A Comparative Phytochemical and Biological Study between Different Solvent Extracts of Leaves and Stems Extracts of Erica arborea L. and Viburnum tinus L. Plants Growing in Tunisia

2020 ◽  
Vol 15 (6) ◽  
pp. 686-691
Author(s):  
Meriem Elaloui ◽  
Amel Ennajah ◽  
Hanene Ghazghazi ◽  
Wiem Issami ◽  
Abir Mekni ◽  
...  
Keyword(s):  
Antioxidant Activity ◽  
Avena Sativa ◽  
Biological Activities ◽  
Inhibitory Effect ◽  
Point Of View ◽  
Biological Study ◽  
Allelopathic Effect ◽  
Total Phenols ◽  
Test Species ◽  
Erica Arborea

Background: Many Tunisian medicinal plants are widespread and are used in modern ethnomedecin due to their interesting biological activities. Considering natural products of plant origin, this study was conceived to evaluate the allelopathic effect of leaf and stem extracts of Erica arborea and Viburnum tinus on the seed germination and seedling development of Avena sativa. We identified the secondary metabolites that were responsible. Methods: Total phenols, flavonoids, tannins contents and antioxidant activity were evaluated using the Folin ciocalteux, Aluminum trichloride, vanillin and scavenging activity on 2, 2-diphenyl- 1picrylhydrazyl (DPPH) radicals methods, respectively. Leaf powders (5, 20, 40, 60 and 100 g) were macerated each with 1000 ml of distilled water for 24 h. The extracts were filtered through Whatman N°1 filter paper, pooled and concentrated under vacuum. Allelopathic bioassays were conducted using the obtained supernatant. Results: The obtained results indicated that acetonic extracts of the Viburnum leaves had the highest levels of total phenols (36.82 mg / g), flavonoïds (11.99 mg / g) and tannins (7.93 mg / g) and recorded a high antioxidant activity (0.054 mg / ml). Both test species showed that all organs had significant inhibitory effect on the development of Avena sativa. The leaves of Viburnum are best from the point of view inhibition of root length (-85.45%) and height of the aerial part (-78.95%). Conclusion: The inhibitory effects of these extracts were manifested much more on the development of seedlings. Extracts from Viburnum tinus leaves were the best inhibitors and could be regarded as promising candidates for natural plant source of antioxidant and herbicide agents.

scholarly journals IN VITRO BIOLOGICAL STUDY OF SEVEN NEPALESE MEDICINAL PLANTS AND ISOLATION OF CHEMICAL CONSTITUENTS FROM CISSAMPELOS PAREIRA

2020 ◽  
pp. 91-97
Author(s):  
MD AMIT ◽  
KHAGA RAJ SHARMA
Keyword(s):  
Antioxidant Activity ◽  
Medicinal Plants ◽  
Toxic Effect ◽  
Plant Extracts ◽  
Brine Shrimp ◽  
Biological Activities ◽  
Alpha Tocopherol ◽  
Biological Study ◽  
Phytochemical Analysis ◽  
Flavonoid Content

