Extract Of Whole Plant Research Articles

Antibacterial activity of methanol extract from Wedelia biflora (L.) DC. growing in the Can Gio Mangrove Biosphere Reserve, Vietnam

The study investigated antibacterial activity of methanol extract of Wedelia biflora (L.) DC. (Wollastonia biflora or Melanthera biflora) growing in the Can Gio Mangrove Biosphere Reserve, Vietnam by using agar well diffusion method. Antimicrobial activity strength of Wedelia biflora (L.) DC. was depended on diameter of antibacterial zone causing by the methanol extract. The findings showed that methanol extract of whole plants, Wedelia biflora (L.) DC. exhibited antibacterial activity against Gram (+) bacteria: Bacillus cereus and Staphylococcus aureus but negative effects on Gram (-) bacteria: Pseudomonas aeruginosa and Escherichia coli. Its antibacterial activity increased with increase in extract concentration. Only extract with concentration of 1000 mg mL-1 had moderately antibacterial strength against B. cereus but the extract with other tested concentrations had antibacterial activity at weak level according to Manuanza’s rating scale of antibacterial zones.

Phytochemical Screening and Pharmacological Activities of Gentiana ornata from Lauribinayak, Rasuwa, Nepal

Gentiana ornata (Wall. ex G. Don) Griseb, also called decorated gentian or showy gentian, has been used as a decoction plant in temperate regions of Nepal. This work aims to evaluate the phytochemical properties, antioxidant values, and pharmacological properties of this plant collected from Lauribinayak, Gosainkunda Rural Municipality, Rasuwa, Nepal. The extract of whole plant was prepared by cold extraction process at 100% ethanol. Then, the qualitative preliminary phytochemical test of plant extract was performed to know its chemical constituents. The total phenolic content using Folin-Ciocalteu method, total flavonoid content using aluminium chloride colorimetric assay and antioxidant potential of the plant extract were also determined by using diphenylpicrylhydrazyl (DPPH) reagent. The pharmacological activities like oral acute toxicity test, antidiarrheal test and anti-ulcer test were also carried out in laboratory animals. The qualitative phytochemical screening showed the presence of flavonoids, steroids, glycosides, anthocyanin, alkaloids, terpenoids, and phenolic constituents. The total phenolic content, total flavonoid content and antioxidant assay value of this plant extract were 242.64±0.280 mg GAE/g, 39.23±0.005 mg QE/g and 42±0.072 µg/mL respectively. The extract showed no morbidity, mortality, toxicity signs, or symptoms in the oral acute toxicity test. Though it could not show considerable antidiarrheal effect by reducing gastrointestinal motility when compared to the standard drug, loperamide, it showed significant anti-ulcer effects by reducing gastric lesions when compared to the standard drug, sucralfate, which may be due to its mucosal protecting nature. Therefore, isolation and purification of phytochemicals responsible for the pharmacological activity of this plant have been recommended.

The antiproliferative effects of Marrubium vulgare, and toxicity screening in zebrafish embryos

Consider the medicinal usefulness and ethnomedicinal uses referring to Marrubium vulgare; the CH3OH extract of whole plant was investigated for the antiproliferative, effect and toxicological screening. Its antiproliferative effect was evaluated against A549 (lung), HepG2 (Liver), MDA-MB-231 (breast) and MCF-7 cancer cell-lines. Doxorubicin was used as a positive control. Toxicological evaluation of the Marrubium vulgare methanol extract (MVM) was carried out in zebrafish embryos. The MVM showed more effective inhibition against MCF-7and MDA-MB-231 breast-cancer cells. The IC50 value ranged from 43.5 to 223.5 μg/mL. In term of IC50 MVM showed a strong antiproliferative effect averse to MDA-MB-231 and MCF-7 in terms of IC50 values (43.5 and 46.5 μg/mL respectively). Lethal concentration of MVM in zebrafish embryos remained 5 µg/ml. The results obtained from zebrafish embryos tests indicates that the extract is toxic at some level and should be used carefully or avoid it during the pregnancy.

