| Literature DB >> 35911652 |
Bahareh Samakar1, Soghra Mehri2,1, Hossein Hosseinzadeh2,1.
Abstract
Metabolic syndrome is a serious health condition, yet a common worldwide disorder. It includes several risk factors such as hypertension, dyslipidemia, and high glucose levels which lead the patients to higher risks of cardiovascular diseases, diabetes, and stroke. Phytotherapy plays an important role in treating components of metabolic syndrome. Nettle (Urtica dioica) is considered a valuable plant due to bioactive compounds such as formic acid and rich sources of flavonoids. To acknowledge the role of nettle in metabolic syndrome, several mechanisms have been suggested such as alterations in potassium and calcium channels which improve hypertension. Antihyperlipidemic properties of nettle are mediated by inhibition of HMGCoA reductase and amelioration of lipid peroxidation via antioxidant effects. Also, one of the flavonoids in nettle, quercetin, is responsible for decreasing total cholesterol. Moreover, nettle is responsible for anti-diabetic effects through processes such as increasing insulin secretion and proliferation of pancreatic β-cells. This review aims to gather different studies to confirm the potential efficacy of nettle in metabolic syndrome.Entities:
Keywords: Diabetes; Hyperlipidemia; Hypertension; Metabolic syndrome; Nettle; Urtica dioica
Year: 2022 PMID: 35911652 PMCID: PMC9282742 DOI: 10.22038/IJBMS.2022.58892.13079
Source DB: PubMed Journal: Iran J Basic Med Sci ISSN: 2008-3866 Impact factor: 2.532
Figure 1Different mechanisms of antihypertensive effects of nettle
The summary of animal and clinical studies regarding anti-hypertension effects of nettle and related mechanisms
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| rat | 4 mg/kg/h or | 1.25 hr | 0.9% NaCl | ↓arterial blood pressure | ↑diuresis and natriuresis | ( |
| rat | 200 mg/kg/day | 4 weeks | ↓cardiac index | ( | |||
| rat | 1, 3, 10, 30 and 50 mg/kg | 6 weeks | high-salt (8 % | ↓mean arterial pressure | calcium channel blocking effects, nitric oxide (NO)-mediated vasorelaxation | ( | |
| rat | 1 and 2 g/l | 30 min | ↓blood pressure | bradycardia | ( | ||
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| ___ | 300 mL/day | 16 weeks | ___ | ↓blood pressure | ( | |
| ___ | 100 mg/kg/day | 8 weeks | ___ | ↓systolic blood pressure | ( |
The summary of animal and clinical studies regarding anti-hyperlipidemic effects of nettle and related mechanisms
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| rat | 100 mg/kg | 10 days | Diet with increased fat content (30%) |
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| rat | 100 or 300 mg/kg | 4 weeks | 10 ml/kg/day of a cocktail (1 L peanut oil, 100 g cholesterol, 30 g propylthiouracil,100 g cholic acid) | hypocholesterolemic effects | ( | ||
| rat | 150 mg/kg/day | 30 days | diet enriched with coconut oil as |
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| rat | 15% (w/w) | 4 weeks |
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| rat | 1.25 g/kg | 4 weeks |
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| rat | triple mixture of 200 mg/kg/day | 4 weeks |
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| rat | 100 mg/kg/day | 28 days |
| improving lipid metabolism | ( | ||
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| ___ | 5 ml TDS | 8 weeks | ___ |
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| ___ | 100 mg/kg/day | 8 weeks | ___ |
