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1.
Asian Pacific Journal of Tropical Biomedicine ; (12): 207-216, 2018.
Article in Chinese | WPRIM | ID: wpr-950443

ABSTRACT

Objective: To elucidate for the first time the phenological stage effect on polyphenol, flavonoid and proanthocyanidin contents of pennyroyal (Mentha pulegium) as well as their antioxidant capacities and insecticidal potentials against Tribolium castaneum and Lasioderma serricorne. Methods: Crude methanol extracts from pennyroyal (Mentha pulegium) aerial parts were evaluated for their antiradical, reducing power activities and repellent potentials against selected coleopteran insects during different phenological stages. Results: Phenolic contents of pennyroyal aerial parts and their antioxidant effects were significantly dependent on maturity stage of the plant. The maximum of phenol production was reached during the full flowering stage. Apigenin was the major phenol in Mentha pulegium with an amount of 6.01 mg/g of dry vegetable matter during this period. Nevertheless, at fructification stage, the highest antioxidant activity was not related to high phenolic content. The repulsive effect of pennyroyal extract showed that Lasioderma serricorne was more susceptible to pennyroyal extract than Tribolium castaneum with corresponding median repellent dose values of 0.124 and 0.006 mg/mL respectively. Moreover, great differences in insect repulsion depending on extract concentrations, exposure time and developmental stage was observed. For the lowest concentration (0.125 mg/mL), the repellent effect against Tribolium reached its maximum (90%) during the fructification stage (after 24 h of exposure) while this repellent effect was 80% during the vegetative stage. Conclusions: Due to the strong insecticidal potential of pennyroyal extracts, this study highlights the therapeutic properties of this plant and encourages its use as a safer, environmental-friendly and efficient insecticide in food industry.

2.
Asian Pacific Journal of Tropical Biomedicine ; (12): 702-707, 2017.
Article in Chinese | WPRIM | ID: wpr-950544

ABSTRACT

Objective To study the phytochemical constituents and in vitro biological activities of hydromethanolic extract and fractions from Algerian Sahara Myrtus nivellei (M. nivellei) collected in Hoggar region and to identify the active fraction that can act as an alternative of commonly used antibiotics and as antileishmanial or antioxidant agents. Methods Phytochemical screening of M. nivellei aerial parts was realised according to the literature. Extract was firstly prepared by using aqueous methanol then fractionated with ethyl acetate and butanol solvents. Total phenolics, tannis and flavonoids, of the hydromethanolic extract and their fractions were determined by Folin–Ciocalteu method as gallic acid equivalents and by aluminium chloride as rutin equivalent respectively. Extract and fractions were tested for their antimicrobial and antiparasital activities against standard bacteria using agar diffusion method and two kinds of leishmania visceral and cutaneous. The antioxidant activities were realized using phosphomolybdenum, FRAP and DPPH tests. Results Preliminary phytochemical screening exhibited the presence of flavonoids, tannins, saponins, and alkaloids. The experimental results showed that plant extract and fractions were high in phenolic compounds and exhibited an important role as antioxidant, antimicrobial and had a moderate antileishmanial activity. Conclusions These observations lead us toward more studies in this field, so that we can get more benefits from our local Algerian medicinal plants.

3.
Pakistan Journal of Pharmaceutical Sciences. 2016; 29 (3): 961-968
in English | IMEMR | ID: emr-179568

ABSTRACT

The study investigated the protective effect of grape seed and skin extract [GSSE] against doxorubicin-induced renal toxicity in healthy rats. Animals were treated with GSSE or not [control], for 8 days, administered with doxorubicin [20mg/kg] in the 4th day, and renal function as well as oxidative stress parameters were evaluated. Data showed that doxorubicin induced renal toxicity by affecting renal architecture and plasma creatinine. Doxorubicin also induced an oxidative stress characterized by an increase in malondialdehyde [MDA], calcium and H2O2 and a decrease in catalase [CAT] and superoxide dismutase [SOD]. Unexpectedly doxorubicin increased peroxidase [POD] and decreased carbonyl protein and plasma urea. Treatment with GSSE counteracted almost all adverse effects induced by doxorubicin. Data suggest that doxorubicin induced an oxidative stress into rat kidney and GSSE exerted antioxidant properties, which seem to be mediated by the modulation of intracellular calcium