Phytochemical investigation, in-vitro antiplasmodial assessment and cytotoxic effect of ethanol extract of whole plant of Crotalaria arenaria (Benth)

Crotataria arenaria (Benth) is a native plant from Northern part of Nigeria which is employed as antimalarial herb in traditional medicine in the communities where it grows. The phytochemical composition, In-vitro antiplasmodial activity and in-vitro cytotoxic effect of the extract and fractions of the whole plant of Crotalaria arenaria were investigated. The mature and fresh whole plant of C. arenaria were collected, air dried and pulverized. The pulverized form of the plant were soaked in ethanol for two weeks and later decanted, filtered and concentrated using rotatory evaporator at 40oC and evaporated to dryness and labeled CRA-1. The dried ethanol solid extract (CRA-1) was patitioned/fractionated using water, chloroform, ethyl acetate, 18% aqueous methanol, n-hexane which afforded chloroform fraction (CRA-1-01), water fraction (CRA-1-02), ethyl acetate fraction (CRA-1-03) aqueous methanol fraction (CRA-1-04) and n-hexane (CRA - 1- 05) and they were dried and tested for their photochemicals and In-vitro antiplasmdial activity against Plasmodium falciparum strain (K1). The ethanol extract and its fractions were found to significantly inhibited/suppressed multi-drug resistant strain of P. falciparium (K1) in the range of 86.73% - 65.31% at varied concentrations of 5000 µg/ml, 2000 µg/ml, 1000 µg/ml and 500 µg/ml. The ethanol extract and its fractions showed the presence of tannins, saponins and alkaloids which could be responsible for the In-vitro antiplasmodial activity of the whole plant extract of C. arenaria and each of its fractions. Ethanol crude extracts of whole plant of Crotalaria arenaria and its fractions were investigated for cytotoxicity in Brine shrimp lethality Test (BSLT). Larvicidal activities were noticed with dosage concentration from 1000 µg/ml down to 10 µg/ml of the plant extract and all its fractions. The relative cytotoxic effects of extract and fractions obtained from whole plant of Crotalaria arenaria were found to be dose-dependent because higher dosage brought about an increase in mortality of Artemia salina Leach. Sea salty water of the crude ethanol extract and its fractions served as the negative control. The chloroform fraction was observed to be most cytotoxic killing 30% of brine shrimp larvae at lowest concentration of 10 µg/ml with average percentage lethality of 46.67%. Aqueous methanol and ethanol crude extract appears to show similar and closely related activities against brine shrimp larvae at highest concentration of 1000 µg/ml. The ethanol crude extract and aqueous methanol fractions are toxic at higher dosage as they were found to induce significant mortality effect (In-vitro) against Artemia salina Leach particularly at concentration of 1000 µg/ml and therefore not safe for oral consumption especially at higher uncontrolled doses but at relatively low/moderate doses. The findings in this present study demonstrated that the extract of C. arenaria (whole plant) and fractions have significant in vitro antiplasmodial activity and this has justified the traditional use of the whole plant extract of Crotaria arenaria in the folklore medicine to cure malaria related illness. The results obtained in this study may serve as key data for utilization of Crotalaria arenaria in the development of bioactive agents which could be used as antimalarial, anticancer, pesticidal, insecticidal and anti-proliferation agents. The study recommended in-vivo antiplasmodial assay of the extract of the whole plant of Crotalaria arenaria to further substantiate the findings of this present study.

Cellular and molecular mechanisms involved in the protective effects of Aerva Lanata Linn.on airways remodeling in experimental model of bronchial asthma in rats

