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1.
Andrologia ; 50(2)2018 Mar.
Article in English | MEDLINE | ID: mdl-28737015

ABSTRACT

This study assessed the effects of caffeine combined with caffeic acid on some biomarkers of male reproductive function using normal albino Wistar rats. Rats were divided into four groups (n = 6) and treated for seven successive days; group 1 represents the control rats; group 2 rats were treated with 50 mg/kg body weight (BW) of caffeine only; group 3 rats were treated with 50 mg/kg BW of caffeic acid, while the rats in group 4 were cotreated with an equal combination of caffeine and caffeic acid. The results revealed significant increase in reproductive hormone, testicular and epididymal nitric oxide levels of the rats. Moreover, decreased oxidative stress in the testes and epididymides of the treated rats was evidenced by significant increase in total and nonprotein thiol levels, catalase and superoxide dismutase activities. Similarly, decreased testicular cholesterol level with concomitant elevation in testicular steroidogenic enzyme activities, glycogen and zinc levels were observed in the treated rats. No morphological changes were observed as revealed by the photomicrographs from light microscopy in treated rats. Nevertheless, the combination therapy exhibited additive/synergistic effect on these biochemical indices than when they were administered singly. This study suggests the combination therapy of caffeine and caffeic acid at the dose tested for improving male reproductive function.


Subject(s)
Antioxidants/pharmacology , Caffeic Acids/pharmacology , Caffeine/pharmacology , Central Nervous System Stimulants/pharmacology , Fertility/drug effects , Animals , Antioxidants/therapeutic use , Biomarkers/analysis , Caffeic Acids/therapeutic use , Caffeine/therapeutic use , Catalase/metabolism , Central Nervous System Stimulants/therapeutic use , Drug Synergism , Drug Therapy, Combination/methods , Epididymis/drug effects , Epididymis/enzymology , Lipid Peroxidation/drug effects , Male , Models, Animal , Nitric Oxide/metabolism , Oxidative Stress/drug effects , Rats , Rats, Wistar , Superoxide Dismutase/metabolism , Testis/drug effects , Testis/enzymology , Testosterone/biosynthesis
2.
Neurotoxicology ; 62: 6-13, 2017 Sep.
Article in English | MEDLINE | ID: mdl-28465162

ABSTRACT

Caffeine and caffeic acid are two bioactive compounds that are present in plant foods and are major constituent of coffee, cocoa, tea, cola drinks and chocolate. Although not structurally related, caffeine and caffeic acid has been reported to elicit neuroprotective properties. However, their different proportional distribution in food sources and possible effect of such interactions are not often taken into consideration. Therefore, in this study, we investigated the effect of caffeine, caffeic acid and their various combinations on activities of some enzymes [acetylcholinesterase (AChE), monoamine oxidase (MAO) ecto-nucleoside triphosphate diphosphohydrolase (E-NTPase), ecto-51-nucleotidase (E-NTDase) and Na+/K+ ATPase relevant to neurodegeneration in vitro in rat brain. The stock concentration of caffeine and caffiec acid and their various proportional combinations were prepared and their interactions with the activities of these enzymes were assessed (in vitro) in different brain structures. The Fe2+ and Cu2+ chelating abilities of the samples were also investigated. The results revealed that caffeine, caffeic acid and their various combinations exhibited inhibitory effect on activities of AChE, MAO, E-NTPase and E-NTDase, but stimulatory effect on Na+/K+ ATPase activity. The combinations also exhibited Fe2+ and Cu2+ chelating abilities. Considering the various combinations, a higher caffeine to caffeic acid ratio produced significantly highest enzyme modulatory effects; these were significantly lower to the effect of caffeine alone but significantly higher than the effect of caffeic acid alone. These findings may provide new insight into the effect of proportional combination of these bioactive compounds as obtained in many foods especially with respect to their neuroprotective effects.


