In Vitro Attenuation of Thermal-Induced Protein Denaturation by Aerial Parts of Artemisia scoparia

2014 ◽  
Vol 20 (1) ◽  
pp. 9-12 ◽  
Author(s):  
Murad Ali Khan ◽  
Haroon Khan ◽  
Shafiq Ahmad Tariq ◽  
Samreen Pervez
Keyword(s):  
Crude Extract ◽  
Protein Denaturation ◽  
Total Flavonoid ◽  
Significant Activity ◽  
Dependent Manner ◽  
Concentration Dependent Manner ◽  
Aqueous Fraction ◽  
Denatured Protein ◽  
Aerial Parts ◽  
Artemisia Scoparia

The goal of this study was to explore the aerial parts of Artemisia scoparia (crude extract, total flavonoid contents, and aqueous fraction) for protein denaturation potential. The crude extract provoked marked attenuation of thermal-induced denatured protein in a concentration-dependent manner with maximum inhibition of 54.05 μg/mL at 500 μg/mL and IC50 of 449.66 μg/mL. When total flavonoid contents were studied, it illustrated most dominant activity concentration dependently with maximum amelioration of 62.16 μg/mL at 500 μg/mL and IC50 of 378.35 μg/mL. The aqueous fraction also exhibited significant activity with maximum of 56.75% inhibition at 500 μg/mL and IC50 of 445.10 μg/mL. It can be concluded on the basis of the results that the crude extract, flavonoid contents, and aqueous fraction of the plant possessed significant inhibition on thermal-induced denatured protein.

Improved Method for Obtaining of Arctigenin from Arctium Lappa L. and its Antiproliferative Effect on Human Hepatocarcinoma HepG2 Cells

2020 ◽  
Vol 16 (3) ◽  
pp. 358-362
Author(s):  
Renan S. Teixeira ◽  
Paulo H.D. Carvalho ◽  
Jair A.K. Aguiar ◽  
Valquíria P. Medeiros ◽  
Ademar A. Da Silva Filho ◽  
...  
Keyword(s):  
Antitumor Activity ◽  
Crude Extract ◽  
Hepg2 Cells ◽  
Liver Carcinoma ◽  
Adhesion Assay ◽  
Dependent Manner ◽  
Concentration Dependent Manner ◽  
Arctium Lappa ◽  
Nih 3T3

Background: Arctigenin is a lignan found in Arctium lappa L. (Asteraceae) that displays anti-inflammatory activities. Previous studies showed that the crude extract of A. Lappa has antitumor activity in human liver carcinoma, lung and stomach cancer cells. The aim of this study was to obtain arctigenin from A. lappa L., as well as to evaluate its antiproliferative effects in cells of liver carcinoma (HepG2) and fibroblasts (NIH/3T3). Methods: Arctigenin was obtained from the hydrolysis of arctiin, which was isolated from the crude extract of A. lappa. The effects of arctigenin and arctiin on HepG2 cell viability and cell adhesion were analyzed by MTT method. Adhesion assay was also carried out to evaluate the antitumor activity. Results: Our results showed that the analytical process to obtain arctigenin was fast and easy. In vitro experiments showed that arctigenin (107-269 μM) decreased HepG2 cells viability and did not cause cytotoxicity on NIH/3T3 cells. Arctigenin (27-269 μM) demonstrated anti-adhesion in HepG2 cells in a concentration-dependent manner, when compared with control. Conclusion: These results suggest a promising pharmacological activity for arctigenin as an antiproliferative compound.

scholarly journals Calcium channels blocked activity: Providing the basis for medicinal use of Abies pindrow in diarrhea and bronchitis

2015 ◽  
Vol 10 (2) ◽  
pp. 430 ◽  
Author(s):  
Sohaib Mushtaq ◽  
Mueen Ahmad Chaudhry ◽  
Hafiz Muhammad Abdul Rahman
Keyword(s):  
Calcium Channels ◽  
Crude Extract ◽  
Dependent Manner ◽  
Response Curves ◽  
Traditional Practice ◽  
Concentration Dependent Manner ◽  
Medicinal Uses ◽  
High K ◽  
Medicinal Use ◽  
Abies Pindrow