Bronchial asthma is a chronic inflammatory respiratory disease characterized by bronchoconstriction and hyperresponsiveness of the bronchial airways. The treatment for bronchial asthma is mainly aimed at relieving symptoms by bronchodilators and controlling asthmatic attacks with anti-inflammatory agents. These therapeutic strategies are associated with several adverse drug effects and high cost that may negatively affect the compliance to therapy. Chronic asthma also results in structural remodeling of the airways which enhances the incidence of refractory asthma and increases morbidity/mortality. It is therefore important to explore adjuncts from alternative forms of therapy to compliment/supplement the conventional treatment. The study assessed the effects of Aerva Lanata Linn., a medicinal plant used in the traditional systems of medicine, on airway remodeling in an experimental model of asthma in rats. Wistar rats were immunized on day 0 with ovalbumin and Al(OH)3 and challenged with aerosolized ovalbumin from day 15 to 22. The rats were treated orally with various doses of standardized aqueous extract of whole plant of Aerva Lanata Linn. or prednisolone (10 mg/kg) for 22 days. After 24 hrs of last challenge, blood, bronchoalveolar lavage (BAL) fluid and lung tissue were collected and assayed for markers of structural remodeling viz, (a) cytokine levels (TGF-β and IL-13); (b) hydroxyproline content, and (c) histopathology. The results showed that Aerva Lanata Linn. markedly reduced the levels of TGF-β, IL-13 in both blood and BAL fluid and hydroxyproline content in lung homogenates. Histopathological examination of lung tissue confirmed the modulatory effects of Aerva Lanata Linn. on airway remodeling as evidenced by reductions in goblet cell hyperplasia, inflammatory cells infiltration and sub epithelial fibrosis, as compared to that in the experimental (disease control) group. The results showed that Aerva Lanata Linn. Attenuated the histopathological changes and biochemical markers of airway remodeling by altering the levels of IL-13 and TGFβ, and the study suggested that it could be beneficial in cases of chronic bronchial asthma.

Phytochemical and in vitro biological profiling of Portulaca grandiflora whole plant extracts

P. grandiflora is a small herbaceous annual herb from Portulacaceae family and found useful in mitigating the health care crisis. The study aimed to determine the phytochemicals and to examine the in vitro antifungal, antibacterial, antioxidant and anticancer potential of Portulaca grandiflora. Crude methanolic, ethanolic and n-Hexane extracts of whole plant were used for this study. Antimicrobial properties were estimated through disk diffusion assay, antioxidant activity was determined by using 2,2-diphenyl-1-picryl-hydrazyl scavenging (DPPH), total antioxidant capability and reducing power assays. From the results it was found that methanolic extract of P. grandiflora showed the highest zone of inhibition against Pseudomonas aeruginosa and Candida albicans i.e. 36 ±1mm and 18 ±1 mm respectively with MIC of 25 μg/ml. The highest amount of gallic acid equivalent phenolic and quercetin equivalent flavonoid content were found in methanolic extract of P. grandiflora i.e. 77 ± 0.68 μg GAE/mg extract and 63 ± 1.08 μg QE/mg extract. The significant DPPH scavenging activity (P< 0.05) wasrecorded for methanolic extract of P. grandiflora (87%). Considerably greater antioxidant capacity (10 ± 1.18 μg AAE/mg) and reducing power (4.06 ± 0.18 μg AAE/mg) was observed in methanolic extract. MTT cell viability assay methanolic extract of P. grandiflora showed the IC50 of 42.70 μg/ml at 72h. Whole plant extracts in different solvents exhibit strong pharmacological properties thus suggesting it as a major source of pharmaceutical industry.

Total Alkaloid content and In vitro Antiplasmodial activity of Grangea maderaspatana collected from Burkina Faso

Effective management of malaria remains a major concern for the scientific community mainly due to the resistance of Plasmodium falciparum to the common antimalarials. Many studies are conducted to identify plants that can fight against this disease. This work aimed to contribute to a better knowledge of antiplasmodial activity of different parts of Grangea maderaspatana (Asteracea). Thus, roots, flowers, leafy branches and whole plant of Grangea maderaspatana were extracted with hexane, dichloromethane, ethyl acetate and methanol. Alkaloid contents and antiplasmodial activity of extracts were respectively determined by bromocresol green method and enzyme-linked immunosorbent assay based on pLDH quantification. Total alkaloid contents ranged from 21.036 in methanolic extract of leafy branches to 1074.752µg qE/g in dichloromethane extract of whole plant. Extracts showed moderate to very active antiplasmodial effects. Antiplasmodial activity evaluated on chloroquino (CQ)-sensitive D10 and CQ-resistant Dd2 strains of Plasmodium falciparum showed that hexane and dichloromethane leafy branches extracts had a better activity. Alkaloid could be potentially responsible for antiplasmodial activity observed. None extract found to be toxic for cells at 50 and 100µg/ml. Dichloromethane extract of leafy branches could be a potential source of antiplasmodial molecules.