Objective: This study aimed to investigate the phytochemical analysis and biological activities of methanol extracts of seven medicinal plants such as Anisomeles indica, Achyranthes bidentata, Sphenomeris chinensis, Cleistocalyx operculatus, Malvaviscus arboreus, Cissampelos pareira, and Tectaria coadunate collected from Tanahun district of Nepal. Methods: Phytochemical analysis was performed by color differentiation methods adopting the standard protocol. Antioxidant activity of plant extracts was evaluated by 2,2-diphenyl-1-picrylhydrazyl radical scavenging assay. Flavonoid content was estimated by aluminum chloride colorimetric method. Antidiabetic activity was evaluated by α-amylase inhibition assay where acarbose was used as standard. Toxic effect was studied by brine shrimp bioassay. Results: Phytochemical analysis showed the presence of alkaloids, polyphenols, flavonoids glycoside, and terpenoid in most of the extracts. T. coadunate and C. pareira exhibited high antioxidant activity with IC50 41.84 and 52.03 μg/ml, respectively. Whereas, the plant extracts of Malvaviscus arboretum, S. chinensis, and A. bidentata exhibited moderate antioxidant activity with IC50 76.07, 81.05, and 89.93 µg/ml, respectively. The result of flavonoid content showed the values ranged A. indica (1.84 mg quercetin equivalent per gram [mg QE/g]) to A. bidentata (5.93 mg QE/g). C. pareira and S. chinensis exhibited the highest α amylase inhibition activity with IC50 471.68 and 517.59 µg/ml, respectively. Whereas, A. indica and M. arboreus showed moderate activity with IC50 626.12 and 952.39 μg/ml, respectively. C. pareira exhibited against Staphylococcus aureus (ATCC 25923) with a zone of inhibition 12 mm/well, and Escherichia coli (ATCC 25922) 9 mm/well but, T. coadunate showed 14 mm/well against S. aureus. The plant extracts of A. bidentata and C. operculatus showed toxic effect against newly hatched brine shrimp larvae. The chemical compounds isolated from C. pareira indicated by gas chromatography-mass spectrometry analysis were 3-isopropoxy-1,1,1,7,7,7-hexamethyl-3,5,5-tris(trimethylsiloxy) tetrasiloxane, alpha-tocopherol, pentadecanoic acid, and 4,22-stigmastadiene-3-one. The major compound was indicated by percent peak area and base m/z value as alpha-tocopherol. Conclusion: Present study revealed that plant extracts are the potential source of antioxidant, antidiabetic, and antibacterial agents showing different biological activities. The results of this study provide partial scientific support for the traditional application of medicinal plants to cure diabetes and infectious diseases, although further studies are needed to assess the mechanism of action.

scholarly journals Storage Effect on Phenols and on the Antioxidant Activity of Extracts fromAnemopsis californicaand Inhibition of Elastase Enzyme

2015 ◽  
Vol 2015 ◽  
pp. 1-8 ◽  
Author(s):  
Carmen Lizette Del-Toro-Sánchez ◽  
Melesio Gutiérrez-Lomelí ◽  
Eugenia Lugo-Cervantes ◽  
Florentina Zurita ◽  
Miguel Angel Robles-García ◽  
...  
Keyword(s):  
Antioxidant Activity ◽  
Phenolic Content ◽  
Good Alternative ◽  
Storage Conditions ◽  
Inhibitory Effect ◽  
The Other ◽  
Storage Effect ◽  
Total Phenols ◽  
Methanolic Extracts ◽  
Anemopsis Californica

The amount of total phenols and flavonoids and the antioxidant activity of leaf, stem, and rhizome methanolic extracts from a commonly consumedAnemopsis californicaunder different storage conditions were investigated. Storage conditions were at 50, 25, 4, and −20°C, protected or not from light, during 180 days. The inhibition of the elastase enzyme was also evaluated. The results demonstrated that leaf, stem, and rhizome methanolic extracts ofAnemopsis californicamaintain approximately up to 97 and 95% stability in phenolic content and antioxidant activity, respectively, when stored during 60 days at −20°C in the dark. Additionally, these extracts, principally from leaf and rhizome, showed an elastase inhibitory effect by 75 and 71.8%, respectively. Therefore, this study provides the basis for further research on the anti-inflammatory activity. On the other hand,Anemopsis californicacould comprise a good alternative of use as antioxidant in foods.

scholarly journals Seasonal Effect on the Biological Activities of Litsea glaucescens Kunth Extracts

2018 ◽  
Vol 2018 ◽  
pp. 1-11 ◽  
Author(s):  
Julio César López-Romero ◽  
Humberto González-Ríos ◽  
Aida Peña-Ramos ◽  
Carlos Velazquez ◽  
Moises Navarro ◽  
...  
Keyword(s):  
Antioxidant Activity ◽  
Cell Lines ◽  
Antiproliferative Activity ◽  
Biological Activities ◽  
Antimicrobial Activities ◽  
Inhibitory Effect ◽  
Biological Properties ◽  
Seasonal Effect ◽  
Microdilution Method ◽  
High Antioxidant Activity

