| Literature DB >> 36079856 |
Abstract
Cardiovascular (CV) system dysfunction can result in the development of cardiovascular diseases (CVDs), a key cause of death around the world. For many people, the most common treatment choices are still based on various plants used in traditional and folk medicine. Interestingly, many of these plants demonstrate various biological activities and pro-health properties; as such, there has been growing scientific interest in their use as medicines, including treatments for CVDs. Due to their varied biological properties, including anti-inflammatory and anticancer potential, the members of the Asteraceae and Cucurbitaceae have long been used in traditional medicine. These properties are believed to derive from the chemical composition of the plants, which includes various flavonoids, phenolic acids, and terpenes. Although many of their pro-health properties have been well described, their effect on the cardiovascular system and CVDs remains unclear. The present work reviews the current literature about the effects of preparations of vegetables of the Asteraceae and Cucurbitaceae families on the cardiovascular system and CVDs. Various species from the two families demonstrate antioxidant and antiplatelet activities in vitro and in vivo, which play key roles in the prophylaxis and treatment of CVDs. Additionally, some species have been evaluated for their anticoagulant activity. This review also describes the biological properties of these vegetables and discusses their anti-hyperlipidemic action, and their potential for obesity prevention and body weight control.Entities:
Keywords: Asteraceae; Cucurbitaceae; antiplatelet activity; cardiovascular disease; cardiovascular system; oxidative stress
Mesh:
Year: 2022 PMID: 36079856 PMCID: PMC9460361 DOI: 10.3390/nu14173601
Source DB: PubMed Journal: Nutrients ISSN: 2072-6643 Impact factor: 6.706
Comparative in vitro and in vivo studies of cardioprotective activity of vegetables from Cucurbitaceae and Asteraceae families.
| Vegetables | Cardioprotective Activity | Type of | Dose | Biological Material | Studies | References |
|---|---|---|---|---|---|---|
| Antioxidant Activity | ||||||
|
| Scavenging free radical, inhibition of lipid peroxidation, and carbonylation of plasma protein | methanol | 1–50 µg/mL | Human plasma | in vitro | [ |
| Scavenging free radicals | methanol | 100 mg/mL | Human serum | in vitro | [ | |
| Scavenging free radicals | water | 20 mg/mL | Human serum | in vitro | [ | |
|
| Decrease in free radical production | ethanol-aqueous | 1–20 μg/μL | PLB985 cells | in vitro | [ |
| Scavenging free radicals, inhibition of lipid peroxidation, and carbonylation of plasma protein | methanol | 1–50 µg/mL | Human plasma | in vitro | [ | |
|
| Scavenging free radicals | methanol/water | 1–5000 µg/mL | - | in vitro | [ |
|
| Scavenging free radicals | methanol/water | 1–5000 µg/mL | - | in vitro | [ |
|
| Scavenging free radicals | methanol/water | 1–5000 µg/mL | - | in vitro | [ |
|
| Inhibition of lipid peroxidation, | methanol, chloroform | 100 mg/mL | Human plasma | in vitro | [ |
|
| Decrease in biomarkers of oxidative stress in blood | methanol | 100%, | Male albino Wistar rats | in vivo | [ |
|
| Decrease in lipid peroxidation biomarkers in liver tissue | no solvent/dry extract | 300 mg/kg | Diabetic albino rats | in vivo | [ |
|
| Decrease in lipid peroxidation | water | 300 mg/kg | Male Sprague–Dawley rats | in vivo | [ |
| Antiplatelet activity | ||||||
|
| Inhibition of adhesion of thrombin- and ADP-activated platelets to fibrinogen | methanol | 1–50 µg/mL | Human blood platelets | in vitro | [ |
| Inhibition of adhesion of thrombin- and ADP-activated platelets to collagen and fibrinogen | methanol | 1–50 µg/mL | Human blood platelets | in vitro | [ | |
|
| Inhibition of platelet aggregation | water | 300 mL of 20 g chicory coffee | Human | in vivo | [ |
|
| Inhibition of ADP-induced platelet aggregation | ethanol | 250, 5000 and 1000 mg/kg | Swiss albino mouse | in vivo | [ |
| Anticoagulant activity | ||||||
|
| Inhibition of total thrombus formation | methanol | 50 µg/mL | Whole blood | in vitro | [ |
| Anti-hyperlipidemic activity | ||||||
|
| Inhibition of lipid accumulation | ethanol-aqueous | 20 μg/μL | HepG2 cells | in vitro | [ |
|
| Improvement of lipid profile | no solvent | 10 g/100 g of diet | male Wistar rats | in vivo | [ |
|
| Decrease in serum triglyceride and cholesterol | methanol | 60 mg/kg | Sprague–Dawley rats | in vivo | [ |
|
| Decrease in triglyceride and cholesterol in blood | ethanol-aqueous | 500 mg/kg | Adult mice | in vivo | [ |
| Antihypertensive activity | ||||||
|
| Decrease of nitric oxide | no solvent | 40 or 100 mg/kg of body weight | Sprague–Dawley rats | in vivo | [ |
|
| Decrease in blood pressure | water | 18% juice | Patients with mild-hypertension | in vivo | [ |
|
| modulation of endothelium-derived relaxing factors | ethanol-aqueous | 50–300 mg/kg | Sprague–Dawley rats | in vivo | [ |
| Anti-obesity and body weight control | ||||||
|
| Decrease in triglycerides content | methanol | 1 pg/mL to 10 μg/mL | 3T3-L1 preadipocytes | in vitro | [ |
|
| Decrease in LDL and triglycerides | methanol | 100, 200, 400 mg/kg | male Wistar rats | in vivo | [ |
|
| Decrease in blood pressure, lower body weight, and LDL level | ethanol/methanol | 100 mg/kg | male Wistar rats | in vivo | [ |
Figure 1The effect of selected vegetables from Cucurbitaceae and Asteraceae family on development of cardiovascular diseases.