An acute and sub-acute toxicological assessment of Reissantia indica plant extract in male Sprague-Dawley rats: Hematological, serum biochemical and histopathology

The traditional use of medicinal plants in Sub-Saharan health management lacks thorough toxicological evaluations, particularly concerning lethal dose levels. This study aims to assess the acute and sub-acute toxicity of Reissantia indica whole-plant extract (RIE) in male Sprague-Dawley rats, with a focal point on delineating its safety profile while exploring potential therapeutic applications.RIE, obtained through precise cold maceration in 70 % ethanol, underwent rigorous analysis, revealing diverse secondary metabolites, including alkaloids, flavonoids, terpenoids, and glycosides. Renowned for antioxidant, anti-inflammatory, and anticancer properties, these compounds enhance RIE's pharmacological potential.In the acute toxicity study, RIE was orally administered at 500 and 5000 mg/kg. Sub-acute toxicity involved oral administration of the extract at various doses (5, 50 and 500 mg/kg) over 28 days, with comprehensive assessments, including hematological, biochemical, and histopathological evaluations.Results from the acute toxicity showed no mortality, suggesting a median lethal dose (LD50) exceeding 5000 mg/kg and indicating a substantial margin of safety. Sub-acute toxicity investigations, spanning 28 days revealed no significant changes in body and organ weights, hematological and biochemical parameters, or histopathological signs compared to the control group. Histological examination of kidney, liver, heart, and lung sections from treated animals showed no signs of degeneration.This study, to our knowledge, pioneers a comprehensive investigation into the toxicity profile of Reissantia indica's whole-plant ethanolic extract, addressing a significant gap in existing literature on medicinal plant safety in the Sub-Saharan region.

GC-MS and HPTLC bioautography-based phytochemical profiling and evaluation of biological activity Neptunia prostrata Linn whole plant and leaves

This work used experimental methods to evaluate the chemical composition of GC-MS, HPTLC-based bioautographaphy, antioxidant, anti-diabetic, and protein denaturation properties of the Neptunia prostrata Linn (family: Mimosaceae) whole plant and leaves. Three methods, namely DPPH, metal chelating, and reducing power assays, were used to estimate the antioxidant effects. In addition, α-amylase, a carbohydrate-hydrolyzing enzyme, was targeted to test the anti-diabetic activity. The protein denaturation assay was used to evaluate the anti-inflammatory activity of the plant. GC-MS, an important analytical tool, was performed to identify bioactive compounds of medicinal plants used in pharmaceutical industries. Biochemical derivatization HPTLC-based bioautography with DPPH was executed to identify antioxidant agents from N. prostrata. The validated HPTLC method was used to quantify identified antioxidant agents. The stability of compounds, preparation of calibration curves, linearity, range, precision, limit of detection, limit of quantification, robustness, and accuracy are examined to develop a robust method. Higher total phenolic content (TPC) content was observed in N. prostrata hydroalcoholic extract of the whole plant (81.12 ± 4.19 mg GAE/g) and methanolic extract of leaves (105.16 ± 3.11 mg GAE/g). Methanolic extract of N. prostrata leaves showed significantly high antioxidant potential for all DPPH (IC50:28.05 ± 1.78 µg/mL), metal chelating (IC50:1598 ± 23.51 µg/mL), and reducing power assay compared to standard ascorbic acid (DPPH assay: IC50:24.14 ± 2.34 µg/mL and metal chelating: IC50:1301.16 ± 6.14 µg/mL). N. prostrata aqueous extract of the whole plant (IC50:179.47 ± 10.59 µg/mL) and leaves (IC50:130.86 ± 3.58 µg/mL) showed significantly high α-amylase inhibitory activity as compared to standard acarbose (IC50:148.62 ± 7.84 µg/mL). Methanolic extract of whole plants (IC50:131.46 ± 11.81 µg/mL) and chloroform extract of leaves (IC50:122.61 ± 8.19 µg/mL) exhibited strong anti-inflammatory activity as compared to standard acetylsalicylic acid (IC50:117.77 ± 4.95 µg/mL). GC-MS analysis revealed the presence of several bioactive compounds, where 2-cyclopenten-1-one, 2-hydroxy showed the most abundant bioactive compounds in the plant with 17.01%. HPTLC-bioautography identified three phenolic acids (chlorogenic acid, gallic acid, and 4-hydroxybenzoic acid) and one flavonoid (naringenin), further quantified with the validated HPTLC method. These findings propose that N. prostrata has therapeutic potential for treating diseases related to oxidative damage, diabetes, and inflammation, which may be due to the presence of bioactive compounds.

