scholarly journals Гематологічні показники та морфологічна характеристика селезінки самок щурів f1 за дії наногерманію цитрату, застосованого у різних дозах

2017 ◽  
Vol 19 (77) ◽  
pp. 45-50
Author(s):  
G. Kotsjumbas ◽  
U. Tesarivska ◽  
M. Humenetska ◽  
M. Shumska
Keyword(s):  
Aqueous Solution ◽  
Marked Decrease ◽  
Hematological Parameters ◽  
Structural Disorder ◽  
Female Rats ◽  
White Pulp ◽  
Histological Changes ◽  
Group V ◽  
Laboratory Rats ◽  
Different Doses

The article presents results of drinking by female rats the water contained different doses of nanogermanium citrate (NGeC). Studies performed on laboratory rats females F1, divided into 5 groups: I – control, II group – aqueous solution of citric acid at a dose 50 µg; III – 10µg Ge; IV – 20µg Ge; V – 200 µg of Ge per kg of body weight. Defined hematological parameters, weight and index mass and histological changes in spleen. From blood leucogram was еstablished that rats from group II, III and IV had incresed the amount of neutrophils and eosinophils. Animals Group V biased marked decrease of lymphocytes and eosinophils, certain decrease of monocytes and increase of neutrophils. Index mass of spleen biased increased in animals IV and V groups. Prolonged drink to female rats aqueous solution of NGeC at a dose of 10 µg/kg promoted the growth of number cells of white pulp and the formation lymph nodes with reactive centers. This indicates an active limphopoetic function of spleen. But a dose of 200 µg/kg – led to structural disorder that manifested hyperemia, edema, easing trabecular content and reduced lymphocytes, macrophages and microphages of white pulp. This points to the dysfunction lymphocytopoiesis.

scholarly journals The effects of Nigella sativa oil administration on some physiological and histological values of reproductive aspects of rats

2011 ◽  
Vol 35 (2) ◽  
pp. 52-60
Author(s):  
Farooq T. Juma
Keyword(s):  
Blood Cells ◽  
Nigella Sativa ◽  
Hematological Parameters ◽  
White Blood Cells ◽  
Female Rats ◽  
Cholesterol Concentration ◽  
Control Group ◽  
Sexual Hormones ◽  
Histological Changes ◽  
Accessory Glands

The goal of this study to investigate the effects of Nigella sativa (Ns) oil on reproductive values, some hematological parameters serum biochemical characteristics, some sexual hormones concentration and histological changes of treated and normal male reproductive organs. The experiment (1) dealt with 20 males and 20 female rats at 21 days of age, 10 rats of each sex were giving orally Ns oil at the rate of 1ml/kg/day for 30 days and the others left as a control group. Insignificant changes were occurred in hematological parameters except the white blood cells (WBCs), were significantly increased in treated groups (P<0.05). The treated groups showed significant increases in total protein and significant decreases in total cholesterol liver enzymes markedly increased in treated rats Significant increases in the levels of LH, FSH and testosterone for males and LH, FSH, estrogen and progesterone for females were recorded. The experiment (2) dealt with effects of Ns oil on 20 adult males and 20 adult female rats that were given same dose of Ns oil for 30 days. There were significant increase in litter size and weight of rats born in treated groups. The experiment (3) dealt with the effects of Ns oil on castrated males fifteen adult rats were divided equally into 3 groups, two groups were castrated while, the third group was left as a control group; one castrated group was treated with same dose of Ns oil for 30 days, there were significant increases in serum testosterone concentration and weight of accessory glands in treated group. Histological changes in the accessory glands of treated groups were evident.In conclusion, the administration of 1ml/kg/day of Ns oil stimulated the secretion of sexual hormones that led to improve protein synthesis of hepatic enzymes, white blood cells count and decrease the serum cholesterol concentration in blood

The Effect of Moderate Vitamin B6 Deficiency on Immunological and Hematological Parameters of Adult Female Rats

1990 ◽  
Vol 587 (1) ◽  
pp. 292-293
Author(s):  
D. S. KELLEY ◽  
M. C. SCHAEFFER ◽  
D. A. SAMPSON ◽  
P. C. TAYLOR ◽  
Y. M. RIVERA
Keyword(s):  
Adult Female ◽  
Vitamin B6 ◽  
Hematological Parameters ◽  
Female Rats ◽  
Vitamin B6 Deficiency

