Intranasal lithium in Ryanodex formulation vehicle inhibits inflammation and pyroptosis in aged 5XFAD mice brains

Abstract Background This study investigates the therapeutic versus side effects of intranasal lithium chloride (LiCl) in Ryanodex formulation vehicle (RFV) to inhibit inflammation and pyroptosis and to ameliorate on cognitive dysfunction and depressive behavior in 5XFAD mice. Method 5XFAD and wild type (WT) B6SJLF1/J mice were treated with intranasal or oral LiCl (3 mM/kg) dissolved in RFV starting at 2 or 9 months old and the continuous treatment lasted for 12 weeks. Behavior was examined for depression, cognition, olfaction, and motor function at the ages of 5 or 12 months. Body weights were monitored monthly. At 6 or 13 months old, blood and brain were harvested. Blood biomarkers for thyroid (TSH: thyroid stimulating hormone) and kidney (creatinine) function were measured by ELISA. Immunoblotting determined the proteins expression levels of type 1 InsP 3 receptors (InsP 3 R‐1), oxidative stress (4‐HNE, MDA), pyroptosis activation pathway regulatory proteins, proinflammatory versus neuroprotective cytokines, and synaptic proteins in aged mice brains. Result Compared to WT mice, significant memory loss and depression behavior existed in both adult and aged 5XFAD mice, and both were abolished by intranasal LiCl in RFV Intranasal LiCl in RFV significantly inhibited the pathological proteins increase of InsP 3 R‐1, MDA‐modified proteins by pyroptosis pathway activation proteins (NLRP3, cleaved caspase‐1, N‐terminal GSDMD) in aged 5XFAD mice brains, in comparison with aged WT mice brains. Furthermore, intranasal LiCl in RFV significantly reduced protein levels of cytotoxic cytokines (IL‐1β, IL‐18, IL‐6, TNF‐α), alleviated the activation of astrogliosis and microgliosis, and increased cytoprotective cytokine IL‐10 and inhibited PSD‐95 synapse protein loss in aged 5XFAD mice brain. Intranasal LiCl did not affect blood TSH but significantly inhibited abnormal age‐dependent increase of blood creatinine in 5XFAD mice. Intranasal LiCl in RFV did not affect body weight, smell, or motor function significantly in either WT or 5XFAD mice. Conclusion Intranasal LiCl in RFV ameliorates memory loss and depressive behavior in 5XFAD mice without side effects or organ toxicity, with chronic use. Intranasal LiCl in RFV effectively inhibited, oxidative stress, inflammation and pyroptosis in aged 5XFAD brains.

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Journal
Alzheimer s & Dementia
Published
2024-12-01
DOI
https://doi.org/10.1002/alz.089654
Primary Topic
Pediatric health and respiratory diseases
Type
article
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article

Intranasal lithium in Ryanodex formulation vehicle inhibits inflammation and pyroptosis in aged 5XFAD mice brains

Kunhong Kim, Piplu Bhuiyan, Liang Ge, Jia Liu et al.
Alzheimer s & Dementia
Pediatric health and respiratory diseases
article

Intranasal lithium in Ryanodex formulation vehicle inhibits inflammation and pyroptosis in aged 5XFAD mice brains

Kunhong Kim, Piplu Bhuiyan, Liang Ge, Jia Liu, Wenjia Zhang, Huafeng Wei, Lauren St. Louis, Rebecca Chae, Ying Wang
article en

Abstract

Abstract Background This study investigates the therapeutic versus side effects of intranasal lithium chloride (LiCl) in Ryanodex formulation vehicle (RFV) to inhibit inflammation and pyroptosis and to ameliorate on cognitive dysfunction and depressive behavior in 5XFAD mice. Method 5XFAD and wild type (WT) B6SJLF1/J mice were treated with intranasal or oral LiCl (3 mM/kg) dissolved in RFV starting at 2 or 9 months old and the continuous treatment lasted for 12 weeks. Behavior was examined for depression, cognition, olfaction, and motor function at the ages of 5 or 12 months. Body weights were monitored monthly. At 6 or 13 months old, blood and brain were harvested. Blood biomarkers for thyroid (TSH: thyroid stimulating hormone) and kidney (creatinine) function were measured by ELISA. Immunoblotting determined the proteins expression levels of type 1 InsP 3 receptors (InsP 3 R‐1), oxidative stress (4‐HNE, MDA), pyroptosis activation pathway regulatory proteins, proinflammatory versus neuroprotective cytokines, and synaptic proteins in aged mice brains. Result Compared to WT mice, significant memory loss and depression behavior existed in both adult and aged 5XFAD mice, and both were abolished by intranasal LiCl in RFV Intranasal LiCl in RFV significantly inhibited the pathological proteins increase of InsP 3 R‐1, MDA‐modified proteins by pyroptosis pathway activation proteins (NLRP3, cleaved caspase‐1, N‐terminal GSDMD) in aged 5XFAD mice brains, in comparison with aged WT mice brains. Furthermore, intranasal LiCl in RFV significantly reduced protein levels of cytotoxic cytokines (IL‐1β, IL‐18, IL‐6, TNF‐α), alleviated the activation of astrogliosis and microgliosis, and increased cytoprotective cytokine IL‐10 and inhibited PSD‐95 synapse protein loss in aged 5XFAD mice brain. Intranasal LiCl did not affect blood TSH but significantly inhibited abnormal age‐dependent increase of blood creatinine in 5XFAD mice. Intranasal LiCl in RFV did not affect body weight, smell, or motor function significantly in either WT or 5XFAD mice. Conclusion Intranasal LiCl in RFV ameliorates memory loss and depressive behavior in 5XFAD mice without side effects or organ toxicity, with chronic use. Intranasal LiCl in RFV effectively inhibited, oxidative stress, inflammation and pyroptosis in aged 5XFAD brains.

Alzheimer s & DementiaVol. 20(S6)
University of Pennsylvania (US)
Openalex Percentile: Top 56%
Pediatric health and respiratory diseases
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