| Literature DB >> 35087593 |
Arka Jyoti Chakraborty1, Tanvir Mahtab Uddin1, B M Redwan Matin Zidan1, Saikat Mitra1, Rajib Das1, Firzan Nainu2, Kuldeep Dhama3, Arpita Roy4, Md Jamal Hossain5, Ameer Khusro6, Talha Bin Emran7.
Abstract
As Allium cepa is one of the most important condiment plants grown and consumed all over the world, various therapeutic and pharmacological effects of A. cepa were reviewed. Onion (Allium cepa) is a high dietary fiber-rich perennial herb that is placed under the family Amaryllidaceae. It contains high concentration of folic acid, vitamin B6, magnesium, calcium, potassium, and phosphorus as well as vitamins and minerals. It is widely used as an antimicrobial agent, but it showed anticancer, antidiabetic, antioxidant, antiplatelet, antihypertensive, and antidepressant effects and neuroprotective, anti-inflammatory, and antiparasitic effects and so on. It is said to have beneficial effects on the digestive, circulatory, and respiratory systems, as well as on the immune system. This review article was devoted to discussing many health benefits and traditional uses of onions in pharmacological perspectives, as well as the safety/toxicological profile. If more detailed research on this perennial herb is conducted, it will open the door to an infinite number of possibilities.Entities:
Year: 2022 PMID: 35087593 PMCID: PMC8789449 DOI: 10.1155/2022/4586318
Source DB: PubMed Journal: Evid Based Complement Alternat Med ISSN: 1741-427X Impact factor: 2.629
Figure 1(a, b) Bioactive compounds of Allium cepa.
Figure 2Major therapeutic effects of Allium cepa.
An overview of recent in vivo and in vitro studies of Allium cepa based on its therapeutic efficacy.
| Field of Study | Subject | Dosage | Outcome | Mechanism of Action | References |
|---|---|---|---|---|---|
| Antimicrobial effect (in vivo) | Broiler chicks | 1.5–2.5 g | Population of | Onion may alter a microflora intestinal, which improves digestion and absorption of nutrients in the intestines | [ |
| Antimicrobial effect (in vitro) |
| Powdered bulb onion | The strain tested had MIC = 93.8 ± 44.2 µg/mL and MBC = 312.5 ± 265 µg/mL showing that | Destroys bacteria by using their most active extract forms, or combining them to achieve latent synergistic effects | [ |
| Food-borne bacterial strains | 15.6–1000 | All bacteria projected inhibition zone, but a greater inhibitory effect was observed for | n.m. | [ | |
| Gram-positive and Gram-negative bacteria | n.m. | Methanolic extract of onion inhibits | Flavonoids, phenolic compounds, quercetin inhibited the growth of Gram positive and Gram-negative bacteria | [ | |
| Gastrointestinal tract pathogens | n.m. | 100% aqueous extracts of green onion bulbs displayed maximum bacterial kill, and its kill rate is slightly higher than the kill rate by positive control for | Flavonoids and phenolic compounds of green onion bulb destroy bacterial membrane and shows antibacterial activity | [ | |
| Antiplatelet activity (in vivo) | Sprague Dawley rats | 6 µg/mL | Significant inhibition of aggregation of platelets | Flavones such as apigenin, chrysin, and phloretin inhibited aggregation of platelets | [ |
| Rats | 5 | Platelet aggregation was inhibited | Inhibition of aggregation-inducing molecules, thromboxane A2 (TXA2), and intracellular Ca2+ by blocking TXA2 synthase (TXAS) and cyclooxygenase-1 (COX-1) activities | [ | |
| Antiplatelet activity (in vitro) | Two healthy nonsmoker donors | n.m. | The dose-response curves developed using different dosages of allium juice vs. the percentage of inhibition of aggregation are calculated for juice levels needed to reduce platelet aggregation by 50% (IC50) | Aglycone part did not take part in inhibiting platelet aggregation. The flavone part of flavonoids of | [ |
