310
页数:13
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