ABSTRACT
Background: Drug-induced reproductive organs toxicities is an important aetiology in investigation of male infertility. The aim is to study levofloxacin effect on male reproductive system in comparison to ciprofloxacin.Methods: Twenty-five male wister rats weighted 230±20 gm and aged 8 weeks were randomly divided into five groups of five. The first group received ciprofloxacin with dose 78.23 mg/kg/day in 2 doses (therapeutic dose). The second group received the double dose of the first group ciprofloxacin. The third group received levofloxacin with dose 39.11 mg/kg/day once daily (OD) (therapeutic dose). The Fourth group received the double dose of the third group levofloxacin. However, the fifth group served as a control and received normal saline with carboxymethylcellulose OD. All treatments were administered orally for 14 days. On the 15th day, blood samples and reproductive organs were obtained from all rats. Testicular tissues were prepared for genetic testing and chemical and microscopical examination.Results: Ciprofloxacin and levofloxacin negatively altered reproductive organ weights, sperm parameters and serum follicle stimulating hormone (FSH) and luteinizing hormone (LH) level (p<0.05). Additionally, serum testosterone level was significantly deceased in ciprofloxacin-treated group (the double dose) (p<0.05) relative to control. The difference between ciprofloxacin and levofloxacin was significant in seminal vesicle weight and serum LH and FSH level (p<0.05). Testicular histopathological changes were also found with the two drugs with different degrees. Effects of levofloxacin and ciprofloxacin were dose-dependent.Conclusions: Both ciprofloxacin and levofloxacin adversely affect andrological function that should be monitored and controlled during application of these drugs.
ABSTRACT
Background: Many drugs are implicated in male infertility and screening for medication history is an important for diagnosis and treatment of the problem. The aim is to study amikacin effect on male reproductive system in comparison to gentamicin.Methods: Twenty-five male wister rats weighted 220±20 gm and aged 8 weeks were randomly divided into five groups of five. The first group received gentamicin in dose 18.25 mg/kg/day once daily (OD) (therapeutic dose). The second group received gentamicin with double dose of the first group. The third group received amikacin in dose 54.75 mg/kg/day OD (therapeutic dose). The Fourth group received amikacin with double dose of the third group. However, the fifth group served as a control and received normal saline (NS) OD. All treatments were administered intraperitoneally (IP) for 14 days. On the 15th day, blood samples and reproductive organs were obtained from all animals. Testicular tissues were prepared for genetic testing and chemical and microscopical examination.Results: Amikacin and gentamicin negatively affected reproductive organs weights, sperm parameters, serum follicle stimulating hormone and luteinizing hormone (LH) level relative to control (p<0.05). However, serum testosterone level was only affected with gentamicin (p<0.05). A significant difference between gentamicin and amikacin was found in sperm count, testis and epididymis weights and serum testosterone and LH level (p<0.05). Testicular histopathological changes were also found with the two drugs with different degrees. Effects of both gentamicin and amikacin were dose-dependent.Conclusions: Both gentamicin and amikacin adversely affect andrological function that should be monitored and controlled during application of these drugs.
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Punica granatum flower and leaf were extracted with hydromethanol 50% and evaluated for antioxidant activity using phosophomolybdenum, DPPH, reducing power, and -OH-scavenging assays; and for antiinflammatory activity using HRBC-MS assay. Both extracts exhibited antioxidant activities indicated by DPPH decolorization and -OH-scavenging and increased Ferric reducing and phosphomolybdenum assays. Also, both extracts showed anti-inflammatory activities indicated by red blood cell membrane stabilization and reduced haemolysis-resultant haemoglobin. All results were concentration-dependent; and the leaf extract was more potent than that of the flower. The IC50 values for the flower and leaf extracts were 777.6 ± 1.48 & 656.4 ± 1.79; 184.3 ± 1.803 & 113.9 ± 2.001; 130.8 ± 1.66 & 81.4 ± 2.1; 132.4 ± 1.55 & 79.67 ± 0.03; and 126.1 ± 1.35 & 67.25 ± 1.28 µg/mL in phosophomolybdenum, DPPH, reducing power, -OH-scavenging and red blood cell-membrane stability assays, respectively. Phytochemical analysis revealed presence of tannins and flavonoids with results more obvious in the leaf extract. These active principle contents may account for the recorded antioxidant and anti-inflammatory activities of both extracts. These findings provide evidence for the possible beneficial applications of the Punica granatum leaf and flower extracts in stress-related disease conditions and for maintenance of normal health status and well-being as well.
A flor e a folha de Punica granatum foram extraídas com hidrometanol 50% e avaliadas quanto à atividade antioxidante usando ensaios de fosfomolibdênio, DPPH, poder redutor e de eliminação de OH; E para atividade anti-inflamatória utilizando ensaio de HRBC-MS. Ambos os extratos exibiram actividades antioxidantes indicadas por descoloração do DPPH e por eliminação de OH e aumento nos ensaios de redução férrica e fosfomolibdênio. Além disso, ambos os extratos mostraram atividades anti-inflamatórias indicadas pela estabilização da membrana dos glóbulos vermelhos e redução da hemoglobina resultante da hemólise. Todos os resultados foram dependentes da concentração; E o extrato foliar era mais potente que o da flor. Os valores de IC50 para os extractos de flores e folhas foram de 777,6 ± 1,48 & 656,4 ± 1,79; 184,3 ± 1,803 e 113,9 ± 2,001; 130,8 ± 1,66 & 81,4 ± 2,1; 132,4 ± 1,55 & 79,67 ± 0,03; E 126,1 ± 1,35 & 67,25 ± 1,28 µg / mL em ensaios de fosfomolibdênio, DPPH, poder redutor, eliminação de OH e de estabilidade de membrana de glóbulos vermelhos, respectivamente. A análise fitoquímica revelou presença de taninos e flavonóides com resultados mais evidentes no extrato foliar. Estes conteúdos de princípio activo podem explicar as actividades antioxidantes e anti-inflamatórias registadas de ambos os extractos. Estes resultados fornecem evidências para as possíveis aplicações benéficas da folha de Punica granatum e extratos de flores em condições de doença relacionadas ao estresse e para a manutenção do estado de saúde normal e bem-estar também.