| Gallstone treatment (in vivo) | Sprague Dawley rats | 7% (w/w) onion powder | Lowered ballooning, hepatic steatosis, and lobular inflammation | Quercetin decreases the levels of hepatic enzymes, serum lipids, steatosis, and inflammation through regulating the expressions of NF-kB, p65, Sirt1, and iNOS | [ |
| Antiparasitic activity (in vitro) |
| 3–5 µg/mL | Zwiebelane in the onion extract killed both types of parasites efficiently | The forming of disulfide bonds between SH classes of essential redox compounds and secondary metabolites containing sulfur are inhibiting trypanothion reductases | [ |
| Antidepressant activity (in vivo) | Albino Wistar mice | 200 mg/kg/day | Immobilization stress substantially reduced | Reduce stress by its potential antioxidant mechanism | [ |
| Anti-inflammatory (in vivo) | Wistar rats | 35–140 mg/kg/day | Reduced the pulmonary inflammatory cells, such as eosinophil, neutrophil, and monocyte and overall WBC | Inhibited NF- | [ |
| BV-2 microglial cells | 50–500 mg/mL | Attenuated neuroinflammation | Onion increases iNOS expression at the protein levels and mRNA in LPS-stimulated BV-2 microglial cells, thus reducing proinflammatory cytokines IL-1-b, TNF-a, and IL-6 | [ | |
| Wistar rats | 150 and 300 mg/kg | Reduced lymphocyte and eosinophil count in the blood and bronchoalveolar lavage fluid (BALF) | n.m. | [ | |
| Inflammatory responses (in vitro) | RAW 264.7 cells | 100 mg/mL | LPS-induced inflammation | Dose-dependent reduction in IL-6, TNF-a, and IL-1-b secretion, as well as NO production | [ |
| Neuroprotective activity (In vivo) | Swiss albino male mice | 200 mg/kg/day | Reduced lipid peroxidation and nitrate/nitrite ratios, as well as increased GSH and catalase activities. The amount of AChE in the body was also decreased. | Quercetin, kaempferol, cycloartenol, phytosterols like lophenol, 24-ethyl cycloartenol, and 24-methyl lophenol have been found to inhibit transcription of genes like FAS, S14, transferrin, apolipoprotein CIII | [ |
| Mice | 300 mg/kg | Protects mice from neuronal harm in I/R induced retinal injury. | Changes the expression of neurotrophic factor | [ | |
| Ashthma (in vivo) | Blomia | 100–1000 mg/kg | Induced asthma | Reduced IL-4, IL-5, IL-13, and IgE levels | [ |
| Inhibitory and stimulatory activity (in vivo) | Mice | 10–200 g | Inhibitory effect on Th2 activity and stimulatory effect on Th1 | Th2 cytokines, IL-4, IL-5, and IL-13, as well as IgE, were inhibited at 1000 µg/mL | [ |
| Osteoclastogenesis (in vitro) | RAW264.7 cells | 100–1000 | Induced inflammatory conditions | Cepa inhibited the development of IL-6 and IL-1a while increasing the production of IL-3 and IL-4 and inhibiting the NF- | [ |
| In breast cancer (in vivo) | Female BALB/ | 0.1 mL/100 g bw | Stimulatory effects on Th1 but inhibitory effects on Th2 activity | Induced decreases in IL-4 and rises in IFN-c levels and IFN-c/IL4 ratio (Th1/Th2 balance) | [ |
| Allergic rhinitis (In vivo) | BALB/c mice | 20–40 mL | Decreased allergic symptoms, Reduced eosinophil penetration of nasal turbinate mucosa, and OVA-specific IgE levels | Levels of IL-4, IL-5, IL-10, IL-13, and IFN-c decreased in groups treated with onion extract | [ |
| Immunomodulatory property (in vitro) | BALB/c mice | 3.5–15 | Showed immunomodulatory properties | Inhibited the development of Th2 cytokines such as IL-4, IL-5, IL-13, and IgE | [ |
| Immunoprotective effects (in vivo) | Wistar rats | 1–100 intraperitoneal | Natural and cyclophosphamide-induced immunosuppression | TNF-a, IL-10, COX-2, IgG and IgA levels in serum were increased by and immune parameters such as myeloid cells (RBC, WBC, and hb), body weight, splenic index, and thymic index in the spleen and thymus were enhanced | [ |
| Lung disorder (in vivo) | Wistar rats | 0.175–0.7 mg/mL | WBC count were improved, but their lymphocytes were reduced ( | A significant decrease in tracheal tolerance, neutrophil and eosinophil counts, but a significant increase in lymphocyte count ( | [ |