Phytochemicals and Haematological Studies of Aqueous Crude Extract of Whole Plant of Euphorbia heterophylla Administered to Wistar Albino Rats

Changes in blood parameters are often triggered when toxic doses of plant extracts are administered to animals thereby calling for the haematological studies. Standard techniques were used for the phytochemical and haematological studies. Tannins, steroids, cardiac glycosides, flavonoids, alkaloids, terpenoids, phenols, reducing sugars and saponins were found in the aqueous crude extract obtained from Euphorbia heterophylla. Dosage increment of the aqueous extract from 10-600 mg/kgbw led to increments in all the haematological parameters (Total white blood cell, red blood cell, packed cell volume, red blood indices, platelets and differential white blood cell) checked in the blood of the experimental Wistar albino rat.The implication of this study is that the extractcan be used as therapeutic agents and the haematological parameters were dose-dependent.

Physicochemical Constituent, Phytochemical Analysis and Antimicrobial Activity in Ethanolic Extract of Cyanotis Axillaris

Cyanotis axillaris belong to family Commellianaceae. The present investigation deal with the physicochemical constituent, phytochemical analysis and antimicrobial activity in ethanolic extract of whole plant of Cynotis axillaris. The plant part decoction used in Ayurveda to cure many diseases [2]. The evaluation of physicochemical constituents was carried out by ash value, extractive value and phytochemical constituent in plant. The antibacterial activity was tested by cup plate agar diffusion method. The antibacterial activity carried out against E. coli, Staphylococcus Aureus, Bacilis subtilis and Proteus species

Cichorium intybus L. significantly alleviates cigarette smoke-induced acute lung injury by lowering NF-κB pathway activation and inflammatory mediators

BackgroundCigarette smoke (CS) is one of the primary causes of acute lung injury (ALI) via provoking pulmonary inflammation and oxidative stress. Despite substantial studies, no effective treatment for ALI is presently available. PurposeNew prospective treatment options for ALI are required. Thus, this project was designed to investigate the in vivo and in vitro protective effects of 70 % methanolic-aqueous crude extract of whole plant of Cichorium intybus (Ci.Mce) against CS-induced ALI. Study design/methods: Initially, male Swiss albino mice were subjected to whole-body CS exposure for 10 continuous days to prepare CS-induced ALI models. Normal saline (10 mL/kg), Ci.Mce (100, 200, 300 mg/kg), and Dexamethasone (1 mg/kg) were orally administered to respective animal groups 1 h prior to CS-exposure. 24 hrs after the last CS-exposure, BALF and lungs were harvested to study the key characteristics of ALI. Next, HPLC analysis was done to explore the phytoconstituents. ResultsCi.Mce exhibited significant reductions in lung macrophage and neutrophil infiltration, lung weight coefficient, and albumin exudation. Additionally, it effectively ameliorated lung histopathological alterations and hypoxemia. Notably, Ci.Mce exerted inhibitory effects on the excessive generation of IL-6, IL-1β, and KC in both CS-induced ALI murine models and CSE-stimulated RAW 264.7 macrophages. Noteworthy benefits included the attenuation of oxidative stress induced by CS, evidenced by decreased levels of MDA, TOS, and MPO, alongside enhanced TAC production. Furthermore, Ci.Mce demonstrated a marked reduction in CS-induced NF-κB expression, both in vivo and in vitro. ConclusionConsequently, Cichorium intybus could be a therapeutic option for CS-induced ALI due to its ability to suppress inflammatory reactions, mitigate oxidative stress, and quell NF-κB p65 activation.

