Effects of Dictyophora polysaccharide on cerebellar Purkinje cell degeneration in a chronic alcohol mouse model

Jian Zhang , Zhihui Dai , Huanhuan Yu , Baofei Sun , Jiuyang Ding , Yuanhe Wang

Animal Models and Experimental Medicine ›› 2025, Vol. 8 ›› Issue (9) : 1656 -1666.

PDF
Animal Models and Experimental Medicine ›› 2025, Vol. 8 ›› Issue (9) : 1656 -1666. DOI: 10.1002/ame2.70021
ORIGINAL ARTICLE

Effects of Dictyophora polysaccharide on cerebellar Purkinje cell degeneration in a chronic alcohol mouse model

Author information +
History +
PDF

Abstract

Background: Recent research showed that the NLRP3 inflammasome was activated in the central nervous system of mice administered chronic ethanol (EtOH). Dictyophora polysaccharides (DIPs) are essential components of the valuable edible fungus Dictyophora, which has antioxidant properties that can delay the aging process of the body. This study aimed to investigate the roles of NLRP3 in chronic EtOH-induced cerebellar Purkinje cell (PC) degeneration and behavioral changes.

Methods: C57BL/6J normal and NLRP3 knockout mice were exposed to EtOH for 14 days. Dictyophora polysaccharide (DIP) and NLRP3 inhibitor were administered to the EtOH mice. The pathology and NLRP3-ASC-caspase-1 signaling pathway proteins were analyzed in EtOH mice cerebellar tissues and behavioral performance was assessed in the mice.

Results: In the EtOH mouse model, we observed increases in the NLRP3 inflammasome proteins, including NLRP3, ASC, caspase-1, mature IL-1β and pro IL-1β, loss of PCs, and motor coordination disorders. We found that DIPs could suppress the NLRP3-ASC-caspase-1 signaling pathway, and alleviate the motor deficits and cerebellar pathological changes in chronic EtOH mice. Next, we used MCC950, a NLRP3 inhibitor, and an NLRP3 knockout strategy to further verify the effects of NLRP3-ASC-caspase-1 signaling in chronic EtOH mice. MCC950 or NLRP3 knockout alleviated the EtOH-induced latency to decreases in fall time, increases in stride width and decreases in stride length. MCC950 or NLRP3 knockout also attenuated PC number loss and suppressed NLRP3 inflammation induced by EtOH. Taken together, pharmacologically or genetically inhibiting NLRP3 alleviated EtOH-induced cerebellar degeneration and behavioral deficits.

Conclusion: These findings indicated that DIPs might diminish EtOH-induced cerebellar degeneration and behavioral deficits through the NLRP3-ASC-caspase-1 signaling pathway, which provides a potential therapeutic target for the prevention and treatment of alcoholism and EtOH-induced cerebellar pathology.

Keywords

alcohol / cerebellum / Dictyophora polysaccharides / inflammasome / motor deficit

Cite this article

Download citation ▾
Jian Zhang, Zhihui Dai, Huanhuan Yu, Baofei Sun, Jiuyang Ding, Yuanhe Wang. Effects of Dictyophora polysaccharide on cerebellar Purkinje cell degeneration in a chronic alcohol mouse model. Animal Models and Experimental Medicine, 2025, 8(9): 1656-1666 DOI:10.1002/ame2.70021

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Rocco A, Compare D, Angrisani D, Sanduzzi Zamparelli M, Nardone G. Alcoholic disease: liver and beyond. World J Gastroenterol. 2014; 20(40): 14652-14659.

[2]

Roerecke M, Rehm J. Alcohol consumption, drinking patterns, and ischemic heart disease: a narrative review of meta-analyses and a systematic review and meta-analysis of the impact of heavy drinking occasions on risk for moderate drinkers. BMC Med. 2014; 12: 182.

[3]

Mukherjee S. Alcoholism and its effects on the central nervous system. Curr Neurovasc Res. 2013; 10(3): 256-262.