| Hepatoprotective (in vivo) | Adult male albino rats | 200–450 mg/kg | Decreased alanine aminotransferase and overall serum bilirubin levels in a dose-dependent way | Decrease in alanine levels. Paracetamol hepatotoxic rats' aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP), lactate dehydrogenase (LDH), and complete serum bilirubin (TSB). | [ |
| Anti-cancer effect (in vitro) | Murine ovarian cancer model | 20 mg/kg | Blocks tumor cell growth | Blocks the activation of M2 macrophages | [ |
| Antidiabetic effect (in vivo) | Diabetic rats | Aqueous extract of onions (25 mg/kg) for 21 days | Reduced blood glucose level | Increased glucose uptake into soleus muscle | [ |
| Rats | 200 mg/kg | Decrease in blood glucose level | Stimulate the formation of pancreatic | [ | |
| Rats | 3 mL/100 g | Decrease in blood glucose level | n.m. | [ | |
| Antihypercholesterolemic effect (in vivo) | Sprague Dawley rats | 4.5 g/kg body weight | Inhibited the formation of atherosclerosis | n.m. | [ |
| Mice | 2% raw or heat processed onions with high cholesterol diet | Reduced the risk of CGS | Decrease cholesterol secretion in bile and increase bile acid excretion | [ | |
| Antioxidant effects (in vivo) | Broiler chicken | 3 g/kg diet | Increased antioxidant enzyme activities | n.m. | [ |
| Antiobesity effects (in vivo) | Rats | 92.6 mg/kg bw/days | Weight gain reduced significantly compared to the rats who were only fed high fat diet | n.m. | [ |
MIC = minimum inhibitory concentration, MBC = minimum bactericidal concentration, IZD = inhibition zone diameter, n.m. = not mentioned, HDL = high density lipoprotein, LDL = low density lipoprotein, ACA = Allium cepa agglutinin, PROE = phenol-rich onion extract, CGS = cholesterol gallstone.
Clinical studies of Allium cepa based on its pharmacological effects.
| Field of Study | Subject | Dosage | Outcome | Mechanism of Action | References |
|---|---|---|---|---|---|
| Cardioprotective effect | 24 healthy pilot | 100 mL onion juice/day | Total cholesterol, waist circumference, and LDL-C reduced substantially | Onion juice contains quercetin which markedly attenuated LDL-c, serum total cholesterol, and HDL-c levels in healthy mild hypercholesterolemic subjects | [ |
| Wound healing | 39 patients | Onion extract ( | Hypertrophic scars and keloids were attenuated properly | Onion extracts inhibit vascular endothelial growth factor (VEGF) production which is the prime cause of HTS and keloids | [ |
| Antihypertensive effects | 70 people | 162 mg/day | Systolic BP was reduced by −3.6 mmHg | Mechanisms remain unclear | [ |
| Anti-inflammatory effects | In human epidermal keratinocytes | 15 mg/mL extract | Stimulatory effect on Th1 and inhibitory effect on Th2 activity | Reduced amounts of IL-6, IL-10, and TNF- | [ |
| Anticancer effects | Human | 10 g/day | Reduced risk of prostate cancer | Activation of detoxifying enzymes by organosulfur compounds | [ |
| Human | Taking a combination of 200 mg synthetic DATS and 100 | Gastric cancer risk is reduced | DATS triggers cancer cell cycle arrest at the G2/M phase | [ | |
| Antihypercholesterolemic effect | 24 hypercholesterolemic patients | 100 mL onion juice for 8 weeks | Reduction in serum TC, LDL-c, LDL-c/HDL-c levels | Increase LDL receptor mRNA expression and increase bile acid synthesis | [ |
| Antiobesity effects | 72 overweight and obese humans | 50 mg | Reduction in body weight, BMI, waist circumference | As an anti-oxidant, quercetin scavenges free radicals and restores the respiration process in the adipocytes | [ |
BW = body weight; n.m. = not mentioned; DATS = diallyl trisulfide; TC = total cholesterol; LDL-c = low density lipoprotein cholesterol; HDL-c = high density lipoprotein cholesterol; HTS = hypertrophic scars; BP = blood pressure; OPE = onion peel extract; ZnO-NPs = zinc oxide nanoparticles.