Antimicrobial Activities of Chloroform Extract of Whole Plant of Sida acuta Burm. f against Selected Clinical Isolates from Laboratory Samples of a Private Hospital in Benin City, Edo State, Nigeria

Antimicrobial Activities of Chloroform Extract of Whole Plant of Sida acuta Burm. f against Selected Clinical Isolates from Laboratory Samples of a Private Hospital in Benin City, Edo State, Nigeria

Red light enhances the antibacterial properties, biofabrication, and stability of Fagonia indica callus-based silver nanoparticles.

Plant-based nanoparticles can be tuned through the frequency of light for efficient synthesis, structural properties, and antibacterial applications. This research assessed the effect of material type (callus and whole-plant extract) and the interaction with a specific range of light wavelength on AgNP synthesis. All types of AgNPs were characterized by their size, shape, associated functional groups, and surface charge. Interestingly, the size of red light and callus-based AgNPs (RC-AgNPs) was smaller (6.32 nm) compared to 14.59 nm for Ultraviolet light and callus-based AgNPs (UV-C-AgNPs). Zeta potential analysis showed that RC-AgNPs had higher stability (-29.2 mV) compared to UV-C-AgNPs (-16.7 mV). Similarly, red light-based AgNPs had higher Oxidation reduction potential in both whole-plant-based and callus-based AgNPs, indicating a more oxidizing nature compared to those synthesized under UV light. This was confirmed by the lower total phenolic and flavonoid content associated with them and their lower antioxidant activity. The higher antibacterial activities and lower minimum inhibitory concentrations of red light-based AgNPs against highly resistant pathogenic bacteria demonstrated the role of red light in enhancing antibacterial activity. These results indicate that AgNPs synthesized in red light and callus extract are more active compared to those synthesized under other wavelengths and/or in whole-plant extracts.

Administration of Ethanolic Extract of Spinacia oleracea Rich in Omega-3 Improves Oxidative Stress and Goblet Cells in Broiler Chickens Infected with Eimeria tenella.

This study investigated the anticoccidial activity of spinach (Spinacia oleracea) whole-plant extract against Eimeria tenella, both in vitro and in vivo. For this purpose, one hundred 8-day-old broiler chicks of both sexes were divided into four groups (n = 25 in each group). Chicks in the first group served as the negative control (non-treated-non-infected). Chicks in the second group were challenged at 18 days old with 5 × 104E. tenella sporulated oocysts. The third group was challenged with 5 × 104 sporulated E. tenella oocysts at 18 days old after receiving spinach extract at a dose of 50 mg/kg at 8 days old. The fourth group received 0.2 mg/kg diclazuril (Coxiril® 0.2%) in their diet two days before being orally infected with 5 × 104 sporulated E. tenella oocysts and this continued till day 10 post-infection (PI). The growth performance, clinical symptoms, oocyst shedding, histological findings, and biochemical parameters were used to evaluate the efficacy on day 8 PI when the infection was at its peak. A gas chromatography examination revealed that omega-3 fatty acids were the main constituents of the spinach extract, followed by oleic acid, palmitic acid, and phytol, with amounts of 23.37%, 17.53%, 11.26%, and 7.97%, respectively. The in vitro investigation revealed that the spinach extract at concentrations of 10% and 5% inhibited the oocyst sporulation by 52.1% and 45.1%, respectively. The 5% concentration was selected for the in vivo trial based on the results of the in vitro study. The infected-untreated group showed high levels of OPG; lower body weight; a greater number of parasite stages; few goblet cells; decreased SOD, CAT, and GPX levels; and increased MDA and NO levels. The spinach-treated group, on the other hand, showed a significant decrease in oocyst output per gram of feces (OPG), increased body weight, decreased parasitic stages, and a nearly normal number of goblet cells. Additionally, it reduced malondialdehyde (MDA) and nitric oxide (NO), while increasing superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GPX). In conclusion, spinach produced significant antioxidant effects, increased body weight, reduced the number of oocysts and parasite stages in the caecum, and restored the number of goblet cells relative to those of an uninfected control. Furthermore, spinach extract inhibits the sporulation percentage of E. tenella oocysts. The ethanolic extract of S. oleracea (whole plant) contained high concentrations of fatty acids, palmitic acid, Phytol, betulin, and ursolic aldehyde, all of which are known to regulate the antioxidant pathway and modulate inflammatory processes and may be the main reason for its anticoccidial activity.

