Background:Black ginseng is a unique processed product of ginseng,a source of health food,medicine and modern cosmetics.Purpose:The purpose of this study was to develop a new application for preventing inflammatory ag...Background:Black ginseng is a unique processed product of ginseng,a source of health food,medicine and modern cosmetics.Purpose:The purpose of this study was to develop a new application for preventing inflammatory aging.Method:To investigate the effects and mechanisms of action of black ginseng extract(BGE)on inflammatory aging,models of inflammatory aging were established in human foreskin fibroblasts cells and reconstructed 3D skin model.Result:The results showed that MMP-1 expression in human foreskin fibroblasts was reduced at a concentration of 4μg/mL BGE.At a concentration of 0.1%,BGE not only inhibited the secretion of PGE 2 in reconstructed 3D skin model damaged by SDS but also promoted the expression of TIMP-1.Furthermore,the composition of three rare ginsenosides in the BGE and their binding affinity to target proteins associated with inflammatory aging were analyzed using high-performance liquid chromatography(HPLC)and molecular docking technique.Conclusion:BGE has potential application value in alleviating skin inflammatory aging.展开更多
Vascular inflammatory aging is strongly associated with multimorbidity,including immunosenescence.Here,bioinformatic analysis indicated elevated expression of the lysozyme(LYZ)gene in age-dependent vascular diseases.L...Vascular inflammatory aging is strongly associated with multimorbidity,including immunosenescence.Here,bioinformatic analysis indicated elevated expression of the lysozyme(LYZ)gene in age-dependent vascular diseases.Lyzl deficiency led to vascular inflammatory aging,including damage to indicators related to oxidative stress,vascular function,and inflammation in the serum and vascular tissues of wild-type(WT)and Lyz1^(-/-)mice.The 16S ribosomal RNA sequencing of intestinal contents revealed increased Bifidobacterium and its metabolism of acetate,butyrate,omega-muricholic acid,propionate,and valeric acid in Lyz1^(-/-)mice compared with that in WT mice.Additionally,RNA sequencing of vascular tissues identified differentially expressed genes in Lyz1^(-/-)mice compared with those in WT mice,as well as enrichment of the common phosphatidylinositol 3-kinase(Pl3K)-Akt signaling pathway.Vascular inflammatory aging phenotypes were detected in the blood vessels of antibiotic-treated and germ-free mice,and the PI3K-Akt signaling pathway was inhibited.Importantly,intravenous LYZ administration worsened the pathological conditions,whereas oral LYZ administration successfully restored the gut microbial balance and reversed the vascular inflammatory aging phenotypes.Collectively,this study establishes LYZ as a novel biomarker for age-related vascular diseases and the gut microbiota-PI3K-Akt axis as a promising therapeutic target.展开更多
文摘Background:Black ginseng is a unique processed product of ginseng,a source of health food,medicine and modern cosmetics.Purpose:The purpose of this study was to develop a new application for preventing inflammatory aging.Method:To investigate the effects and mechanisms of action of black ginseng extract(BGE)on inflammatory aging,models of inflammatory aging were established in human foreskin fibroblasts cells and reconstructed 3D skin model.Result:The results showed that MMP-1 expression in human foreskin fibroblasts was reduced at a concentration of 4μg/mL BGE.At a concentration of 0.1%,BGE not only inhibited the secretion of PGE 2 in reconstructed 3D skin model damaged by SDS but also promoted the expression of TIMP-1.Furthermore,the composition of three rare ginsenosides in the BGE and their binding affinity to target proteins associated with inflammatory aging were analyzed using high-performance liquid chromatography(HPLC)and molecular docking technique.Conclusion:BGE has potential application value in alleviating skin inflammatory aging.
基金supported by the National Natural Sciences Foundation of China(82305072,82305064,and 82300345)the Natural Science Foundation of Jiangsu Province(BK20230184)+6 种基金the Science and Technology Development project of Jiangsu Provincial Administration of Traditional Chinese Medicine(YB2020043)the Wuxi Municipal Health Commission Scientific Research Fund Youth Project(Q202106 and Q202225)The Taihu Lake Talent Project of Wuxi Science and Technology Bureau(K20221027)the Medical Key Discipline Program of Wuxi Health Commission(HB2023044 and HB2023051)the Chongqing Natural Science Foundation(CSTB2024NSCQMSX0368)the high-level hospital clinical research fees of Fu Wai Hospital,CAMS(grant 2023-GSP-QN-23)the Doctoral Talent Startup Fund of Affiliated Hospital of Jiangnan University.
文摘Vascular inflammatory aging is strongly associated with multimorbidity,including immunosenescence.Here,bioinformatic analysis indicated elevated expression of the lysozyme(LYZ)gene in age-dependent vascular diseases.Lyzl deficiency led to vascular inflammatory aging,including damage to indicators related to oxidative stress,vascular function,and inflammation in the serum and vascular tissues of wild-type(WT)and Lyz1^(-/-)mice.The 16S ribosomal RNA sequencing of intestinal contents revealed increased Bifidobacterium and its metabolism of acetate,butyrate,omega-muricholic acid,propionate,and valeric acid in Lyz1^(-/-)mice compared with that in WT mice.Additionally,RNA sequencing of vascular tissues identified differentially expressed genes in Lyz1^(-/-)mice compared with those in WT mice,as well as enrichment of the common phosphatidylinositol 3-kinase(Pl3K)-Akt signaling pathway.Vascular inflammatory aging phenotypes were detected in the blood vessels of antibiotic-treated and germ-free mice,and the PI3K-Akt signaling pathway was inhibited.Importantly,intravenous LYZ administration worsened the pathological conditions,whereas oral LYZ administration successfully restored the gut microbial balance and reversed the vascular inflammatory aging phenotypes.Collectively,this study establishes LYZ as a novel biomarker for age-related vascular diseases and the gut microbiota-PI3K-Akt axis as a promising therapeutic target.