<p><em>Abies pindrow</em> is widely used in traditional practice for the treatment of diarrhea and bronchitis and the present study was designed to validate its folkloric uses. The crude extract of <em>A. pindrow</em> inhibit spontaneously contracting (1-10 mg/mL) and high K<sup>+</sup> (80 mM)-induced pre-contracted rabbit jejun-um (3 mg/mL) in concentration dependent manner. A rightward shift in Ca<sup>+2</sup> concentration response curves was seen in the presence of crude extract (0.1-0.3), similar to verapamil. In isolated tracheal tissue, <em>A. pindrow</em> inhibited, high K<sup>+</sup> and carbachol (1 µM)-induced contractions, at 3 mg/mL and 10 mg/mL respectively, similar to that caused by verapamil. These results indicate the presence of calcium channels blocked activity in crude extract of <em>A. pindrow</em>, which provide sound basis for medicinal uses of<em> A. pindrow</em> in diarrhea and bronchitis.   </p><p> </p>

scholarly journals Identification of Major α-Glucosidase Inhibitors from Stem Bark of Panamanian Mangrove Plant Pelliciera rhizophorae

2019 ◽  
Vol 14 (1) ◽  
pp. 1934578X1901400
Author(s):  
Lilia Cherigo ◽  
Sergio Martínez-Luis
Keyword(s):  
Stem Bark ◽  
Spectrometric Analysis ◽  
Dependent Manner ◽  
Mangrove Plant ◽  
Concentration Dependent Manner ◽  
Pentacyclic Triterpenes ◽  
Aerial Parts ◽  
Glucosidase Inhibitors ◽  
Pelliciera Rhizophorae ◽  
First Time

In our continuous search for α-glucosidase inhibitors, three active pentacyclic triterpenes were isolated from stem bark samples of the Panamanian mangrove Pelliciera rhizophorae Triana & Planchon. These compounds were identified by both spectroscopic and spectrometric analysis. Of the isolated compounds, only betulinic acid has been previously isolated from P. rhizophorae leaves while both betulin (IC50 2.09 μM) and lupeol (IC50 0.58 μM) were isolated from this plant for the first time. All three pentacyclic triterpenes inhibited the α-glucosidase enzyme in a concentration-dependent manner, and their inhibitory activity was higher than that of the antidiabetic drug acarbose (IC50 241.6 μM). Kinetic analysis established that betulin and lupeol acted as competitive inhibitors. Finally, docking analysis suggested that all three triterpenes bind at the same site as acarbose does in the human intestinal α-glucosidase (PDB: 3TOP). This work contributes further evidence similar to previous studies that point out that the aerial parts of P. rhizophorae might be potential agents in controlling hyperglycemia in diabetic persons.

In vivo Analgesic and Anti-Inflammatory Activities of Ursolic Acid and Oleanoic Acid from Miconia albicans (Melastomataceae)

2006 ◽  
Vol 61 (7-8) ◽  
pp. 477-482 ◽  
Author(s):  
Maria Anita L. Vasconcelos ◽  
Vanessa A. Royo ◽  
Daniele S. Ferreira ◽  
Antonio E. Miller Crotti ◽  
Márcio L. Andrade e Silva ◽  
...  
Keyword(s):  
Ursolic Acid ◽  
Crude Extract ◽  
Methylene Chloride ◽  
Second Phase ◽  
Dependent Manner ◽  
In Vivo Models ◽  
Isomeric Mixture ◽  
Aerial Parts ◽  
Anti Inflammatory