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| ___ | 8 weeks | ___ | ↑HDL | ( | |||
| ___ | 1g TDS | 12 weeks | ___ |
| oxidation of fatty acids via activating PPAR | ( | |
| ___ | 8 mg/day | 8 weeks | ___ |
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PPAR: peroxisome proliferator-activated receptor
The summary of animal and clinical studies regarding anti-diabetic effects of nettle and related mechanisms
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| rats | 40-60 ml/day | 4 weeks | Fructose (66%) |
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| rats | 50, 100 or 200 mg/kg/day | 2 weeks | Fructose (10%) |
| ↓FIRI | ( | |
| rats | 10% | 8 weeks | Fructose (21%) | ↓serum and urine glucose | ( | ||
| rats | 250 mg/kg | 2 hr | Alloxan |
| ↓intestinal glucose absorption | ( | |
| mice | 150 mg/kg | 8 days | Alloxan | ↓serum glucose | prevented GluT2 gene expression | ( | |
| mice | 20 mg/kg | 1 week | Alloxan | ↓serum glucose, ↓fructosamine | ( | ||
| rabbits | 4 ml/kg | 5 hr | Dextrose | ↑serum glucose | ( | ||
| rats | 1 week | STZ (40 mg/kg) | ↓serum glucose | ↑insulin secretion | ( | ||
| rats | 12.5 ml/kg/day | 4 weeks | STZ (50 mg/kg) | ↓serum glucose recovered islet volumes and β-cell numbers | ↑insulin secretion, | ( | |
| rats | 100 mg/kg/day | 5 weeks | STZ (80 mg/kg) | ↓serum glucose | protective effect on β-cells | ( | |
| rats | 15 mg/kg/day | 8 weeks | STZ (50 mg/kg) | slight to moderate rearrangement of pancreatic islets | protective effect on pancreatic islets | ( | |
| rats | 1.25 g/kg | 4 weeks | STZ (90 mg/kg) | ↓fasting serum glucose | ( | ||
| rats | 100 mg/kg/day | 5 days | STZ (80 mg/kg) | ↓serum glucose | proliferation of β-cells | ( | |
| rats | 100 mg/kg/day | 4 weeks | STZ (60 mg/kg) | ↓serum glucose | ( | ||
| rats | 0.40-0.60 ml/day | 4 weeks | STZ (65 mg/kg) | ↓fasting serum glucose | ( | ||
| mice | 6.25% | 4 weeks | STZ (200 mg/kg) | ↑serum glucose | ( | ||
| rats | 625 mg/kg, 1.25 g/kg | 4 weeks | STZ (50 mg/kg) | ↓serum glucose | ↑insulin secretion, ↑glucose uptake, | ( | |
| rats | 100 mg/kg | 4 weeks | STZ (60 mg/kg) | ↓serum glucose | ↓GSK-3 beta level | ( | |
| rats | 500, 1000 mg/kg orally, | single dose | STZ | hypoglycemic effect with a stronger response in IP models | ( | ||
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| ___ | 100 mg/kg/day | 8 weeks | ___ | no significant effect on fasting blood glucose | ↓insulin resistance | ( |
| ___ | 100 mg/kg/day | 8 weeks | ___ | ↓fasting blood glucose | ( | ||
| ___ | 10 g/day | 8 weeks | ___ | ↓blood glucose, ↓body weight | ( | ||
| ___ | 500 mg TDS | 3 months | ___ | ↓fasting blood glucose, | inhibition of α-glucosidase, PPAR-γ agonistic properties, ↑insulin secretion | ( | |
| ___ | 10 gr/day | 8 weeks | ___ | ↓blood glucose | ( | ||
| ___ | 8 weeks | ___ | ↓mean serum fasting blood glucose, | ( | |||
| ___ | 1 capsule (200mg/600mg) TDS | 90 days | ___ | ↓blood glucose | ( | ||
| ___ | 3 Glucolevel tablets/day | 4 weeks | ___ | regulated glucose-homeostasis | ( |
FIRI: Fasting insulin resistance index, GluT2: Glucose transporter 2, STZ: Streptozotocin, IP: Intraperitoneally, 2hPPG: 2 hr postprandial glucose, HbA1c: Hemoglobin A1C, PPAR: Peroxisome proliferator-activated receptor, GSK-3 beta: Glycogen synthase kinase 3 beta, TDS: 3 times a day
Figure 2Different mechanisms of antihyperglycemic effects of nettle