首页|期刊导航|中国中药杂志|基于代谢组学与p38 MAPK/NF-κB信号通路探讨土槐丹四物汤治疗血热型银屑病的机制研究

基于代谢组学与p38 MAPK/NF-κB信号通路探讨土槐丹四物汤治疗血热型银屑病的机制研究OA

Mechanism study on treating psoriasis of blood-heat type with Tuhuaidan Siwu Decoction based on metabolomics and p38 MAPK/NF-κB signaling pathway

中文摘要英文摘要

该研究旨在探究土槐丹四物汤对心得安诱导的小鼠病证结合银屑病模型的血清代谢组学和丝裂原活化蛋白激酶p38(p38 MAPK)/核因子κB(NF-κB)信号通路的影响,并探讨其作用机制.将 40 只KM小鼠随机分为空白组、模型组、阳性药组、治疗组,每组 10 只.采用 5%盐酸普萘洛尔诱导银屑病模型同时干姜甘草煎液灌胃、紫外线灯照射建立血热证模型,造模 7 d,治疗组与阳性药组分别给予相应药物干预,空白组和模型组则予生理盐水,持续 14 d.记录小鼠皮损并进行皮损严重程度指数(PASI)评分;检测脾脏指数;苏木精-伊红(HE)染色观察皮损的病理变化并进行Baker评分;酶联免疫吸附测定法(ELISA)检测小鼠血清肿瘤坏死因子-α(TNF-α)、白细胞介素(IL)-1β、IL-6、IL-17 的表达;蛋白免疫印迹(Western blot)法检测p38 MAPK、p-p38 MAPK、NF-κB抑制蛋白α(IκBα)、NF-κB p65、p-NF-κB p65 的表达;进行小鼠血清代谢组学分析,筛选差异代谢物和银屑病相关代谢通路.结果显示,与空白组比较,模型组PASI评分、脾脏指数明显上升,皮肤组织病理出现棘层增厚、角化不全或角化过度、炎性细胞浸润等表现,Baker 评分明显上升,TNF-α、IL-1β、IL-6、IL-17 的表达水平明显上升,p38 MAPK、NF-κB p65 的磷酸化水平明显上调,IκBα的水平明显下调.与模型组比较,阳性药组和治疗组PASI评分、脾脏指数明显下降,皮肤病理变化改善,Baker评分明显下降,TNF-α、IL-1β、IL-6、IL-17 的表达水平明显下降,p38 MAPK、NF-κB p65 的磷酸化水平明显下调,IκBα的水平明显上调.血清代谢组学显示,空白组与模型组有 42 个差异代谢物,21 个上调,21 个下调,与甘油磷脂代谢,花生四烯酸代谢,柠檬酸循环,缬氨酸、亮氨酸和异亮氨酸降解等代谢通路有关;模型组与治疗组有 38个差异代谢物,15 个上调,23 个下调,主要与甘油磷脂代谢,缬氨酸、亮氨酸和异亮氨酸降解,泛醌及其他萜醌生物合成,泛酸和辅酶A生物合成等代谢通路有关.其中共同代谢通路有甘油磷脂代谢,缬氨酸、亮氨酸和异亮氨酸降解等.综上表明,土槐丹四物汤可能通过p38 MAPK/NF-κB信号通路调控TNF-α、IL-1β、IL-6、IL-17 细胞因子的表达和甘油磷脂代谢治疗银屑病.

This study aims to investigate the effects of Tuhuaidan Siwu Decoction on serum metabolomics and p38 mitogen-activated protein kinase(p38 MAPK)/nuclear factor kappa B(NF-κB)signaling pathway in propranolol-induced mouse model of psoriasis with syndrome,and to investigate its mechanism of action.Forty KM mice were randomly divided into a blank group,a model group,a positive group,and a treatment group,with 10 mice in each group.The psoriasis model was induced by 5%propranolol hydrochloride,and the blood heat syndrome model was established by intragastric administration of Zingiberis Rhizoma and Glycyrrhizae Radix et Rhizoma decoction combined with ultraviolet lamp irradiation.After 7 days of modeling,the treatment group and the positive group were given corresponding drug interventions,while the blank group and the model group were given normal saline,for 14 consecutive days.The skin lesions of mice were recorded and scored using the psoriasis area and severity index(PASI).Spleen index was detected.Pathological changes of skin lesion tissues were observed by hematoxylin-eosin(HE)staining and scored by Baker scores.The expression of tumor necrosis factor-α(TNF-α),interleukin(IL)-1β,IL-6,and IL-17 in mouse serum was detected by enzyme-linked immunosorbent assay(ELISA).The expression of p38 MAPK,p-p38 MAPK,inhibitor of nuclear factor kappa B alpha(IκBα),NF-κB p65,and p-NF-κB p65 was detected by Western blot.Serum metabolomics analysis of mice was performed to screen differential metabolites and psoriasis-related metabolic pathways.The results showed that compared with the blank group,the model group showed significantly increased PASI score and spleen index,manifestations of parakeratosis or hyperkeratosis,acanthosis,inflammatory cell infiltration in skin histopathology,a significantly increased Baker score,significantly increased expression levels of TNF-α,IL-1β,IL-6,and IL-17,significantly up-regulated phosphorylation levels of p38 MAPK and NF-κB p65,and a significantly down-regulated IκBα level.Compared with the model group,the positive group and the treatment group exhibited significantly decreased PASI scores and spleen indices,improved skin pathological changes,significantly decreased Baker scores,significantly decreased expression levels of TNF-α,IL-1β,IL-6,and IL-17,significantly down-regulated phosphorylation levels of p38 MAPK and NF-κB p65,and significantly up-regulated IκBα levels.Serum metabolomics showed that there were 42 differential metabolites between the blank group and the model group,with 21 of them up-regulated and 21 down-regulated,which were related to metabolic pathways such as glycerophospholipid metabolism,arachidonic acid metabolism,citrate cycle(TCA cycle),and valine,leucine,and isoleucine degradation.There were 38 differential metabolites between the model group and the treatment group,with 15 of them up-regulated and 23 down-regulated,which were mainly related to metabolic pathways such as glycerophospholipid metabolism,valine,leucine,and isoleucine degradation,biosynthesis of ubiquinone and other terpenoid-quinones,and biosynthesis of pantothenate and CoA.Among them,the common metabolic pathways included glycerophospholipid metabolism,valine,leucine,and isoleucine degradation,etc.In conclusion,Tuhuaidan Siwu Decoction may treat psoriasis by regulating the expression of TNF-α,IL-1β,IL-6,and IL-17 and glycerophospholipid metabolism through the p38 MAPK/NF-κB signaling pathway.

李思源;樊晓杰;焦滕震;何海艳;张雨冰;贾颖

山西中医药大学 第一临床学院,山西 晋中 030619山西中医药大学 第一临床学院,山西 晋中 030619山西中医药大学 第一临床学院,山西 晋中 030619山西中医药大学 第一临床学院,山西 晋中 030619山西中医药大学 第一临床学院,山西 晋中 030619山西中医药大学 第一临床学院,山西 晋中 030619

土槐丹四物汤银屑病代谢组学p38MAPK/NF-κB5%盐酸普萘洛尔

Tuhuaidan Siwu Decoctionpsoriasismetabolomicsp38 MAPK/NF-κB5%propranolol hydrochloride

《中国中药杂志》 2026 (6)

1757-1765,9

山西省自然科学基金面上项目(202403021211186)山西中医药大学中医外科学学科建设项目(2025XKJS-13)山西省研究生实践创新项目(X2025SJ019)

10.19540/j.cnki.cjcmm.20251121.901

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