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Pharmacological Activity | Tested Substance | In vivo/ In vitro | Model or sample | Active concentration | Administration (In vivo) | References |
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Anti-inflammatory effect | PAR extract with voucher specimens | In vitro | BV2 cells (Mouse microglial cell line) | 100 μg/ml | | [28] |
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| PCC extract | In vivo, in vitro | 12-O-Tetradecanoylphorbol-13-acetate-induced mouse ear edema | (i) TPA and AA tests: 0.5 mg/ear (ii) TPA multiple application: 1 mg/ear (iii) DTH test: 1 mg/ear | Topical application | [29] |
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| PCC extract with voucher specimens | In vivo, in vitro | lipopolysaccharides-induced systemic inflammation mice model and macrophage RAW 264.7 cells | 1,10,100 μg/mL | Oral administration | [30] |
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| Ethanol extract of PCC with voucher specimens | In vivo | 12-O-tetradecanoyl-phorbol-13-acetate- induced ear edema in mice | 200-400 mg/kg | Administered intragastrically | [3] |
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| PAR methanol extract with voucher specimens | In vitro, in vivo | ICR mice and male Wistar rats | IC50: Methanol extract 20.9 ± 3.8 μg/mL; Non-alkaloids 22.0 μg/mL; Limonin 15.8 ± 5.2 μm; Obakunone 2.6 ± 1.1 μm | Oral administration | [11] |
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| PCC methanol extract with voucher specimens | In vivo | Lipopolysaccharides- induced acute airway inflammation on a mouse model | 100, 200 and 400 mg/kg | Administrated by gavage | [31] |
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| Demethyleneberberine | In vivo | Acute colitis mice model | 150,300 mg/kg | Oral administration | [32] |
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Anti-bacterial effect | Ethanol Extract of PAR; Aqueous extract of PAR | In vitro | Enterococcus faecium, Staphylococcus aureus, Streptococcus pyogenes, Escherichia coli, Klebsiella pneumonia, Pseudomonas aeruginosa | MIC and MBC: 3.676 mg/ml and 7.353 mg/ml for ethanol extract; 6.25 mg/ml and 50 mg/ml for aqueous extract | | [33] |
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| PCC extract with voucher specimens | In vitro | Streptococcus. mitis, Streptococcus. sanguis, Streptococcus. mutans, Streptococcus. gingivalis | 2.5 g/ml | | [34] |
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| PCC extract | In vitro | Mycoplasma hominis | 0.24-250 mg/ml | | [35] |
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| Aqueous extract of PCC | In vivo, In vitro | S. Typhimurium 21 infected mouse model | 2.5 or 5 mg/day | Administrated by gavage | [36] |
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| Berberine in PAR | In vitro | Staphylococcus aureus | 32 to 128 μg/mL | | [37] |
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| Berberine in PCS | In vitro | P. aeruginosa | 100 ml | | [38] |
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| PCC | In vitro | Propionibacterium acnes | MIC50%: 24 μg/mL MIC90%: 190 μg/mL | | [39] |
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Anti-fungal effect | Berberine hydrochloride, palmatine hydrochloride | In vitro, In vivo | Microsporum Canis –induced dermatitis in rabbits | 1 mg/ml | Administered through the sterile pipette tip | [40] |
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Anti-viral effect | Ethanol extract of PAR; Aqueous extract of PAR | In vitro | African green monkey kidney cells | 6.73 ± 0.87 mg/ml for aqueous extract; 4.26 ± 0.59 mg/ml for ethanol extract | | [33] |
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| Aqueous extract of PAR with voucher specimens | In vitro, in vivo | H1N1, H5N2, H7N3 or H9N2 infected BALB/c mice | 0.8 μg/g in a total volume of 200 μl at 1, 3 and 5 days before infection | Oral administration | [41] |
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Anti-tumor effect | PCS extract with voucher specimens | In vitro | (i) Leukemic cell lines K562 (ii) Leukemic cell lines HEL (iii) Breast cancer cell line MDA (iv) Prostate cancer cell line PC3 | (i) IC50 of Compound 1: 7.66 ±2.08; (ii) IC50 of compound 3: 14.30 ± 1.93; (iii) IC50 of compound 4: 11.81 ± 2.79 | | [42] |
