scholarly journals In vitro Studies on Antioxidant Potential of Aqueous Extract of Bridelia ferruginea Stem Bark in Brain and Liver of Wistar-albino Rats using Sodium Nitroprusside as Pro-oxidant

Author(s):  
Adesola Oluwaseun Adeleye

Thiobarbituric acid reactive species (TBARS) assay was used to study the antioxidant potential of Bridelia ferruginea, a widely used medicinal plant in Nigeria, sub-tropical Africa and parts of Asia. The aqueous extract of Bridelia ferruginea stem bark showed inhibition against the formation of TBARS induced by the pro-oxidant, sodium nitroprusside, in the liver and brain tissue homogenates of the locally bred male and female albino-Wistar rats. The inhibition of TBARS is an indication of the antioxidant potential of the plant extract. The extent of antioxidant potential depends on concentrations, showing varying degrees of inhibition with different concentrations. It showed a 54.16% inhibition in the liver and 60.65% in the brain, both at a concentration of 0.33 mg/ml, with IC50 values of 3.00 ± 1.58 mg/ml and 2.99 ± 1.59 mg/ml for the liver and brain homogenates respectively. The results suggest the effectiveness of the aqueous extract of Bridelia ferruginea stem bark in reversing the effect of lipid peroxidation that may result from sodium nitroprusside overload.

2016 ◽  
Vol 14 (1) ◽  
pp. 93-97 ◽  
Author(s):  
A. A. Biu ◽  
L. B. Buratai ◽  
P. N. Onyedim ◽  
I. U. Hambali ◽  
S. I. Ngulde ◽  
...  

The crude aqueous extract of Guiera senegalensis stem bark was evaluated for its phytochemistry, acute toxicity and in vitro antitrypanosomal efficacy in this study. Tests for alkaloids, flavonoids, tannins, phlabotannins, saponins, steroids, cardenolides, terpenoids, cardiac glycosides, and anthraquinones were conducted. A total of 15 albino rats of both sexes were used and grouped into 5 (A to E) of 3 rats each. Groups A-D were intraperitoneally treated with graded doses of 100, 200, 400, 800mg/kg body weight of the crude aqueous extract of G. senegalensis stem bark. Group E was treated with Physiological Saline Solution serving as the control. All groups were observed for 24 hours for clinical signs and death to determine the median lethal dose (LD50). An in vitro experiment was carried out with 2 drops of blood from a donor rat added to 5 ml of phosphate buffer glucose solution out of which 0.2ml was finally used at 40, 20, 10, 5, 2.5, 0.625, 0.313, 0.156 and 0.078 concentrations of the extract. The phytochemical screening for bioactive substances had tannins, terpenoids, alkaloids, flavonoids, saponins, anthraquinones and cardiac glycosides.  Phlabotannins and cardenolides were not detected. The clinical signs observed were sluggishness, awkward posture, loss of appetite, starry hair coat and terminal death within 24 hours with LD50 value of 600mg/kg. The in vitro antitrypanosomal efficacy of the extract showed 100% inhibition of motility against Trypanosoma brucei at 20mg/ml. In conclusion, the crude aqueous extract of G. senegalensis stem bark contains phytochemical components that exhibit inhibitory trypanosomal activity. 


2013 ◽  
Vol 2013 ◽  
pp. 1-7 ◽  
Author(s):  
Seun F. Akomolafe ◽  
Ganiyu Oboh ◽  
Afolabi A. Akindahunsi ◽  
Ayodele J. Akinyemi ◽  
Oluwatosin G. Tade

Cissus populnea are plants associated with a myriad of medicinal uses in different parts of the world and are good sources of carotenoids, triterpenoids, and ascorbic acid. The antioxidant properties and inhibitory effect of water extractible phytochemicals from stem bark of C. populnea on FeSO4 and sodium nitroprusside- (SNP-) induced lipid peroxidation in rat testes were investigated in vitro. The results revealed that the extract was able to scavenge DPPH radical, chelate Fe2+ and also had a high reducing power. Furthermore, the incubation of the testes tissue homogenate in the presence of FeSO4 and SNP, respectively, caused a significant increase in the malondialdehyde (MDA) contents of the testes. However, the aqueous extract of the stem bark of C. populnea caused a significant decrease in the MDA contents of both Fe2+ (EC50 = 0.027 mg/mL) and SNP- (EC50 = 0.22 mg/mL) induced lipid peroxidation in the rat testes homogenates in a dose-dependent manner. The water extractible phytochemicals from C. populnea protect the testes from oxidative stress and this could be attributed to their high antioxidant activity: DPPH-scavenging ability, Fe2+-chelating and -reducing power. Therefore, oxidatively stress in testes could be potentially managed/prevented by this plant.


