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This study was designed to evaluate the changes in adenylate levels, adenylate energy charge (AEC) and glycolytic enzymes in control and infected mice and treatment with Citrus reticulata or the oleo-resin extract from Myrrh of Commiphora molmol tree (Mirazid), as a new antischistosomal drug. Alternations in the hepatic content of adenine nucleotides (ATP, ADP and AMP), Pi, phosphate potential, AEC, glucose, glycogen, AMP-deaminase, adenosine deaminase and total protein contents were investigated in a trial to point out the effect of infection with Schistosoma mansoni parasite as a hypoxia inducer in mice liver tissues. Moreover, the role of Citrus reticulata and Commiphora (Mirazid), natural plant extracts in improving the energy status in S. mansoni infected mice was studied, since Citrus reticulata was previously reported to possess anti-leukemia, antimicrobial and antibacterial activities, whereas Commiphora extract (Mirazid) – antifasciolicidal ones.
 The current study was undertaken to elucidate a possible neuroprotective role of dehydroepiandrosterone (DHEA) against the development of Alzheimer's disease in experimental rat model. Alzheimer's disease was produced in young female ovariectomized rats by intraperitoneal administration of AlCl3 (4.2 mg/kg body weight) daily for 12 weeks. Half of these animals also received orally DHEA (250 mg/kg body weight, three times weekly) for 18 weeks. Control groups of animals received either DHAE alone, or no DHEA, or were not ovariectomized. After such treatment the animals were analyzed for oxidative stress biomarkers such as hydrogen peroxide, nitric oxide and malondialdehyde, total antioxidant capacity, reduced glutathione, glutathione peroxidase, glutathione reductase, superoxide dismutase and catalase activities, antiapoptotic marker Bcl-2 and brain derived neurotrophic factor. Also brain cholinergic markers (acetylcholinesterase and acetylcholine) were determined. The results revealed significant increase in oxidative stress parameters associated with significant decrease in the antioxidant enzyme activities in Al-intoxicated ovariectomized rats. Significant depletion in brain Bcl-2 and brain-derived neurotrophic factor levels were also detected. Moreover, significant elevations in brain acetylcholinesterase activity accompanied with significant reduction in acetylcholine level were recorded. Significant amelioration in all investigated parameters was detected as a result of treatment of Al-intoxicated ovariectomized rats with DHEA. These results were confirmed by histological examination of brain sections. These results clearly indicate a neuroprotective effect of DHEA against Alzheimer's disease.
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