The aim of this work was to use in vivo models to evaluate the analgesic and anti-inflammatory activities of ursolic acid (UA) and oleanoic acid (OA), the major compounds isolated as an isomeric mixture from the crude methylene chloride extract of Miconia albicans aerial parts, in an attempt to clarify if these compounds are responsible for the analgesic properties displayed by this plant. Ursolic acid inhibited abdominal constriction in a dose-dependent manner, and the result obtained at a content of 40 mg kg-1 was similar to that produced by administration of acetylsalicylic acid at a content of 100 mg kg-1. Both acids reduced the number of paw licks in the second phase of the formalin test, and both of them displayed a significant anti-inflammatory effect at a content of 40 mg kg-1. It is noteworthy that the administration of the isolated mixture, containing 65% ursolic acid/35% oleanolic acid, did not display significant analgesic and anti-inflammatory activities. On the basis of the obtained results, considering that the mixture of UA and OA was poorly active, it is suggested that other compounds, rather than UA and OA, should be responsible for the evaluated activities in the crude extract, since the crude extract samples displayed good activities.

scholarly journals Physiological and Biochemical Changes in Moth Bean (Vigna aconitifolia L.) under Cadmium Stress

2016 ◽  
Vol 2016 ◽  
pp. 1-13 ◽  
Author(s):  
Poornima D. Vijendra ◽  
Kavitha M. Huchappa ◽  
Roopa Lingappa ◽  
Giridhara Basappa ◽  
Sathisha G. Jayanna ◽  
...  
Keyword(s):  
Growth Parameters ◽  
Cadmium Stress ◽  
Protein Carbonyls ◽  
Dependent Manner ◽  
Concentration Dependent Manner ◽  
Vigna Aconitifolia ◽  
Moth Bean ◽  
Aerial Parts ◽  
Drought Resistant ◽  
Physiological And Biochemical

Moth bean (Vigna aconitifolia L.), a drought resistant legume, possesses high nutritional value. Cadmium (Cd) is a nonessential and the most toxic heavy metal in plants. The present study was to test the hypothesis of whether moth bean being a drought resistant legume can withstand the cadmium stress. Ten-day-old moth bean seedlings were subjected to cadmium stress and investigated for a period of 15 days every 3-day intervals. Cadmium quantification in moth bean tissues suggests root accumulation and translocation to aerial parts in a concentration dependent manner. Results of physiological and biochemical studies revealed that cadmium has affected the growth parameters like shoot and root lengths and tissue dry weights. Significant alternations in relative water content and cell membrane stability were observed in stressed seedlings. Similarly superoxide radical, lipoxygenase activity, membrane lipid peroxidation products, protein carbonyls, and reduced glutathione and nonprotein thiols were found increased in stressed seedlings compared to controls. However, hydrogen peroxide and ascorbic acid levels were not altered significantly in both stressed and control seedlings. Cadmium translocation ability from roots to aerial parts and elevated levels of nonenzymatic antioxidants in stressed seedlings suggest the cadmium stress withstanding ability of moth bean.

In vitro myometrial inhibition by the partitioned aqueous fraction of Anthocleista djalonensis leaves

2010 ◽  
Vol 88 (9) ◽  
pp. 880-887
Author(s):  
Enitome Evi Bafor ◽  
Lucky Osaro Okunrobo
Keyword(s):  
Uterine Contraction ◽  
Calcium Influx ◽  
Inhibitory Effect ◽  
Dependent Manner ◽  
Response Curves ◽  
Concentration Dependent Manner ◽  
Aqueous Fraction ◽  
Uterine Contractions ◽  
Β Adrenergic Receptors

This study investigated the effect on the uterus of the aqueous fraction of the partitioned methanol crude extract of the leaves of Anthocleista djalonensis (AD) and the possible mechanism of AD activity. AD inhibited the concentration–response curves induced by oxytocin and CaCl2 on the rat uterus in vitro and significantly reduced the EC50 in a concentration-dependent manner (p < 0.05). A similar effect was observed with salbutamol and verapamil on the concentration–response curves obtained for oxytocin and CaCl2. The inhibitory effect of AD was not attenuated in the presence of propranolol. AD, salbutamol, and verapamil also produced a concentration-dependent relaxation on K+-induced sustained uterine contraction. In Ca2+-free medium, AD and salbutamol similarly inhibited oxytocin-induced contraction, but verapamil failed to produce this effect. The present results suggest that AD, being a mixture of phytochemicals, probably exerts inhibitory activity on in vitro uterine contractions of the nonpregnant, diethylstilboestrol-treated rat by multiple mechanisms that do not involve interaction with β-adrenergic receptors and do not solely depend on inhibition of calcium influx.