2013 ◽  
Vol 85 (3) ◽  
pp. 945-954 ◽  
Author(s):  
ISABELA K.R. AGRA ◽  
LUANA L.S. PIRES ◽  
PAULO S.M. CARVALHO ◽  
EURIPEDES A. SILVA-FILHO ◽  
SALETE SMANIOTTO ◽  
...  

The decoction of the stem barks from Bowdichia virgilioides KUNTH is a folk remedy used to treat inflammatory disorders in Latin American and Brazil. In the present study, the wound healing activity of aqueous extract of the stem bark from B. virgilioides, called AEBv, was evaluated by the rate of healing by wound contraction and period of epithelization at different days post-wound using the wound excisional model. On day 9, the AEBv-treated animals exhibited significative reduction in the wound area when compared with controls. In wound infected with S. aureus, the AEBv significantly improved the wound contraction when compared to the saline-treated mice. The histological analysis showed that AEBv induced a collagen deposition, increase in the fibroblast count and few inflammatory cells than compared to saline-treated group. The expression of collagen type I was increased in the group treated with AEBv as indicated by immunohistochemical staining. In vitro, the AEBv was effective only against S. aureus but not against P. aeruginosa. Together, the results of this study demonstrate, for the first time, the healing and antimicrobiological effects of aqueous extract of the stem bark from B. virgilioides in the therapy of skin wounds.


2009 ◽  
Vol 79 (1) ◽  
pp. 48-56 ◽  
Author(s):  
Chaturvedi

In the present study, protective effects of bitter melon (Momordica charantia) extract on lipid peroxidation induced by immobilization stress in rats have been assessed. Graded doses of extract (50, 100, and 150 mg/kg body weight) were administered orally to rats subjected to immobilization stress for two hours for seven consecutive days. Stress was applied by keeping the rats in a cage where no movement was possible. After seven days, rats were killed by decapitation after ether anesthesia. Blood and liver were collected to measure thiobarbituric acid reactive substances, reduced glutathione, and catalase. In vitro effects of M. charantia extract on lipid peroxidation in liver homogenate of normal, control, and rats pretreated with extract were carried out against cumene hydroperoxide-induced lipid peroxidation. Results reveal that in vivo M. charantia inhibited stress-induced lipid peroxidation by increasing the levels of reduced glutathione and activities of catalase. These results were further supported by in vitro results. In vitro inhibition of lipid peroxidation was indicated by low levels of thiobarbituric acid in the liver homogenate from pretreated rats and normal rats when incubated with both cumene hydroperoxide and extract. Inhibition was also noted in the homogenate where the rats were pretreated but the mixture contained no extract. Thus this plant provides protection by strengthening the antioxidants like reduced glutathione and catalase. Inclusion of this plant in the daily diet would be beneficial.


Author(s):  
Mohammed Aliyu Sulaiman ◽  
Daniel Dahiru ◽  
Mohammed Auwal Ibrahim ◽  
Ahmed Ibrahim Hayatu

