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Main component | Study subject | Material and method | Result | References |
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CFE | Overweight adults | Daily supplementation (16 weeks) | A significant effect on body weight maintenance was observed | [20] |
CFE | Adults (97) | 500 mg for 8 weeks | Significant reduction in stress and anxiety | [28] |
CFE | A 14-year-old female (PWS) | CFE supplementation over 12 years | Significant effect against hyperphagia and obesity | [32] |
Hydroalcoholic extract of C. fimbriata | Animal model (40 rats) | HFD-induced cardiac damage was analyzed | Cardiac protective outcomes were observed | [62] |
C. fimbriata | Human colon cancer cells | MTT cell viability assay was performed on KB cell lines | Good antiproliferative activity against KB mouth cell line | [88] |
Hydroalcoholic extract of C. fimbriata | Animal model (Wister rats) | Oxidative stress markers GSH, LO, PO, SDH, and AR were examined | Reduced oxidative and pancreatic damage caused by HFD | [89] |
Hydroalcoholic extract of C. fimbriata | Animal model (HFD diabetic rats) | Carbohydrate metabolism was analyzed in rats with HFD | Significantly restore the levels of glycogen in the liver and muscles | [18] |
Ethanolic leaf extract of C. fimbriata | Human colon cancer cell | Antiproliferative effects were evaluated using MTT assays | Reduced cell proliferation by inducing cytotoxicity of COLO 320 cells | [88] |
Commercially available CFE | Animal model (female rats) | Modulation of brain neuropeptides NPY and ORX | Significant reduction in weight gain | [55] |
Ethanolic leaf extract of C. fimbriata | Vitro approach | Alpha-amylase and alpha-glucosidase inhibitory assay with acarbose as control | Potent antihyperglycemic activity | [23] |
Hydroalcoholic extract of C. fimbriata | Animal model (male Wister rats) | Renal functional and oxidative stress markers were checked | Effectively alleviated the HFD-induced renal damage | [35] |
CFE and metformin | Wister rats | Lipid profile was analyzed | Significant reduction in lipid profile | [39] |
CFE | Male Wister rats | Oxidative stress markers were checked | Significant protection against HF diet | [34] |
CFE | Animal and human | Snord116 deletion | Significant alteration in appetite | [90] |
CFE | PWS children and adolescents | Appetite behavior was recorded | Significant reduction in hyperphagia | [30] |
CFE | Overweight and obese individuals | Anthropometry, appetite, and biochemical investigation done | No significant changes in the biochemical and clinical parameters | [91] |
CFE | Animal model | Glucose, leptin, and triglycerides were measured | Significant reduction in insulin resistance and oxidative stress | [14] |
CFE | Animal model | Metabolic parameters were assessed | Significant reduction in food intake and blood pressure | [92] |
CFE | Animal model | Hepatotoxic, diabetic, and renal toxicities were analyzed | Significant reduction in diabetes | [87] |
CFE | Animal model | Renal and liver function tests were measured | Significant reduction in body weight and lipid profile | [93] |
CFE | Animal model | Serum lipid profile and blood glucose were measured | Significant alteration in lipid profile and body weight | [94] |
CFE | Overweight and obese individuals | 500 mg capsules twice for 12 weeks | CFE showed a reduction in BMI, weight gain, hip circumference, and systolic blood pressure | [95] |
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