This study shows the seasonal effect on the antioxidant, antiproliferative, and antimicrobial activities of L. glaucescens Kunth (LG) leaves extracts. Their antioxidant activity was evaluated through the DPPH, FRAP, and ORAC assays. Their phenolic content (PC) was determined by means of the Folin-Ciocalteu method, and the main phenolic compounds were identified through a HPLC-DAD analysis. Antiproliferative activity was determined by MTT assay against HeLa, LS 180, M12.C3.F6, and ARPE cell lines. Antimicrobial potential was evaluated against Staphylococcus aureus and Escherichia coli using a microdilution method. All the LG extracts presented high antioxidant activity and PC, with quercitrin and epicatechin being the most abundant. Antioxidant activity and PC were affected by the season; particularly autumn (ALGE) and summer (SULGE) extracts exhibited the highest values (p<0.05). All extracts presented moderate antiproliferative activity against the cell lines evaluated, HeLa being the most susceptible of them. However, ALGE and SULGE were the most active too. About antimicrobial activity, SULGE (MIC90<800 μg/mL; MIC50 < 400 μg/mL), and SLGE (MIC50 < 1000 μg/mL) showed a moderate inhibitory effect against S. aureus. These findings provide new information about the seasonal effect on the PC and biological properties of LG extracts. Clearly, antioxidant activity was the most important with respect to the other two.

scholarly journals Phytochemical Screening and Antidiabetic, Antihyperlipidemic, and Antioxidant Properties ofAnthyllis henoniana(Coss.) Flowers Extracts in an Alloxan-Induced Rats Model of Diabetes

2018 ◽  
Vol 2018 ◽  
pp. 1-14 ◽  
Author(s):  
Ameur Ben Younes ◽  
Maryem Ben Salem ◽  
Hanen El Abed ◽  
Raoudha Jarraya
Keyword(s):  
Antioxidant Activity ◽  
Ethyl Acetate ◽  
Ethyl Acetate Extract ◽  
Biological Activities ◽  
Antioxidant Properties ◽  
Inhibitory Effect ◽  
Diabetic Rats ◽  
Histological Results

Background. This study investigates the biological activities ofAnthyllis henonianaflowers extracts.Materials and Methods. Antioxidant activity and thein vitroinhibitory effect of key digesting enzymes related to postprandial hyperglycemia were determined. Diabetic rats were orally and daily given the best extract from flowers ofAnthyllis henonianaat a dose of acarbose for one month.Results. Among the extracts, the ethyl acetate one displayed remarkable antioxidant activity including DPPH (IC50= 2.34 mg/mL) and was more effective in inhibitingα-glucosidase (IC50= 17μg/mL) thanα-amylase (IC50= 920μg /mL) activities.In vivo, the results proved that ethyl acetate extract at doses of 400 mg/kg bw decreased significantly the blood glucose level and lipid profile levels and increased the activities of antioxidant enzymes. These protective impacts ofAnthyllis henonianaethyl acetate flowers extract were confirmed by histological results.Conclusion. This study demonstrates, for the first time, thatAnthyllis henonianaflowers ethyl acetate extract is effective in inhibiting hyperglycemia and oxidative stress caused by diabetes.

scholarly journals Antioxidant activity, antibacterial and inhibitory effect of intestinal disaccharidases of extracts obtained from Eugenia uniflora L. Seeds