Subject(s)
Acetylcholinesterase/metabolism , Adenosine Triphosphatases/metabolism , Brain/drug effects , Caffeic Acids/pharmacology , Caffeine/pharmacology , Central Nervous System Stimulants/pharmacokinetics , Monoamine Oxidase/metabolism , Animals , Copper/metabolism , Dose-Response Relationship, Drug , Drug Combinations , Iron/metabolism , Rats , Rats, Wistar , Spectrophotometry
3.
Andrologia ; 49(10)2017 Dec.
Article in English | MEDLINE | ID: mdl-28164351

ABSTRACT

This study investigated the effects of Tetracarpidium conophorum leaf extract on infertility induced by ethanol in male rats. Thirty rats were randomly divided into six groups of five animals each: Group 1 (positive control) received 0.9% saline only; Group 2 (ethanol alone) were given only 30% ethanol orally at 7 ml/kg body weight per day, thrice in a week; groups 3, 4 and 5 were given ethanol and co-treated with 50, 500 and 1,000 mg/kg body weight of leaf extract, respectively, while Group 6 was given ethanol and co-treated with a fertility drug, clomiphene citrate. Ethanol treatment resulted in significant (p < .05) decrease in LDH activity, G-6PDH activity, glycogen content, 3ß and 17ß HSD activities and testicular and epididymal Zn and Se contents and furthermore decrease in testicular sperm count, viability and marked increment in total sperm abnormalities, rate of sperm analysis parameters and consequently decreased reproductive hormone levels. Interestingly, co-administration of ethanol with either T. conophorum extract or drug almost ameliorated the toxic assault imposed by ethanol on reproductive organs and improved seminal qualities of the rats.


Subject(s)
Clomiphene/therapeutic use , Ethanol , Euphorbiaceae , Infertility, Male/drug therapy , Plant Extracts/therapeutic use , Spermatozoa/drug effects , Testis/drug effects , Animals , Clomiphene/pharmacology , DNA Fragmentation/drug effects , Glycogen/metabolism , Infertility, Male/chemically induced , L-Lactate Dehydrogenase/metabolism , Male , Oxidative Stress/drug effects , Plant Extracts/pharmacology , Rats , Sperm Count , Sperm Motility/drug effects , Spermatozoa/metabolism , Testis/metabolism
4.
BMC Complement Altern Med ; 15: 439, 2015 Dec 18.
Article in English | MEDLINE | ID: mdl-26682909

ABSTRACT

BACKGROUND: Tetracarpidium conophorum (Mull. Arg.) Hutch. & Dalz is one of the many medicinal plants used for ages in folklore as male fertility enhancers. The current study evaluates the effect of the plant leaf extract on alcohol - induced reproductive toxicity in male rats. METHODS: Thirty rats were randomly divided into six groups of five animals each; Group 1 (positive control) received normal saline only; Group 2 (ethanol alone) were given only 30 % ethanol orally at 7 ml/kg body weight per day, thrice in a week; Group 3, 4, 5 were given ethanol and co-treated with 50 mg/kg, 500 mg/kg and 1000 mg/kg body weight of leaf extract respectively while Group 6 were given ethanol and co-treated with a fertility drug, clomiphene citrate. All the drugs were given daily and the experiment lasted for twenty one consecutive days. RESULTS: Alcohol ingestion resulted in a significant (p < 0.05) decrease in water, food intake and marked elevation of lipid peroxidation as assessed by the accumulation of malondialdehyde (MDA) in the reproductive tissues. Precisely, MDA level was elevated in the testis, epididymis, seminal vesicle and prostate gland by 81 %, 63 %, 95 % and 91 %, respectively. Furthermore, levels of total protein, reduced glutathione (GSH), vitamin C and activities of antioxidant enzymes in the reproductive tissues were significantly (p < 0.0001) reduced in ethanol-ingested rats. Interestingly, co-administration of T. conophorum with ethanol led to almost complete inhibition of lipid peroxidation thereby enhancing antioxidant status of the reproductive tissues. CONCLUSION: Overall, T. conophorum ameliorates oxidative reproductive toxicity induced by ethanol in male rats and its ameliorative effect comparable well with the fertility drug, clomiphene citrate.


Subject(s)
Ethanol/adverse effects , Euphorbiaceae/chemistry , Infertility, Male/drug therapy , Plant Extracts/administration & dosage , Animals , Ascorbic Acid/metabolism , Humans , Infertility, Male/chemically induced , Infertility, Male/metabolism , Lipid Peroxidation/drug effects , Male , Malondialdehyde/metabolism , Oxidative Stress/drug effects , Plant Leaves/chemistry , Rats , Rats, Wistar
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