scholarly journals Anti-Inflammatory and Neuroprotective Effects of Constituents Isolated fromRhodiola rosea

2013 ◽  
Vol 2013 ◽  
pp. 1-9 ◽  
Author(s):  
Yeonju Lee ◽  
Jae-Chul Jung ◽  
Soyong Jang ◽  
Jieun Kim ◽  
Zulfiqar Ali ◽  
...  
Keyword(s):  
Biological Activity ◽  
Crude Extract ◽  
Therapeutic Potential ◽  
Neuroprotective Effect ◽  
Rhodiola Rosea ◽  
Dependent Manner ◽  
Neuroprotective Effects ◽  
Concentration Dependent Manner ◽  
Bv2 Cells ◽  
Proinflammatory Factors

To determine the biological activity ofRhodiola rosea, the protein expression of iNOS and proinflammatory cytokines was measured after the activation of murine microglial BV2 cells by LPS under the exposure of constituents ofRhodiola rosea: crude extract, rosin, rosarin, and salidroside (each 1–50 μg/mL). The LPS-induced expression of iNOS and cytokines in BV2 cells was suppressed by the constituents ofRhodiola roseain a concentration-dependent manner. Also the expression of the proinflammatory factors iNOS, IL-1β, and TNF-αin the kidney and prefrontal cortex of brain in mice was suppressed by the oral administration ofRhodiola roseacrude extract (500 mg/kg). To determine the neuroprotective effect of constituents ofRhodiola rosea, neuronal cells were activated by L-glutamate, and neurotoxicity was analyzed. The L-glutamate-induced neurotoxicity was suppressed by the treatment with rosin but not by rosarin. The level of phosphorylated MAPK, pJNK, and pp38 was increased by L-glutamate treatment but decreased by the treatment with rosin and salidroside. These results indicate thatRhodiola roseamay have therapeutic potential for the treatment of inflammation and neurodegenerative disease.

scholarly journals Photosynlhetic Inhibitory Activity of Dihydro-β-agarofurans Sesquiterpenes from Maytenus dislicha and Maytenus boaria (Celastraceae)

2000 ◽  
Vol 55 (7-8) ◽  
pp. 631-637 ◽  
Author(s):  
Carlos Céspedes ◽  
Lahoucine Achnine ◽  
Julio Alarcón ◽  
José Becerra ◽  
Blas Lotina-Hennsen
Keyword(s):  
Electron Transport ◽  
Inhibitory Activity ◽  
Hill Reaction ◽  
Dependent Manner ◽  
Concentration Dependent Manner ◽  
Structural Requirements ◽  
Aerial Parts ◽  
Site Of Action ◽  
Order Of Magnitude ◽  
Photosynthetic Activities

Abstract The effects of 9β-benzoyloxy-la, 2α, 6β, 8α, 15-pentaacetoxy-dihydro-β-agarofuran and 9β furoyloxy-1α, 6β, 8α-triacetoxy-dihydro-β-agarofuran, major phytogrowth inhibitors isolated from the aerial parts of Maytenus disticha (Celastraceae) and seeds of Maytenus boaria (Celastaraceae), respectively, on different photosynthetic activities of isolated spinach chloroplasts have been investigated. Photophosphorylation and electron transport (basal, phosphorylating and uncoupled) were inhibited in a concentration dependent manner by both compounds, therefore acting as Hill reaction inhibitors. The site of action of these natural compounds was located in the span from P680 to QA. 9β-benzoyloxy-1,2,6,8,15-pentaacetoxydihydro-β-agarofuran was one order of magnitude more potent (I50 = 2.6 μм) than 9β-furoyloxy-1,6,8,-triacetoxydihydro-β-agarofuran, suggesting that the substitution at C-9 and the acetoxy groups at carbons 2 and 15 are important structural requirements for the displayed inhibitory activity.

scholarly journals Pharmacological insights into Merremia vitifolia (Burm.f.) Hallier f. leaf for its antioxidant, thrombolytic, anti-arthritic and anti-nociceptive potential