2020 ◽  
Author(s):  
J. Lazzarotto-Figueiró ◽  
A. P. Capelezzo ◽  
M. S. Z. Schindler ◽  
J. F. C. Fossá ◽  
D. Albeny-Simões ◽  
...  
Keyword(s):  
Antioxidant Activity ◽  
Inhibitory Action ◽  
Biological Activities ◽  
Industrial Sector ◽  
Inhibitory Effect ◽  
Eugenia Uniflora ◽  
Positive Strain ◽  
Phytochemical Profile ◽  
Wide Geographic Distribution ◽  
Intestinal Disaccharidases

Abstract The use of medicinal plants for disease prevention, treatment and cure is an ancient practice used by humanity, and many plants species are used in bioprospecting research. In this context, its stands out Eugenia uniflora L., populary known as pitangueira and belongs to the Myrtaceae family, with a wide geographic distribution and native of Brazil. In view of the therapeutic qualities of the plant and the lack of the studies on its seeds, the present study had as objective to evaluate the phytochemical profile of the extracts of Eugenia uniflora L. seeds, from different solvents, as well as their antibacterial activity, antioxidant and its inhibitory effect of intestinal disaccharidases. Results showed a high content of phenolic compounds and total flavonoids, thus characterizing antioxidant activity, also highlighting the best bacteriostatic action for the Gram positive strain of Staphylococcus aureus in the ethanolic fraction. Regarding the disaccharidases, a strong inhibitory action was observed for all concentrations, evidencing a antihyperglycemic potential. The present research allowed to concluded that Eugenia uniflora L. seeds have promising biological activities for the industrial sector, but a more detailed investigation is needed regarding their bioactive compounds.

SYNTHESIS AND ANTIOXIDANT ACTIVITY OF SOME NEW SULFONAMIDE DERIVATIVES

2021 ◽  
Author(s):  
Jovana M. Muškinja ◽  
◽  
Jelena S. Katanić Stanković ◽  
Zoran R. Ratković
Keyword(s):  
Antioxidant Activity ◽  
Antioxidant Activities ◽  
Biological Activities ◽  
Point Of View ◽  
Important Class ◽  
Dpph Radical ◽  
Sulfa Drugs ◽  
Nmr Methods ◽  
In Vitro Antioxidant Activity

Sulfonamide derivatives are a very important class of compounds with pronounced biological activities and, for this reason, they have very useful pharmaceutical applications. They are the basis of several groups of drugs and are known as sulfa-drugs. From this point of view, the present study focuses on the synthesis of some novel structural hybrids incorporating two very important groups, sulfonamide, and pyrazoline. The new sulfonamide-based pyrazolines were synthesized in very good yields. The structures of the sulfonamide compounds were confirmed by IR and NMR methods. Synthesized compounds were tested for their antioxidant activities using two different methods, DPPH radical and ABTS radical cation scavenging assays. The results showed relatively good in vitro antioxidant activity.

Improvement of cytoprotective and antioxidant activity of Rosa canina L. and Salix alba L. by controlled differential sieving process against H2O2-induced oxidative stress in mouse primary splenocytes

2017 ◽  
Vol 87 (3-4) ◽  
pp. 191-200 ◽  
Author(s):  
Nidhal Soualeh ◽  
Aliçia Stiévenard ◽  
Elie Baudelaire ◽  
Rachid Soulimani ◽  
Jaouad Bouayed
Keyword(s):  
Antioxidant Activity ◽  
Antioxidant Activities ◽  
Biological Activities ◽  
Good Alternative ◽  
Activity Levels ◽  
Salix Alba ◽  
Rosa Canina ◽  
Free Process ◽  
Plant Powders ◽  
Sieving Process

