| Literature DB >> 35683996 |
Fatiha Brahmi1, Anne Vejux2, Imen Ghzaiel2,3, Mohamed Ksila2,4, Amira Zarrouk3,5, Taoufik Ghrairi4, Soukena Essadek2,6, Stéphane Mandard7, Valerio Leoni8, Giuseppe Poli9, Dominique Vervandier-Fasseur10, Omar Kharoubi11, Adil El Midaoui12,13, Atanas G Atanasov14, Smail Meziane15, Norbert Latruffe2, Boubker Nasser6, Balkiss Bouhaouala-Zahar16, Olfa Masmoudi-Kouki4, Khodir Madani1,17, Lila Boulekbache-Makhlouf1, Gérard Lizard2.
Abstract
Coronavirus illness (COVID-19) is an infectious pathology generated by intense severe respiratory syndrome coronavirus 2 (SARS-CoV-2). This infectious disease has emerged in 2019. The COVID-19-associated pandemic has considerably affected the way of life and the economy in the world. It is consequently crucial to find solutions allowing remedying or alleviating the effects of this infectious disease. Natural products have been in perpetual application from immemorial time given that they are attested to be efficient towards several illnesses without major side effects. Various studies have shown that plant extracts or purified molecules have a promising inhibiting impact towards coronavirus. In addition, it is substantial to understand the characteristics, susceptibility and impact of diet on patients infected with COVID-19. In this review, we recapitulate the influence of extracts or pure molecules from medicinal plants on COVID-19. We approach the possibilities of plant treatment/co-treatment and feeding applied to COVID-19. We also show coronavirus susceptibility and complications associated with nutrient deficiencies and then discuss the major food groups efficient on COVID-19 pathogenesis. Then, we covered emerging technologies using plant-based SARS-CoV-2 vaccine. We conclude by giving nutrient and plants curative therapy recommendations which are of potential interest in the COVID-19 infection and could pave the way for pharmacological treatments or co-treatments of COVID-19.Entities:
Keywords: COVID-19; anti-inflammatory effect; antioxidant activity; antiviral activity; diet; medicinal plants; nutrients
Mesh:
Substances:
Year: 2022 PMID: 35683996 PMCID: PMC9182601 DOI: 10.3390/nu14112194
Source DB: PubMed Journal: Nutrients ISSN: 2072-6643 Impact factor: 6.706
Figure 1Mechanism of infection by SARS-CoV-2.
Medicinal plants efficient against COVID-19 infection.
| Latin/Vernacular Names | Nature of Extracts or Components | Mode of Action | Refs. |
|---|---|---|---|
| Purified seselin | Inhibitory potential over multiple SARS-COV-2 targets such as SARS-CoV-2S spike protein, COVID-19 main protease and free enzyme of the SARS-CoV-2 (2019-nCoV) main protease. | [ | |
| Pyrethrin | Acts as ligands with viral proteins to prevent the binding of host receptors and the fusion leading to viral replication. | [ | |
| Andrographolide/Andrographiside | ACE inhibition/SARS-3CLpro inhibition of the NOD-like receptor protein 3 (NLRP3), caspase-1 and interleukin-1β (IL-1β) particules. | [ | |
| Hydroalcoholic crude extract | ACE inhibition/IC50 = 82.88%. | [ | |
| Polyphenol (Rutin), theaflavin-3,30-digallate, tannic acid, [−]-epigallocatechin gallate) | ACE inhibition, SARS-3CLpro inhibition. | [ | |
| Emetine | Displayed strong anti-CoV activity by blocking MERSCoV entry consistent with pseudovirus entry assays. | [ | |
| Hesperetin, hesperidin Rhoifolin, Neohesperidin | SARS-3CLpro inhibition in a dose-dependent manner. | [ | |
| Curcumin and its analogue | In a molecular docking study, curcumin and few of its derivatives are suggested as SARS-CoV-2 spike protein inhibitors. | [ | |
| Cynaroside | ACE inhibition/IC50 = 49.7% | [ | |
| - | SARS-3CLpro inhibition/ | [ | |
| Flavone (Scutellarin) | ACE inhibition. | [ | |
| Herbacetin | 3CL inhibitory activity. | [ | |