Subject(s)
In Vitro Techniques , Oxidative Stress , Anti-Inflammatory Agents , AntioxidantsABSTRACT
Background: To shed some light on full characterization and utilization of nonsteroidal anti-inflammatory drugs (NSAIDs) in veterinary medicine, this study, therefore, was designed to clarify the pharmacological effects of two NSAIDs (one selective, that is meloxicam, and the other is non-selective, that is piroxicam) on intestinal contractility of rabbit as a farm animal species. Methods: Rabbits were humanely slaughtered, and segments from different parts of intestinal tracts were dissected out and an intestinal segment of about 2 cm long was fixed in an organ bath containing warm oxygenated Tyrode’s solution at 37°C. The tissue was subjected to a resting tension of 2 g and allowed to equilibrate for 30 min and then the effects of graded increased concentrations of piroxicam and meloxicam were demonstrated on the normal rhythmic motility of the isolated intestinal segments. The sites of action of piroxicam and meloxicam were tried. Results: Piroxicam and meloxicam exhibited concentration-dependent relaxations of intestinal smooth muscle segments with minimal and maximal effects of more potency by prioxicam than meloxicam. Calculated inhibitory concentration 50% were 15.45 and 23.10 μg/ml bath for piroxicam and meloxicam, respectively. Effects of either piroxicam or meloxicam did not involve cholinergic, adrenergic, histaminergic, nitrergic, or purinergic pathways as the application of the corresponding agonists/ antagonists did not affect the inhibitory response of piroxicam and meloxicam. It was assumed that the effects of the drugs were attributed to the direct effects of the drugs on the intestines in addition to inhibiting endogenous prostaglandin synthesis activity via their cyclo-oxygenase inhibiting properties. Conclusions: Data of the present study may indicate that piroxicam and meloxicam could be used effectively and safely in rabbits for their anti-inflammatory actions in small therapeutic doses. However, in large doses, they (particularly, piroxicam) may produce depressant effects on gastrointestinal tract motility that should be taken in consideration in the case of introducing these drugs in therapy with larger doses.
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Background: The concept of effects of Agaricus on inflammatory responses is still controversial. This study, therefore, was designed to assess the potential of the anti-inflammatory effect of Agaricus 100% extract on acute inflammation using the model of carrageenan-induced paw edema in rats. Methods: Four groups among five (six rats each) have been injected with carrageenan (0.1 mL of 3% solution), intra-plantar in the right hind paw; the first group was injected with saline instead in the same manner and kept as control. An hour earlier, rats received different treatments, either saline (inflamed control), or diclofenac (inflamed, standard-treated), or Agaricus extract (5 mL/kg as small dose or 10 mL/kg as a large dose). The volume of the developed paw edema has been measured at an hour interval fashion (1~6 hrs) and at 24 hrs. Results: Agaricus extract showed inhibitory effects on the carrageenan-induced edema in time- and dose-dependent manner, at the late phase (2~ hrs) of the inflammatory response (small dose) and at both early (~2 hrs) and late phases (large dose). The effects were comparable to those of diclofenac being 11.74, 08.46, 08.99, 09.72 and 09.89% at 2-6 hrs (small dose); 14.04, 23.91, 21.92, 17.99, 15.63 and 16.96% at 1-6 hrs (large dose); 16.85, 31.30, 35.38, 35.97, 34.72 and 34.63% (diclofenac). The anti-inflammatory effect of Agaricus could be attributed to its phytochemical content which may inhibit the inducible inflammatory mediators (as prostaglandins and nitric oxide) in the late phase (small dose) and/or inhibiting both early (histamine and oxygen free radicals) and late mediators (large dose). Conclusions: These data may indicate that Agaricus extract has the potential of anti-inflammatory activity that could be applied in acute inflammatory disorders.
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Background: This study was designed to identify the active contents of Citrullus colocynthis plant and to examine their teratogenicity in rats. The fruit pulp of the poisonous plant was collected randomly from Suq-Alkhamis district, Tripoli, Libya. Methods: The glucoside colocynthin was isolated by lead acetate method while the alkaloids and saponins were isolated by maceration method. These active principles were then identified by chemical tests, color reactions and thin layer chromatography. Possible teratogenic effects of the fruit pulp extract was investigated by its administration to twelve pregnant rats on the 7th day of gestation at a dose of 40.6 mg/kg body weight that is equivalent to one fourth of the LD50 of the extract. Results: Gross anatomical observation on the 20th day of gestation revealed a high percentage of resorbed fetuses, smaller size and weight fetuses as well as absence of coccygeal vertebrae, metacarpal and metatarsal bones, and carpal and tarsal bones. Conclusions: It could be concluded that the extract of fruit pulp of Citrullus colocynthis, obtained from Libya, contain glucosidal as well as other principles that may cause teratogenic effects if given during at the early stage of pregnancy.