International Journal of Phytomedicine and Phytotherapy
Pharmacological activities | BPEO/ Piperine | In vitro/ In vivo | Target/ Model | Control(s) | IC 50/Dosage | Results / Remarks | Reference |
---|---|---|---|---|---|---|---|
Antioxidant | BPEO | In vitro | DPPH scavenging | Not reported | EC50 : 103.3 µg/ml | Noteworthy radical activity observed. Though control details are not reported | [50] |
Anti-inflammatory | Piperine | In vitro | B16F-10 melanoma cells | Not reported | MIC: 2, 5, 10 mg/µl | Piperine showed dose dependent inhibition against B16F-10 melanoma cell lines. However proper control details not reported | [51] |
Anti-inflammatory | BPEO | In vivo | Carrageenan induced acute inflammatory Balb/C mice | Positive: Carrageenan | 100, 500, 1000 mg/kg body weight | The dose 500 mg/kg body weight was performed significant inhibition (72 %) at 3rd hour compared to control | [52] |
Anti-inflammatory | BPEO | In vivo | Formalin induced chronic inflammatory Balb/C mice | Positive: Formalin | 100, 500, 1000 mg/kg body weight | 500 mg/kg body weight BPEO produced 50 % inhibition of paw edema compared to control | [52] |
Anti-inflammatory | BPEO | In vivo | Dextran induced acute inflammatory Balb/C mice | Positive: Dextran | 100, 500, 1000 mg/kg body weight | 1000 mg/kg body weight significantly reduced the paw thickness 73.4 % at 3rd hour compared to the control | [52] |
Antibacterial activity | BPEO | In vitro | Alcaligenes faecalis, Acinetobacter calcoacetica, Beneckea natriegens, B. subtilis, Brevibacterium linens, Clostridium sporogenes, Citrobacter freundii, E. carotovora, Enterococcus faecalis, E. coli, Micrococcus luteus | Not reported | Not reported | Highest zone of inhibition (19.7 mm) was obtained against P. aeruginosa. However, in this study dosage and control was not reported. It reduces reliability of results | [53] |
Anticancer activity | Piperine | In vivo | DMBA induced carcinogenesis in Syrian golden hamsters | Postive: DMBA Negative : Distilled water | 50Â mg / kg, oral administration for 14 weeks | Results showed that piperine totally inhibited the oral carcinoma formation | [20] |
Anticancer activity | Piperene | In vtiro | MCF-7 cell line | Negative : Distilled water | IC50: 1.21 µM for 24 h exposure | Piperine exhibited significant synergistic effects in combination with paclitaxel on human breast cancer cell line MCF-7 | [54] |
Anticancer activity | Piperene | In vtiro | HER overexpressing breast cancer cell lines (MCF-7 and SKBR-3) | Negative : Distilled water | IC50 : 200 µM & 50 µM for MCF-7 and SKBR-3 cell lines respectively, 48 h exposure | Piperine strongly inhibited proliferation and induced apoptosis through caspase-3 activation and PARP cleavage. Also, piperine inhibited HER2 gene expression. This study suggested that piperine may be a potential agent for the prevention and treatment of human breast cancer with HER2 overexpression | [55] |
Antiobesity activity | Piperine | In vivo | Obesity-induced dyslipidemia in high-fat diet rats | Not reported | 40Â mg / kg for 3 weeks | Supplementation of piperine with high fat diet significantly reduced body weight and total cholesterol. Though control details not reported | [56] |
Antiaging and wrinkling | BPEO | In vitro | Human neutrophil elastase | Negative: Distilled water | 1 µg/ml | BPEP showed noteworthy elastase inhibitory activity. However, dosage of the experiment is not scientifically accepted | [57] |
Antihypertensive activity | Piperine | In vivo | Anesthetize induced Sprague-Dawley male rats | Positive: Acetylcholine | 1 to 10Â mg/kg body weight | Intravenous administration of piperine caused a dose-dependent decrease in mean arterial pressure (MAP) in normotensive anesthetized rats. Also, higher dose (30Â mg/kg) of piperine did not cause any further change in MAP. However, this study not reported detailed dosages along with experiment duration. | [19] |
Antiasthmatic activity | Piperine | In vivo | Asthma induced Balb/c mice | Positive: Ovalbumin + vehicle | 4.5 & 2.25 mg/kg, oral administration, five times a week for 8 weeks | Piperine-treated group had suppressed eosinophil infiltration, allergic airway inflammation and airway hyper responsiveness, and these occurred by suppression of the production of interleukin-4, interleukin-5, immunoglobulin E and histamine, than comparing with control group | [58] |
Antidepressant & cognitive | Piperine | In vivo | Male wistar rats | Positive: Diazepam | 5, 10 & 20Â mg/kg body weight once daily for 4 weeks | All the treatment showed anti-depression like activity and cognitive enhancing activity | [23] |
Antidepressant activity | Piperine | In vivo | Corticosterone-induced depression in mice | Negative: Distilled water | 10Â mg/kg body weight for 24Â h. | Significant decrease in sucrose consumption and increase in immobility time in the forced swim test and tail suspension test | [59] |
Antidepressant activity | Piperine | In vivo | Pilocarpine (350Â mg/kg i.p.) induced rats | Positive: Pilocarpine | 25Â mg/kg, p.o. for 10 days | In comparison with pilocarpine, piperine significantly reduced lipid peroxidase and catalase activity, and increased GSH level, brain-plasma phenytoin and number of viable neurons | [60] |
Anticonvulsant activity | Piperine | In vivo | Pentylenetetrazole (PTZ)- and picrotoxin (PIC)-induced seizure in mice | Negative: Normal Saline | 30, 50 and 70Â mg/kg, i.p. | Piperine protected animals from PTZ induced seizures in a dose-dependent manner. PTZ-induced convulsion in piperine treated animals was significantly different compared to saline treated animals | [61] |
Insecticidal activity | BPEO | In vivo | Sitophilus zeamais | Negative: Distilled water | LD50: 26.4 µl/g for 48 h | BPEO showed some insecticide activity (contact toxicity) against Sitophilus zeamais | [62] |