| Tetra- | Binding with surface spike protein of SARS-CoV. | [ | |
| Glycyrrhizin | Inhibition of COVID-19 replication and entry to its host cells. | [ | |
| Herbacetin | SARS-3CLpro inhibition. | [ | |
| Chlorogenic acid | ACE inhibition. | [ | |
| The aqueous extract | Inhibition of RNA-dependent RNA polymerase (RdRp), 3CL-like protease and viral polymerase. | [ | |
| Hypericin | C-terminal and N-terminal domains of 2019-nCoV NSP 14 can bind Hypericin. | [ | |
| Phenol (indigo, sinigrin, aloe emodin, hesperetin, sinigrin), 2,2-Di(3-indolyl)-3-indolone, phaitanthrin D | Inhibit the cleavage activity of SARS-3CLpro enzyme/IC50 = 53.8 ± 4.2 μg/mL. | [ | |
| Flavonoids such as rhoifolin, pectolinarin, Epigallocatechin gallate, Gallocatechin gallate, quercetin and herbacetin | Inhibition of SARS-3CLpro activity. | [ | |
| Glycyrrhizic acid derivatives | Reduction or inhibition of penetration and viral attachment (IC50 = 2.4 ± 0.2 μg/mL). | [ | |
| Nigellidine and α-hederin | High potential to act as COVID-19 treatment in docking studies. | [ | |
| Tulsinol and dihydroeugenol | Effective against SARS CoV 2 in molecular docking studies. | [ | |
| Emodin | Inhibit interaction of SARS-CoV spike protein and ACE2. | [ | |
| Bavachinin, psoralidin | The ethanol extracts of these secondary metabolites show high activity | [ | |
| Anthraquinone (Emodin) | Positive ACE inhibitor in combination with ACEI/ARB agents. | [ | |
| Ethanol extract | Significant reduction in virus yield, plaque formation and virus attachment. | [ | |
| Baicalin, cosmosiin | ACE inhibition and SARS-3CLpro inhibition. | [ | |
| Quercetin and TSL-1 | Inhibition of the cellular entry of SARS-CoV. | [ | |
| Amentoflavone and Apigenin | Showed the most potent 3CLpro inhibitory effect. | [ | |
| Tylophorine | Tylophorine-based biomolecules exhibit broad spectrum potential for inhibiting coronaviruses. | [ | |
| Luteolin | Avidly binds with surface spike protein of SARS-CoV. | [ | |
| Withanone and withaferin | Effective against SARS CoV-2 in bioinformatic studies. | [ |
Mode of action of some nutrients tested against COVID-19.
| Nutrients Types | Mode of Action against | Refs. |
|---|---|---|
| Macronutrients | ||
| Protein | Oral and IV glutathione, glutathione precursors (N-acetyl-cysteine) block NF-κB. | [ |
| Polyunsaturated fatty acids | Suppress inflammation and augment phagocytosis. | [ |
| Probiotics | Inhibit SARS-CoV-2 main protease, S1 glycoprotein and angiotensin-converting enzyme. | [ |
| Micronutrients | ||
| Vitamin B-complexes |
Vit B1 acts as a carbonic anhydrase isoenzyme inhibitor. | [ |
| Vitamin C | Inhibits cytokine storm through reducing | [ |
| Vitamin D | Vitamin D tablets can be taken to reduce | [ |
| Vitamin E | Inactivation of 15-lipoxygenase by the reduction of Fe3+ to Fe2+ leading to ferroptosis prevention. | [ |
| Magnesium | Reduction in lung inflammation response and oxidative stress, and inhibition of bronchial smooth muscle contraction; favors bronchodilation. | [ |
| Zinc | Doxycycline, a tetracycline antibiotic, is known to chelate Zn from matrix metalloproteinases, which may help in part to inhibit the COVID-19 infection by limiting its ability to replicate in the host. | [ |
| Selenium | Enhance adaptive immunity by reinvigorating cytotoxic cells and moderating the release of inflammatory cytokines by the innate immune system. | [ |
| B12 supplements (500 μg), vitamin D (1000 IU) and magnesium | Reduce COVID-19 symptom severity and the need for oxygen and intensive care support. | [ |
| Vitamin C and E | Ameliorate cardiac injuries of critically ill COVID-19 patients. | [ |
| Copper, Iodine, Selenium, Zinc | Immune enhancers towards SARS CoV 2. | [ |
Figure 2Different food classes with positive effects in the treatment of the COVID-19 infection.