Pharmacological effects | Active extract/fraction/compounds | Mechanism | Effective dose | Material or mode | Study design | References |
---|---|---|---|---|---|---|
Anti-inflammatory effects | Psoralen | Reduced the release of inflammatory factors and inflammatory cell infiltration | 5, 10, 20 mg/kg | Dextran sulfate sodium-induced ulcerative colitis mice | In vivo | [77] |
Isopsoralen | Targeted MIF and reduced the release of inflammatory factors | 10, 20 μM; 5, 20 mg/kg | Fibroblast-like synoviocytes; Collagen-induced arthritis mice | In vitro; In vivo | [78] | |
Imperatorin | Inhibited COX-2, iNOS, and NF-κB activity and reduced circulating cytokines | ED50 = 4.53 mg/kg | Acetic acid and formalin -induced mice | In vivo | [79] | |
Bavachinin A | Suppressed phosphorylation of p38 and JNK and inhibited expression and secretion of inflammatory factors in macrophages | 6.25, 12.5, 25 μM | RAW264.7 cells stimulated by LPS | In vitro | [80] | |
Corylin | Inhibited pro-caspase-1 self-shear activation | 20 μM | NLRP3, NLRC4, AIM2 inflammasomes with immortalized bone marrow-derived macrophages | In vitro | [81] | |
Bakuchiol | Activated SIRT1 signaling pathway | 1, 5, 10 μM | LPS-induced cardiomyocyte inflammation myocytes | In vitro | [82] | |
Antibacterial effects | Psoralen | Inhibited the growth of biofilms | MIC = 6.25 μg/mL | Planktonic porphyromonas gingivalis and porphyromonas gingivalis | In vitro | [83] |
Isopsoralen | Inhibited the growth of biofilms | MIC = 3.125 μg/mL | Planktonic porphyromonas gingivalis and porphyromonas gingivalis | In vitro | [83] | |
Isobavachalcone | Changed the bacterial morphology, destroy the cell membrane, increased the permeability of cell wall and the amount of soluble protein leakage in the cell | MIC = 0.078 mg/mL | Staphylococcus aureus, escherichia coli and pseudomonas aeruginosa | In vitro | [84] | |
Antiviral effects | Isopsoralen | Inhibited the lytic replication of the virus | IC50 = 28.95 μM | Murine gammaherpesvirus 68 | In vitro | [86] |
Psoralen | Increased the neutralizing antibody titer of each dengue serotype | 50 μg/mL | Mice and nonhuman primates | In vivo | [87] | |
Psoralen | Down-regulated the expression of FOXO1 replication | IC50 = 63.7 ± 14.53 μm | HepG2.2.15 cells | In vitro | [88] | |
Antioxidant effects | Bavachinin A | Increased the activity of antioxidant enzymes and mitochondrial membrane potential | 10–6 M | Aβ-induced PC12 cells | In vitro | [90] |
Corylisoflavone A | Reduced ROS levels through mitochondrial and non-mitochondrial pathways and regulated Nrf2 signaling pathway | 10–3, 10–2, 10–1 μM | UVB-induced HaCaT cells | In vitro | [91] | |
Bakuchiol | Activated the SIRT3/SOD2 signaling pathway | 20 mg/kg | Doxorubicin-induced cardiotoxicity in mice | In vivo | [92] | |
Isopsoralen | Regulated the PPAR-γ/Wnt pathway | 10 mg/kg | Ovariectomized rats | In vivo | [93] | |
Anticancereffects | ||||||
Block cell cycle | Psoralen | Inhibited Wnt/β-catenin pathway | IC10 = 8 μg/mL; IC10 = 12 μg/mL | MCF-7 cells; MDA-MB-231 cells | In vitro | [94] |
Psoralen | Blocked the G0/G1 and G2/M phases | 10, 30, 50 and 100 μg/ml | PC3 cells | In vitro | [95] | |
Bakuchiol | Induced S-phase arrest through the p38-ROS-p53 pathway and inhibited cell proliferation through the JNK pathway | 30 μmol/L | MCF-7 cells | [96] | ||
Induction of apoptosis | Psoralen | Induced apoptosis via caspase-3, p53, Bax, and Bcl-2 pathway | 10, 30, 50 and 100 μg/mL | SMMC-7721 cells | In vitro | [97] |
Psoralen | Depolymerized the cytoskeletal protein F-actin | 25, 30, 50 μg/mL | BGC-803 cells | In vitro | [98] | |
Psoralen | Triggered endoplasmic reticulum stress | 10, 20, 40 and 80 μM | SMMC-7721 cells | In vitro | [99] | |
Isobavachalcone | Regulated Sirtuins-related signaling pathway | 60 μM | H460 cell | In vitro | [100] | |
Isobavachalcone | Promoted the phosphorylation of AKT and its downstream GSK-3β, activated autophagy | 10, 12, 14 μM | SW480cells | In vitro | [101] | |
Isobavachalcone | Inhibited RSK2 activity and regulated the expression of c-Jun and Bcl-2/Bax | 20, 40 μM | CNE-2Z cells | In vitro | [102] | |
Inhibit cell migration and invasion | Psoralen | Suppressed the expression levels of MKI67, PCNA, MMP2 and MMP9 | 30 μg/ml | HTB-47 and CRL-1932 cells | In vitro | [103] |
