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1.
Zhonghua Nan Ke Xue ; 23(9): 817-820, 2017 Sep.
Artigo em Chinês | MEDLINE | ID: mdl-29726664

RESUMO

OBJECTIVE: To investigate the association of the abnormal length of human Y chromosome with semen quality and the outcome of assisted reproductive technology (ART). METHODS: Based on the karyotype, we assigned the patients undergoing ART to a normal control, a long Y chromosome (Y>18), and a short Y chromosome group (Y<22). We compared the semen parameters and numbers of embryos and high-quality embryos among the three groups of patients and performed statistical analysis of the obtained data using Chi-square distribution and t-test. RESULTS: Compared with the control, the Y>18 group showed a significantly lower incidence rate of asthenozoospermia (31.03% vs 8.33%, P <0.05) and a larger number of high-quality embryos (5.46 ± 4.54 vs 7.40 ± 5.49, P<0.05). Both the incidence rate of azoospermia and number of total embryos were remarkably lower in the control than in the Y<22 group (1.87% vs 16.47%, P <0.05; 8.60 ± 7.03 vs 10.00 ± 6.58, P<0.05). No statistically significant differences were found in the pregnancy rate between the Y>18 and Y<22 groups (P>0.05). CONCLUSIONS: Short Y chromosome may affect spermatogenesis, but the length of Y chromosome does not negatively influence the outcome of ART.


Assuntos
Azoospermia/genética , Cromossomos Humanos Y , Técnicas de Reprodução Assistida , Análise do Sêmen/normas , Aberrações dos Cromossomos Sexuais , Astenozoospermia/genética , Distribuição de Qui-Quadrado , Feminino , Humanos , Cariótipo , Cariotipagem , Masculino , Gravidez , Taxa de Gravidez , Sêmen , Espermatogênese , Resultado do Tratamento
2.
Eur J Med Chem ; 46(4): 1172-80, 2011 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-21316818

RESUMO

A series of polyhalo 1,3-diazaheterocycle fused isoquinolin-1(2H)-imines were evaluated in vitro against human tumour cell lines including A431, K562, HL60, HepG2 and Skov-3. As a result, some of the target compounds such as 5b, 5c, 5i, 5o, 6c, 6h and 7f showed stronger cytotoxicity against K562, H562 and Skov-3 cells in comparison with cisplatin, and the others displayed moderate cytotoxicity to A431 and HepG2. Biological investigations using the representative compounds 5c, 6c and 6h were also performed in mice bearing S(180) and H(22) tumours. The results indicated that these three compounds inhibit S(180) and H(22) growth. In addition, compounds 6c and 6h have very low acute toxicities. The preliminary analysis of structure-activity relationships is also discussed.


Assuntos
Antineoplásicos/química , Antineoplásicos/farmacologia , Halogênios/química , Isoquinolinas/química , Isoquinolinas/farmacologia , Animais , Antineoplásicos/síntese química , Benzeno/química , Proliferação de Células/efeitos dos fármacos , Humanos , Concentração Inibidora 50 , Isoquinolinas/síntese química , Camundongos , Relação Estrutura-Atividade , Ensaios Antitumorais Modelo de Xenoenxerto
4.
Bioorg Med Chem Lett ; 20(1): 48-51, 2010 Jan 01.
Artigo em Inglês | MEDLINE | ID: mdl-19948403

RESUMO

A series of polyhalo heterocyclic ketene aminals (polyhalo-HKAs) were synthesized under solvent-free conditions and evaluated in vitro against a panel of human tumor cell lines. Trifluoro-HKAs were the most cytotoxic compounds, followed by difluoro-HKAs and trichloro-HKAs. Trichloro-HKAs were more potent against the tumor cell lines Skov-3, Hep-2, K562, and A431 than difluoro-HKAs. An ethoxycarbonyl at the 2-position of the polyhalo HKAs gave the highest activity. Ethoxycarbonyl substituted 5o, bearing three fluorine atoms on the isophthalonitrile ring, was found to be the most potent derivative with IC(50) values lower than 3.7microg/mL against five human tumor cell lines making it more active than cisplatin (DDP).