Neospora caninum (Protozoa: Apicomplexa) infections in rats

1990 ◽  
Vol 68 (7) ◽  
pp. 1595-1599 ◽  
Author(s):  
David S. Lindsay ◽  
J. P. Dubey
Keyword(s):  
Rattus Norvegicus ◽  
Neospora Caninum ◽  
Clinical Signs ◽  
Hepatic Necrosis ◽  
Female Rats ◽  
Methylprednisolone Acetate ◽  
Laboratory Rats ◽  
Experimental Inoculation ◽  
Caninum Tachyzoites ◽  
Subcutaneous Inoculation

The susceptibility of laboratory rats (Rattus norvegicus) to experimental inoculation with tachyzoites of Neospora caninum was examined. Groups of female rats were intramuscularly injected with 0, 2, or 4 mg of methylprednisolone acetate (MPA) 7 days prior to, and on the day of, subcutaneous inoculation with 0 or 1.5 × 105 tachyzoites. Clinical signs of disease or deaths did not occur in rats given nothing or only N. caninum tachyzoites. Rats given only 4 mg MPA failed to grow as well as rats given nothing or only N. caninum tachyzoites but were otherwise healthy. All of 20 rats given 4 mg MPA and tachyzoites died of hepatitis and pneumonia within 12 days postinoculation. Hepatic necrosis was the most striking lesion seen in these rats, and other milder lesions consisted of pneumonia, encephalitis, and myositis. The response of rats given 2 mg MPA and tachyzoites was less severe. Three of 20 rats died with encephalitis, myositis, hepatitis, and pancreatitis. Mild lesions, but no N. caninum tachyzoites, were seen in 3 of 14 rats inoculated only with tachyzoites. Rats given the 4 mg MPA treatment and inoculated with N. caninum tachyzoites appear to be suitable subjects for examining acute neosporosis and could be used in studies designed to examine treatment of acute disease.

scholarly journals Diuretic activity of the bark of Eysenhardtia polystachya

2016 ◽  
Vol 11 (1) ◽  
pp. 212 ◽  
Author(s):  
Saudy Saret Pablo-Pérez ◽  
María Mirian Estévez-Carmona ◽  
María Estela Meléndez-Camargo
Keyword(s):  
Body Weight ◽  
Filtration Rate ◽  
Treated Group ◽  
Female Rats ◽  
Control Group ◽  
Electrolyte Balance ◽  
Urinary Flow ◽  
Diuretic Activity ◽  
Sodium And Potassium ◽  
Different Doses

<p class="Abstract">The aim of this study was to evaluate the diuretic activity of <em>Eysenhardtia polystachya</em> bark aqueous extract at different doses in a rat model. Different doses of <em>E. polystachya</em> (125, 250, 500 and 750 mg/kg body weight), furosemide (4 mg/kg) and vehicle were administered per os to female rats (n=6 animals per group). After 6 hours in metabolic cages, the effect on urinary flow, glomerular filtration rate and electrolyte balance of sodium and potassium were assessed in all animals. <em>E. polystachya</em> at the doses of 500 and 750 mg/kg induced diuretic activity, since markedly increased (p&lt;0.05) the urinary flow rate, similar to that of furosemide treated group. Only the dose of 750 mg/kg produced an increment in urinary excretion of sodium but not of potassium compared with control group. These findings indicate that<em> E. polystachya</em> bark-induced diuretic activity, providing evidence for its folkloric use.</p><p> </p>

Final Report on the Safety Assessment of Potassium Silicate, Sodium Metasilicate, and Sodium Silicate1

2005 ◽  
Vol 24 (1_suppl) ◽  
pp. 103-117 ◽  
Keyword(s):  
Aqueous Solution ◽  
Human Skin ◽  
Sodium Silicate ◽  
Safety Assessment ◽  
Sodium Metasilicate ◽  
Potassium Silicate ◽  
Female Rats ◽  
Male Rats ◽  
Molar Ratio ◽  
Eye Irritation