4.
Pakistan Journal of Pharmaceutical Sciences. 2015; 28 (6): 1971-1978
in English | IMEMR | ID: emr-174503

ABSTRACT

Doxorubicin [Dox] is an anthracycline used in chemotherapy, although it causes toxicity and oxidative stress. Grape seed and skin extract [GSSE] is a mixture of polyphenolic compounds with antioxidant properties. To evaluate the hepato-toxicity of Dox on healthy rats as well as the protective effect of GSSE, rats were treated with GSSE [500mg/kg bw] during 8 days. At the 4[th] day of treatment, they received a single dose of Dox [20 mg/kg bw]. After the treatment [9[th] day], livers were collected and processed for oxidative stress status. Dox increased MDA [+ 900%], decreased catalase [-60%] and increased peroxidase [+90%] and superoxide dismutase [+100%] activities. In this latter case Dox mainly increased the iron isoform. Furthermore Dox altered intracellular mediators as catalytic free iron [-75%], H[2]O[2] [-75%] and calcium [+30%]. Dox also affected liver function by elevating plasma triacylglycerol and transaminases and liver morphology by altering its typical architecture. Importantly all Dox-induced liver disturbances were alleviated upon GSSE treatment. Dox induced liver toxicity and an oxidative stress mainly characterized by increased lipoperoxidation but not protein carbonylation. GSSE efficiently protected the liver from Dox-induced toxicity and appeared as a safe adjuvant that could be incorporated into chemotherapy protocols

5.
IJPR-Iranian Journal of Pharmaceutical Research. 2013; 12 (4): 867-875
in English | IMEMR | ID: emr-139866

ABSTRACT

In this study, we investigated the cardioprotective effects of resveratrol. Rats were intraperitoneally administered with resveratrol [25 mg/kg bw] or vehicle [ethanol 10%] for 7 days and their heart subjected to ischemia/reperfusion injury. Isolated hearts were langendorff perfused, left ventricular functions as heart rate and developed pressure, as well as, heart antioxidant status were determined. Data showed that resveratrol improved recovery of post-ischemic ventricular functions when compared to control. Resveratrol also improved myocardial lipoperoxidation, free iron and antioxidant enzyme activities. Resveratrol decreased significantly catalase while it increased peroxidase and superoxide dismutase activities. In this later case, native PAGE analysis of superoxide dismutase isoforms revealed that resveratrol up regulated iron and manganese isoforms. Resveratrol exerted potential cardioprotection partly by its antioxidant properties

6.
Indian J Biochem Biophys ; 2006 Dec; 43(6): 386-90
Article in English | IMSEAR | ID: sea-28213

ABSTRACT

Garlic has been extensively used as a medicinal plant. Most of its numerous beneficial effects such as antioxidant, antibacterial, antitumoral involve sulfur-derived amino acids. In the present work, we reevaluated the acute effects of aqueous extract of garlic on plasma glucose and cholesterol levels in normal rats. Control (vehicle H2O) or garlic extract-treated group at 100-120 mg protein/kg body wt were intraperitoneally injected (IP) and glucose, cholesterol, insulin and nitric oxide metabolites levels were determined after a short-term duration of 6 h. We confirmed that garlic contained an active fraction, exerting both glucose and cholesterol-lowering activity. The glucose-lowering effect was triggered by an increase in insulinemia. Preliminary study indicated that the active agent was different from S-allyl-cysteine-sulfoxide, the active principle implicated in hypoglycaemic and hypolipidemic effects of garlic or arginine. The mechanism of action seemed to involve nitric oxide (NO), which increased time and dose-dependently. The garlic effects were abolished by diphenyleneiodonium chloride (DPI = 1 mg/kg body wt), a specific inhibitor of NO production, suggesting the involvement of constitutive nitric oxide synthase.


Subject(s)
Animals , Blood Glucose/drug effects , Cholesterol/blood , Female , Garlic/chemistry , Male , Nitric Oxide/physiology , Plant Extracts/administration & dosage , Rats , Rats, Wistar
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