Assuntos
Antineoplásicos/síntese química , Etilenos/química , Compostos Heterocíclicos/síntese química , Imidazolidinas/síntese química , Cetonas/química , Micro-Ondas , Nitrilas/síntese química , Antineoplásicos/química , Antineoplásicos/farmacologia , Linhagem Celular Tumoral , Ensaios de Seleção de Medicamentos Antitumorais , Compostos Heterocíclicos/química , Compostos Heterocíclicos/farmacologia , Humanos , Imidazolidinas/química , Imidazolidinas/farmacologia , Nitrilas/química , Nitrilas/farmacologia , Relação Estrutura-Atividade
5.
Bioorg Med Chem Lett ; 19(7): 1892-5, 2009 Apr 01.
Artigo em Inglês | MEDLINE | ID: mdl-19269816

RESUMO

A series of novel phenacylimidazolium derivatives, bearing an aryl or alkyl substituent at position-1 and a phenacyl substituent at position-3 of the imidazole ring, has been prepared and evaluated in vitro against a panel of human tumor cell lines. Phenacylimidazolium bromides bearing a highly sterically hindered aryl group at position-1 and an electron-rich phenacyl or naphthylacyl substituent at position-3 of imidazole ring proved to be more active than imidazolium bromides with other substituted groups. In particular, compound 5j was found to be the most potent compounds with IC(50) values lower than 5.0 microM against 8 strains human tumor cell lines and more active than cisplatin (DDP).


Assuntos
Antineoplásicos/síntese química , Antineoplásicos/toxicidade , Imidazóis/síntese química , Imidazóis/toxicidade , Antineoplásicos/química , Linhagem Celular Tumoral , Cisplatino/farmacologia , Ensaios de Seleção de Medicamentos Antitumorais , Humanos , Imidazóis/química , Relação Estrutura-Atividade
6.
J Asian Nat Prod Res ; 11(12): 1028-31, 2009 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-20183272

RESUMO

A novel aryltetralone lignan, pedunculine A (1), together with a known lignan cagayanone A (2), was isolated from the leaves and twigs of Litsea pedunculata. The structure of the new lignan was elucidated on the basis of spectroscopic methods and single-crystal X-ray diffraction.


Assuntos
Medicamentos de Ervas Chinesas/isolamento & purificação , Lignanas/isolamento & purificação , Litsea/química , Cristalografia por Raios X , Ensaios de Seleção de Medicamentos Antitumorais , Medicamentos de Ervas Chinesas/química , Medicamentos de Ervas Chinesas/farmacologia , Células HL-60 , Humanos , Lignanas/farmacologia , Conformação Molecular , Estrutura Molecular , Ressonância Magnética Nuclear Biomolecular , Folhas de Planta/química , Caules de Planta/química
7.
Biol Pharm Bull ; 30(6): 1084-90, 2007 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-17541158

RESUMO

In the case of left ventricle remodeling after myocardial infarction, cardiomyocyte apoptosis is attributed to increased cardiac workload by the stimulus such as chronic hypoxia. B-Type natriuretic peptide, being known as a reliable prognostic of cardiovascular pathology, plays an important role in the myocardial infarction. However, the action of B-type natriuretic peptide on cardiomyocytes undergoing apoptosis is unclear. In the present study, B-type natriuretic peptide have exhibited the enhancive effects on the mild hypoxia-induced cardiomyocyte apoptosis with the manifestation of facilitating phosphatidylserine evagination and increasing typical fragmented nuclei. In addition, B-type natriuretic peptide aggravated the dissipation of delta psi(m), the depletion of intracellular ATP and the increase of caspase-3 activity. 8-Bromo-cGMP, which increased cGMP independent of B-type natriuretic peptide, could mimic B-type natriuretic peptide's effects; whereas cGMP-dependent protein kinase inhibitor, Rp-8-br-cGMP inhibited that. Further study revealed the enhancive effect of BNP on down-regulation of Bcl-2 mRNA expression in the presence of mild hypoxia. In conclusion, the present study demonstrated that B-type natriuretic peptide aggravated the cardiomyocyte apoptosis by influencing hypoxia-induced mitochondrial death pathway, which is true at least in this oxygen deprivation model; and this effect was partially realized through intracellular cGMP.