[4]

Egervari G, Siciliano CA, Whiteley EL, Ron D. Alcohol and the brain: from genes to circuits. Trends Neurosci. 2021; 44(12): 1004-1015.

[5]

Cohen SM, DePhilippis D, Deng Y, et al. Perspectives on contingency management for alcohol use and alcohol-associated conditions among people in care with HIV. Alcohol Clin Exp Res (Hoboken). 2023; 47(9): 1783-1797.

[6]

Deng W, Jin L, Zhuo H, Vasiliou V, Zhang Y. Alcohol consumption and risk of stomach cancer: a meta-analysis. Chem Biol Interact. 2021; 336: 109365.

[7]

Gonzalez-Palacios S, Compan-Gabucio LM, Torres-Collado L, et al. The protective effect of dietary folate intake on gastric cancer is modified by alcohol consumption: a pooled analysis of the StoP consortium. Int J Cancer. 2024; 155: 1367-1375.

[8]

Urvalek AM, Osei-Sarfo K, Tang XH, Zhang T, Scognamiglio T, Gudas LJ. Identification of ethanol and 4-Nitroquinoline-1-oxide induced epigenetic and oxidative stress markers during Oral cavity carcinogenesis. Alcohol Clin Exp Res. 2015; 39(8): 1360-1372.

[9]

Lin X, Wang H, Zou L, et al. The NRF2 activator RTA-408 ameliorates chronic alcohol exposure-induced cognitive impairment and NLRP3 inflammasome activation by modulating impaired mitophagy initiation. Free Radic Biol Med. 2024; 220: 15-27.

[10]

Ding J, Shen L, Ye Y, et al. Inflammasome inhibition prevents motor deficit and cerebellar degeneration induced by chronic methamphetamine administration. Front Mol Neurosci. 2022; 15: 861340.

[11]

Amin-Esmaeili M, Farokhnia M, Susukida R, et al. Reduced drug use as an alternative valid outcome in individuals with stimulant use disorders: findings from 13 multisite randomized clinical trials. Addiction. 2024; 119(5): 833-843.

[12]

Deng C, Fu H, Xu J, Shang J, Cheng Y. Physiochemical and biological properties of phosphorylated polysaccharides from Dictyophora indusiata. Int J Biol Macromol. 2015; 72: 894-899.

[13]

Wang G, Zuo P, Ding K, et al. Intervention study of Dictyophora polysaccharides on arsenic-induced liver fibrosis in SD rats. Biomed Res Int. 2022; 2022: 7509620.

[14]

Chatterton BJ, Nunes PT, Savage LM. The effect of chronic ethanol exposure and thiamine deficiency on myelin-related genes in the cortex and the cerebellum. Alcohol Clin Exp Res. 2020; 44(12): 2481-2493.

[15]

Jung ME. Alcohol withdrawal and cerebellar mitochondria. Cerebellum. 2015; 14(4): 421-437.

[16]

Niedzwiedz-Massey VM, Douglas JC, Rafferty T, Kane CJM, Drew PD. Ethanol effects on cerebellar myelination in a postnatal mouse model of fetal alcohol spectrum disorders. Alcohol. 2021; 96: 43-53.

[17]

Nobrega C, Nascimento-Ferreira I, Onofre I, et al. Silencing mutant ataxin-3 rescues motor deficits and neuropathology in Machado-Joseph disease transgenic mice. PLoS One. 2013; 8(1): e52396.

[18]

Sugimoto H, Kawakami K. Low-cost protocol of footprint analysis and hanging box test for mice applied the chronic restraint stress. J Vis Exp. 2019; 143: 23-35.

[19]

Deacon RM. Measuring motor coordination in mice. J Vis Exp. 2013; 75: e2609.

[20]

Ding J, Hu S, Meng Y, et al. Alpha-Synuclein deficiency ameliorates chronic methamphetamine induced neurodegeneration in mice. Toxicology. 2020; 438: 152461.