Phytoconstituent Profiles Associated with Relevant Antioxidant Potential and Variable Nutritive Effects of the Olive, Sweet Almond, and Black Mulberry Gemmotherapy Extracts.

The extracts of whole plants or specific organs from different plant species are gaining increasing attention for their phytotherapy applications. Accordingly, we prepared standardized gemmotherapy extracts (GTEs) from young shoots/buds of olive (Olea europaea), sweet almond (Prunus amygdalus), and black mulberry (Morus nigra), and analyzed the corresponding phytonutrient profiles. We identified 42, 103, and 109 phytonutrients in the olive, almond, and black mulberry GTEs, respectively, containing amino acids, vitamins, polyphenols, flavonoids, coumarins, alkaloids, iridoids, carboxylic acids, lignans, terpenoids, and others. In order to assess the physiological effects generated by the GTEs, we developed a translational nutrition model based on Drosophila melanogaster and Cyprinus carpio. The results indicate that GTEs could influence, to a variable extent, viability and ATP synthesis, even though both are dependent on the specific carbohydrate load of the applied diet and the amino acid and polyphenol pools provided by the GTEs. It seems, therefore, likely that the complex chemical composition of the GTEs offers nutritional properties that cannot be separated from the health-promoting mechanisms that ultimately increase viability and survival. Such an approach sets the paves the way for the nutritional genomic descriptions regarding GTE-associated health-promoting effects.

Phytochemical, biological, and in-silico analysis of Colutea armata Hemsl. & Lace: A possible source of bioactive natural compounds

The Colutea genus of plants has been studied for its medicinal qualities, particularly antifungal. The current study is the first to examine and contrast the biological functions and chemical makeup of whole-plant extracts of Colutea armata Hemsl. & Lace. made with dichloromethane (DCM) solvent and methanol (MeOH) solvent. The ability of the extracts under study to block specific enzymes, such as α-glucosidase, tyrosinase, acetylcholinesterase (AChE), butyrylcholinesterase (BChE), and phosphodiesterase. Likewise, spectrophotometric techniques were used to estimate the total bioactive components and potential for antioxidants (DPPH). Additionally, GC–MS metabolomics was done to establish the composition of potential secondary metabolites. Moreover, the in-silico docking studies confirmed the specific compound responsible for biological activities. The varying concentrations of alkaloidal, phenolic and flavonoid components were found in MeOH and DCM extracts, which might be responsible for the notable DPPH, α-glucosidase, and tyrosinase inhibitory potentials. In the contrast, moderate AChE, BChE, and phosphodiesterase inhibition were noted. Additionally, the extracts presented considerable antifungal (S. cerevisiae) and anti-bacterial (K. pneumoniae, S. typhi, E. coli, and S. aureus). In addition, GC–MS profiling of both the MeOH and the DCM extracts revealed the tentative presence of 19 and 33 secondary metabolites, respectively, mostly phenolic, flavonoid, glycoside, terpenes, steroids, and alkaloids, this may be the cause of the plant extract under study's reported biological potential. To conclude, our findings highlighted C. armata as a lead source for naturally bioactive compounds that may open the door to industrial uses.

Antimicrobial Efficacy and HPLC Analysis of Polyphenolic Compounds in a Whole-Plant Extract of Eryngium campestre

