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The mechanism of MASM in treating multiple sclerosis by regulating astrocyte activation through Wnt5a/FZD5 pathway
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Teng-xiang CHEN, Run-yong LUO, Shi-guo LI, Yi-xing HUANG, Si-fan FU, Xin-wei LI, Xiao-ting LIN, Ruo-ying HU, Li-hong NAN*, Ya-ping CHEN*
Acta Pharmaceutica Sinica | 2026, 61(2) : 515 - 522
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Acta Pharmaceutica Sinica | 2026, 61(2): 515-522
• Original Articles •
The mechanism of MASM in treating multiple sclerosis by regulating astrocyte activation through Wnt5a/FZD5 pathway
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Teng-xiang CHEN, Run-yong LUO, Shi-guo LI, Yi-xing HUANG, Si-fan FU, Xin-wei LI, Xiao-ting LIN, Ruo-ying HU, Li-hong NAN*, Ya-ping CHEN*
Affiliations
  • College of Pharmacy, Fujian University of Traditional Chinese Medicine, Fuzhou 350122, China
Published: 2026-02-12 doi: 10.16438/j.0513-4870.2025-1123
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This study systematically investigated the therapeutic mechanism of matrine derivative, (6aS, 10S, 11aR, 11bR, 11cS)-10-methylaminododecahydro-3a, 7a-diaza-benzo (de) anthracene-8-thione (MASM), in experimental autoimmune encephalomyelitis (EAE) through multi-dimensional analysis. The myelin oligodendrocyte glycoprotein MOG35-55/pertussis toxin-induced EAE mouse model was established, and neurological impairment was confirmed using Kono's 5-point scoring system, mice with scores between 0.5 and 3.5 were considered successful models. These mice were randomly divided into six groups: EAE control, MASM groups (1.5, 3 and 6 mg·kg-1), a positive control group (fingolimod, 1.0 mg·kg-1), and a normal control group. Drug administration was initiated on the day of grouping, once daily for 21 consecutive days. The Kono's score was used to evaluate the neurological function; HE staining and electron microscopy was used to observe the pathological changes of spinal cord; transforming growth factor-β1 and monocyte chemoattractant protein-1 content was detected by ELISA. The gene expression of H2T23 was detected by qRT-PCR, the binding interactions between MASM and human frizzled homolog (FZD5) was evaluated by molecular docking, and protein expression levels of glial fibrillary acidic protein (GFAP), complement 3 (C3), wingless type mouse mammary tumor virus integration site family member 5a (Wnt5a), FZD5, protein kinase Cα (PKCα), and the phosphorylation level of glycogen synthase kinase 3 (GSK3β) were detected by Western blot. MASM significantly improved neurological function, reduced spinal cord inflammation and demyelination, and downregulated astrocyte activation markers (GFAP, C3, H2T23) (P < 0.05, P < 0.01) and Wnt5a/FZD5 pathway components (Wnt5a, FZD5, PKCα, p-GSK3β) (P < 0.05, P < 0.01). MASM demonstrates strong binding capacity to FZD. These findings suggest that MASM alleviates EAE by inhibiting astrocyte polarization via the Wnt5a/FZD5 pathway. The animal study was approved by the Animal Ethics Committee of Fujian University of Traditional Chinese Medicine (approval number: FJTCMIACUC 2023319).

multiple sclerosis  /  experimental autoimmune encephalomyelitis  /  (6aS, 10S, 11aR, 11bR, 11cS)-10-methylaminododecahydro-3a, 7a-diaza-benzo (de) anthracene-8-thione  /  astrocyte  /  Wnt5a/FZD5 pathway
陈腾翔, 罗润永, 李世国, 黄益兴, 傅思凡, 李鑫炜, 林小婷, 胡若莹, 南丽红, 陈亚萍. MASM通过Wnt5a/FZD5途径调控星形胶质细胞活化抗多发性硬化症的机制研究. 药学学报, 2026 , 61 (2) : 515 -522 . DOI: 10.16438/j.0513-4870.2025-1123
Teng-xiang CHEN, Run-yong LUO, Shi-guo LI, Yi-xing HUANG, Si-fan FU, Xin-wei LI, Xiao-ting LIN, Ruo-ying HU, Li-hong NAN, Ya-ping CHEN. The mechanism of MASM in treating multiple sclerosis by regulating astrocyte activation through Wnt5a/FZD5 pathway[J]. Acta Pharmaceutica Sinica, 2026 , 61 (2) : 515 -522 . DOI: 10.16438/j.0513-4870.2025-1123
Year 2026 volume 61 Issue 2
171
86
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doi: 10.16438/j.0513-4870.2025-1123
  • Receive Date:2025-09-19
  • Online Date:2026-09-21
  • Published:2026-02-12
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  • Received:2025-09-19
  • Revised:2025-12-03
Affiliations
    College of Pharmacy, Fujian University of Traditional Chinese Medicine, Fuzhou 350122, China
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表12种不同金属材料的力学参数
科
Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)
属
Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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