Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/5735
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dc.contributor.authorAcheampong, Desmond O.
dc.contributor.author.Barfour, Isaac K
dc.contributor.authorBoye, Alex
dc.contributor.authorAsiamah, Ernest .
dc.contributor.authorArmah, Francis A.
dc.contributor.authorAdokoh, Christian K.
dc.contributor.authorOluyemi, Joy F.
dc.contributor.authorAdrah, Benjamin
dc.contributor.authorOpoku, Richard
dc.contributor.authorAdakudugu, Emmanuel
dc.date.accessioned2021-07-26T12:49:30Z
dc.date.available2021-07-26T12:49:30Z
dc.date.issued2019-09-25
dc.identifier.issn23105496
dc.identifier.urihttp://hdl.handle.net/123456789/5735
dc.description15p:, ill.en_US
dc.description.abstractBackground. Benign prostatic hyperplasia (BPH) is a common urological disorder reported among ageing men. Objective. The study assessed histoprotective effect of lime essential oil (LEO) in a rat model of testosterone-induced benign prostatic hyperplasia (BPH) and evaluated its ability to reverse testosterone-mediated changes in the testis, kidney, and liver. Materials and methods. Adult Sprague Dawley (aged 12 weeks, 240–390 g) male rats were intramuscularly injected with testosterone enanthate (TE) (10 mg/kg) reconstituted in olive oil for ten days to establish benign prostatic hyperplasia (serum PSA level ≥ 1.24 ng/ml) in. After confirmation of BPH (sustained serum PSA level ≥ 1.24 ng/ml), rats in all groups (LEO: 30, 100, and 300 mg/kg,po,n � 6; fnasteride: 15 mg/kg,po,n � 6) except model (BPH without treatment) and sham (no BPH and no treatment) groups were treated for 21 days. At the end of treatment, rats were anesthetised and blood was collected ia cardiac puncture to determine serum PSA and total antioxidant capacity (TAC) levels. *e prostate gland, testis, kidney, and liver were harvested, weighed, histologically processed and stained with H&E. Results. LEO- and fnasteride-treated groups recorded lesser mean prostatic weights relative to their model group. Baseline mean serum PSA level of LEO- and fnasteride-treated groups reduced significantly (p <0.05) relative to model group. Serum TAC levels were also higher in LEO- and fnasteride-treated groups relative to model group. LEO-treated groups had less thickened glandular epithelium, smaller acini, fewer prostatic secretions and more fibro muscular stroma relative to model group. LEO and fnasteride treatment produced improved histomorphological characteristics of testis, kidney, and liver compared to model group.Conclusion. By the current results, Citrus aurantifolia LEO may possess active agents that can be explored for translational medicine against BPHen_US
dc.language.isoenen_US
dc.publisherUniversity of Cape Coasten_US
dc.titleHistoprotective Effect of Essential Oil from Citrus Aurantifoliain Testosterone-induced Benign Prostatic Hyperplasia Raten_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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