As a result of normal metabolic processes, the human body produces reactive oxygen species capable of oxidizing biomolecules that can damage DNA, cells and also contribute to the development of chronic diseases. The process can be attenuated or perhaps reversed by herbs and diets containing components that can scavenge reactive oxygen species. In this study, the total antioxidant capacity (TAC), total polyphenolic content (TPC) and total flavonoids content (TFC) of aqueous, ethanol, nHexane extract as well as ethanol extract fractions of Vitex doniana leaves were determined. Ethanol extract showed the highest 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical scavenging activity (69.01±1.13) followed by aqueous extract (66.14±1.12) and n-hexane extract (50.05±2.11). The total flavonoids content is in the order; aqueous (304±4.14) > ethanol (276 ±4.69) > n-Hexane (88±3.45). Hence, the total phenolic content is in a similar order as that of total antioxidant capacity. Chloroform : ethyl acetate fraction has the highest antioxidant capacity (165mg/ml). methanol : H 2 O fraction (76mg/ml) and 100% methanol (76mg/ml). Similarly, the total flavonoids content is in the order of fractions; 1>6>4>13>12>2 and others. Total phenolics were in the order of fractions; 1>5>4>12>7>2. There was a strong relationship (R 2 = 0.77) between total antioxidant activity and total flavonoid contents and (R 2 = 0.6517) for total phenolic content of the fractions. The present study demonstrated that V. doniana leaves extracts contain high amounts of flavonoids and phenolic compounds so that these compounds are efficient free radical scavengers.

Background: Benign prostate hyperplasia (BPH) is an age-related disease of unknown etiology, characterized by prostate enlargement. The effect of Prosopis africana (PA), Vernonia amydalina (VA) and Ocimum gratissmum (OG), plant extracts on haematological parameters of BPH animal model was investigated. Methods: BPH was induced in 45 male Wistar rats (250-350 g) by exogenous injection of testosterone and estradiol in staggered doses for 3 weeks. To confirm BPH induction, some animals were sacrificed; histological inspection of prostate gland and PSA was carried out. Forty BPH induced rats were divided into 8 groups. Group 1 and 2, 3 and 4, 5 and 6 were treated with 50 mg/kg bw and 100 mg/kg bw doses of PA, VA and OG extracts respectively. Group 7 received finasteride (0.1 mg/kg bw). Group 8 BPH control and five rats without induction constitute group 9, the normal control and both received distilled water. After 45 days, the rats were anaesthetised by a brief exposure to trichloromethane vapour and 5 ml of blood was collected from the rats through cardiac puncture and dispensed into well-labelled EDTA containers to avoid coagulation. All analyses were completed within 24 h of sample collection. Results: Results showed that induction of BPH caused a significant (P< 0.05) enlargement of prostate gland when compared to normal control. All extracts produced significant (P<0.05) reduction in the weight of the enlarged prostate when compared to the BPH control. There were significant (P ˂0.05) decline in RBC, PCV and Hb of BPH control when compared to the normal control and treated groups. In the treated groups the administration of the extracts and standard drug exhibited an increase in RBC, PCV and Hb concentration when compared with the BPH control. Also there was significant (P < 0.05) increase in the WBC, neutrophils, platelets, monocytes, lymphocytes and eosinophils levels in BPH control when compared to normal control and treated groups. In all treated groups there was significant decrease in WBC, neutrophils, platelets, monocytes, lymphocytes and eosinophils concentration levels when compared with the BPH control group. Conclusion: The result of this study indicates that the extracts have the potential to reverse the inflammation caused by BPH and also have the capacity to boost the numbers of red blood cells probably by inhibiting the hemolysis caused by inflammatory factors or by enhancing the production of red blood cell from the bone marrow.

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Background:The most significant risk factor for developing benign prostatic hyperplasia (BPH) is an advanced age. As BPH and aberrant changes in reactive oxygen species become more common with ageing, oxygen species signalling may play an important role in the development and progression of this disease. In this study, we investigated the effect of Nigerian indigenous plant; Vernonia amygdalina (VA) on oxidative stress indices in BPH induced rats. Methods: BPH was induced in male rats weighing 200-300 g by exogenous administration of testosterone and estradiol via subcutaneous injection at a dose of 400 µg/kg testosterone (T) and

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