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1.
Int Immunopharmacol ; 134: 112183, 2024 Jun 15.
Article in English | MEDLINE | ID: mdl-38705031

ABSTRACT

Psoriasis is a chronic inflammatory skin disease substantially affecting the quality of life, with no complete cure owing to its complex pathogenesis. Cornuside, a major bioactive compound present in Cornus officinalis Sieb. et Zucc., which is a well-known traditional Chinese medicine with a variety of biological and pharmacological activities, such as anti-apoptotic, antioxidant, and anti-inflammatory properties. However, its effects on psoriasis remain unclear. Our preliminary analysis of network pharmacology showed that cornuside may be involved in psoriasis by regulating the inflammatory response and IL-17 signaling pathway. Thus, we investigated the protective role and mechanism of cornuside in the pathogenesis of psoriasis in an imiquimod (IMQ)-induced psoriasis mouse model. In-vivo experiments demonstrated that cornuside-treated mice had reduced skin erythema, scales, thickness, and inflammatory infiltration. The Psoriasis Area Severity Index score was significantly lower than that of the IMQ group. Flow cytometry analysis indicated that cornuside effectively inhibited Th1- and Th17-cell infiltration and promoted aggregation of Th2 cells in skin tissues. Cornuside also inhibited the infiltration of macrophages to the skin. Furthermore, in-vitro experiments indicated that cornuside also decreased the polarization of M1 macrophages and reduced the levels of associated cytokines. Western blotting demonstrated that cornuside suppressed the phosphorylation of c-Jun N-terminal kinase (JNK) and extracellular receptor kinase (ERK) in bone marrow-derived macrophages. Our findings indicate that cornuside has a protective effect against IMQ-induced psoriasis by inhibiting M1 macrophage polarization through the ERK and JNK signaling pathways and modulating the infiltration of immune cells as well as the expression of inflammatory factors.


Subject(s)
Anti-Inflammatory Agents , Imiquimod , Mice, Inbred BALB C , Psoriasis , Skin , Th17 Cells , Animals , Psoriasis/drug therapy , Psoriasis/chemically induced , Psoriasis/immunology , Skin/drug effects , Skin/pathology , Skin/immunology , Anti-Inflammatory Agents/therapeutic use , Anti-Inflammatory Agents/pharmacology , Mice , Th17 Cells/immunology , Th17 Cells/drug effects , Disease Models, Animal , Macrophages/drug effects , Macrophages/immunology , Cornus/chemistry , Humans , Interleukin-17/metabolism , Cytokines/metabolism , Female , Signal Transduction/drug effects , Th1 Cells/immunology , Th1 Cells/drug effects , Male
2.
Environ Sci Pollut Res Int ; 30(26): 68667-68676, 2023 Jun.
Article in English | MEDLINE | ID: mdl-37126176

ABSTRACT

This study uses the green finance reform and innovation pilot zone policy approved by the State Council in 2017 as a quasi-natural experiment to explore whether the implementation of the policy has improved the level of green finance development and environmental quality in Chinese cities at the prefecture level and above. The results show that the green financial reform and innovation pilot zone policy can significantly improve the level of regional green financial development and environmental quality, and the results are robust. Further heterogeneity analysis finds that the green financial reform and innovation pilot zone policy have heterogeneous effects on the level of green financial development and environmental quality in different regions, sizes, environmental regulation intensity, financial development levels, and cities of different administrative levels. Based on this conclusion, suggestions are made that the scope should be further expanded and green finance policies should be formulated differently.


Subject(s)
Fiscal Policy , Policy , China , Cities , Economic Development , Environmental Policy
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