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| PCC extract | In vivo, in vitro | Prostate cancer cell infested Male BALB/c-nude mice model | 1.6 g/kg per day for 28 days | Administered intragastrically | [43] |
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| Aqueous extract of PCS with voucher specimens | In vitro In vivo | Sarcoma 180 ascites cells implanted Mice model | 2 mg/100g; 5 mg/100g; 10 mg/100g | Injected intraperitoneally daily for 10 days | [44] |
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Anti-gout effect | Compounds of Si-Miao-Wan (containing PCC) | In vivo | Male Sprague-Dawley rats | 1.0 ml/100 g | Oral administration | [45] |
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| PCS extract with voucher specimens | In vivo | Uricase inhibitor potassium oxonate induced male ICR mice model | 480 mg/kg | Oral or intraperitoneal administration | [46] |
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Anti-ulcer effect | Ethanol extract of PCC with voucher specimens | In vivo In vitro | Acetic acid-induced chronic gastric ulcers on Sprague Dawley rats model | 30 mg/kg/day | Administered intragastrically once a day for seven days. | [47] |
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| Aqueous extract of PCC | In vivo | Ethanol-induced gastric lesions on Male Wistar rats model | 100 mg/kg | Oral administration | [48] |
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Anti-oxidant effect | Ethanol extract of PAR; Aqueous extract of PAR | In vitro | For anti-microbial Enterococcus faecium, Staphylococcus aureus, Streptococcus pyogenes, Escherichia coli, Klebsiella pneumonia, and Pseudomonas aeruginosa; Anti-herpes simplex virus tested on African green monkey kidney cells | 25 mg/ml | | [33] |
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| Phellodendrine isolated from PCC extract | In vivo | AAPH-induced oxidative stress on zebrafish embryo model | 200 μg/mL | Waterborne exposure | [49] |
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Sun screening effect | PCC extract + 50% ethanol | In vitro | PC extract+50% ethanol | 0.5 mg/ml | | [50] |
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| PCC extract | In vivo | UVB lamp inflicted skin lesions on the dorsal of the rats model | 200, 400 or 800 mg/kg, once daily for 11 days | Oral administration | [51] |
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Bone-growth effect | PCC extract | In vivo | 72 intact 21-day-old female Sprague–Dawley rats | 100 and 300 mg/kg | Oral administration | [52] |
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Hemostatic effect | PCC Carbonisatus-carbon dots | In vivo In vitro | Mouse tail amputation and liver scratch on male Kunming mice models | 5, 2 and 1 mg/kg | Subcutaneous administration | [53] |
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Neuroprotective effect | PCC extract with voucher specimens | In vitro | PC-12 cells | 10 and 30 μg/mL | | [54] |
PCC and PAC extract with voucher specimens | In vitro | PC-12 cells | 0.1 and 1 g/ml for 2 hours | | [55] |
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Counter-atopic dermatitis effect | Salt processed PAC extract with voucher specimens | In vivo | 2,4-dinitrochlorobenzene induced skin lesions on the NC/Nga mice model | 200 μl | Topical administration | [56] |
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Counter-diabetic nephropathy effect | PAR aqueous extract | In vivo | Streptozotocin-induced diabetes on male Sprague-Dawley rats model | 379 mg/kg | Oral administration | [57] |
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| Berberine | In vivo | Streptozotocin-induced diabetes on male Wistar rats model | 200 mg/kg once a day for 12 weeks | Oral intubation | [58] |
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Immunity suppressing effect | Phellodendrine and cyclophosphamide isolated from PCC in saline water | In vivo | ddY mice, BALB/c mice, and Hartlay guinea pigs | (i) 0.1 ml/10 g for mice (ii) 1 ml for guinea pigs | Administered intraperitoneally | [59] |
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Anti-asthmatic effect | n-butyl alcohol extract of PCS with voucher specimens | In vivo | BALB/c mice asthmatic model induced by saline solution | The IC50 of n-butyl alcohol extract of PCS was 12.2 ± 1.3 μg/mL | intranasally | [6] |
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