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Curcuma longa normalized cimetidine-induced pituitarytesticular dysfunction: Relevance in nutraceutical therapy
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作者 Ngozi Joy Onwuemene christian eseigbe imafidon Abiodun Oladele Ayoka 《Animal Models and Experimental Medicine》 CSCD 2019年第3期191-200,共10页
Background:The increasing incidence of chemically induced infertility is both a social threat and a threat to the continuation of life itself.Treatment or management therapy is often expensive.This study investigated ... Background:The increasing incidence of chemically induced infertility is both a social threat and a threat to the continuation of life itself.Treatment or management therapy is often expensive.This study investigated the effects of acetone extract of a local plant(Curcuma longa)in a Wistar rat model of cimetidine‐induced pituitarytesticular dysfunction.Methods:Thirty‐five male Wistar rats were divided into 7 groups of 5 rats.After a phytochemical screening of an acetone extract of C.Longa,cimetidine and the extract at three doses,200,400 and 600 mg/kg,were orally co‐administered to the rats for 28 consecutive days.Comparisons were made(at P<0.05)against a control(2 mL/kg distilled water),a standard treatment group(cimetidine+50 mg/kg vitamin C),a toxic group(60 mg/kg cimetidine)and a group receiving extract alone.Results:Cimetidine administration was associated with deleterious alterations to sperm motility,sperm count and sperm viability,as well as derangements in the plasma levels of FSH,LH and testosterone(P<0.05).Both brain and testicular GSH and TBARS levels were significantly altered following cimetidine administration,and distortions were seen in the pituitary and testicular histoarchitecture.These changes were significantly normalized by co‐administration of graded doses of the extract,with an associated improvement of both pituitary and testicular histology.Conclusion:Acetone extract of C.Longa normalized cimetidine‐induced pituitarytesticular dysfunction in Wistar rats.This presents the extract as a potential nutraceutical choice against chemically induced reproductive toxicity. 展开更多
关键词 CURCUMA longa nutraceutics PITUITARY TESTIS WISTAR rats
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Age-related changes in urinary protein excretion in relation to indices of renal function in Wistar rats
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作者 Olaoluwa Sesan Olukiran Rufus Ojo Akomolafe +2 位作者 Olutosin Samuel Ilesanmi christian eseigbe imafidon Quadri Kunle Alabi 《Animal Models and Experimental Medicine》 2018年第4期295-304,共10页
Background: The study determined the fractions of proteins in the urine and plasma of rats at different ages, measured the plasma and urine concentrations of markers of renal function, with a view to determining the i... Background: The study determined the fractions of proteins in the urine and plasma of rats at different ages, measured the plasma and urine concentrations of markers of renal function, with a view to determining the influence of proteinuria on renal function.Methods: Eighty Wistar rats were used for this study. Groups 1 and 2 each consisted of eight 1-month-old male and female rats; 3 and 4 had eight 3-month-old male and female rats; 5 and 6 had eight 6-month-old male and female rats; 7 and 8 had eight 9-month old male and female rats; and 9 and 10 had eight 12-month-old male and female rats.Results: A fraction of the molecular weight of protein in the urine of rats aged 1, 9 and 12 months was higher than that of 3 and 6 months. The total protein concentration in the urine of male and female rats aged 9 and 12 months was significantly higher than that of rats aged 1 and 3 months. The urine creatinine concentrations of male and female rats aged 9 months were significantly higher when compared with that of 1, 3, 6 and 12 months.Conclusion: Our results suggest that the 3-month-old rats seem less affected by proteinuria, because they had the least urine protein, and consistent and reduced plasma and urine concentrations of markers of renal function. The results of this study may provide a foundation for future mechanistic inquiries as to why this age group was the least affected by proteinuria. 展开更多
关键词 CREATININE ELECTROPHORESIS PROTEIN rats UREA
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