[21]

Wallace K, Veerisetty S, Paul I, May W, Miguel-Hidalgo JJ, Bennett W. Prenatal infection decreases calbindin, decreases Purkinje cell volume and density and produces long-term motor deficits in Sprague-Dawley rats. Dev Neurosci. 2010; 32(4): 302-312.

[22]

Al-Kharashi L, Attia H, Alsaffi A, et al. Pentoxifylline and thiamine ameliorate rhabdomyolysis-induced acute kidney injury in rats via suppressing TLR4/NF-kappaB and NLRP-3/caspase-1/gasdermin mediated-pyroptosis. Toxicol Appl Pharmacol. 2023; 461: 116387.

[23]

de Carvalho Ribeiro M, Szabo G. Role of the Inflammasome in liver disease. Annu Rev Pathol. 2022; 17: 345-365.

[24]

Liu J, Li X, Ding L, Li W, Niu X, Gao D. GRK2 participation in cardiac hypertrophy induced by isoproterenol through the regulation of Nrf2 signaling and the promotion of NLRP3 inflammasome and oxidative stress. Int Immunopharmacol. 2023; 117: 109957.

[25]

Solopov PA, Colunga Biancatelli RML, Catravas JD. Alcohol increases lung angiotensin-converting enzyme 2 expression and exacerbates severe acute respiratory syndrome coronavirus 2 spike protein subunit 1-induced acute lung injury in K18-hACE2 transgenic mice. Am J Pathol. 2022; 192(7): 990-1000.

[26]

Yu C, Chen P, Miao L, Di G. The role of the NLRP3 Inflammasome and programmed cell death in acute liver injury. Int J Mol Sci. 2023; 24(4): 1-20.

[27]

Munshi S, Albrechet-Souza L, Dos-Santos RC, et al. Acute ethanol modulates synaptic inhibition in the basolateral amygdala via rapid NLRP3 Inflammasome activation and regulates anxiety-like behavior in rats. J Neurosci. 2023; 43(47): 7902-7912.

[28]

Priyanka SH, Thushara AJ, Rauf AA, Indira M. Alcohol induced NLRP3 inflammasome activation in the brain of rats is attenuated by ATRA supplementation. Brain Behav Immun Health. 2020; 2: 100024.

[29]

Zhang J, Hu T, Wang Y, et al. Investigating the neurotoxic impacts of arsenic and the neuroprotective effects of Dictyophora polysaccharide using SWATH-MS-based proteomics. Molecules. 2022; 27(5): 1-21.

[30]

Zhang X, Yang H, Wang Y, et al. Proteomic study on the mechanism of arsenic neurotoxicity in the rat cerebral cortex and the protective mechanism of Dictyophora polysaccharides against arsenic neurotoxicity. ACS Chem Neurosci. 2023; 14(12): 2302-2319.

[31]

Mohammadi R, Heidari MH, Sadeghi Y, Abdollahifar MA, Aghaei A. Evaluation of the spatial arrangement of Purkinje cells in ataxic rat's cerebellum after Sertoli cells transplantation. Folia Morphol (Warsz). 2018; 77(2): 194-200.

[32]

Todd D, Clapp M, Dains P, Karacay B, Bonthius DJ. Purkinje cell-specific deletion of CREB worsens alcohol-induced cerebellar neuronal losses and motor deficits. Alcohol. 2022; 101: 27-35.

[33]

Bonthius DJ, Winters Z, Karacay B, Bousquet SL, Bonthius DJ. Importance of genetics in fetal alcohol effects: null mutation of the nNOS gene worsens alcohol-induced cerebellar neuronal losses and behavioral deficits. Neurotoxicology. 2015; 46: 60-72.

RIGHTS & PERMISSIONS

2025 The Author(s). Animal Models and Experimental Medicine published by John Wiley & Sons Australia, Ltd on behalf of The Chinese Association for Laboratory Animal Sciences.

AI Summary AI Mindmap
PDF

15

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/