2020 ◽  
Author(s):  
Sahida Akter ◽  
Israt Jahan ◽  
Riniara Khatun ◽  
Mohammad Forhad Khan ◽  
Laiba Arshad ◽  
...  
Keyword(s):  
Acetic Acid ◽  
Protein Denaturation ◽  
Antioxidant Activities ◽  
Reducing Power ◽  
Clot Lysis ◽  
Dependent Manner ◽  
Aqueous Fraction ◽  
Writhing Test ◽  
Dose Dependent

Merremia vitifolia (Burm.f.) Hallier f., an ethnomedicinally important plant, used in the tribal areas to treat various ailments including fever, headache, eye inflammation, rheumatism, dysentery, jaundice and urinary diseases. The present study explored the biological efficacy of the aqueous fraction of M. vitifolia leaves (AFMV) through in vitro and in vivo experimental models. The thrombolytic and anti-arthritic effects of AFMV were evaluated by using the clot lysis technique and inhibition of protein denaturation technique, respectively. The anti-nociceptive activity of AFMV was investigated in Swiss Albino mice by acetic acid-induced writhing test and formalin-induced paw licking test. The antioxidant activities of AFMV, including 2,2-diphenyl-1-picrylhydrazyl (DPPH) free radical and total reducing power, were also tested. The qualitative phytochemical assays exhibited AFMV contains secondary metabolites such as alkaloid, carbohydrate, flavonoid, tannin, triterpenoids and phenols. In addition, AFMV showed strong antioxidant effects with the highest scavenging activity (IC50 146.61 µg/mL) and reducing power was increased with a dose-dependent manner. AFMV also revealed notable clot lysis effect and substantial anti-arthritic activity at higher doses (500 µg/mL) as  compared to the control. The results demonstrated a promising reduction of the number of writhing and duration of paw licking in acetic acid-induced writhing test and formalin-induced paw licking test in a dose-dependent manner, respectively. In conclusion, AFMV provides the scientific basis of its folkloric usage,  suggesting it as the vital source of dietary supplement.

scholarly journals Phytochemical and Pharmacological Investigations of Crude Aqueous Extract of Momordica charantia

2020 ◽  
Vol 3 (1) ◽  
Keyword(s):  
Crude Extract ◽  
Skin Diseases ◽  
Protein Denaturation ◽  
Ex Vivo ◽  
Continuous Process ◽  
Momordica Charantia ◽  
Clot Lysis ◽  
Phytochemical Analysis ◽  
Dependent Manner ◽  
Anti Inflammatory

The search for new therapeutic remedies from natural sources is a continuous process. Momordica charantia under the family Cucurbitaceous is commonly known as tita korola in Bangladesh. Traditionally, it is used to treat many diseases, including diabetes and obesity, infections, cough, respiratory diseases, wounds and skin diseases, ulcer, gout and rheumatism, spasm, and cancer. This study aimed at the evalualtion of toxicity, anti-inflammatory, membrane stabilizing and thrombolytic activity of M. charantia aqueous leaf extract by applying a number of in vitro and ex vivo test systems. For this, toxicity analysis was done in Allium cepa, while anti-inflammatory, and membrane stabilizing and clotlysis capacity were tested by using egg albumin and human erythrocytes, respectively. Additionally, preliminary phytochemical analysis was also done. The results suggest that the crude aqueous crude extract of M. charantia possesses alkaloid, flavonoid, terpinoid, saponins, glycoside, tannins, and reducing sugars. The crude extract exhibited toxicity in A. cepa in a concentration and time-dependent manner. No adaptation capacity of DNA damage was seen during the exposure time (24-72 h). The extract at 0.03 – 0.14% (v/v) significantly (p <0.05, p <0.01, p <0.001) inhibited protein denaturation, membrane lysis and clot lysis capacity in a concentration-dependent manner. Of note, the extract exerted toxic effects at high concentrations, while protective effects against toxic and cytotoxic effects at low concentrations. M. charantia may be one of the potential sources of phytotherapeutic agents for various diseases, including oxidative stress, inflammatory diseases and cancer

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