2015
DOI: 10.1155/2015/175950
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Phenolic Extract fromMoringa oleiferaLeaves Inhibits Key Enzymes Linked to Erectile Dysfunction and Oxidative Stress in Rats’ Penile Tissues

Abstract: This study was designed to determine the antioxidant properties and inhibitory effects of extract from Moringa oleifera leaves on angiotensin-I-converting enzyme (ACE) and arginase activities in vitro. The extract was prepared and phenolic (total phenols and flavonoid) contents, radical (nitric oxide (NO), hydroxyl (OH)) scavenging abilities, and Fe2+-chelating ability were assessed. Characterization of the phenolic constituents was done via high performance liquid chromatography-diode array detection (HPLC-DA… Show more

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Cited by 107 publications
(84 citation statements)
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“…Hence, the inhibition of arginase activity can be additional therapeutic targets for the management of ED as this could increase the bioavailability of L-arginine, contribute to the production of NO via reaction catalyzed by NOS, where overall result could facilitate penile erection. Inhibition of arginase activity by the studied extracts is in line with some reports of plant extracts, which are rich in phenolics including epicatechin, quercetin, quercitrin and isoquercitrin and their arginase inhibitory potential (Shin et al 2011;Oboh et al 2015;Akomolafe et al 2016). Hence, the observed high flavonoid content and abundant presence of flavonoid compounds such as (-)-epicatechin, rutin, quercetin and quercitrin in UPP may be responsible for its higher arginase inhibitory activity.…”
Section: Discussionsupporting
confidence: 86%
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“…Hence, the inhibition of arginase activity can be additional therapeutic targets for the management of ED as this could increase the bioavailability of L-arginine, contribute to the production of NO via reaction catalyzed by NOS, where overall result could facilitate penile erection. Inhibition of arginase activity by the studied extracts is in line with some reports of plant extracts, which are rich in phenolics including epicatechin, quercetin, quercitrin and isoquercitrin and their arginase inhibitory potential (Shin et al 2011;Oboh et al 2015;Akomolafe et al 2016). Hence, the observed high flavonoid content and abundant presence of flavonoid compounds such as (-)-epicatechin, rutin, quercetin and quercitrin in UPP may be responsible for its higher arginase inhibitory activity.…”
Section: Discussionsupporting
confidence: 86%
“…In the ED, the increased activity of arginase reduces production of NO, as arginase catalyzes the conversion of arginine to urea and ornithine, thereby reducing arginine levels that could be used for NO production by NO synthase (NOs). Arginase competes with NOs for L-arginine substrate, therefore, inhibition of arginase could up-regulate NO production (Sakai et al 2004;Oboh et al 2015). Inhibition of acetylcholinesterase (AChE) is another target for the treatment of ED as it regulates the levels of ACh, which trigger NO-dependent smooth muscle relaxation in erection process (Vargas et al 2004).…”
Section: Introductionmentioning
confidence: 99%
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