Background: Oxidative stress is involved in the pathogenesis of hypertension, myocardial ischemia-reperfusion injury, atherosclerosis, muscular dystrophy, aging and other associated diseases. Vitex doniana is used in Adamawa, northern Nigeria to treat oxidative stress associated diseases. However, the antioxidative effects of the plant have not been scientifically examined in oxidative stress experimental animal models. The aim of this study is to investigate the in vitro and in vivo antioxidant activities of aqueous and ethanol stem bark extracts of Vitex doniana in oxidative stress model of rats. Methods: The study used 35 adult albino rats weighing 175 ± 25 g, of which 30 were induced with oxidative stress by intraperitoneal injection of doxorubicin (10 mg/kg) for three consecutive days. Animals were treated by oral administration of silymarin (100 mg/kg) and Vitex doniana aqueous or ethanol extract (100 mg/kg and 200 mg/kg) for 14 consecutive days before they were sacrificed on the 15th day and blood was analyzed for biochemical indices of oxidative stress. Results: The results of the phytochemistry showed the presence of alkaloids, tannins, flavonoids, steroids, phenols, saponins, terpenoids, glycosides: and total flavonoids (52.70 ± 1.60 mg/ml and 75.40 ± 0.80 mg/ml), total phenols (21.45 ± 1.54 mg/ml and 26.50 ± 1.22 mg/ml) for aqueous and ethanol stem bark extracts respectively. The extracts scavenged DPPH radical, reduced Fe3+ and inhibited lipid peroxidation. Doxorubicin significantly (p<0.05) lowered the levels of SOD, CAT, GR and TAS and significantly (p<0.05) but, increased the level of LPO. Oral treatment with Vitex doniana extracts significantly (p<0.05) increased the activities of CAT, GR, SOD and TAS while LPO was significantly (p<0.05) lowered. Vitex doniana stem bark extracts significantly (p<0.05) improved the biochemical derangements observed in the induced untreated animals in comparable manner to that of Silymarin. Conclusion: The present study provides the scientific rationale for the use of Vitex doniana stem bark in traditional medicine and has a viable antioxidative capacity both in vitro and in vivo.


2019 ◽  
Vol 2019 ◽  
pp. 1-7
Author(s):  
Mahamad Abba Talba ◽  
David Miaffo ◽  
Sylviane Laure Poualeu Kamani ◽  
Albert Kamanyi ◽  
Sylvie Léa Wansi

Cissus polyantha (Vitaceae) is a plant used in Cameroonian traditional medicine for the treatment of diabetes. The aims of this study were to evaluate the in vitro antioxidant and antidiabetic activities of the aqueous extract of Cissus polyantha leafy stems. The enzyme inhibitory activity was determined in vitro on α-amylase and α-glucosidase enzymes, followed by confirmative study in vivo on normal rats (oral starch and sucrose tolerance tests at doses of 111, 222, and 444 mg/kg). The ferric reducing antioxidant power and the 2,2-diphenyl-1-picrylhydrazyl (DPPH) antiradical activity of the extract were examined to evaluate the antioxidant potential of the extract. The total content of phenols, flavonoids, and tannins of the extract were also determined. The results showed an inhibitory effect of the extract on the α-amylase and α-glucosidase activities with IC50 values of 216.14 and 182.40 μg/mL, respectively. The extract at doses of 222 and 444 mg/kg induced a significant decrease in postprandial glycaemia during the starch and sucrose tolerance tests. A remarkable antiradical activity of the extract was obtained although lower than that of the standard product. The aqueous extract of leafy stems of Cissus polyantha has an interesting inhibitory activity on the α-amylase and α-glucosidase enzymes, as well as an antioxidant potential, thus validating its use in traditional medicine for the treatment of diabetes mellitus and its complications.


2014 ◽  
Vol 2014 ◽  
pp. 1-5 ◽  
Author(s):  
Victor Ambrose Maikai ◽  
Beatty Viv Maikai ◽  
Patricia Ishyaku Kobo

Trypanosomosis is a debilitating disease affecting mainly livestock and humans in tropical Africa. Chemically synthesized drugs and medicinal plants have been used in the treatment and control of this disease. In this study, thein vitroeffect of aqueous extracts and fraction IV extract ofXimenia americanastem bark onTrypanosoma congolenseDNA was investigated. The extracts were incubated with the parasitesin vitroat 300 mg/mL aqueous extract and 25 mg/mL fraction IV portion for 30, 60, and 120 mins. The DNA of the trypanosomes was isolated and digested using ECOR1 enzyme and subsequently PCR was carried out. Results showed that aqueous extract and fraction IV portion immobilized 55% and 90% of the trypanosomes after 30-minute incubation. Subsequent isolation of the parasite DNA and agarose gel electrophoresis did not reveal that cell death was as a result of DNA fragmentation. This suggests that cell death was by another mechanism of action.


2014 ◽  
Vol 8 (4) ◽  
pp. 84-87
Author(s):  
O. I. Olarewaju ◽  
O. I. Oloyede ◽  
O. A Ojo ◽  
S. A Onikanni ◽  
B. O Ajiboye

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