Abstract. In this study, cytoprotective and antioxidant activities of Rosa canina (RC) and Salix alba (SA), medicinal plants, were studied on mouse primary splenocytes by comparing Controlled Differential Sieving process (CDSp), which is a novel green solvent-free process, versus a conventional technique, employing hydroethanolic extraction (HEE). Thus, preventive antioxidant activity of three plant powders of homogeneous particle sizes, 50–100 µm, 100–180 µm and 180–315 µm, dissolved directly in the cellular buffer, were compared to those of hydroethanolic (HE) extract, at 2 concentrations (250 and 500 µg/mL) in H2O2-treated spleen cells. Overall, compared to HE extract, the superfine powders, i. e., fractions < 180 µm, at the lowest concentration, resulted in greater reactive oxygen species (ROS) elimination, increased glutathione peroxidase (GPx) activity and lower malondialdehyde (MDA) production. Better antioxidant and preventive effects in pre-treated cells were found with the superfine powders for SA (i. e., 50–100 µm and 100–180 µm, both p < 0.001), and with the intermediate powder for RC (i. e., 100–180 µm, p < 0.05) versus HE extract. The activity levels of catalase (CAT) and superoxide dismutase (SOD) in pretreated splenocytes exposed to H2O2, albeit reduced, were near to those in unexposed cells, suggesting that pretreatment with the fine powders has relatively restored the normal levels of antioxidant-related enzymes. These findings supported that CDSp improved the biological activities of plants, avoiding the use of organic solvents and thus it could be a good alternative to conventional extraction techniques.

Regioselective Synthesis of Potent 4,5,6,7-Tetrahydroindazole Derivatives via Microwave-assisted Vilsmeier-Haack Reaction and their Antioxidant Activity Evaluation

2019 ◽  
Vol 16 (3) ◽  
pp. 194-201 ◽  
Author(s):  
Renu Bala ◽  
Vandana Devi ◽  
Pratibha Singh ◽  
Navjot Kaur ◽  
Pawandeep Kaur ◽  
...  
Keyword(s):  
Antioxidant Activity ◽  
Microwave Irradiation ◽  
Biological Activities ◽  
Reaction Times ◽  
Conventional Heating ◽  
High Chemical ◽  
Microwave Assisted ◽  
Work Up ◽  
Active Methylene ◽  
By Products

Background: Tetrahydroindazole, a member of the fused-pyrazole system, is a least studied class of heterocyclic compounds owing to its scarcity in nature. However, a large number of synthetically prepared tetrahydroindazoles are known to show a variety of biological activities such as interleukin- 2 inducible T-Cell kinase inhibitors, AMPA receptor positive allosteric modulators, antitumor, antituberculosis, anti-inflammatory and antimicrobial activities. Vilsmeier-Haack reaction is one of the most important chemical reactions used for formylation of electron rich arenes. Even though Vilsmeier- Haack reaction was studied on a wide variety of hydrazones derived from active methylene compounds, literature lacks the examples of the use of 4-substituted cyclohexanones as a substrate for the synthesis of 4,5,6,7-tetrahydroindazoles. The study of the reaction of Vilsmeier-Haack reagent with hydrazones derived from cyclic keto compounds having active methylene has been considered the interested topic of investigation. In the present study, ethyl cyclohexanone-4-carboxylate was treated with one equivalent of various hydrazines for two hours and the resulted hydrazones were further treated with an OPC-VH reagent (Vilsmeier-Haack reagent isolated from phthaloyl dichloride and N,Ndimethylformamide) afforded 4,5,6,7-tetrahydroindazoles in excellent yields. The synthesized compounds 4a-f and 5a-f were screened for their antioxidant activities using the DPPH radical scavenging assay. The target compounds were synthesized regioselectively using 4+1 approach in excellent yields. A number of experiments using both conventional heating as well as microwave irradiation methods were tried and on comparison, microwave irradiation method was found excellent in terms of easy work up, high chemical yields, shortened reaction times, clean and, no by-products formation. Some of the synthesized compounds showed significant antioxidant activity. The microwave assisted synthesis of 4,5,6,7-tetrahydroindazoles from ethyl cyclohexanone-4-carboxylate has been reported under mild conditions in excellent yield. Easy work up, high chemical yield, shortened reaction times, clean and no by-products formation are the major advantages of this protocol. These advantages may make this method useful for chemists who are interested in developing novel 4,5,6,7-tetrahydroindazole based drugs.

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