Isopsoralen | Up-regulated the expression of LncRNA THOR and down-regulated the expression of miR-153-5p | 10、30、90 μg/ml | Tu686 cells | In vitro | [104] | |
Imperatorin | Downregulated the expression of HMGB2 | 25, 50 µM | SKBR3 cells | In vitro | [105] | |
Photosensitive effects | Psoralen | Inhibited cell proliferation, reducted DNA synthesis and inducted inflammatory cell apoptosis | 0.4 mg/kg | Patients with psoriasis | In vivo | [106] |
Psoralen | Normalized the expression of abnormal NGF and Sema3A in the epidermis | 0.4 mg/kg | Patients with atopic dermatitis | In vivo | [107] | |
Estrogen-like effects | Psoralen | Bind to ERα and inhibited the activation of TLR4-IRAK4-NF-κB pathway | 3.125, 6.25, 12.5 μg/mL | Human periodontalligament cells | In vitro | [110] |
Isopsoralen | Activated ERα and regulated the PI3K/AKT pathway | 5, 10 mg/kg | Mice with spinal cord injury | In vivo | [111] | |
Regulation of cardiovascular system functions | 70% ethanol extracts of PCL | Induced vasodilation through endothelium-dependent and non-dependent pathways | 10–600 μg/mL | Rat aortic rings | In vitro | [113] |
Psoralen | Exerted vasodilatory effects via endothelium-dependent NO pathway and promoted eNOS protein expression | 0.1, 1, 10 μM | Rat thoracic aortas | In vitro | [114] | |
Bakuchiol | Exerted vasodilatory effects via non-endothelium dependent pathway of opening inwardly rectifying potassium channel | 0.1, 1, 10 μM | Rat thoracic aortas | In vitro | [114] | |
Isobavachalcone | Promoted HUVEC migration, reduced the secretion of inflammatory factors, and down-regulated NOD1/RIP2 signaling pathway.resistance | 2.5, 5, 10 μM | LPS-induced HUVEC cells | In vitro | [115] | |
Regulation of nervous system functions | 70% ethanol extracts of PCL | Improved the learning and memory ability by increasing the expressions of ERα, ERβ, FSHR and LHR | 0.5 g/kg | APP/PS1mice | In vivo | [117] |
70% ethanol extracts of PCL | Increased the content of 5-hydroxytryptamine in serum and hippocampus | 15, 30, 60 mg/kg | Mice | In vivo | [118] | |
Psoralen | Inhibited neural stem cell proliferation and promoted stem cell differentiation | 10, 50, 100 nM | Adult neural stem cells | In vitro | [119] | |
Psoralen | Reduced the expression of APP, BACE1 and Aβ protein through the ERβ-mediated P-ERK pathway | 1 μM | Aβ-induced PC12 cells | In vitro | [120] | |
Imperatorin | Mitigated proinflammatory cytokines, oxidative stress and modulated brain-derived neurotropic factor | 5, 10 mg/kg | LPS-induced mice | In vivo | [121] | |
Regulation of immune system functions | Psoralen | Regulated Th1/Th2 cell balance and inhibited the release of inflammatory factors TNF-α, IL-6 and IL-1β | 40 mg/kg | Type II collagen-induced rheumatoid arthritis in mice | In vivo | [123] |
Imperatorin | Suppressed anaphylactic reaction and IgE-mediated allergic responses by inhibiting multiple steps of FceRI Signaling in Mast Cell | 15, 30, 60 mg/kg | Passive cutaneous anaphylaxis in mice | In vivo | [124] | |
PCp-I (a polysaccharide from PCL) | Activated RAW264.7 cells through NF-κB/MAPK signalling pathway | 100, 200, 400 and 800 μg/m L | RAW264.7 cells | In vitro | [125] | |
Regulation of motor system functions | Psoralen | Promote osteoclast bone resorption and osteoblast bone differentiation through the ERK pathway | 2.5, 5, 10, 20 and 40 μM | BMM cells and MC3T3-E1 cells | In vitro | [127] |
Psoralen | Increased the expression of PPARγ, osteocalcin, and trabecular bone area | 35 mg/kg | Rabbits with steroid-induced avascular necrosis of the femoral head | In vivo | [128] | |
Psoralen | Promoted the proliferation of bone marrow mesenchymal stem cells and induced bone marrow mesenchymal stem cells to differentiate into cartilage | 10 μM | Rat bone marrow mesenchymal stem cells | In vitro | [129] | |
Isopsoralen | Inhibited the Axin2/PPAR-γ signaling pathway and activating the Wnt signaling pathway | 25 mg/kg | Dexamethasone sodium injection-induced in rats | In vivo | [130] | |
Isopsoralen | Inhibited RANKL-induced osteoclast differentiation by inhibiting the NF-κB signaling pathway | 30 μM | Primary mouse mononuclear macrophages | In vitro | [131] | |
Neobavaisoflavone | Interfered the activation of key signaling pathways mediated by RANKL/RANK | 30 mg/kg; 2, 4, 8 μM | Ovariectomized in mice; RAW264.7 cells and BMMC cells | In vivo; In vitro | [132] |