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1.
Nutrients ; 13(9)2021 Aug 26.
Artigo em Inglês | MEDLINE | ID: mdl-34578850

RESUMO

Kaff-e-Maryam (Anastatica hierochuntica L.) is extensively used to treat a range of health problems, most notably to ease childbirth and alleviate reproductive system-related disorders. This study aimed to evaluate the effect of A. hierochuntica ethanolic (KEE), and aqueous (KAE) extracts on CCl4-induced oxidative stress and nephrotoxicity in rats using the biochemical markers for renal functions and antioxidant status as well as histopathological examinations of kidney tissue. A. hierochuntica contained 67.49 mg GAE g-1 of total phenolic compounds (TPC), 3.51 µg g-1 of total carotenoids (TC), and 49.78 and 17.45 mg QE g-1 of total flavonoids (TF) and total flavonols (TFL), respectively. It resulted in 128.71 µmol of TE g-1 of DPPH-RSA and 141.92 µmol of TE g-1 of ABTS-RSA. A. hierochuntica presented superior antioxidant activity by inhibiting linoleic acid radicals and chelating oxidation metals. The HPLC analysis resulted in 9 and 21 phenolic acids and 6 and 2 flavonoids in KEE and KAE with a predominance of sinapic and syringic acids, respectively. Intramuscular injection of vit. E + Se and oral administration of KEE, KAE, and KEE + KAE at 250 mg kg-1 body weight significantly restored serum creatinine, urea, K, total protein, and albumin levels. Additionally, they reduced malondialdehyde (MOD), restored reduced-glutathione (GSH), and enhanced superoxide dismutase (SOD) levels. KEE, KAE, and KEE + KAE protected the kidneys from CCl4-nephrotoxicity as they mainly attenuated induced oxidative stress. Total nephroprotection was about 83.27%, 97.62%, and 78.85% for KEE, KAE, and KEE + KAE, respectively. Both vit. E + Se and A. hierochuntica extracts attenuated the histopathological alteration in CCl4-treated rats. In conclusion, A. hierochuntica, especially KAE, has the potential capability to restore oxidative stability and improve kidney function after CCl4 acute kidney injury better than KEE. Therefore, A. hierochuntica has the potential to be a useful therapeutic agent in the treatment of drug-induced nephrotoxicity.


Assuntos
Antioxidantes/farmacologia , Brassicaceae/química , Nefropatias/tratamento farmacológico , Estresse Oxidativo/efeitos dos fármacos , Fenóis/farmacologia , Extratos Vegetais/farmacologia , Plantas Medicinais/química , Animais , Tetracloreto de Carbono , Modelos Animais de Doenças , Etanol , Rim/efeitos dos fármacos , Masculino , Ratos , Água
2.
Biol Trace Elem Res ; 199(4): 1370-1376, 2021 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-32632750

RESUMO

This study aimed to investigate the effect of zinc (Zn), selenium (Se), and vitamin E (Vit E) administration on semen quality and fertility in male dromedary camels with impotentia generandi (IG, post-coital infertility). Factors that may affect response to treatment were investigated. Thirty-three IG-affected and five fertile camels were included. Case history was obtained, and breeding sound examination was performed. Semen was collected using electroejaculation. IG-camels were classified according to initial sperm count, body condition score, age, duration of infertility, IG-type, and testicular size. IG-camels were treated with a combination of intramuscular injections of Vit E (α-tocopherol acetate, 1 mg/kg bw) and Se (sodium selenite, 0.088 mg/kg bw) once every week for three successive weeks and by daily oral administration of 360 mg of zinc gluconate for 5 successive weeks. Semen quality was estimated before and after treatment. IG-treated camels were allowed to mate females in estrus, and conception rates were calculated. The results showed that sperm cell concentration, sperm motility, and viability significantly increased, while sperm abnormality significantly decreased after treatment (P < 0.01). Positive correlations were observed between initial sperm cell count and post-treated sperm count (P = 0.001), sperm motility (P = 0.01), and viability (P = 0.002). Other variables and their interactions did not affect response to treatment. Conception rates improved after treatment. In conclusion, Zn, Se, and Vit E administration improved semen quality and fertility in male dromedary camels with impotentia generandi. Initial sperm count can be used to predict the degree of camel response to treatment.


Assuntos
Camelus , Infertilidade Masculina , Selênio , Análise do Sêmen , Animais , Feminino , Fertilidade , Infertilidade Masculina/veterinária , Masculino , Selênio/farmacologia , Sêmen , Contagem de Espermatozoides , Motilidade dos Espermatozoides , Espermatozoides , Vitamina E/farmacologia , Zinco/farmacologia
3.
Plants (Basel) ; 9(11)2020 Nov 10.
Artigo em Inglês | MEDLINE | ID: mdl-33182768