Potassium Silicate, Sodium Metasilicate, and Sodium Silicate combine metal cations with silica to form inorganic salts used as corrosion inhibitors in cosmetics. Sodium Metasilicate also functions as a chelating agent and Sodium Silicate as a buffering and pH adjuster. Sodium Metasilicate is currently used in 168 formulations at concentrations ranging from 13% to 18%. Sodium Silicate is currently used in 24 formulations at concentrations ranging from 0.3% to 55%. Potassium Silicate and Sodium Silicate have been reported as being used in industrial cleaners and detergents. Sodium Metasilicate is a GRAS (generally regarded as safe) food ingredient. Aqueous solutions of Sodium Silicate species are a part of a chemical continuum of silicates based on an equilibrium of alkali, water, and silica. pH determines the solubility of silica and, together with concentration, determines the degree of polymerization. Sodium Silicate administered orally is readily absorbed from the alimentary canal and excreted in the urine. The toxicity of these silicates has been related to the molar ratio of SiO2/Na2O and the concentration being used. The Sodium Metasilicate acute oral LD50 ranged from 847 mg/kg in male rats to 1349.3 mg/kg in female rats and from 770 mg/kg in female mice to 820 mg/kg in male mice. Gross lesions of variable severity were found in the oral cavity, pharynx, esophagus, stomach, larynx, lungs, and kidneys of dogs receiving 0.25 g/kg or more of a commercial detergent containing Sodium Metasilicate; similar lesions were also seen in pigs administered the same detergent and dose. Male rats orally administered 464 mg/kg of a 20% solution containing either 2.0 or 2.4 to 1.0 ratio of sodium oxide showed no signs of toxicity, whereas doses of 1000 and 2150 mg/kg produced gasping, dypsnea, and acute depression. Dogs fed 2.4 g/kg/day of Sodium Silicate for 4 weeks had gross renal lesions but no impairment of renal function. Dermal irritation of Potassium Silicate, Sodium Metasilicate, and Sodium Silicate ranged from negligible to severe, depending on the species tested and the molar ratio and concentration tested. Sodium Metasilicate was negative in the local lymph node assay (LLNA), but a delayed-type hypersensitivity response was observed in mice. Potassium Silicate was nonirritating in two acute eye irritation studies in rabbits. Sodium Metasilicate (42.4% H20) was corrosive to the rabbit eye. Sodium Silicate was a severe eye irritant in some eye irritation studies, but was irritating or nonirritating in others. A skin freshener containing Sodium Silicate was nonirritating. Sodium Metasilicate was nonmutagenic in bacterial cells. Rats given Sodium Silicate (600 and 1200 ppm of added silica) in the drinking water in reproductive studies produced a reduced number of offspring: to 67% of controls at 600 ppm and to 80% of controls at 1200 ppm. Three adult rats injected intratesticularly and subcutaneously with 0.8 mM/kg of Sodium Silicate showed no morphological changes in the testes and no effect on the residual spermatozoa in the ductus deferens. Sodium Metasilicate (37% in a detergent) mixed with water was a severe skin irritant when tested on intact and abraded human skin, but 6%, 7%, and 13% Sodium Silicate were negligible skin irritants to intact and abraded human skin. Sodium Silicate (10% of a 40% aqueous solution) was negative in a repeat-insult predictive patch test in humans. The same aqueous solution of Sodium Silicate was considered a mild irritant under normal use conditions in a study of cumulative irritant properties. The Cosmetic Ingredient Review (CIR) Expert Panel recognized the irritation potential of these ingredients, especially in leave-on products. However, because these ingredients have limited dermal absorption and Sodium Metasilicate is a GRAS direct food substance, the Panel deemed the ingredients safe for use in cosmetic products in the practices of use and concentration described in this safety assessment, when formulated to avoid irritation.

scholarly journals Pyrrolizidine Alkaloid-Induced Hepatotoxicity Associated with the Formation of Reactive Metabolite-Derived Pyrrole–Protein Adducts

