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The S1P1 regulator IMMH002 and its therapeutic effect and mechanism on autoimmune hepatitis
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Chun-yu ZHANG1, 2, Nan XIANG2, 3, Shu-ying LI2, Xiao-guang CHEN2, *, Jing JIN2, *, Tai-gang LIANG1, *
Acta Pharmaceutica Sinica | 2023, 58(12) : 3608 - 3618
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Acta Pharmaceutica Sinica | 2023, 58(12): 3608-3618
The S1P1 regulator IMMH002 and its therapeutic effect and mechanism on autoimmune hepatitis
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Chun-yu ZHANG1, 2, Nan XIANG2, 3, Shu-ying LI2, Xiao-guang CHEN2, *, Jing JIN2, *, Tai-gang LIANG1, *
Affiliations
  • 1. School of Pharmaceutical Science, Medicinal Basic Research Innovation Center of Chronic Kidney Disease, Ministry of Education, Shanxi Medical University, Taiyuan 030001, China
  • 2. State Key Laboratory of Bioactive Substances and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China
  • 3. Key Laboratory of Molecular Pharmacology and Drug Evaluation (Yantai University), Ministry of Education, Collaborative Innovation Center of Advanced Drug Delivery System and Biotech Drugs in Universities of Shandong, Yantai University, Yantai 264005, China
Published: 2023-12-12 doi: 10.16438/j.0513-4870.2023-1197
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This study assessed and explored the pharmacological effects and mechanisms of action of IMMH002 {2-amino-2-(2-(4ʹ-(2-ethyloxazol-4-yl)-[1, 1ʹ-biphenyl]-4-yl)ethyl)propane-1, 3-dio}, a selective sphingosine-1-phosphate receptor subtype 1 (S1P1) modulator, in a concanavalin A (ConA)-induced autoimmune hepatitis (AIH) mouse model. The experimental protocol strictly adhered to the guidelines of the Ethics Committee for Animal Research of the Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College (Approval No.: 00004046). Male ICR mice were pre-treated with the drug for four days, followed by induction of AIH through tail vein injection of ConA protein. Liver function, hepatic tissue pathology, peripheral blood parameters, as well as immunoglobulin G (IgG), inflammatory cytokines, T cell distribution, and inflammatory pathways were evaluated in mice. Results demonstrated that IMMH002 significantly reduced liver function indicators such as alanine aminotransferase (ALT) and aspartate aminotransferase (AST), alleviated hepatic tissue inflammation and necrotic damage, decreased serum IgG levels, and lowered the expression of inflammatory mediators including interleukin 6 (IL-6), tumor necrosis factor α (TNF-α), interleukin 1β (IL-1β), and interferon γ (IFN-γ). Additionally, it facilitated T lymphocyte homing, downregulated the phosphorylation of nuclear factor kappa-B (NF-κB), IκB kinase β (IKKβ) and nuclear factor inhibitor protein-α (IκBα) proteins in hepatic tissue and cellular inflammation models. Collectively, IMMH002 effectively ameliorated ConA-induced autoimmune hepatitis in mice, exhibiting extensive anti-inflammatory and anti-necrotic effects, thereby laying a theoretical foundation for AIH clinical treatment.

autoimmune hepatitis  /  sphingosine-1-phosphate receptor subtype 1  /  2-amino-2-(2-(4ʹ-(2-ethyloxazol-4-yl)-[1, 1ʹ-biphenyl]-4-yl)ethyl)propane-1, 3-dio  /  liver injury  /  lymphocyte homing
Chun-yu ZHANG, Nan XIANG, Shu-ying LI, Xiao-guang CHEN, Jing JIN, Tai-gang LIANG. The S1P1 regulator IMMH002 and its therapeutic effect and mechanism on autoimmune hepatitis[J]. Acta Pharmaceutica Sinica, 2023 , 58 (12) : 3608 -3618 . DOI: 10.16438/j.0513-4870.2023-1197
Year 2023 volume 58 Issue 12
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Article Info
doi: 10.16438/j.0513-4870.2023-1197
  • Receive Date:2023-10-23
  • Online Date:2025-11-21
  • Published:2023-12-12
Article Data
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History
  • Received:2023-10-23
  • Revised:2023-11-13
Funding
Affiliations
    1. School of Pharmaceutical Science, Medicinal Basic Research Innovation Center of Chronic Kidney Disease, Ministry of Education, Shanxi Medical University, Taiyuan 030001, China
    2. State Key Laboratory of Bioactive Substances and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China
    3. Key Laboratory of Molecular Pharmacology and Drug Evaluation (Yantai University), Ministry of Education, Collaborative Innovation Center of Advanced Drug Delivery System and Biotech Drugs in Universities of Shandong, Yantai University, Yantai 264005, China
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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

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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