RESUMO

Piper cubeba L. fruit is an important species used in folk medicine for different types of pains such as rheumatism, chills, flu, colds, muscular aches, and fever. This study examines the chemical constituents, antioxidant activity, and potential inhibitory effect against human peroxiredoxin 5, a key enzyme of P. cubeba essential oil from fruits. Using gas chromatography coupled with mass spectrometry (GC-MS), the principal components were methyleugenol (41.31%) and eugenol (33.95%), followed by (E)-caryophyllene (5.65%), p-cymene-8-ol (3.50%), 1,8-cineole (2.94%), and α-terpinolene (1.41%). Results showed similar scavenging activity via 2,2-diphenyl-1-picrylhydrazyl DPPH radical scavenging activity (IC50 = 110.00 ± 0.08 µg/mL), as well as very potent antioxidant activity against both ferric reducing/antioxidant power (FRAP) (106.00 ± 0.11 µg/mL) and ß-carotene bleaching (IC50 = 315.00 ± 2.08 µg/mL) assays when compared to positive butylated hydroxytoluene and ascorbic acid. The molecular docking approach has also been performed to screen the antioxidant activities of the major and potent compounds against human protein target peroxiredoxin 5. Results showed good binding profiles and attributed the strongest inhibitory activity to ß-caryophyllene oxide (-5.8 kcal/mol), followed respectively by isocembrol and α-selinene (-5.4 kcal/mol), and viridiflorol (-5.1 kcal/mol). Furthermore, ADME (absorption, distribution, metabolism and excretion)-related physicochemical and pharmacokinetic properties have been assessed and support our in vitro findings. This work demonstrates the powerful antioxidant potency of cubeba pepper and paves the way for the discovery and development of antioxidant agent with high potency.

4.
Trop Anim Health Prod ; 51(5): 1167-1172, 2019 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-30645711

RESUMO

The aim of this study was to investigate the profiles of cadmium (Cd), lead (Pb), selenium (Se), zinc (Zn), copper (Cu), molybdenum (Mo), iron (Fe), and manganese (Mn) in serum of dromedary camels with impotentia generandi and their associations with the clinical findings and semen analysis data. Sixteen male dromedary camels with impotentia generandi (IG group) and 5 fertile camels (FERT group) were used. The external and internal genital organs were examined using visual inspection, palpation, and ultrasonography. Semen was collected by electroejaculation and examined for volume, count, motility, viability, and abnormality. Blood was collected from all camels and serum was harvested. All serum samples were digested by concentrated acids and analyzed for heavy metals and trace elements by flame emission atomic absorption spectrophotometer. Results showed that the mean heavy metal and trace element concentrations in serum were in the following descending order Fe > Zn > Cu > Cd > Mo > Se > Mn > Pb. Cd was higher in IG than in FERT males (P = 0.02). Se was greater in FERT than in IG groups (P = 0.003). Zn was higher in in FERT than in IG groups (P = 0.001). There were positive correlations between Zn and sperm count (r = 0.59, P = 0.005) and sperm motility (r = 0.57, P = 0.005) and a tendency for negative correlation between Zn and sperm abnormalities (r = - 0.44, P = 0.05). In conclusion, Cd might be implicated as a cause of infertility in male camels. Deficiencies of Se and Zn may also have adverse impacts on male camel reproduction.


Assuntos
Camelus , Infertilidade Masculina/veterinária , Metais Pesados/sangue , Selênio/sangue , Sêmen/fisiologia , Oligoelementos/sangue , Animais , Infertilidade Masculina/sangue , Masculino , Análise do Sêmen/veterinária
5.
Sci Rep ; 6: 37435, 2016 11 25.
Artigo em Inglês | MEDLINE | ID: mdl-27886210

RESUMO

Melanocortin 4 receptor (MC4R) variants contribute to human obesity, and rats lacking functional MC4R (Mc4rK314X/K314X) are obese. We investigated the hypothesis that low energy expenditure (EE) and physical activity contribute to this obese phenotype in male rats, and determined whether lack of functional MC4R conferred protection from weight loss during 50% calorie restriction. Though Mc4rK314X/K314X rats showed low brown adipose Ucp1 expression and were less physically active than rats heterozygous for the mutation (Mc4r+/K314X) or wild-type (Mc4r+/+) rats, we found no evidence of lowered EE in Mc4rK314X/K314X rats once body weight was taken into account using covariance. Mc4rK314X/K314X rats had a significantly higher respiratory exchange ratio. Compared to Mc4r+/+ rats, Mc4rK314X/K314X and Mc4r+/K314X rats lost less lean mass during calorie restriction, and less body mass when baseline weight was accounted for. Limited regional overexpression of Mc3r was found in the hypothalamus. Although lower physical activity levels in rats with nonfunctional MC4R did not result in lower total EE during free-fed conditions, rats lacking one or two functional copies of Mc4r showed conservation of mass, particularly lean mass, during energy restriction. This suggests that variants affecting MC4R function may contribute to individual differences in the metabolic response to food restriction.


Assuntos
Tecido Adiposo Marrom/metabolismo , Peso Corporal/genética , Metabolismo Energético/genética , Hipotálamo/metabolismo , Receptor Tipo 4 de Melanocortina/deficiência , Animais , Restrição Calórica/métodos , Expressão Gênica , Heterozigoto , Homozigoto , Masculino , Fenótipo , Condicionamento Físico Animal , Ratos , Ratos Transgênicos , Receptor Tipo 4 de Melanocortina/genética , Proteína Desacopladora 1/genética , Proteína Desacopladora 1/metabolismo
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