Due to the constant increase in the number of plant diseases and the lack of available treatments, there has been a growing interest in plant extracts over the past few decades. Numerous studies suggest that plant extract molecules possess valuable antimicrobial activities, particularly against fungi and bacteria. This suggests that these biomaterials could potentially serve as attractive therapeutic options for the treatment of phytopathogen infections. In the present study, we investigated and analyzed the methanolic extract of Eryngium campestre L. whole plant extract using HPLC. The analysis revealed the presence of several polyphenolic constituents, with benzoic acid, catechol, quercetin, vanillic acid, resveratrol, naringenin, and quinol being the most abundant. The amounts of these constituents were determined to be 2135.53, 626.728, 579.048, 356.489, 323.41, 153.038, and 128.77 mg/kg, respectively. Furthermore, we isolated and identified different plant fungal and bacterial isolates from symptomatic potato plants, which were accessioned as Rhizoctonia solani (OQ880458), Fusarium oxysporum (OQ820156) and Fusarium solani (OQ891085), Ralstonia solanacearum (OQ878653), Dickeya solani (OQ878655), and Pectobacterium carotovorum (OQ878656). The antifungal activity of the extract was assessed using fungal growth inhibitions (FGI) at concentrations of 100, 200, and 300 µg/mL. The results showed that at the lowest concentration tested (100 µg/mL), the extract exhibited the highest effectiveness against R. solani with an FGI of 78.52%, while it was least effective against F. solani with an FGI of 61.85%. At the highest concentration tested, the extract demonstrated the highest effectiveness against R. solani and F. oxysporum, with FGIs of 88.89% and 77.04%, respectively. Additionally, the extract displayed a concentration-dependent inhibitory effect on all three bacterial pathogens. At the highest concentration tested (3000 µg/mL), the extract was able to inhibit the growth of all three bacterial pathogens, although the inhibition zone diameter varied. Among the bacterial pathogens, D. solani exhibited the highest sensitivity to the extract, as it showed the largest inhibition zone diameter at most of the extract concentrations. These findings highlight the potential of the E. campestre extract as a source of natural antimicrobial agents for controlling various plant pathogens. Consequently, it offers a safer alternative to the currently employed protective methods for plant disease management.

Phytochemical Profiling, In-vitroAntioxidant and Cytotoxic Effects of Luisia tenuifolia Extracts Against Human Skin Squamous Carcinoma.

The present study establishes the phytochemical screening, TLC profiling, in-vitroradical scavenging, and anticancer activities in the successive extracts of whole plant of L. tenuifolia Blume. The preliminary phytochemical screening followed by quantitative estimation of bioactive secondary metabolites revealed higher abundance of phenolic (13.22 ± 0.21mg GAE/g of extract), flavonoid (8.09 ± 0.13mg QE/g of extract), and tannin (7.53 ± 0.08mg GAE/g of extract) contents in ethyl acetate extract of L. tenuifolia which might be attributed to the difference in the polarity and efficacy of the solvents used in successive Soxhlet extraction. Antioxidant activity assessed by DPPH assay and ABTS assay revealed that the ethanol extract exhibited the highest radical scavenging activity with an IC50 value of 18.7µg/mL and 33.83µg/mL respectively. FRAP assay carried out on the extracts showed the maximum reducing power exhibited by the ethanol extract with a FRAP value of 1162.30 ± 20.73 FeSO4 E mg/g dw. MTT assay showed that the ethanol extract exhibited promising cytotoxic effect in A431 human skin squamous carcinoma cells with an IC50 value of 24.29µg/mL. Collectively, our findings strongly suggest that the ethanol extract and its one or more active phytoconstituent can be used as a potential therapeutic to treat skin cancer.

Polyacetylenes from the adventitious roots of Centella asiatica with glucose uptake stimulatory activity.

Centella asiatica (L.) Urban is an herbaceous perennial plant of the Apiaceae family that has diverse medicinal uses. Its active components are saponin, phenolics, and polyacetylenes. Plant cell cultures have been exploited for the efficient production of metabolites with pharmacological activity. In this work, we prepared adventitious root cultures of C. asiatica and analyzed their content and biological activity. Adventitious root extracts were found to increase glucose uptake by differentiated L6 skeletal muscle cells and to be more efficient than the extract of whole plants. Chromatographic fractionation of the extracts from adventitious roots of C. asiatica led to the isolation of two known polyacetylenes, araliadiol (1) and 8-acetoxy-1,9-pentadecadiene-4,6-diyn-3-ol (2), in addition to a new polyacetylene, which we have named centellidiol (3). All the three polyacetylenes stimulated glucose uptake in a dose-dependent manner. The methanol extract of adventitious roots contained 0.53% and 0.82% of compounds 1 and 2, respectively, which are values that were 15 and 21 times higher that are found in mother plants. We therefore suggest that the high content of these polyacetylenes contributes to the high efficacy of C. asiatica adventitious root cultures. Overall, adventitious root cultures of C. asiatica can be part of a secure supply of effective ingredients including polyacetylenes.