Assuntos
Apoptose/efeitos dos fármacos , Miócitos Cardíacos/efeitos dos fármacos , Peptídeo Natriurético Encefálico/farmacologia , Animais , Animais Recém-Nascidos , Morte Celular/efeitos dos fármacos , Hipóxia Celular/efeitos dos fármacos , Células Cultivadas , Ratos , Ratos Sprague-Dawley
8.
Neurosci Lett ; 397(1-2): 135-9, 2006.
Artigo em Inglês | MEDLINE | ID: mdl-16384643

RESUMO

Treadmill exercise and neuromuscular electrical stimulation are common clinical approaches for stroke rehabilitation. Both animal and clinical studies have shown the functional improvements after these interventions. However, the neurochemical effects on the ischemic brain had not been well studied. This study aimed at evaluating the effects of treadmill exercise and neuromuscular electrical stimulation (NMES), and studying their effects during a 2-week training, on the levels of common neurotransmitters (aspartate, glutamate, taurine and gamma-aminobutyric acid (GABA)) in the hippocampus following transient focal cerebral ischemia. Either treadmill exercise or neuromuscular electrical stimulation was prescribed to the rats 24 h after cerebral ischemia whereas Control group remained in cages for 2 weeks. Microdialysis technique was used to collect dialysates from ipsilesional hippocampus in vivo. It was found that the glutamate level was increased significantly during treadmill exercise and then returned to baseline level. Both interventions did not trigger significant effects on aspartate and glutamate basal levels during the 2 weeks. The relatively high taurine level in Control groups may suggest that the interventions might suppress the taurine release in hippocampus. GABA and aspartate levels did not showed significant changes over the 2 weeks in all groups. These results provide insights to explain the neurochemical effects on the ischemic injured brain during the course of rehabilitation.


Assuntos
Química Encefálica/efeitos da radiação , Estimulação Elétrica/métodos , Acidente Vascular Cerebral/fisiopatologia , Animais , Modelos Animais de Doenças , Ácido Glutâmico , Masculino , Microdiálise/métodos , Condicionamento Físico Animal , Ratos , Ratos Sprague-Dawley , Acidente Vascular Cerebral/metabolismo , Acidente Vascular Cerebral/terapia , Taurina/metabolismo , Fatores de Tempo , Ácido gama-Aminobutírico/metabolismo
9.
Zhonghua Kou Qiang Yi Xue Za Zhi ; 40(3): 187-90, 2005 May.
Artigo em Chinês | MEDLINE | ID: mdl-15938871

RESUMO

OBJECTIVE: To observe the management results of hemangioma in infants and children. METHODS: Forty-nine cases of hemangioma in infants and children managed from 1986 to 2004 were reviewed. During the management period, the incidence and first visit age and sex were recorded. The location and volume of the lesions were photographed and followed up at an interval of 3 to 12 months until the complete involution of the tumor. The treatment modalities used included local injection of prednisone in 16 cases, surgery in 6 cases, and the remaining 33 cases were observed without treatment. RESULTS: Thirty-three cases receiving no treatment involuted naturally. The complete involution age was found from 9 months to 10 years with average age of 5.4 years. The cosmetic results after involution were good. CONCLUSIONS: Most hemangiomas do not need treatment and can involute naturally. However, in cases with severe complications such as expansion, destruction and obstructive or congestive heart failure, treatment is indicated.


Assuntos
Neoplasias Faciais/fisiopatologia , Hemangioma/fisiopatologia , Neoplasias Labiais/fisiopatologia , Regressão Neoplásica Espontânea/fisiopatologia , Neoplasias Parotídeas/fisiopatologia , Criança , Pré-Escolar , Neoplasias Faciais/diagnóstico , Neoplasias Faciais/terapia , Feminino , Seguimentos , Hemangioma/diagnóstico , Hemangioma/terapia , Humanos , Lactente , Neoplasias Labiais/diagnóstico , Neoplasias Labiais/terapia , Masculino , Neoplasias Parotídeas/diagnóstico , Neoplasias Parotídeas/terapia , Estudos Retrospectivos
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