Toxins ◽  
2021 ◽  
Vol 13 (10) ◽  
pp. 723
Author(s):  
Jiang Ma ◽  
Mi Li ◽  
Na Li ◽  
Wood Yee Chan ◽  
Ge Lin
Keyword(s):  
Natural Products ◽  
Pyrrolizidine Alkaloids ◽  
Pyrrolizidine Alkaloid ◽  
Protein Adducts ◽  
Dependent Manner ◽  
Histological Changes ◽  
Histological Results ◽  
Dose Dependent ◽  
Different Doses ◽  
Alt Activity

Pyrrolizidine alkaloids (PAs) with 1,2-unsaturated necine base are hepatotoxic phytotoxins. Acute PA intoxication is initiated by the formation of adducts between PA-derived reactive pyrrolic metabolites with cellular proteins. The present study aimed to investigate the correlation between the formation of hepatic pyrrole–protein adducts and occurrence of PA-induced liver injury (PA-ILI), and to further explore the use of such adducts for rapidly screening the hepatotoxic potency of natural products which contain PAs. Aqueous extracts of Crotalaria sessiliflora (containing one PA: monocrotaline) and Gynura japonica (containing two PAs: senecionine and seneciphylline) were orally administered to rats at different doses for 24 h to investigate PA-ILI. Serum alanine aminotransferase (ALT) activity, hepatic glutathione (GSH) level, and liver histological changes of the treated rats were evaluated to assess the severity of PA-ILI. The levels of pyrrole–protein adducts formed in the rats’ livers were determined by a well-established spectrophotometric method. The biological and histological results showed a dose-dependent hepatotoxicity with significantly different toxic severity among groups of rats treated with herbal extracts containing different PAs. Both serum ALT activity and the amount of hepatic pyrrole–protein adducts increased in a dose-dependent manner. Moreover, the elevation of ALT activity correlated well with the formation of hepatic pyrrole–protein adducts, regardless of the structures of different PAs. The findings revealed that the formation of hepatic pyrrole–protein adducts—which directly correlated with the elevation of serum ALT activity—was a common insult leading to PA-ILI, suggesting a potential for using pyrrole–protein adducts to screen hepatotoxicity and rank PA-containing natural products, which generally contain multiple PAs with different structures.

Acute and sub-chronic toxicity of the aqueous extract of Ficus vogelii (Miq.) Miq. stem bark in rats

2021 ◽  
Vol 10 (2) ◽  
pp. 89-97
Author(s):  
EL Lappa ◽  
◽  
C Bogning Zangueu ◽  
EL Nguemfo ◽  
JJ Kojom Wanche ◽  
...  
Keyword(s):  
Body Weight ◽  
Aqueous Extract ◽  
Chronic Toxicity ◽  
Hematological Parameters ◽  
Lethal Dose ◽  
Relative Weight ◽  
Stem Bark ◽  
The Body ◽  
Female Rats ◽  
Male Rats

Ficus vogelii is a medicinal plant mainly found in tropical Africa and reported to treat inflammatory complaints. This study aims to evaluate the acute and sub-chronic toxicity of the aqueous extract of Ficus vogelii stem bark in wistar rats. For acute study, aqueous extract at a single dose of 5000 mg/kg body weight was administered to female rats and observed for 14 days. In the sub-chronic study, the extract was administered daily to both sex rats at the doses of 100, 200, 400, and 600 mg/kg body weight for 28 consecutive days. Body weight was measured weekly, while hematological, biochemical, and histopathological parameters were analyzed after euthanize. Aqueous extract of Ficus vogelii at all tested doses didn’t produced any mortality or significant change on the body weight and relative weight of rats on acute and sub-chronic studies. The lethal dose 50 was estimated greater than 5000 mg/kg (DL50˃5000 mg/kg). Hematological parameters were recorded non-significant in all treated rats. Aqueous extract at 600 mg/kg significantly changed transaminases and alkaline phosphatase activities, these changes were reversible in satellites. The concentrations of bilirubin was increased at 200 and 600 mg/kg in male rats, at 100, 400 mg/kg in female rats. The levels of lipids markers didn’t changed, except the significant decrease of LDL-cholesterol. Histological examination didn’t showed any change in the architecture of the liver and kidney of rats treated compared to control. Thus aqueous extract of Ficus vogelii stem bark didn’t produced adverse effects in rats after oral acute and sub-chronic treatment.

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